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Hormone Research
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March 18, 2003
Adrenoleukodystrophy: the most frequent genetic cause of Addison's disease
Patrick Aubourg, Jean-Louis Chaussain
Brain Pathology (Zurich, Switzerland)
|
July 15, 2010
General aspects and neuropathology of X-linked adrenoleukodystrophy
Isidro Ferrer, Patrick Aubourg, Aurora Pujol
Biochimica Et Biophysica Acta
|
April 10, 2012
X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects
Stephan Kemp, Johannes Berger, Patrick Aubourg
Human Molecular Genetics
|
April 5, 2011
Gene therapy for leukodystrophies
Alessandra Biffi, Patrick Aubourg, Nathalie Cartier
Brain Pathology (Zurich, Switzerland)
|
July 15, 2010
Current and future pharmacological treatment strategies in X-linked adrenoleukodystrophy
Johannes Berger, Aurora Pujol, Patrick Aubourg, et al.
Journal of Molecular Recognition : JMR
|
November 24, 2004
T-cell receptor Vbeta gene usage in CSF lymphocytes in X-linked adrenoleukodystrophy
Fabienne Picard, Sylvie Guidoux, Thierry Martin, et al.
Orphanet Journal of Rare Diseases
|
March 12, 2011
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene
Caroline Sevin, Sacha Ferdinandusse, Hans R Waterham, et al.
Journal of the Endocrine Society
|
December 22, 2017
A Somewhat Bizarre Case of Graves Disease Due to Vitamin Treatment
Abdallah Al-Salameh, Laurent Becquemont, Sylvie Brailly-Tabard, et al.
Journal of Neuroscience Research
|
September 18, 2016
Gene therapy for metachromatic leukodystrophy
Jonathan B Rosenberg, Stephen M Kaminsky, Patrick Aubourg, et al.
Human Molecular Genetics
|
April 1, 2005
Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy
Muriel Asheuer, Ivan Bieche, Ingrid Laurendeau, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 71) with videos related to
Sort By:
Page
of 8
Hormone Research
|
March 18, 2003
Adrenoleukodystrophy: the most frequent genetic cause of Addison's disease
Patrick Aubourg, Jean-Louis Chaussain
Brain Pathology (Zurich, Switzerland)
|
July 15, 2010
General aspects and neuropathology of X-linked adrenoleukodystrophy
Isidro Ferrer, Patrick Aubourg, Aurora Pujol
Biochimica Et Biophysica Acta
|
April 10, 2012
X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects
Stephan Kemp, Johannes Berger, Patrick Aubourg
Human Molecular Genetics
|
April 5, 2011
Gene therapy for leukodystrophies
Alessandra Biffi, Patrick Aubourg, Nathalie Cartier
Brain Pathology (Zurich, Switzerland)
|
July 15, 2010
Current and future pharmacological treatment strategies in X-linked adrenoleukodystrophy
Johannes Berger, Aurora Pujol, Patrick Aubourg, et al.
Journal of Molecular Recognition : JMR
|
November 24, 2004
T-cell receptor Vbeta gene usage in CSF lymphocytes in X-linked adrenoleukodystrophy
Fabienne Picard, Sylvie Guidoux, Thierry Martin, et al.
Orphanet Journal of Rare Diseases
|
March 12, 2011
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene
Caroline Sevin, Sacha Ferdinandusse, Hans R Waterham, et al.
Journal of the Endocrine Society
|
December 22, 2017
A Somewhat Bizarre Case of Graves Disease Due to Vitamin Treatment
Abdallah Al-Salameh, Laurent Becquemont, Sylvie Brailly-Tabard, et al.
Journal of Neuroscience Research
|
September 18, 2016
Gene therapy for metachromatic leukodystrophy
Jonathan B Rosenberg, Stephen M Kaminsky, Patrick Aubourg, et al.
Human Molecular Genetics
|
April 1, 2005
Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy
Muriel Asheuer, Ivan Bieche, Ingrid Laurendeau, et al.
Page
of 8