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You searched for subject:(amyotrophic lateral sclerosis). Showing records 1 – 30 of 405 total matches.

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1. Duffy, Amanda Marie. Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring.

Degree: Department of Neuroscience, 2018, Brown University

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of the upper and lower motor neurons resulting in weakness, paralysis and death within two to five… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis

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

APA (6th Edition):

Duffy, A. M. (2018). Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:792852/

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):

Duffy, Amanda Marie. “Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring.” 2018. Thesis, Brown University. Accessed January 19, 2020. https://repository.library.brown.edu/studio/item/bdr:792852/.

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

MLA Handbook (7th Edition):

Duffy, Amanda Marie. “Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring.” 2018. Web. 19 Jan 2020.

Vancouver:

Duffy AM. Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring. [Internet] [Thesis]. Brown University; 2018. [cited 2020 Jan 19]. Available from: https://repository.library.brown.edu/studio/item/bdr:792852/.

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

Council of Science Editors:

Duffy AM. Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring. [Thesis]. Brown University; 2018. Available from: https://repository.library.brown.edu/studio/item/bdr:792852/

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


Baylor University

2. [No author]. Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes.

Degree: 2018, Baylor University

 Cu, Zn superoxide dismutase (SOD1) is a ubiquitous metalloprotein, which is responsible for protecting living cells from oxidative stress via disproportionation of superoxide ions. Misfolding… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis.

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APA (6th Edition):

author], [. (2018). Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/10435

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):

author], [No. “Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. ” 2018. Thesis, Baylor University. Accessed January 19, 2020. http://hdl.handle.net/2104/10435.

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

MLA Handbook (7th Edition):

author], [No. “Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. ” 2018. Web. 19 Jan 2020.

Vancouver:

author] [. Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. [Internet] [Thesis]. Baylor University; 2018. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2104/10435.

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

Council of Science Editors:

author] [. Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. [Thesis]. Baylor University; 2018. Available from: http://hdl.handle.net/2104/10435

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


Boston University

3. Chang, Joshua Sua. A review of therapeutics targeting excitotoxicity in amyotrophic lateral sclerosis.

Degree: MS, Medical Sciences, 2019, Boston University

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects between 14,000 to 15,000 Americans. The upper and lower motor neurons degenerate, which eventually… (more)

Subjects/Keywords: Medicine; ALS; Amyotrophic lateral sclerosis

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APA (6th Edition):

Chang, J. S. (2019). A review of therapeutics targeting excitotoxicity in amyotrophic lateral sclerosis. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/36171

Chicago Manual of Style (16th Edition):

Chang, Joshua Sua. “A review of therapeutics targeting excitotoxicity in amyotrophic lateral sclerosis.” 2019. Masters Thesis, Boston University. Accessed January 19, 2020. http://hdl.handle.net/2144/36171.

MLA Handbook (7th Edition):

Chang, Joshua Sua. “A review of therapeutics targeting excitotoxicity in amyotrophic lateral sclerosis.” 2019. Web. 19 Jan 2020.

Vancouver:

Chang JS. A review of therapeutics targeting excitotoxicity in amyotrophic lateral sclerosis. [Internet] [Masters thesis]. Boston University; 2019. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2144/36171.

Council of Science Editors:

Chang JS. A review of therapeutics targeting excitotoxicity in amyotrophic lateral sclerosis. [Masters Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/36171


University of Edinburgh

4. Van Der Hulst, Egberdina Jozefa. Heterogeneity of cognitive impairment in amyotrophic lateral sclerosis.

Degree: PhD, 2012, University of Edinburgh

 This PhD thesis examines the relationship between Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal dementia (FTD). ALS is a rapidly progressive neurodegenerative movement disorder characterized by… (more)

Subjects/Keywords: 616.8; amyotrophic lateral sclerosis; cognition; neuropsychology

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APA (6th Edition):

Van Der Hulst, E. J. (2012). Heterogeneity of cognitive impairment in amyotrophic lateral sclerosis. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/6388

Chicago Manual of Style (16th Edition):

Van Der Hulst, Egberdina Jozefa. “Heterogeneity of cognitive impairment in amyotrophic lateral sclerosis.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed January 19, 2020. http://hdl.handle.net/1842/6388.

MLA Handbook (7th Edition):

Van Der Hulst, Egberdina Jozefa. “Heterogeneity of cognitive impairment in amyotrophic lateral sclerosis.” 2012. Web. 19 Jan 2020.

Vancouver:

Van Der Hulst EJ. Heterogeneity of cognitive impairment in amyotrophic lateral sclerosis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1842/6388.

Council of Science Editors:

Van Der Hulst EJ. Heterogeneity of cognitive impairment in amyotrophic lateral sclerosis. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/6388


University of Edinburgh

5. Fowler, Elizabeth. Cognitive and Affective Theory of Mind in Amyotrophic Lateral Sclerosis.

Degree: 2012, University of Edinburgh

 Research has demonstrated that approximately one third of Amyotrophic Lateral Sclerosis (ALS) patients exhibit subtle changes in cognition and social and emotional behaviours, similar to… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Theory of Mind

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APA (6th Edition):

Fowler, E. (2012). Cognitive and Affective Theory of Mind in Amyotrophic Lateral Sclerosis. (Thesis). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8415

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):

Fowler, Elizabeth. “Cognitive and Affective Theory of Mind in Amyotrophic Lateral Sclerosis.” 2012. Thesis, University of Edinburgh. Accessed January 19, 2020. http://hdl.handle.net/1842/8415.

