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You searched for subject:(Neuroblastoma). Showing records 1 – 30 of 265 total matches.

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Universitat de Valencia

1. Yáñez Peralta, Yania. Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma .

Degree: 2016, Universitat de Valencia

 El neuroblastoma (NB) es un tumor neuroectodérmico de las células embrionarias derivadas de la cresta neural. Constituye el tumor sólido extracraneal más frecuente en la… (more)

Subjects/Keywords: Neuroblastoma; biomarcadores

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APA (6th Edition):

Yáñez Peralta, Y. (2016). Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/56672

Chicago Manual of Style (16th Edition):

Yáñez Peralta, Yania. “Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma .” 2016. Doctoral Dissertation, Universitat de Valencia. Accessed June 25, 2019. http://hdl.handle.net/10550/56672.

MLA Handbook (7th Edition):

Yáñez Peralta, Yania. “Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma .” 2016. Web. 25 Jun 2019.

Vancouver:

Yáñez Peralta Y. Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2016. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10550/56672.

Council of Science Editors:

Yáñez Peralta Y. Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma . [Doctoral Dissertation]. Universitat de Valencia; 2016. Available from: http://hdl.handle.net/10550/56672


University of Toronto

2. Wolter, Jennifer. Modulation of p53 Family Proteins in the Treatment of Neuroblastoma.

Degree: 2013, University of Toronto

Neuroblastoma is the most common type of extra-cranial solid tumour in children. Additional investigation is required to fully understand the genetics and tumour biology of… (more)

Subjects/Keywords: Neuroblastoma; 0307

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APA (6th Edition):

Wolter, J. (2013). Modulation of p53 Family Proteins in the Treatment of Neuroblastoma. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/75241

Chicago Manual of Style (16th Edition):

Wolter, Jennifer. “Modulation of p53 Family Proteins in the Treatment of Neuroblastoma.” 2013. Doctoral Dissertation, University of Toronto. Accessed June 25, 2019. http://hdl.handle.net/1807/75241.

MLA Handbook (7th Edition):

Wolter, Jennifer. “Modulation of p53 Family Proteins in the Treatment of Neuroblastoma.” 2013. Web. 25 Jun 2019.

Vancouver:

Wolter J. Modulation of p53 Family Proteins in the Treatment of Neuroblastoma. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1807/75241.

Council of Science Editors:

Wolter J. Modulation of p53 Family Proteins in the Treatment of Neuroblastoma. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/75241

3. Cartum, Jairo. Variáveis de prognóstico em crianças maiores de um ano portadoras de neuroblastoma disseminado.

Degree: PhD, Pediatria, 2011, University of São Paulo

Introdução: Os neuroblastomas apresentam grande diversidade de comportamento clínico, evoluindo desde remissão espontânea à rápida progressão e morte. Heterogeneidade clínica e biológica tem implicado em… (more)

Subjects/Keywords: Child; Criança; Neuroblastoma; Neuroblastoma; Prognosis; Prognóstico

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APA (6th Edition):

Cartum, J. (2011). Variáveis de prognóstico em crianças maiores de um ano portadoras de neuroblastoma disseminado. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5141/tde-18022011-152029/ ;

Chicago Manual of Style (16th Edition):

Cartum, Jairo. “Variáveis de prognóstico em crianças maiores de um ano portadoras de neuroblastoma disseminado.” 2011. Doctoral Dissertation, University of São Paulo. Accessed June 25, 2019. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-18022011-152029/ ;.

MLA Handbook (7th Edition):

Cartum, Jairo. “Variáveis de prognóstico em crianças maiores de um ano portadoras de neuroblastoma disseminado.” 2011. Web. 25 Jun 2019.

Vancouver:

Cartum J. Variáveis de prognóstico em crianças maiores de um ano portadoras de neuroblastoma disseminado. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2019 Jun 25]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-18022011-152029/ ;.

Council of Science Editors:

Cartum J. Variáveis de prognóstico em crianças maiores de um ano portadoras de neuroblastoma disseminado. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-18022011-152029/ ;


University of Hong Kong

4. Kwong, Rebecca Sze-Wai. Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells.

Degree: Master of Medical Sciences, 2012, University of Hong Kong

Background Mesenchymal stem cells (MSC) were first discovered in the 1970s by scientist A.J. Friedenstein and his colleagues. Friedenstein isolated the first mesenchymal stem cells… (more)

Subjects/Keywords: Neuroblastoma.; Stem cells.

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APA (6th Edition):

Kwong, R. S. (2012). Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. (Masters Thesis). University of Hong Kong. Retrieved from Kwong, R. S. W.. (2012). Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4854148 ; http://dx.doi.org/10.5353/th_b4854148 ; http://hdl.handle.net/10722/180078

Chicago Manual of Style (16th Edition):

Kwong, Rebecca Sze-Wai. “Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells.” 2012. Masters Thesis, University of Hong Kong. Accessed June 25, 2019. Kwong, R. S. W.. (2012). Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4854148 ; http://dx.doi.org/10.5353/th_b4854148 ; http://hdl.handle.net/10722/180078.

MLA Handbook (7th Edition):

Kwong, Rebecca Sze-Wai. “Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells.” 2012. Web. 25 Jun 2019.

