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You searched for subject:(Hepatolenticular degeneration). Showing records 1 – 7 of 7 total matches.

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1. Machado, Alexandre Aluizio Costa. Manifestações neurológicas na doença de Wilson: estudo clínico e correlações genotípicas.

Degree: PhD, Neurologia, 2008, University of São Paulo

A doença de Wilson, moléstia hereditária, caracteriza-se pela deficiência de excreção de cobre pelo fígado, originária da mutação do gene ATP7B. As manifestações neurológicas na… (more)

Subjects/Keywords: Degeneração hepatolenticular; Genótipo; Genotype; Hepatolenticular degeneration; Manifestações neurológicas; Mutação; Mutation; Neurologic manifestations

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APA (6th Edition):

Machado, A. A. C. (2008). Manifestações neurológicas na doença de Wilson: estudo clínico e correlações genotípicas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5138/tde-12012009-141218/ ;

Chicago Manual of Style (16th Edition):

Machado, Alexandre Aluizio Costa. “Manifestações neurológicas na doença de Wilson: estudo clínico e correlações genotípicas.” 2008. Doctoral Dissertation, University of São Paulo. Accessed January 27, 2021. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-12012009-141218/ ;.

MLA Handbook (7th Edition):

Machado, Alexandre Aluizio Costa. “Manifestações neurológicas na doença de Wilson: estudo clínico e correlações genotípicas.” 2008. Web. 27 Jan 2021.

Vancouver:

Machado AAC. Manifestações neurológicas na doença de Wilson: estudo clínico e correlações genotípicas. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2021 Jan 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-12012009-141218/ ;.

Council of Science Editors:

Machado AAC. Manifestações neurológicas na doença de Wilson: estudo clínico e correlações genotípicas. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-12012009-141218/ ;


Indian Institute of Science

2. Singh, Nivedita. Genetic Analysis of Wilson Disease in a South Indian Population and Molecular Characterization of 13 Novel ATP7B Mutations.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Wilson disease (WD) is an autosomal recessive disorder characterized by deposition of copper in the body, mainly in the liver and brain. WD patients present… (more)

Subjects/Keywords: Wilson Disease; TRIM36; ATP7B Mutations; PLA2G6; Non-Wilsonian Hepatolenticular Degeneration; Molecular Reproduction

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APA (6th Edition):

Singh, N. (2018). Genetic Analysis of Wilson Disease in a South Indian Population and Molecular Characterization of 13 Novel ATP7B Mutations. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3273

Chicago Manual of Style (16th Edition):

Singh, Nivedita. “Genetic Analysis of Wilson Disease in a South Indian Population and Molecular Characterization of 13 Novel ATP7B Mutations.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed January 27, 2021. http://etd.iisc.ac.in/handle/2005/3273.

MLA Handbook (7th Edition):

Singh, Nivedita. “Genetic Analysis of Wilson Disease in a South Indian Population and Molecular Characterization of 13 Novel ATP7B Mutations.” 2018. Web. 27 Jan 2021.

Vancouver:

Singh N. Genetic Analysis of Wilson Disease in a South Indian Population and Molecular Characterization of 13 Novel ATP7B Mutations. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Jan 27]. Available from: http://etd.iisc.ac.in/handle/2005/3273.

Council of Science Editors:

Singh N. Genetic Analysis of Wilson Disease in a South Indian Population and Molecular Characterization of 13 Novel ATP7B Mutations. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3273

3. Vieira, Jakeliny. Cuprúria em pais de pacientes com doença de Wilson antes e depois da administração oral de d-penicilamina.

Degree: Mestrado, Gastroenterologia Clínica, 2007, University of São Paulo

A doença de Wilson (DW) é distúrbio da excreção biliar de cobre, de herança autossômica recessiva, devido a mutações no gene ATP7B. O cobre que… (more)

Subjects/Keywords: Ceruloplasmin; Ceruloplasmina; Chelating agents; Cobre/urina; Copper/urine; Degeneração hepatolenticular; Heptolenticular degeneration; Penicilamina/urina; Penicillamine/urine; Quelantes

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APA (6th Edition):

Vieira, J. (2007). Cuprúria em pais de pacientes com doença de Wilson antes e depois da administração oral de d-penicilamina. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5147/tde-20082007-144528/ ;

Chicago Manual of Style (16th Edition):

Vieira, Jakeliny. “Cuprúria em pais de pacientes com doença de Wilson antes e depois da administração oral de d-penicilamina.” 2007. Masters Thesis, University of São Paulo. Accessed January 27, 2021. http://www.teses.usp.br/teses/disponiveis/5/5147/tde-20082007-144528/ ;.

