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Neurology
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November 24, 2004
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease
H Hochstrasser, P Bauer, U Walter, et al.
Brain Pathology (Zurich, Switzerland)
|
November 6, 1998
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients
T Schmidt, G B Landwehrmeyer, I Schmitt, et al.
Molecular Genetics and Metabolism
|
February 9, 2020
The Undiagnosed Diseases Network International: Five years and more!
D Taruscio, G Baynam, H Cederroth, et al.
Neurology
|
March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families
M Dichgans, L Schöls, J Herzog, et al.
Neuroreport
|
August 16, 2000
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease
R Krüger, A M Menezes-Saecker, L Schöls, et al.
American Journal of Medical Genetics
|
September 5, 1997
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome
Y Y Fang, S Bain, E A Haan, et al.
European Journal of Neurology
|
January 15, 2014
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood
B P C van de Warrenburg, J van Gaalen, S Boesch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 18, 2009
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
R Schüle, N Schlipf, M Synofzik, et al.
Cellular and Molecular Life Sciences : CMLS
|
May 15, 2010
Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice
K Schaeferhoff, S Michalakis, N Tanimoto, et al.
Archives of Neurology
|
October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds
L Schöls, S Gispert, M Vorgerd, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 144) with videos related to
Sort By:
Page
of 15
Neurology
|
November 24, 2004
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease
H Hochstrasser, P Bauer, U Walter, et al.
Brain Pathology (Zurich, Switzerland)
|
November 6, 1998
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients
T Schmidt, G B Landwehrmeyer, I Schmitt, et al.
Molecular Genetics and Metabolism
|
February 9, 2020
The Undiagnosed Diseases Network International: Five years and more!
D Taruscio, G Baynam, H Cederroth, et al.
Neurology
|
March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families
M Dichgans, L Schöls, J Herzog, et al.
Neuroreport
|
August 16, 2000
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease
R Krüger, A M Menezes-Saecker, L Schöls, et al.
American Journal of Medical Genetics
|
September 5, 1997
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome
Y Y Fang, S Bain, E A Haan, et al.
European Journal of Neurology
|
January 15, 2014
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood
B P C van de Warrenburg, J van Gaalen, S Boesch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 18, 2009
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
R Schüle, N Schlipf, M Synofzik, et al.
Cellular and Molecular Life Sciences : CMLS
|
May 15, 2010
Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice
K Schaeferhoff, S Michalakis, N Tanimoto, et al.
Archives of Neurology
|
October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds
L Schöls, S Gispert, M Vorgerd, et al.
Page
of 15