Vancouver:

Kwong RS. Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2019 Jun 25]. Available from: Kwong, R. S. W.. (2012). Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4854148 ; http://dx.doi.org/10.5353/th_b4854148 ; http://hdl.handle.net/10722/180078.

Council of Science Editors:

Kwong RS. Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. [Masters Thesis]. University of Hong Kong; 2012. Available from: Kwong, R. S. W.. (2012). Interaction of bone marrow-derived mesenchymal stem cells on neuroblastoma cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4854148 ; http://dx.doi.org/10.5353/th_b4854148 ; http://hdl.handle.net/10722/180078


University of New South Wales

5. Shahbazi, Jeyran. Epigenetic regulators contributing to MYCN-driven neuroblastoma.

Degree: Biotechnology & Biomolecular Sciences, 2014, University of New South Wales

Neuroblastoma is the most common solid tumour in children under the age of five. N-Myc oncoprotein induces neuroblastoma initiation and progression. Myc oncoproteins and histone… (more)

Subjects/Keywords: MYC; Neuroblastoma; Epigenetics

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APA (6th Edition):

Shahbazi, J. (2014). Epigenetic regulators contributing to MYCN-driven neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54587 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35327/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Shahbazi, Jeyran. “Epigenetic regulators contributing to MYCN-driven neuroblastoma.” 2014. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/54587 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35327/SOURCE02?view=true.

MLA Handbook (7th Edition):

Shahbazi, Jeyran. “Epigenetic regulators contributing to MYCN-driven neuroblastoma.” 2014. Web. 25 Jun 2019.

Vancouver:

Shahbazi J. Epigenetic regulators contributing to MYCN-driven neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/54587 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35327/SOURCE02?view=true.

Council of Science Editors:

Shahbazi J. Epigenetic regulators contributing to MYCN-driven neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/54587 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35327/SOURCE02?view=true


University of New South Wales

6. Koach, Jessica. Characterising the role of PA2G4 and its interaction with MYCN in neuroblastoma progression.

Degree: Women's & Children's Health, 2016, University of New South Wales

Neuroblastoma, an embryonal tumour of the sympathetic nervous system, is the most common solid tumour in childhood. MYCN oncogene amplification is found in one third… (more)

Subjects/Keywords: PA2G4; Neuroblastoma; MYCN

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APA (6th Edition):

Koach, J. (2016). Characterising the role of PA2G4 and its interaction with MYCN in neuroblastoma progression. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56333 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40579/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Koach, Jessica. “Characterising the role of PA2G4 and its interaction with MYCN in neuroblastoma progression.” 2016. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/56333 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40579/SOURCE02?view=true.

MLA Handbook (7th Edition):

Koach, Jessica. “Characterising the role of PA2G4 and its interaction with MYCN in neuroblastoma progression.” 2016. Web. 25 Jun 2019.

Vancouver:

Koach J. Characterising the role of PA2G4 and its interaction with MYCN in neuroblastoma progression. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/56333 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40579/SOURCE02?view=true.

Council of Science Editors:

Koach J. Characterising the role of PA2G4 and its interaction with MYCN in neuroblastoma progression. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/56333 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40579/SOURCE02?view=true


University of New South Wales

7. Byrne, Frances Louise. Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis.

Degree: Children's Cancer Institute Australia for Medical Research, 2012, University of New South Wales

Neuroblastoma is a highly metastatic childhood cancer that originates from primitive cells of the neural crest and contributes to 15% of all paediatric cancer deaths.… (more)

Subjects/Keywords: Stathmin; Neuroblastoma; Metastasis

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APA (6th Edition):

Byrne, F. L. (2012). Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Byrne, Frances Louise. “Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis.” 2012. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true.

MLA Handbook (7th Edition):

Byrne, Frances Louise. “Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis.” 2012. Web. 25 Jun 2019.

Vancouver:

Byrne FL. Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true.

Council of Science Editors:

Byrne FL. Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true


University of New South Wales

8. Bell, Jessica Lilian. Characterising the role of trim16 in differentiation, proliferation and tumour development in neuroblastoma.

Degree: Children's Cancer Institute Australia for Medical Research, 2012, University of New South Wales

Neuroblastoma is the most common solid tumour in childhood and represents a significant 15% of all cancer deaths in children. Retinoids are used in the… (more)

Subjects/Keywords: Cancer; Neuroblastoma; TRIM16

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APA (6th Edition):

Bell, J. L. (2012). Characterising the role of trim16 in differentiation, proliferation and tumour development in neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51965 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10635/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Bell, Jessica Lilian. “Characterising the role of trim16 in differentiation, proliferation and tumour development in neuroblastoma.” 2012. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/51965 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10635/SOURCE01?view=true.

MLA Handbook (7th Edition):

Bell, Jessica Lilian. “Characterising the role of trim16 in differentiation, proliferation and tumour development in neuroblastoma.” 2012. Web. 25 Jun 2019.

Vancouver:

Bell JL. Characterising the role of trim16 in differentiation, proliferation and tumour development in neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/51965 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10635/SOURCE01?view=true.