MLA Handbook (7th Edition):

Vieira, Jakeliny. “Cuprúria em pais de pacientes com doença de Wilson antes e depois da administração oral de d-penicilamina.” 2007. Web. 27 Jan 2021.

Vancouver:

Vieira J. Cuprúria em pais de pacientes com doença de Wilson antes e depois da administração oral de d-penicilamina. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2021 Jan 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-20082007-144528/ ;.

Council of Science Editors:

Vieira J. Cuprúria em pais de pacientes com doença de Wilson antes e depois da administração oral de d-penicilamina. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-20082007-144528/ ;

4. Adewusi, Emmanuel Adekanmi. Evaluation of the effect of Pelargonium reniforme Curtis extract on alcohol induced liver damage in Nkonkobe Municipality Eastern Cape Province South Africa.

Degree: MS, Ethno-Botany, 2009, University of Fort Hare

 Alcohol abuse is a very common practice (just like in many other parts of the world) in Nkonkobe Municipality, Eastern Cape Province, South Africa. This… (more)

Subjects/Keywords: Plants – Therapeutic use; Alcoholism – South Africa – Eastern Cape; Hepatolenticular degeneration; Pelargoniums; Plant extracts; Plant bioassay; Medicinal plants – South Africa – Eastern Cape

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APA (6th Edition):

Adewusi, E. A. (2009). Evaluation of the effect of Pelargonium reniforme Curtis extract on alcohol induced liver damage in Nkonkobe Municipality Eastern Cape Province South Africa. (Masters Thesis). University of Fort Hare. Retrieved from http://hdl.handle.net/10353/263

Chicago Manual of Style (16th Edition):

Adewusi, Emmanuel Adekanmi. “Evaluation of the effect of Pelargonium reniforme Curtis extract on alcohol induced liver damage in Nkonkobe Municipality Eastern Cape Province South Africa.” 2009. Masters Thesis, University of Fort Hare. Accessed January 27, 2021. http://hdl.handle.net/10353/263.

MLA Handbook (7th Edition):

Adewusi, Emmanuel Adekanmi. “Evaluation of the effect of Pelargonium reniforme Curtis extract on alcohol induced liver damage in Nkonkobe Municipality Eastern Cape Province South Africa.” 2009. Web. 27 Jan 2021.

Vancouver:

Adewusi EA. Evaluation of the effect of Pelargonium reniforme Curtis extract on alcohol induced liver damage in Nkonkobe Municipality Eastern Cape Province South Africa. [Internet] [Masters thesis]. University of Fort Hare; 2009. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10353/263.

Council of Science Editors:

Adewusi EA. Evaluation of the effect of Pelargonium reniforme Curtis extract on alcohol induced liver damage in Nkonkobe Municipality Eastern Cape Province South Africa. [Masters Thesis]. University of Fort Hare; 2009. Available from: http://hdl.handle.net/10353/263

5. Lucato, Leandro Tavares. Análise comparativa entre as imagens convencionais de ressonância magnética do encéfalo e a espectroscopia de prótons na doença de Wilson.

Degree: PhD, Radiologia, 2003, University of São Paulo

 A doença de Wilson (DW) é rara, de herança autossômica recessiva, com prevalência estimada de 1 em 30.000 nascidos vivos, causada por distúrbio no metabolismo… (more)

Subjects/Keywords: Análise espectral; Cobre/toxicidade; Copper/toxicity; Degeneração hepatolenticular; Hepatolenticular degeneration; Imagem por ressonância magnética; Magnetic resonance spectroscopy; Prevalence; Prevalência; Spectrum analysis

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APA (6th Edition):

Lucato, L. T. (2003). Análise comparativa entre as imagens convencionais de ressonância magnética do encéfalo e a espectroscopia de prótons na doença de Wilson. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5151/tde-17092014-094357/ ;

Chicago Manual of Style (16th Edition):

Lucato, Leandro Tavares. “Análise comparativa entre as imagens convencionais de ressonância magnética do encéfalo e a espectroscopia de prótons na doença de Wilson.” 2003. Doctoral Dissertation, University of São Paulo. Accessed January 27, 2021. http://www.teses.usp.br/teses/disponiveis/5/5151/tde-17092014-094357/ ;.

MLA Handbook (7th Edition):

Lucato, Leandro Tavares. “Análise comparativa entre as imagens convencionais de ressonância magnética do encéfalo e a espectroscopia de prótons na doença de Wilson.” 2003. Web. 27 Jan 2021.

Vancouver:

Lucato LT. Análise comparativa entre as imagens convencionais de ressonância magnética do encéfalo e a espectroscopia de prótons na doença de Wilson. [Internet] [Doctoral dissertation]. University of São Paulo; 2003. [cited 2021 Jan 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5151/tde-17092014-094357/ ;.