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

MLA Handbook (7th Edition):

Fowler, Elizabeth. “Cognitive and Affective Theory of Mind in Amyotrophic Lateral Sclerosis.” 2012. Web. 19 Jan 2020.

Vancouver:

Fowler E. Cognitive and Affective Theory of Mind in Amyotrophic Lateral Sclerosis. [Internet] [Thesis]. University of Edinburgh; 2012. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1842/8415.

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

Council of Science Editors:

Fowler E. Cognitive and Affective Theory of Mind in Amyotrophic Lateral Sclerosis. [Thesis]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/8415

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


University of Rochester

6. Shapovalov, Yuriy. The Role of Neuroinflammation in the Pathogenesis of Amyotrophic Lateral Sclerosis.

Degree: PhD, 2010, University of Rochester

Amyotrophic lateral sclerosis (ALS) has remained an incurable disease since its first description by Jean Martin Charcot in 1869. It is characterized by progressive muscle… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Neuroinflammation; Cyclooxygenases; Prostaglandins

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APA (6th Edition):

Shapovalov, Y. (2010). The Role of Neuroinflammation in the Pathogenesis of Amyotrophic Lateral Sclerosis. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/11848

Chicago Manual of Style (16th Edition):

Shapovalov, Yuriy. “The Role of Neuroinflammation in the Pathogenesis of Amyotrophic Lateral Sclerosis.” 2010. Doctoral Dissertation, University of Rochester. Accessed January 19, 2020. http://hdl.handle.net/1802/11848.

MLA Handbook (7th Edition):

Shapovalov, Yuriy. “The Role of Neuroinflammation in the Pathogenesis of Amyotrophic Lateral Sclerosis.” 2010. Web. 19 Jan 2020.

Vancouver:

Shapovalov Y. The Role of Neuroinflammation in the Pathogenesis of Amyotrophic Lateral Sclerosis. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1802/11848.

Council of Science Editors:

Shapovalov Y. The Role of Neuroinflammation in the Pathogenesis of Amyotrophic Lateral Sclerosis. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/11848


Penn State University

7. Wiley, Nicholas J. Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model.

Degree: MS, Neuroscience, 2008, Penn State University

Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and fatal neurological disease characterized by the selective death of motor neurons. There is substantial evidence that… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; SOD1; liposome; minocycline; microglia

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APA (6th Edition):

Wiley, N. J. (2008). Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8464

Chicago Manual of Style (16th Edition):

Wiley, Nicholas J. “Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model.” 2008. Masters Thesis, Penn State University. Accessed January 19, 2020. https://etda.libraries.psu.edu/catalog/8464.

MLA Handbook (7th Edition):

Wiley, Nicholas J. “Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model.” 2008. Web. 19 Jan 2020.

Vancouver:

Wiley NJ. Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model. [Internet] [Masters thesis]. Penn State University; 2008. [cited 2020 Jan 19]. Available from: https://etda.libraries.psu.edu/catalog/8464.

Council of Science Editors:

Wiley NJ. Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model. [Masters Thesis]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8464


McMaster University

8. Soofi, Ammarah Yasmin. Examining the impact of rehabilitation interventions on quality of life (QoL) in people with amyotrophic lateral sclerosis (ALS).

Degree: MSc, 2016, McMaster University

The purpose of this thesis is to examine how rehabilitation interventions, specifically physiotherapy (PT), occupational therapy (OT), and speech and language pathology (SLP) or a… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; rehabilitation; quality of life

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APA (6th Edition):

Soofi, A. Y. (2016). Examining the impact of rehabilitation interventions on quality of life (QoL) in people with amyotrophic lateral sclerosis (ALS). (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/20636

Chicago Manual of Style (16th Edition):

Soofi, Ammarah Yasmin. “Examining the impact of rehabilitation interventions on quality of life (QoL) in people with amyotrophic lateral sclerosis (ALS).” 2016. Masters Thesis, McMaster University. Accessed January 19, 2020. http://hdl.handle.net/11375/20636.

MLA Handbook (7th Edition):

Soofi, Ammarah Yasmin. “Examining the impact of rehabilitation interventions on quality of life (QoL) in people with amyotrophic lateral sclerosis (ALS).” 2016. Web. 19 Jan 2020.

Vancouver:

Soofi AY. Examining the impact of rehabilitation interventions on quality of life (QoL) in people with amyotrophic lateral sclerosis (ALS). [Internet] [Masters thesis]. McMaster University; 2016. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/11375/20636.

Council of Science Editors:

Soofi AY. Examining the impact of rehabilitation interventions on quality of life (QoL) in people with amyotrophic lateral sclerosis (ALS). [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20636


Univerzitet u Beogradu

9. Kostić-Dedić, Svetlana I., 1967-. Прогностички фактори и њихова корелација са преживљавањем болесника са амиотрофичном латералном склерозом Дедић.