Council of Science Editors:

Bell JL. Characterising the role of trim16 in differentiation, proliferation and tumour development in neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/51965 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10635/SOURCE01?view=true


University of New South Wales

9. Lau, Diana Tsz-Tak. Genetic factors influencing the risk and clinical outcome of childhood neuroblastoma.

Degree: Women's & Children's Health, 2013, University of New South Wales

Neuroblastoma is the most common solid tumour in infancy, yet the cause of the disease remains largely unknown. This thesis examines whether genetic factors involved… (more)

Subjects/Keywords: Folate; Neuroblastoma; Genetics

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APA (6th Edition):

Lau, D. T. (2013). Genetic factors influencing the risk and clinical outcome of childhood neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11053/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Lau, Diana Tsz-Tak. “Genetic factors influencing the risk and clinical outcome of childhood neuroblastoma.” 2013. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/52380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11053/SOURCE01?view=true.

MLA Handbook (7th Edition):

Lau, Diana Tsz-Tak. “Genetic factors influencing the risk and clinical outcome of childhood neuroblastoma.” 2013. Web. 25 Jun 2019.

Vancouver:

Lau DT. Genetic factors influencing the risk and clinical outcome of childhood neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/52380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11053/SOURCE01?view=true.

Council of Science Editors:

Lau DT. Genetic factors influencing the risk and clinical outcome of childhood neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11053/SOURCE01?view=true


University of New South Wales

10. Gao, Jixuan. Investigating the biological roles of ABCE1 in neuroblastoma.

Degree: Women's & Children's Health, 2018, University of New South Wales

 Amplification of MYCN is one of the strongest prognostic factors for poor outcome in neuroblastoma, the most common extra-cranial solid tumour in children. With less… (more)

Subjects/Keywords: MYCN; ABCE1; Neuroblastoma

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APA (6th Edition):

Gao, J. (2018). Investigating the biological roles of ABCE1 in neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/61935 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57814/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Gao, Jixuan. “Investigating the biological roles of ABCE1 in neuroblastoma.” 2018. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/61935 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57814/SOURCE02?view=true.

MLA Handbook (7th Edition):

Gao, Jixuan. “Investigating the biological roles of ABCE1 in neuroblastoma.” 2018. Web. 25 Jun 2019.

Vancouver:

Gao J. Investigating the biological roles of ABCE1 in neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/61935 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57814/SOURCE02?view=true.

Council of Science Editors:

Gao J. Investigating the biological roles of ABCE1 in neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/61935 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57814/SOURCE02?view=true


University of Hawaii – Manoa

11. Yoshioka, Masahiro. Downregulation of MYCN oncogene by retinoic acid in neuroblastoma.

Degree: 2015, University of Hawaii – Manoa

Ph.D. University of Hawaii at Manoa 2014.

Neuroblastoma is the most common extracranial solid tumor for children. Up to 30% of neuroblastoma tumors show the… (more)

Subjects/Keywords: MYCN oncogene; retinoic acid; neuroblastoma

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APA (6th Edition):

Yoshioka, M. (2015). Downregulation of MYCN oncogene by retinoic acid in neuroblastoma. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/101161

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yoshioka, Masahiro. “Downregulation of MYCN oncogene by retinoic acid in neuroblastoma.” 2015. Thesis, University of Hawaii – Manoa. Accessed June 25, 2019. http://hdl.handle.net/10125/101161.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yoshioka, Masahiro. “Downregulation of MYCN oncogene by retinoic acid in neuroblastoma.” 2015. Web. 25 Jun 2019.

Vancouver:

Yoshioka M. Downregulation of MYCN oncogene by retinoic acid in neuroblastoma. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10125/101161.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yoshioka M. Downregulation of MYCN oncogene by retinoic acid in neuroblastoma. [Thesis]. University of Hawaii – Manoa; 2015. Available from: http://hdl.handle.net/10125/101161

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

12. 談沛詩.; Tam, Pui-see, Patricia. Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma.

Degree: Master of Medical Sciences, 2009, University of Hong Kong

published_or_final_version

Surgery

Master

Master of Medical Sciences

Subjects/Keywords: Neuroblastoma - Pathophysiology.

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APA (6th Edition):

談沛詩.; Tam, Pui-see, P. (2009). Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. (Masters Thesis). University of Hong Kong. Retrieved from Tam, P. P. [談沛詩]. (2009). Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4290523 ; http://dx.doi.org/10.5353/th_b4290523 ; http://hdl.handle.net/10722/56981

Chicago Manual of Style (16th Edition):

談沛詩.; Tam, Pui-see, Patricia. “Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma.” 2009. Masters Thesis, University of Hong Kong. Accessed June 25, 2019. Tam, P. P. [談沛詩]. (2009). Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4290523 ; http://dx.doi.org/10.5353/th_b4290523 ; http://hdl.handle.net/10722/56981.

MLA Handbook (7th Edition):

談沛詩.; Tam, Pui-see, Patricia. “Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma.” 2009. Web. 25 Jun 2019.

Vancouver:

談沛詩.; Tam, Pui-see P. Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. [Internet] [Masters thesis]. University of Hong Kong; 2009. [cited 2019 Jun 25]. Available from: Tam, P. P. [談沛詩]. (2009). Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4290523 ; http://dx.doi.org/10.5353/th_b4290523 ; http://hdl.handle.net/10722/56981.