Council of Science Editors:

Lucato LT. Análise comparativa entre as imagens convencionais de ressonância magnética do encéfalo e a espectroscopia de prótons na doença de Wilson. [Doctoral Dissertation]. University of São Paulo; 2003. Available from: http://www.teses.usp.br/teses/disponiveis/5/5151/tde-17092014-094357/ ;


IUPUI

6. LeVora, Jennifer K. THE ROLE OF SMF 1, SMF-2, SMF-3 IN METAL-INDUCED WHOLE ANIMAL VULNERABILITY AND DOPAMINE NEURON DEGENERATION IN CAENORHABDITIS ELEGANS.

Degree: 2012, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The etiology of many neurodegenerative diseases is unknown, but a number of studies indicate that a combination of both genetic… (more)

Subjects/Keywords: dopamine; C. elegans; SMF; aluminum; copper; Parkinson's Disease; Dopamine; Neurotoxicology; Cell death; Parkinson's disease; Metal ions  – Physiological effect; Nervous system  – Degeneration  – Molecular aspects; Oxidative stress; Metals  – Toxicology; Homeostasis; Caenorhabditis elegans; Mitochondrial pathology; Copper  – Physiological effect; Hepatolenticular degeneration; Alzheimer's disease

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APA (6th Edition):

LeVora, J. K. (2012). THE ROLE OF SMF 1, SMF-2, SMF-3 IN METAL-INDUCED WHOLE ANIMAL VULNERABILITY AND DOPAMINE NEURON DEGENERATION IN CAENORHABDITIS ELEGANS. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/3177

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):

LeVora, Jennifer K. “THE ROLE OF SMF 1, SMF-2, SMF-3 IN METAL-INDUCED WHOLE ANIMAL VULNERABILITY AND DOPAMINE NEURON DEGENERATION IN CAENORHABDITIS ELEGANS.” 2012. Thesis, IUPUI. Accessed January 27, 2021. http://hdl.handle.net/1805/3177.

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

MLA Handbook (7th Edition):

LeVora, Jennifer K. “THE ROLE OF SMF 1, SMF-2, SMF-3 IN METAL-INDUCED WHOLE ANIMAL VULNERABILITY AND DOPAMINE NEURON DEGENERATION IN CAENORHABDITIS ELEGANS.” 2012. Web. 27 Jan 2021.

Vancouver:

LeVora JK. THE ROLE OF SMF 1, SMF-2, SMF-3 IN METAL-INDUCED WHOLE ANIMAL VULNERABILITY AND DOPAMINE NEURON DEGENERATION IN CAENORHABDITIS ELEGANS. [Internet] [Thesis]. IUPUI; 2012. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1805/3177.

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

Council of Science Editors:

LeVora JK. THE ROLE OF SMF 1, SMF-2, SMF-3 IN METAL-INDUCED WHOLE ANIMAL VULNERABILITY AND DOPAMINE NEURON DEGENERATION IN CAENORHABDITIS ELEGANS. [Thesis]. IUPUI; 2012. Available from: http://hdl.handle.net/1805/3177

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

7. Deguti, Marta Mitiko. "Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P".

Degree: PhD, Gastroenterologia Clínica, 2004, University of São Paulo

A doença de Wilson é um distúrbio da excreção biliar de cobre devido a um defeito na proteína ATP7B. Em caráter pioneiro na América do… (more)

Subjects/Keywords: Brasil; Brazil; Degeneração hepatolenticular/genética; Estudos prospectivos; Estudos retrospectivos; Fenótipo; Genótipo; Genotype; Haplótipos/genética; Haplotypes/genetics; Hepatolenticular degeneration/genetics; Mutação/genética; Mutation/genetics; Phenotype; Polimorfismo de fragmento de restrição; Polymerase chain reaction/methods; Polymorphism restriction fragment length; Prospective studies; Reação em cadeia por polimerase transcriptase reversa/métodos; Reação em cadeia por polimerase/métodos; Retrospective studies; Reverse transcriptase polymerase chain reaction/methods

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APA (6th Edition):

Deguti, M. M. (2004). "Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/ ;

Chicago Manual of Style (16th Edition):

Deguti, Marta Mitiko. “"Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P".” 2004. Doctoral Dissertation, University of São Paulo. Accessed January 27, 2021. http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/ ;.

MLA Handbook (7th Edition):

Deguti, Marta Mitiko. “"Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P".” 2004. Web. 27 Jan 2021.

Vancouver:

Deguti MM. "Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P". [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2021 Jan 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/ ;.

Council of Science Editors:

Deguti MM. "Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P". [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/ ;

.