Degree: Medicinski fakultet, 2014, Univerzitet u Beogradu

НЕУРОЛОГИЈА - неуродегенеративне болести / Neurology - neurodegenerative disease

УВОД: Aмиoтрофична латерална склероза (ALS) је прогресивно неуродегенеративно оболење са просечним средњим временом преживљавања од 3… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; survival; prognostic factors

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APA (6th Edition):

Kostić-Dedić, Svetlana I., 1. (2014). Прогностички фактори и њихова корелација са преживљавањем болесника са амиотрофичном латералном склерозом Дедић. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:6991/bdef:Content/get

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):

Kostić-Dedić, Svetlana I., 1967-. “Прогностички фактори и њихова корелација са преживљавањем болесника са амиотрофичном латералном склерозом Дедић.” 2014. Thesis, Univerzitet u Beogradu. Accessed January 19, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:6991/bdef:Content/get.

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

MLA Handbook (7th Edition):

Kostić-Dedić, Svetlana I., 1967-. “Прогностички фактори и њихова корелација са преживљавањем болесника са амиотрофичном латералном склерозом Дедић.” 2014. Web. 19 Jan 2020.

Vancouver:

Kostić-Dedić, Svetlana I. 1. Прогностички фактори и њихова корелација са преживљавањем болесника са амиотрофичном латералном склерозом Дедић. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2020 Jan 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:6991/bdef:Content/get.

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

Council of Science Editors:

Kostić-Dedić, Svetlana I. 1. Прогностички фактори и њихова корелација са преживљавањем болесника са амиотрофичном латералном склерозом Дедић. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:6991/bdef:Content/get

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


Columbia University

10. Smerdon, John W. Axon Initial Segment Plasticity in Mouse Models of Amyotrophic Lateral Sclerosis.

Degree: 2019, Columbia University

Amyotrophic Lateral Sclerosis (ALS) is a debilitating and fatal neurodegenerative disease affecting upper and lower motor neurons. Though studied for over two decades since the… (more)

Subjects/Keywords: Neurosciences; Amyotrophic lateral sclerosis; Axons; Electrophysiology

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APA (6th Edition):

Smerdon, J. W. (2019). Axon Initial Segment Plasticity in Mouse Models of Amyotrophic Lateral Sclerosis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-fwsp-9k41

Chicago Manual of Style (16th Edition):

Smerdon, John W. “Axon Initial Segment Plasticity in Mouse Models of Amyotrophic Lateral Sclerosis.” 2019. Doctoral Dissertation, Columbia University. Accessed January 19, 2020. https://doi.org/10.7916/d8-fwsp-9k41.

MLA Handbook (7th Edition):

Smerdon, John W. “Axon Initial Segment Plasticity in Mouse Models of Amyotrophic Lateral Sclerosis.” 2019. Web. 19 Jan 2020.

Vancouver:

Smerdon JW. Axon Initial Segment Plasticity in Mouse Models of Amyotrophic Lateral Sclerosis. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2020 Jan 19]. Available from: https://doi.org/10.7916/d8-fwsp-9k41.

Council of Science Editors:

Smerdon JW. Axon Initial Segment Plasticity in Mouse Models of Amyotrophic Lateral Sclerosis. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-fwsp-9k41


University of New South Wales

11. Ahmed, Rebekah. Eating and metabolism across the frontotemporal dementia and amyotropic lateral sclerosis spectrum.

Degree: Prince of Wales Clinical, 2016, University of New South Wales

 Metabolic changes have been identified across a number of neurodegenerative conditions. It is not known how these changes arise, whether they represent the result of… (more)

Subjects/Keywords: metabolism; Frontotemporal dementia; Amyotrophic lateral sclerosis

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APA (6th Edition):

Ahmed, R. (2016). Eating and metabolism across the frontotemporal dementia and amyotropic lateral sclerosis spectrum. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56912 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42024/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Ahmed, Rebekah. “Eating and metabolism across the frontotemporal dementia and amyotropic lateral sclerosis spectrum.” 2016. Doctoral Dissertation, University of New South Wales. Accessed January 19, 2020. http://handle.unsw.edu.au/1959.4/56912 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42024/SOURCE02?view=true.

MLA Handbook (7th Edition):

Ahmed, Rebekah. “Eating and metabolism across the frontotemporal dementia and amyotropic lateral sclerosis spectrum.” 2016. Web. 19 Jan 2020.

Vancouver:

Ahmed R. Eating and metabolism across the frontotemporal dementia and amyotropic lateral sclerosis spectrum. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2020 Jan 19]. Available from: http://handle.unsw.edu.au/1959.4/56912 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42024/SOURCE02?view=true.

Council of Science Editors:

Ahmed R. Eating and metabolism across the frontotemporal dementia and amyotropic lateral sclerosis spectrum. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/56912 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42024/SOURCE02?view=true


National University of Ireland – Galway

12. Madill, Martin. Developing and characterizing cellular models for neurodegenerative diseases.

Degree: 2016, National University of Ireland – Galway

 The focus of this work was to develop and validate in vitro cell culture models of neurodegenerative diseases, with a focus on Amyotrophic Lateral Sclerosis(more)

Subjects/Keywords: Amyotrophic lateral sclerosis; Medicine; Neurodegenerative diseases; Sclerosis; Regenerative medicine

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APA (6th Edition):

Madill, M. (2016). Developing and characterizing cellular models for neurodegenerative diseases. (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/5790

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):

Madill, Martin. “Developing and characterizing cellular models for neurodegenerative diseases. ” 2016. Thesis, National University of Ireland – Galway. Accessed January 19, 2020. http://hdl.handle.net/10379/5790.

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

MLA Handbook (7th Edition):

Madill, Martin. “Developing and characterizing cellular models for neurodegenerative diseases. ” 2016. Web. 19 Jan 2020.