Council of Science Editors:

談沛詩.; Tam, Pui-see P. Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. [Masters Thesis]. University of Hong Kong; 2009. Available from: Tam, P. P. [談沛詩]. (2009). Developing an in vivo reporter system for the monitoring of therapeutic effects on neuroblastoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4290523 ; http://dx.doi.org/10.5353/th_b4290523 ; http://hdl.handle.net/10722/56981

13. Yáñez Peralta, Yania. Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma.

Degree: 2018, TDX

 El neuroblastoma (NB) es un tumor neuroectodérmico de las células embrionarias derivadas de la cresta neural. Constituye el tumor sólido extracraneal más frecuente en la… (more)

Subjects/Keywords: Neuroblastoma; biomarcadores; UNESCO::CIENCIAS MÉDICAS

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APA (6th Edition):

Yáñez Peralta, Y. (2018). Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma. (Thesis). TDX. Retrieved from http://hdl.handle.net/10803/571195

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yáñez Peralta, Yania. “Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma.” 2018. Thesis, TDX. Accessed June 25, 2019. http://hdl.handle.net/10803/571195.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yáñez Peralta, Yania. “Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma.” 2018. Web. 25 Jun 2019.

Vancouver:

Yáñez Peralta Y. Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma. [Internet] [Thesis]. TDX; 2018. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10803/571195.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yáñez Peralta Y. Búsqueda de nuevos biomarcadores con utilidad pronóstica en el Neuroblastoma. [Thesis]. TDX; 2018. Available from: http://hdl.handle.net/10803/571195

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

14. Vojvodic, Milijana. Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets.

Degree: 2010, University of Toronto

Neuroblastoma (NB) is the most common extra-cranial solid tumor in children. Recently discovered neuroblastoma tumor-initiating cells (NB-TICs) have many properties of cancer stem cells and… (more)

Subjects/Keywords: Neuroblastoma; Phospho-proteomics; 0307

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APA (6th Edition):

Vojvodic, M. (2010). Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30136

Chicago Manual of Style (16th Edition):

Vojvodic, Milijana. “Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets.” 2010. Masters Thesis, University of Toronto. Accessed June 25, 2019. http://hdl.handle.net/1807/30136.

MLA Handbook (7th Edition):

Vojvodic, Milijana. “Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets.” 2010. Web. 25 Jun 2019.

Vancouver:

Vojvodic M. Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1807/30136.

Council of Science Editors:

Vojvodic M. Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/30136


University of Sydney

15. Dagg, Rebecca Ann. The extensive proliferation of human cancer cells with ever-shorter telomeres .

Degree: 2017, University of Sydney

 Cellular immortalisation is currently regarded as an essential step in malignant transformation and is consequently considered a hallmark of cancer. Acquisition of replicative immortality is… (more)

Subjects/Keywords: telomere; telomerase; ALT; neuroblastoma

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APA (6th Edition):

Dagg, R. A. (2017). The extensive proliferation of human cancer cells with ever-shorter telomeres . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17341

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Dagg, Rebecca Ann. “The extensive proliferation of human cancer cells with ever-shorter telomeres .” 2017. Thesis, University of Sydney. Accessed June 25, 2019. http://hdl.handle.net/2123/17341.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Dagg, Rebecca Ann. “The extensive proliferation of human cancer cells with ever-shorter telomeres .” 2017. Web. 25 Jun 2019.

Vancouver:

Dagg RA. The extensive proliferation of human cancer cells with ever-shorter telomeres . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2123/17341.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Dagg RA. The extensive proliferation of human cancer cells with ever-shorter telomeres . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17341

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Debrecen

16. Hornok, Zita. Nephroblastoma és neuroblastoma műtéti kezelése a DE OEC-en 1998 és 2012 között .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Rerospektív vizsgálattal értékeltem ki a DE OEC Gyermekgyógyászati Intézet Gyermeksebészeti Osztályán 1998. január 01. és 2012. december 31. között nephroblastoma és neuroblastoma miatt végzett műtéti… (more)

Subjects/Keywords: nephroblastoma; neuroblastoma

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APA (6th Edition):

Hornok, Z. (n.d.). Nephroblastoma és neuroblastoma műtéti kezelése a DE OEC-en 1998 és 2012 között . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/233943

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hornok, Zita. “Nephroblastoma és neuroblastoma műtéti kezelése a DE OEC-en 1998 és 2012 között .” Thesis, University of Debrecen. Accessed June 25, 2019. http://hdl.handle.net/2437/233943.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hornok, Zita. “Nephroblastoma és neuroblastoma műtéti kezelése a DE OEC-en 1998 és 2012 között .” Web. 25 Jun 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Hornok Z. Nephroblastoma és neuroblastoma műtéti kezelése a DE OEC-en 1998 és 2012 között . [Internet] [Thesis]. University of Debrecen; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2437/233943.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Hornok Z. Nephroblastoma és neuroblastoma műtéti kezelése a DE OEC-en 1998 és 2012 között . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/233943

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Clemson University

17. DeCroes, Olivia Grace. Development of poly(lactic acid)-poly(ethylene glycol) nanoparticles for the delivery of non- toxic drug in combination therapy for the treatment of glioblastoma and neuroblastoma.

