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Brain : a Journal of Neurology
|
August 8, 2018
GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia
Ilse Eidhof, Jonathan Baets, Erik-Jan Kamsteeg, et al.
Annals of Neurology
|
May 4, 2004
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene
Ana Ferreiro, Chantal Ceuterick-de Groote, Jared J Marks, et al.
Archives of Neurology
|
May 12, 2010
Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Ilse Gijselinck, Sebastiaan Engelborghs, Githa Maes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 1, 2006
Linezolid-induced inhibition of mitochondrial protein synthesis
An S De Vriese, Rudy Van Coster, Joel Smet, et al.
BMC Clinical Pathology
|
June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defects
Frank Roels, Patrick Verloo, François Eyskens, et al.
Journal of Alzheimer'S Disease : JAD
|
August 29, 2016
A Decade of Cerebrospinal Fluid Biomarkers for Alzheimer's Disease in Belgium
Charisse Somers, Hanne Struyfs, Joery Goossens, et al.
Nature Genetics
|
October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathy
Marc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
October 25, 2011
Neuropathology in classical and variant ataxia-telangiectasia
Mijke M M Verhagen, Jean-Jacques Martin, Marcel van Deuren, et al.
Journal of Neurology
|
October 9, 2013
Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy
Maike F Dohrn, Christoph Röcken, Jan L De Bleecker, et al.
Alzheimer'S Research & Therapy
|
September 12, 2020
Amyloid-β<sub>1-43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations
Federica Perrone, Maria Bjerke, Elisabeth Hens, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 107) with videos related to
Sort By:
Page
of 11
Brain : a Journal of Neurology
|
August 8, 2018
GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia
Ilse Eidhof, Jonathan Baets, Erik-Jan Kamsteeg, et al.
Annals of Neurology
|
May 4, 2004
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene
Ana Ferreiro, Chantal Ceuterick-de Groote, Jared J Marks, et al.
Archives of Neurology
|
May 12, 2010
Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Ilse Gijselinck, Sebastiaan Engelborghs, Githa Maes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 1, 2006
Linezolid-induced inhibition of mitochondrial protein synthesis
An S De Vriese, Rudy Van Coster, Joel Smet, et al.
BMC Clinical Pathology
|
June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defects
Frank Roels, Patrick Verloo, François Eyskens, et al.
Journal of Alzheimer'S Disease : JAD
|
August 29, 2016
A Decade of Cerebrospinal Fluid Biomarkers for Alzheimer's Disease in Belgium
Charisse Somers, Hanne Struyfs, Joery Goossens, et al.
Nature Genetics
|
October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathy
Marc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
October 25, 2011
Neuropathology in classical and variant ataxia-telangiectasia
Mijke M M Verhagen, Jean-Jacques Martin, Marcel van Deuren, et al.
Journal of Neurology
|
October 9, 2013
Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy
Maike F Dohrn, Christoph Röcken, Jan L De Bleecker, et al.
Alzheimer'S Research & Therapy
|
September 12, 2020
Amyloid-β<sub>1-43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations
Federica Perrone, Maria Bjerke, Elisabeth Hens, et al.
Page
of 11