Vancouver:

Madill M. Developing and characterizing cellular models for neurodegenerative diseases. [Internet] [Thesis]. National University of Ireland – Galway; 2016. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/10379/5790.

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

Council of Science Editors:

Madill M. Developing and characterizing cellular models for neurodegenerative diseases. [Thesis]. National University of Ireland – Galway; 2016. Available from: http://hdl.handle.net/10379/5790

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


University of Florida

13. Altshuler, Marcelle. Influence on Phenotype on the Postnatal Developmental Period in Mice Expressing Human M337V TDP-43.

Degree: 2013, University of Florida

 Frontotemporal lobar degeneration (FTLD) is a neurodegenerative disease that is characterized in many cases by the cytoplasmic aggregation, cleavage, nuclear clearance and ubiquitination of Tar… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; Antibodies; Diseases; Humans; Mice; Pathology; Phenotypes; Torsades de Pointes; Transgenes; Ubiquitins; Amyotrophic lateral sclerosis; DNA-binding proteins; Mice

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APA (6th Edition):

Altshuler, M. (2013). Influence on Phenotype on the Postnatal Developmental Period in Mice Expressing Human M337V TDP-43. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00057069

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):

Altshuler, Marcelle. “Influence on Phenotype on the Postnatal Developmental Period in Mice Expressing Human M337V TDP-43.” 2013. Thesis, University of Florida. Accessed January 19, 2020. http://ufdc.ufl.edu/AA00057069.

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

MLA Handbook (7th Edition):

Altshuler, Marcelle. “Influence on Phenotype on the Postnatal Developmental Period in Mice Expressing Human M337V TDP-43.” 2013. Web. 19 Jan 2020.

Vancouver:

Altshuler M. Influence on Phenotype on the Postnatal Developmental Period in Mice Expressing Human M337V TDP-43. [Internet] [Thesis]. University of Florida; 2013. [cited 2020 Jan 19]. Available from: http://ufdc.ufl.edu/AA00057069.

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

Council of Science Editors:

Altshuler M. Influence on Phenotype on the Postnatal Developmental Period in Mice Expressing Human M337V TDP-43. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00057069

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


Macquarie University

14. Parakh, Sonam. Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis.

Degree: 2016, Macquarie University

Theoretical thesis.

Bibliography: pages 239-279.

General introduction  – Chapter 2. Methods and materials  – Chapter 3. PDI is protective against major familial ALS causing proteins… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis  – Pathogenesis; Protein disulfide isomerase; Superoxide dismutas; amyotrophic lateral sclerosis; protein disulphide isomerase; SODI

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APA (6th Edition):

Parakh, S. (2016). Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/1115418

Chicago Manual of Style (16th Edition):

Parakh, Sonam. “Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis.” 2016. Doctoral Dissertation, Macquarie University. Accessed January 19, 2020. http://hdl.handle.net/1959.14/1115418.

MLA Handbook (7th Edition):

Parakh, Sonam. “Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis.” 2016. Web. 19 Jan 2020.

Vancouver:

Parakh S. Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis. [Internet] [Doctoral dissertation]. Macquarie University; 2016. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1959.14/1115418.

Council of Science Editors:

Parakh S. Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis. [Doctoral Dissertation]. Macquarie University; 2016. Available from: http://hdl.handle.net/1959.14/1115418


University of Edinburgh

15. Parry, Katherine Elizabeth. Investigation of the interactions of DVAP-33A, the orthologue of human VAPB.

Degree: PhD, 2011, University of Edinburgh

Amyotrophic Lateral Sclerosis is the most common type of motor neuron disease, characterized by progressive degeneration of the upper and lower motor neurons. Sufferers present… (more)

Subjects/Keywords: 616.8; Amyotrophic Lateral Sclerosis; ALS; motor neuron disease; protein

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APA (6th Edition):

Parry, K. E. (2011). Investigation of the interactions of DVAP-33A, the orthologue of human VAPB. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5538

Chicago Manual of Style (16th Edition):

Parry, Katherine Elizabeth. “Investigation of the interactions of DVAP-33A, the orthologue of human VAPB.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 19, 2020. http://hdl.handle.net/1842/5538.

MLA Handbook (7th Edition):

Parry, Katherine Elizabeth. “Investigation of the interactions of DVAP-33A, the orthologue of human VAPB.” 2011. Web. 19 Jan 2020.

Vancouver:

Parry KE. Investigation of the interactions of DVAP-33A, the orthologue of human VAPB. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1842/5538.

Council of Science Editors:

Parry KE. Investigation of the interactions of DVAP-33A, the orthologue of human VAPB. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5538


University of Alberta

16. Bohaichuk, Amanda R. The effects of a volitional breathing technique on swallowing and respiratory coordination in individuals with amyotrophic lateral sclerosis: A pilot investigation.

Degree: MS, Department of Speech Pathology and Audiology, 2012, University of Alberta

 Individuals with amyotrophic lateral sclerosis (ALS) often present with aberrant respiratory-swallowing relationships. In this pilot study, eight individuals with ALS learned a volitional breathing technique… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; dysphagia; swallow-respiration coordination; lung volume

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APA (6th Edition):

Bohaichuk, A. R. (2012). The effects of a volitional breathing technique on swallowing and respiratory coordination in individuals with amyotrophic lateral sclerosis: A pilot investigation. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/rj4305185

Chicago Manual of Style (16th Edition):

Bohaichuk, Amanda R. “The effects of a volitional breathing technique on swallowing and respiratory coordination in individuals with amyotrophic lateral sclerosis: A pilot investigation.” 2012. Masters Thesis, University of Alberta. Accessed January 19, 2020. https://era.library.ualberta.ca/files/rj4305185.