Degree: MS, Bioengineering, 2014, Clemson University

 lioblastoma and neuroblastoma are both solid-form tumors. Glioblastomas primarily reside in the brain, while neuroblastomas are found in the sympathetic nervous system. Both glioblastoma and… (more)

Subjects/Keywords: Glioblastoma; Nanomedicine; Nanoparticle; Neuroblastoma

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APA (6th Edition):

DeCroes, O. G. (2014). Development of poly(lactic acid)-poly(ethylene glycol) nanoparticles for the delivery of non- toxic drug in combination therapy for the treatment of glioblastoma and neuroblastoma. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/2616

Chicago Manual of Style (16th Edition):

DeCroes, Olivia Grace. “Development of poly(lactic acid)-poly(ethylene glycol) nanoparticles for the delivery of non- toxic drug in combination therapy for the treatment of glioblastoma and neuroblastoma.” 2014. Masters Thesis, Clemson University. Accessed June 25, 2019. https://tigerprints.clemson.edu/all_theses/2616.

MLA Handbook (7th Edition):

DeCroes, Olivia Grace. “Development of poly(lactic acid)-poly(ethylene glycol) nanoparticles for the delivery of non- toxic drug in combination therapy for the treatment of glioblastoma and neuroblastoma.” 2014. Web. 25 Jun 2019.

Vancouver:

DeCroes OG. Development of poly(lactic acid)-poly(ethylene glycol) nanoparticles for the delivery of non- toxic drug in combination therapy for the treatment of glioblastoma and neuroblastoma. [Internet] [Masters thesis]. Clemson University; 2014. [cited 2019 Jun 25]. Available from: https://tigerprints.clemson.edu/all_theses/2616.

Council of Science Editors:

DeCroes OG. Development of poly(lactic acid)-poly(ethylene glycol) nanoparticles for the delivery of non- toxic drug in combination therapy for the treatment of glioblastoma and neuroblastoma. [Masters Thesis]. Clemson University; 2014. Available from: https://tigerprints.clemson.edu/all_theses/2616


University of Debrecen

18. Magyari, Ágota. A neuroblastoma korszerű kezelése és új terápiás lehetőségei .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

Irodalmi áttekintés arról, hogy jelenleg milyen új terápiás lehetőségek állnak rendelkezésre, amelyek meghosszabbíthatják a neuroblastomában szenvedők túlélését. Bemutatás, hogy eddig milyen eredményeket sikerült elérni az új szerekkel. Advisors/Committee Members: Szegedi, István (advisor), Debreceni Egyetem::Orvos- és Egészségtudományi Centrum::Általános Orvostudományi Kar::Gyermekgyógyászati Intézet (advisor).

Subjects/Keywords: neuroblastoma; kemoterápia

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APA (6th Edition):

Magyari, . (n.d.). A neuroblastoma korszerű kezelése és új terápiás lehetőségei . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/201542

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Magyari, Ágota. “A neuroblastoma korszerű kezelése és új terápiás lehetőségei .” Thesis, University of Debrecen. Accessed June 25, 2019. http://hdl.handle.net/2437/201542.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Magyari, Ágota. “A neuroblastoma korszerű kezelése és új terápiás lehetőségei .” Web. 25 Jun 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Magyari . A neuroblastoma korszerű kezelése és új terápiás lehetőségei . [Internet] [Thesis]. University of Debrecen; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2437/201542.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Magyari . A neuroblastoma korszerű kezelése és új terápiás lehetőségei . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/201542

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Boston University

19. Shetty, Kunal. Amino acid residues critical for anaplastic lymphoma kinase receptor cleavage.

Degree: 2015, Boston University

 The overexpression and phosphorylation of the wild type Anaplastic Lymphoma Kinase (ALK) receptor in neuroblastoma has been associated with a worse prognosis for patients suffering… (more)

Subjects/Keywords: Biochemistry; ALK; Cleavage; Neuroblastoma

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APA (6th Edition):

Shetty, K. (2015). Amino acid residues critical for anaplastic lymphoma kinase receptor cleavage. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16272

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Shetty, Kunal. “Amino acid residues critical for anaplastic lymphoma kinase receptor cleavage.” 2015. Thesis, Boston University. Accessed June 25, 2019. http://hdl.handle.net/2144/16272.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Shetty, Kunal. “Amino acid residues critical for anaplastic lymphoma kinase receptor cleavage.” 2015. Web. 25 Jun 2019.

Vancouver:

Shetty K. Amino acid residues critical for anaplastic lymphoma kinase receptor cleavage. [Internet] [Thesis]. Boston University; 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2144/16272.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Shetty K. Amino acid residues critical for anaplastic lymphoma kinase receptor cleavage. [Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16272

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Cambridge

20. Lee, Liam Changwoo. Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens .

Degree: 2017, University of Cambridge

 Recent whole-exome sequencing studies of hundreds of high-risk neuroblastoma (hNB) patients have identified Anaplastic Lymphoma Kinase (ALK) as the only directly ‘druggable’ target with a… (more)

Subjects/Keywords: CRISPR; ALK; Drug-resistance; Neuroblastoma

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APA (6th Edition):

Lee, L. C. (2017). Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267921

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Liam Changwoo. “Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens .” 2017. Thesis, University of Cambridge. Accessed June 25, 2019. https://www.repository.cam.ac.uk/handle/1810/267921.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Liam Changwoo. “Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens .” 2017. Web. 25 Jun 2019.

Vancouver:

Lee LC. Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Jun 25]. Available from: https://www.repository.cam.ac.uk/handle/1810/267921.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee LC. Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens . [Thesis]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267921

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat Politècnica de València

21. Martínez Díaz, Rafael. Análisis, propuesta y desarrollo de técnicas de medición objetiva en imágenes 123/-mIBG, para pacientes con neuroblastoma .

Degree: 2015, Universitat Politècnica de València

 [EN] In neuroblastoma management various medical imaging modalities are involved. Among them, scans of 123I-mBG continue being today the most specific and sensitive, so they… (more)

Subjects/Keywords: Gammagrafía; MIBG; Neuroblastoma; Cuantificación

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APA (6th Edition):

Martínez Díaz, R. (2015). Análisis, propuesta y desarrollo de técnicas de medición objetiva en imágenes 123/-mIBG, para pacientes con neuroblastoma . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/58984

Chicago Manual of Style (16th Edition):

Martínez Díaz, Rafael. “Análisis, propuesta y desarrollo de técnicas de medición objetiva en imágenes 123/-mIBG, para pacientes con neuroblastoma .” 2015. Doctoral Dissertation, Universitat Politècnica de València. Accessed June 25, 2019. http://hdl.handle.net/10251/58984.

MLA Handbook (7th Edition):

Martínez Díaz, Rafael. “Análisis, propuesta y desarrollo de técnicas de medición objetiva en imágenes 123/-mIBG, para pacientes con neuroblastoma .” 2015. Web. 25 Jun 2019.

Vancouver:

Martínez Díaz R. Análisis, propuesta y desarrollo de técnicas de medición objetiva en imágenes 123/-mIBG, para pacientes con neuroblastoma . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10251/58984.

Council of Science Editors:

Martínez Díaz R. Análisis, propuesta y desarrollo de técnicas de medición objetiva en imágenes 123/-mIBG, para pacientes con neuroblastoma . [Doctoral Dissertation]. Universitat Politècnica de València; 2015. Available from: http://hdl.handle.net/10251/58984


University of New South Wales

22. Swain, Ashleigh. Synergistic Action of Anti-Microtubule and Anti-Tropomyosin Agents on Neuroblastoma.

Degree: Medical Sciences, 2018, University of New South Wales

 We have developed a new therapeutic cancer strategy based on targeting a core component of the cancer cell actin cytoskeleton, tropomyosin Tpm3.1. The first-in-class series… (more)

Subjects/Keywords: Synergy; Neuroblastoma; Tropomyosin; Vincristine

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APA (6th Edition):

Swain, A. (2018). Synergistic Action of Anti-Microtubule and Anti-Tropomyosin Agents on Neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60205 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51069/SOURCE2?view=true

Chicago Manual of Style (16th Edition):

Swain, Ashleigh. “Synergistic Action of Anti-Microtubule and Anti-Tropomyosin Agents on Neuroblastoma.” 2018. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/60205 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51069/SOURCE2?view=true.

MLA Handbook (7th Edition):

Swain, Ashleigh. “Synergistic Action of Anti-Microtubule and Anti-Tropomyosin Agents on Neuroblastoma.” 2018. Web. 25 Jun 2019.

Vancouver:

Swain A. Synergistic Action of Anti-Microtubule and Anti-Tropomyosin Agents on Neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/60205 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51069/SOURCE2?view=true.

Council of Science Editors:

Swain A. Synergistic Action of Anti-Microtubule and Anti-Tropomyosin Agents on Neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/60205 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51069/SOURCE2?view=true


University of New South Wales

23. Murray, Jayne. Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma.

Degree: Women's & Children's Health, 2017, University of New South Wales

Neuroblastoma, a disease of the neural crest and the most common solid tumour of infancy, accounts for 7-10% of all childhood cancer. The disease arises… (more)

Subjects/Keywords: Runx1t1; Neuroblastoma; ENU mutagenesis

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APA (6th Edition):

Murray, J. (2017). Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60088

Chicago Manual of Style (16th Edition):

Murray, Jayne. “Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma.” 2017. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/60088.

MLA Handbook (7th Edition):

Murray, Jayne. “Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma.” 2017. Web. 25 Jun 2019.

Vancouver:

Murray J. Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/60088.

Council of Science Editors:

Murray J. Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/60088


University of New South Wales

24. Fife, Christopher. The role of the microtubule destabilising protein stathmin in neuroblastoma metastasis.

Degree: Women's & Children's Health, 2015, University of New South Wales

Neuroblastoma, the most common extra-cranial solid tumour in children, accounts for 15% of paediatric cancerdeaths. Survival for patients with distant metastases carries a very poor… (more)

Subjects/Keywords: Neuroblastoma; Stathmin; Metastasis; Cytoskeleton

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APA (6th Edition):

Fife, C. (2015). The role of the microtubule destabilising protein stathmin in neuroblastoma metastasis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55096 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36527/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Fife, Christopher. “The role of the microtubule destabilising protein stathmin in neuroblastoma metastasis.” 2015. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/55096 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36527/SOURCE02?view=true.

MLA Handbook (7th Edition):

Fife, Christopher. “The role of the microtubule destabilising protein stathmin in neuroblastoma metastasis.” 2015. Web. 25 Jun 2019.