MLA Handbook (7th Edition):

Bohaichuk, Amanda R. “The effects of a volitional breathing technique on swallowing and respiratory coordination in individuals with amyotrophic lateral sclerosis: A pilot investigation.” 2012. Web. 19 Jan 2020.

Vancouver:

Bohaichuk AR. The effects of a volitional breathing technique on swallowing and respiratory coordination in individuals with amyotrophic lateral sclerosis: A pilot investigation. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Jan 19]. Available from: https://era.library.ualberta.ca/files/rj4305185.

Council of Science Editors:

Bohaichuk AR. The effects of a volitional breathing technique on swallowing and respiratory coordination in individuals with amyotrophic lateral sclerosis: A pilot investigation. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/rj4305185

17. Bokuda, Kota. Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis. : 筋萎縮性側索硬化症における線維束電位の定量的解析および筋力との関連について.

Degree: 博士(医学), 2017, Niigata University / 新潟大学

学位の種類: 博士(医学). 報告番号: 甲第4257号. 学位記番号: 新大院博(医)甲第735号. 学位授与年月日: 平成29年3月23日

Neurological Sciences 37(12) 1939-1945 2016

This study aimed to quantitatively analyze fasciculation potentials (FPs) and to investigate… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; Electromyography; Fasciculation potential; Muscle strength; Quantitative analysis

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APA (6th Edition):

Bokuda, K. (2017). Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis. : 筋萎縮性側索硬化症における線維束電位の定量的解析および筋力との関連について. (Thesis). Niigata University / 新潟大学. Retrieved from http://hdl.handle.net/10191/47588

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):

Bokuda, Kota. “Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis. : 筋萎縮性側索硬化症における線維束電位の定量的解析および筋力との関連について.” 2017. Thesis, Niigata University / 新潟大学. Accessed January 19, 2020. http://hdl.handle.net/10191/47588.

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

MLA Handbook (7th Edition):

Bokuda, Kota. “Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis. : 筋萎縮性側索硬化症における線維束電位の定量的解析および筋力との関連について.” 2017. Web. 19 Jan 2020.

Vancouver:

Bokuda K. Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis. : 筋萎縮性側索硬化症における線維束電位の定量的解析および筋力との関連について. [Internet] [Thesis]. Niigata University / 新潟大学; 2017. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/10191/47588.

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

Council of Science Editors:

Bokuda K. Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis. : 筋萎縮性側索硬化症における線維束電位の定量的解析および筋力との関連について. [Thesis]. Niigata University / 新潟大学; 2017. Available from: http://hdl.handle.net/10191/47588

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


Oregon State University

18. Robinson, Kristine M. The detection of superoxide and implications for amyotrophic lateral sclerosis.

Degree: PhD, Biochemistry, 2007, Oregon State University

 Mutations to superoxide dismutase were the first proven cause of Lou Gehrig’s disease (amyotrophic lateral sclerosis; ALS) implicating superoxide in the selective death of motor… (more)

Subjects/Keywords: superoxide; Amyotrophic lateral sclerosis

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APA (6th Edition):

Robinson, K. M. (2007). The detection of superoxide and implications for amyotrophic lateral sclerosis. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/5003

Chicago Manual of Style (16th Edition):

Robinson, Kristine M. “The detection of superoxide and implications for amyotrophic lateral sclerosis.” 2007. Doctoral Dissertation, Oregon State University. Accessed January 19, 2020. http://hdl.handle.net/1957/5003.

MLA Handbook (7th Edition):

Robinson, Kristine M. “The detection of superoxide and implications for amyotrophic lateral sclerosis.” 2007. Web. 19 Jan 2020.

Vancouver:

Robinson KM. The detection of superoxide and implications for amyotrophic lateral sclerosis. [Internet] [Doctoral dissertation]. Oregon State University; 2007. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1957/5003.

Council of Science Editors:

Robinson KM. The detection of superoxide and implications for amyotrophic lateral sclerosis. [Doctoral Dissertation]. Oregon State University; 2007. Available from: http://hdl.handle.net/1957/5003


University of Oxford

19. Scaber, Jakub. The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations.

Degree: PhD, 2017, University of Oxford

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative condition that affects corticospinal and spinal motor neurons and leads to death within 30 months of symptom onset… (more)

Subjects/Keywords: TDP-43; C9orf72; Motor Neuron Disease; Amyotrophic Lateral Sclerosis

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APA (6th Edition):

Scaber, J. (2017). The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:c5dd8dcf-c3e0-4ff7-ba9d-bfd3cb9914e8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736111

Chicago Manual of Style (16th Edition):

Scaber, Jakub. “The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations.” 2017. Doctoral Dissertation, University of Oxford. Accessed January 19, 2020. https://ora.ox.ac.uk/objects/uuid:c5dd8dcf-c3e0-4ff7-ba9d-bfd3cb9914e8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736111.

MLA Handbook (7th Edition):

Scaber, Jakub. “The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations.” 2017. Web. 19 Jan 2020.