Vancouver:

Fife C. The role of the microtubule destabilising protein stathmin in neuroblastoma metastasis. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/55096 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36527/SOURCE02?view=true.

Council of Science Editors:

Fife C. The role of the microtubule destabilising protein stathmin in neuroblastoma metastasis. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55096 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36527/SOURCE02?view=true


University of New South Wales

25. Sun, Yuting. The Roles of Histone Deacetylase 5 and the Histone Methyltransferase Adaptor WDR5 in Myc oncogenesis.

Degree: Children's Cancer Institute Australia for Medical Research, 2014, University of New South Wales

 N-Myc induces neuroblastoma by regulating the expression of target genes and proteins, and N-Myc protein is degraded by Fbxw7 and NEDD4 and stabilized by Aurora… (more)

Subjects/Keywords: WDR5; N-Myc; HDAC5; Neuroblastoma

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APA (6th Edition):

Sun, Y. (2014). The Roles of Histone Deacetylase 5 and the Histone Methyltransferase Adaptor WDR5 in Myc oncogenesis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54064 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12804/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Sun, Yuting. “The Roles of Histone Deacetylase 5 and the Histone Methyltransferase Adaptor WDR5 in Myc oncogenesis.” 2014. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/54064 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12804/SOURCE02?view=true.

MLA Handbook (7th Edition):

Sun, Yuting. “The Roles of Histone Deacetylase 5 and the Histone Methyltransferase Adaptor WDR5 in Myc oncogenesis.” 2014. Web. 25 Jun 2019.

Vancouver:

Sun Y. The Roles of Histone Deacetylase 5 and the Histone Methyltransferase Adaptor WDR5 in Myc oncogenesis. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/54064 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12804/SOURCE02?view=true.

Council of Science Editors:

Sun Y. The Roles of Histone Deacetylase 5 and the Histone Methyltransferase Adaptor WDR5 in Myc oncogenesis. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/54064 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12804/SOURCE02?view=true


University of New South Wales

26. Cheung, Leanna. The isolation and characterisation of novel small molecule inhibitors of the MYCN transcriptional pathway for the potential treatment of childhood neuroblastoma.

Degree: Children's Cancer Institute Australia for Medical Research, 2011, University of New South Wales

Neuroblastoma is the most common extracranial solid tumour in the paediatric population, and is a highly aggressive disease that originates from the precursor cells of… (more)

Subjects/Keywords: Targeted Therapy; MYCN; Neuroblastoma

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cheung, L. (2011). The isolation and characterisation of novel small molecule inhibitors of the MYCN transcriptional pathway for the potential treatment of childhood neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51623 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10290/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Cheung, Leanna. “The isolation and characterisation of novel small molecule inhibitors of the MYCN transcriptional pathway for the potential treatment of childhood neuroblastoma.” 2011. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/51623 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10290/SOURCE02?view=true.

MLA Handbook (7th Edition):

Cheung, Leanna. “The isolation and characterisation of novel small molecule inhibitors of the MYCN transcriptional pathway for the potential treatment of childhood neuroblastoma.” 2011. Web. 25 Jun 2019.

Vancouver:

Cheung L. The isolation and characterisation of novel small molecule inhibitors of the MYCN transcriptional pathway for the potential treatment of childhood neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/51623 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10290/SOURCE02?view=true.

Council of Science Editors:

Cheung L. The isolation and characterisation of novel small molecule inhibitors of the MYCN transcriptional pathway for the potential treatment of childhood neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51623 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10290/SOURCE02?view=true


Case Western Reserve University

27. Alabran, Jennifer L. HUMAN NEUROBLASTOMA CELLS RAPIDLY ENTER CELL CYCLE ARREST AND APOPTOSIS FOLLOWING EXPOSURE TO C-28 DERIVATIVES OF THE SYNTHETIC TRITERPENOID CDDO.

Degree: MSs, Pathology, 2010, Case Western Reserve University

 Synthetic triterpenoids, such as 2-cyano-3, 12-dioxooleana-1, 9-dien-28-oic acid (CDDO) and its derivatives, belong to an extremely potent class of new anti-cancer therapeutic agents characterized by… (more)

Subjects/Keywords: CDDO; NEUROBLASTOMA; TRITERPENOID; CELLS; NEUROBLASTOMA CELLS; tumor; Cancers

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Alabran, J. L. (2010). HUMAN NEUROBLASTOMA CELLS RAPIDLY ENTER CELL CYCLE ARREST AND APOPTOSIS FOLLOWING EXPOSURE TO C-28 DERIVATIVES OF THE SYNTHETIC TRITERPENOID CDDO. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1253290381

Chicago Manual of Style (16th Edition):

Alabran, Jennifer L. “HUMAN NEUROBLASTOMA CELLS RAPIDLY ENTER CELL CYCLE ARREST AND APOPTOSIS FOLLOWING EXPOSURE TO C-28 DERIVATIVES OF THE SYNTHETIC TRITERPENOID CDDO.” 2010. Masters Thesis, Case Western Reserve University. Accessed June 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1253290381.

MLA Handbook (7th Edition):

Alabran, Jennifer L. “HUMAN NEUROBLASTOMA CELLS RAPIDLY ENTER CELL CYCLE ARREST AND APOPTOSIS FOLLOWING EXPOSURE TO C-28 DERIVATIVES OF THE SYNTHETIC TRITERPENOID CDDO.” 2010. Web. 25 Jun 2019.

Vancouver:

Alabran JL. HUMAN NEUROBLASTOMA CELLS RAPIDLY ENTER CELL CYCLE ARREST AND APOPTOSIS FOLLOWING EXPOSURE TO C-28 DERIVATIVES OF THE SYNTHETIC TRITERPENOID CDDO. [Internet] [Masters thesis]. Case Western Reserve University; 2010. [cited 2019 Jun 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1253290381.

Council of Science Editors:

Alabran JL. HUMAN NEUROBLASTOMA CELLS RAPIDLY ENTER CELL CYCLE ARREST AND APOPTOSIS FOLLOWING EXPOSURE TO C-28 DERIVATIVES OF THE SYNTHETIC TRITERPENOID CDDO. [Masters Thesis]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1253290381


Universidade do Rio Grande do Sul

28. Almeida, Viviane Rösner. Combinação de moduladores epigenéticos com ativação de receptor retinoide em neuroblastoma : efeitos sobre proliferação e diferenciação celular.

Degree: 2016, Universidade do Rio Grande do Sul

Neuroblastoma (NB) é a forma mais indiferenciada de tumores neuroblásticos e a principal causa de morte por câncer pediátrico. Alterações epigenéticas interagem em todas as… (more)

Subjects/Keywords: Diferenciação celular; Neuroblastoma; Neuroblastoma; Epigenetics; Cancer infantil; Retinoids; Cell differentiation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Almeida, V. R. (2016). Combinação de moduladores epigenéticos com ativação de receptor retinoide em neuroblastoma : efeitos sobre proliferação e diferenciação celular. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/150708

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Almeida, Viviane Rösner. “Combinação de moduladores epigenéticos com ativação de receptor retinoide em neuroblastoma : efeitos sobre proliferação e diferenciação celular.” 2016. Thesis, Universidade do Rio Grande do Sul. Accessed June 25, 2019. http://hdl.handle.net/10183/150708.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Almeida, Viviane Rösner. “Combinação de moduladores epigenéticos com ativação de receptor retinoide em neuroblastoma : efeitos sobre proliferação e diferenciação celular.” 2016. Web. 25 Jun 2019.

Vancouver:

Almeida VR. Combinação de moduladores epigenéticos com ativação de receptor retinoide em neuroblastoma : efeitos sobre proliferação e diferenciação celular. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2016. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10183/150708.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Almeida VR. Combinação de moduladores epigenéticos com ativação de receptor retinoide em neuroblastoma : efeitos sobre proliferação e diferenciação celular. [Thesis]. Universidade do Rio Grande do Sul; 2016. Available from: http://hdl.handle.net/10183/150708

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Columbia University

29. Zhang, Shuobo. Transcription factor activating protein 4 is synthetic lethal and a master regulator of MYCN amplified neuroblastoma.

Degree: 2015, Columbia University

 Despite the identification of MYCN amplification as an adverse prognostic marker in neuroblastoma, no drugs that target MYCN have yet been developed. Here, by combining… (more)

Subjects/Keywords: Neuroblastoma – Genetic aspects; Transcription factors; Nervous system – Cancer; Neuroblastoma; Cytology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zhang, S. (2015). Transcription factor activating protein 4 is synthetic lethal and a master regulator of MYCN amplified neuroblastoma. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8VX0FPF

Chicago Manual of Style (16th Edition):

Zhang, Shuobo. “Transcription factor activating protein 4 is synthetic lethal and a master regulator of MYCN amplified neuroblastoma.” 2015. Doctoral Dissertation, Columbia University. Accessed June 25, 2019. https://doi.org/10.7916/D8VX0FPF.

MLA Handbook (7th Edition):

Zhang, Shuobo. “Transcription factor activating protein 4 is synthetic lethal and a master regulator of MYCN amplified neuroblastoma.” 2015. Web. 25 Jun 2019.

Vancouver:

Zhang S. Transcription factor activating protein 4 is synthetic lethal and a master regulator of MYCN amplified neuroblastoma. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Jun 25]. Available from: https://doi.org/10.7916/D8VX0FPF.

Council of Science Editors:

Zhang S. Transcription factor activating protein 4 is synthetic lethal and a master regulator of MYCN amplified neuroblastoma. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8VX0FPF

30. Kratimenos, Panagiotis. Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα.

Degree: 2015, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Background: Neuroblastoma (NB) is the most common extracranial tumor in children, arising from the neural crest of the sympathetic ganglia and accounts for 7-10% of… (more)

Subjects/Keywords: Νευροβλάστωμα; Παχιλλίνη; Neuroblastoma; Src kinase; FAK; Paxillin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kratimenos, P. (2015). Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/43066

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kratimenos, Panagiotis. “Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα.” 2015. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed June 25, 2019. http://hdl.handle.net/10442/hedi/43066.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kratimenos, Panagiotis. “Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα.” 2015. Web. 25 Jun 2019.

Vancouver:

Kratimenos P. Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10442/hedi/43066.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kratimenos P. Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. Available from: http://hdl.handle.net/10442/hedi/43066

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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