Vancouver:

Scaber J. The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Jan 19]. Available from: https://ora.ox.ac.uk/objects/uuid:c5dd8dcf-c3e0-4ff7-ba9d-bfd3cb9914e8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736111.

Council of Science Editors:

Scaber J. The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations. [Doctoral Dissertation]. University of Oxford; 2017. Available from: https://ora.ox.ac.uk/objects/uuid:c5dd8dcf-c3e0-4ff7-ba9d-bfd3cb9914e8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736111


University of Minnesota

20. Cheong, Ian. Noninvasive Assessment of Neurochemical Biomarkers in Humans with Amyotrophic Lateral Sclerosis: Correlates of Clinical Heterogeneity.

Degree: PhD, Neuroscience, 2018, University of Minnesota

 Noninvasive neuroimaging techniques can provide objective measures of disease status that are critical for the development of neurological disease therapies. They can also unlock important… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; biomarkers; magnetic resonance imaging; magnetic resonance spectroscopy; neurochemistry

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APA (6th Edition):

Cheong, I. (2018). Noninvasive Assessment of Neurochemical Biomarkers in Humans with Amyotrophic Lateral Sclerosis: Correlates of Clinical Heterogeneity. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/201066

Chicago Manual of Style (16th Edition):

Cheong, Ian. “Noninvasive Assessment of Neurochemical Biomarkers in Humans with Amyotrophic Lateral Sclerosis: Correlates of Clinical Heterogeneity.” 2018. Doctoral Dissertation, University of Minnesota. Accessed January 19, 2020. http://hdl.handle.net/11299/201066.

MLA Handbook (7th Edition):

Cheong, Ian. “Noninvasive Assessment of Neurochemical Biomarkers in Humans with Amyotrophic Lateral Sclerosis: Correlates of Clinical Heterogeneity.” 2018. Web. 19 Jan 2020.

Vancouver:

Cheong I. Noninvasive Assessment of Neurochemical Biomarkers in Humans with Amyotrophic Lateral Sclerosis: Correlates of Clinical Heterogeneity. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/11299/201066.

Council of Science Editors:

Cheong I. Noninvasive Assessment of Neurochemical Biomarkers in Humans with Amyotrophic Lateral Sclerosis: Correlates of Clinical Heterogeneity. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/201066


University of Rochester

21. Winkler, Ethan A.; Zlokovic, Berislav V. Blood-Spinal Cord Barrier Dysfunction in Neurodegeneration.

Degree: PhD, 2012, University of Rochester

 The central nervous system (CNS) vasculature forms distinct barriers regulating exchange between circulating blood plasma and the cellular constituents of the CNS. CNS-vascular barriers are… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Pericytes; Blood-Spinal Cord Barrier

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APA (6th Edition):

Winkler, Ethan A.; Zlokovic, B. V. (2012). Blood-Spinal Cord Barrier Dysfunction in Neurodegeneration. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/25518

Chicago Manual of Style (16th Edition):

Winkler, Ethan A.; Zlokovic, Berislav V. “Blood-Spinal Cord Barrier Dysfunction in Neurodegeneration.” 2012. Doctoral Dissertation, University of Rochester. Accessed January 19, 2020. http://hdl.handle.net/1802/25518.

MLA Handbook (7th Edition):

Winkler, Ethan A.; Zlokovic, Berislav V. “Blood-Spinal Cord Barrier Dysfunction in Neurodegeneration.” 2012. Web. 19 Jan 2020.

Vancouver:

Winkler, Ethan A.; Zlokovic BV. Blood-Spinal Cord Barrier Dysfunction in Neurodegeneration. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1802/25518.

Council of Science Editors:

Winkler, Ethan A.; Zlokovic BV. Blood-Spinal Cord Barrier Dysfunction in Neurodegeneration. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/25518


University of Southern California

22. Pence, Shannon Michelle. Learning to fall.

Degree: MA, Journalism (Broadcast Journalism), 2010, University of Southern California

 It’s progressive. It’s debilitating. It’s fatal. This is a journey of learning to live and learning to fall with an incurable neurodegenerative muscular disease, known… (more)

Subjects/Keywords: living with amyotrophic lateral sclerosis; Lou Gehrig'; s disease

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APA (6th Edition):

Pence, S. M. (2010). Learning to fall. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/376292/rec/3789

Chicago Manual of Style (16th Edition):

Pence, Shannon Michelle. “Learning to fall.” 2010. Masters Thesis, University of Southern California. Accessed January 19, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/376292/rec/3789.

MLA Handbook (7th Edition):

Pence, Shannon Michelle. “Learning to fall.” 2010. Web. 19 Jan 2020.

Vancouver:

Pence SM. Learning to fall. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2020 Jan 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/376292/rec/3789.

Council of Science Editors:

Pence SM. Learning to fall. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/376292/rec/3789


Boston University

23. Lee, Michael Jisoo. Increased risk for neurodegenerative diseases in professional athletes.

Degree: 2015, Boston University

 BACKGROUND: Although concussion and sport-related traumatic brain injury is being acknowledged as a major public issue, especially in professional football players, current study is mostly… (more)

Subjects/Keywords: Neurosciences; Athletes; Concussion; Alzheimer's disease; Amyotrophic lateral sclerosis; Chronic traumatic encephalopathy

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APA (6th Edition):

Lee, M. J. (2015). Increased risk for neurodegenerative diseases in professional athletes. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16147

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, Michael Jisoo. “Increased risk for neurodegenerative diseases in professional athletes.” 2015. Thesis, Boston University. Accessed January 19, 2020. http://hdl.handle.net/2144/16147.

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

MLA Handbook (7th Edition):

Lee, Michael Jisoo. “Increased risk for neurodegenerative diseases in professional athletes.” 2015. Web. 19 Jan 2020.

Vancouver:

Lee MJ. Increased risk for neurodegenerative diseases in professional athletes. [Internet] [Thesis]. Boston University; 2015. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2144/16147.

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

Council of Science Editors:

Lee MJ. Increased risk for neurodegenerative diseases in professional athletes. [Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16147

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


The Ohio State University

24. Chang, Yueming. Investigation of two early events in amyotrophic lateral sclerosis -MRNA oxidation and up-regulation of a novel protective factor MSUR1-.

Degree: PhD, Ohio State Biochemistry Program, 2007, The Ohio State University

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disorder that is characterized by progressive degeneration of motor neurons. Overexpression of some of ALS-linked mutant SOD1… (more)

Subjects/Keywords: Biology, Neuroscience; RNA Oxidation; Amyotrophic lateral sclerosis; SOD1(G93A); neurodegeneration

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APA (6th Edition):

Chang, Y. (2007). Investigation of two early events in amyotrophic lateral sclerosis -MRNA oxidation and up-regulation of a novel protective factor MSUR1-. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1196182155

Chicago Manual of Style (16th Edition):

Chang, Yueming. “Investigation of two early events in amyotrophic lateral sclerosis -MRNA oxidation and up-regulation of a novel protective factor MSUR1-.” 2007. Doctoral Dissertation, The Ohio State University. Accessed January 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1196182155.

MLA Handbook (7th Edition):

Chang, Yueming. “Investigation of two early events in amyotrophic lateral sclerosis -MRNA oxidation and up-regulation of a novel protective factor MSUR1-.” 2007. Web. 19 Jan 2020.

Vancouver:

Chang Y. Investigation of two early events in amyotrophic lateral sclerosis -MRNA oxidation and up-regulation of a novel protective factor MSUR1-. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2020 Jan 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1196182155.

Council of Science Editors:

Chang Y. Investigation of two early events in amyotrophic lateral sclerosis -MRNA oxidation and up-regulation of a novel protective factor MSUR1-. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1196182155


Universiteit Utrecht

25. Diekstra, F.P. Amyotrophic lateral sclerosis: genetic susceptibility factors and pleiotropy.

Degree: 2015, Universiteit Utrecht

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive muscle weakness, spasticity, dysarthria and, ultimately, respiratory muscle insufficiency. These symptoms are caused… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; ALS; motor neuron disease; genetics; pleiotropy; GWAS

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APA (6th Edition):

Diekstra, F. P. (2015). Amyotrophic lateral sclerosis: genetic susceptibility factors and pleiotropy. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/321622

Chicago Manual of Style (16th Edition):

Diekstra, F P. “Amyotrophic lateral sclerosis: genetic susceptibility factors and pleiotropy.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed January 19, 2020. http://dspace.library.uu.nl:8080/handle/1874/321622.

MLA Handbook (7th Edition):

Diekstra, F P. “Amyotrophic lateral sclerosis: genetic susceptibility factors and pleiotropy.” 2015. Web. 19 Jan 2020.

Vancouver:

Diekstra FP. Amyotrophic lateral sclerosis: genetic susceptibility factors and pleiotropy. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2020 Jan 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/321622.

Council of Science Editors:

Diekstra FP. Amyotrophic lateral sclerosis: genetic susceptibility factors and pleiotropy. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/321622


Penn State University

26. Su, Xiaowei William. Investigating the interplay of intrinsic to extrinsic factors influencing amyotrophic lateral sclerosis disease progression.

Degree: PhD, Molecular Medicine, 2014, Penn State University

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder affecting motor neurons in the spinal cord, brainstem and motor cortex. The disease induces paralysis, and… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; H63D HFE; biomarker; ferritin; HMG-CoA reductase inhibitor

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APA (6th Edition):

Su, X. W. (2014). Investigating the interplay of intrinsic to extrinsic factors influencing amyotrophic lateral sclerosis disease progression. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/22400

Chicago Manual of Style (16th Edition):

Su, Xiaowei William. “Investigating the interplay of intrinsic to extrinsic factors influencing amyotrophic lateral sclerosis disease progression.” 2014. Doctoral Dissertation, Penn State University. Accessed January 19, 2020. https://etda.libraries.psu.edu/catalog/22400.

MLA Handbook (7th Edition):

Su, Xiaowei William. “Investigating the interplay of intrinsic to extrinsic factors influencing amyotrophic lateral sclerosis disease progression.” 2014. Web. 19 Jan 2020.

Vancouver:

Su XW. Investigating the interplay of intrinsic to extrinsic factors influencing amyotrophic lateral sclerosis disease progression. [Internet] [Doctoral dissertation]. Penn State University; 2014. [cited 2020 Jan 19]. Available from: https://etda.libraries.psu.edu/catalog/22400.

Council of Science Editors:

Su XW. Investigating the interplay of intrinsic to extrinsic factors influencing amyotrophic lateral sclerosis disease progression. [Doctoral Dissertation]. Penn State University; 2014. Available from: https://etda.libraries.psu.edu/catalog/22400

27. Sandoe, Jackson L. Developing Human Stem Cell Derived Motor Neuron Models of Amyotrophic Lateral Sclerosis.

Degree: PhD, Biology, Molecular and Cellular, 2014, Harvard University

 Human neurodegenerative disorders are among the most difficult to study. In particular, the inability to readily obtain the faulty cell types most relevant to these… (more)

Subjects/Keywords: Cellular biology; Amyotrophic Lateral Sclerosis; Disease Modeling; Pluripotent Stem Cells

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APA (6th Edition):

Sandoe, J. L. (2014). Developing Human Stem Cell Derived Motor Neuron Models of Amyotrophic Lateral Sclerosis. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070028

Chicago Manual of Style (16th Edition):

Sandoe, Jackson L. “Developing Human Stem Cell Derived Motor Neuron Models of Amyotrophic Lateral Sclerosis.” 2014. Doctoral Dissertation, Harvard University. Accessed January 19, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070028.

MLA Handbook (7th Edition):

Sandoe, Jackson L. “Developing Human Stem Cell Derived Motor Neuron Models of Amyotrophic Lateral Sclerosis.” 2014. Web. 19 Jan 2020.

Vancouver:

Sandoe JL. Developing Human Stem Cell Derived Motor Neuron Models of Amyotrophic Lateral Sclerosis. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Jan 19]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070028.

Council of Science Editors:

Sandoe JL. Developing Human Stem Cell Derived Motor Neuron Models of Amyotrophic Lateral Sclerosis. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070028

28. C. Tarlarini. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS.

Degree: 2014, Università degli Studi di Milano

Amyotrophic lateral sclerosis (ALS) is an adult‑onset, rapidly progressive and ultimately fatal neurodegenerative disorder characterised by degeneration of upper and lower motor neurons. This leads… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; ALS; genetic; mutation; Settore BIO/10 - Biochimica

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APA (6th Edition):

Tarlarini, C. (2014). MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/232574

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):

Tarlarini, C.. “MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS.” 2014. Thesis, Università degli Studi di Milano. Accessed January 19, 2020. http://hdl.handle.net/2434/232574.

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

MLA Handbook (7th Edition):

Tarlarini, C.. “MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS.” 2014. Web. 19 Jan 2020.

Vancouver:

Tarlarini C. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2434/232574.

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

Council of Science Editors:

Tarlarini C. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/232574

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

29. C. Tiloca. EXOME SEQUENCING APPROACH TO IDENTIFY CAUSATIVE GENES FOR AMYOTROPHIC LATERAL SCLEROSIS.

Degree: 2015, Università degli Studi di Milano

 Introduzione: La Sclerosi laterale amiotrofica (SLA) è una malattia neurodegenerativa progressiva e fatale caratterizzata dalla perdita selettiva dei motoneuroni nella corteccia cerebrale, nel tronco cerebrale… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; neurodegenerative disease; exome-sequencing; Settore MED/26 - Neurologia

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

APA (6th Edition):

Tiloca, C. (2015). EXOME SEQUENCING APPROACH TO IDENTIFY CAUSATIVE GENES FOR AMYOTROPHIC LATERAL SCLEROSIS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/253040

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):

Tiloca, C.. “EXOME SEQUENCING APPROACH TO IDENTIFY CAUSATIVE GENES FOR AMYOTROPHIC LATERAL SCLEROSIS.” 2015. Thesis, Università degli Studi di Milano. Accessed January 19, 2020. http://hdl.handle.net/2434/253040.

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

MLA Handbook (7th Edition):

Tiloca, C.. “EXOME SEQUENCING APPROACH TO IDENTIFY CAUSATIVE GENES FOR AMYOTROPHIC LATERAL SCLEROSIS.” 2015. Web. 19 Jan 2020.

Vancouver:

Tiloca C. EXOME SEQUENCING APPROACH TO IDENTIFY CAUSATIVE GENES FOR AMYOTROPHIC LATERAL SCLEROSIS. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2434/253040.

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

Council of Science Editors:

Tiloca C. EXOME SEQUENCING APPROACH TO IDENTIFY CAUSATIVE GENES FOR AMYOTROPHIC LATERAL SCLEROSIS. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/253040

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


Louisiana State University

30. Watkins, Emily. Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt.

Degree: MA, Speech and Hearing Science, 2018, Louisiana State University

  Abstract Purpose: The aim of this study is to detect and track speech changes using acoustic and perceptual measures in an individual (a local… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Acoustic Vowel Space Area; Formant Trajectories

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

APA (6th Edition):

Watkins, E. (2018). Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt. (Masters Thesis). Louisiana State University. Retrieved from https://digitalcommons.lsu.edu/gradschool_theses/4836

Chicago Manual of Style (16th Edition):

Watkins, Emily. “Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt.” 2018. Masters Thesis, Louisiana State University. Accessed January 19, 2020. https://digitalcommons.lsu.edu/gradschool_theses/4836.

MLA Handbook (7th Edition):

Watkins, Emily. “Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt.” 2018. Web. 19 Jan 2020.

Vancouver:

Watkins E. Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt. [Internet] [Masters thesis]. Louisiana State University; 2018. [cited 2020 Jan 19]. Available from: https://digitalcommons.lsu.edu/gradschool_theses/4836.

Council of Science Editors:

Watkins E. Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt. [Masters Thesis]. Louisiana State University; 2018. Available from: https://digitalcommons.lsu.edu/gradschool_theses/4836

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