Search research articles
Contact Us
Filters
Showing results (41-50 of 78) with videos related to
Page
of 8
Sort By:
Journal of Medical Genetics
|
May 24, 2001
Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2
K A Scoggan, T Chandra, R Nelson, et al.
Muscle & Nerve. Supplement
|
January 3, 2001
Clinical and pathological observations in men lacking the gap junction protein connexin 32
A F Hahn, P J Ainsworth, C C Naus, et al.
Journal of the Neurological Sciences
|
September 6, 2006
Cold-induced sweating syndrome: a report of two cases and demonstration of genetic heterogeneity
A F Hahn, D L Jones, P M Knappskog, et al.
Archives of Neurology
|
November 1, 1985
Nemaline myopathy with associated cardiomyopathy. Report of clinical and detailed autopsy findings
A J Stoessl, A F Hahn, D Malott, et al.
Neurology
|
November 23, 2000
Multifocal motor neuropathy improved by IVIg: randomized, double-blind, placebo-controlled study
P Federico, D W Zochodne, A F Hahn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1996
Respiratory electrophysiological studies in Guillain-Barré syndrome
U Zifko, R Chen, H Remtulla, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1992
Detection of hereditary motor sensory neuropathy type I in childhood
T E Feasby, A F Hahn, C F Bolton, et al.
Acta Neuropathologica
|
March 29, 2001
Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis
A F Hahn, P J Ainsworth, C F Bolton, et al.
Human Genetics
|
October 6, 1998
Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene
P J Ainsworth, C F Bolton, B C Murphy, et al.
Neurology
|
January 26, 2005
Rigid spine muscular dystrophy due to SEPN1 mutation presenting as cor pulmonale
S L Venance, W J Koopman, B A Miskie, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 78) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
May 24, 2001
Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2
K A Scoggan, T Chandra, R Nelson, et al.
Muscle & Nerve. Supplement
|
January 3, 2001
Clinical and pathological observations in men lacking the gap junction protein connexin 32
A F Hahn, P J Ainsworth, C C Naus, et al.
Journal of the Neurological Sciences
|
September 6, 2006
Cold-induced sweating syndrome: a report of two cases and demonstration of genetic heterogeneity
A F Hahn, D L Jones, P M Knappskog, et al.
Archives of Neurology
|
November 1, 1985
Nemaline myopathy with associated cardiomyopathy. Report of clinical and detailed autopsy findings
A J Stoessl, A F Hahn, D Malott, et al.
Neurology
|
November 23, 2000
Multifocal motor neuropathy improved by IVIg: randomized, double-blind, placebo-controlled study
P Federico, D W Zochodne, A F Hahn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1996
Respiratory electrophysiological studies in Guillain-Barré syndrome
U Zifko, R Chen, H Remtulla, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1992
Detection of hereditary motor sensory neuropathy type I in childhood
T E Feasby, A F Hahn, C F Bolton, et al.
Acta Neuropathologica
|
March 29, 2001
Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis
A F Hahn, P J Ainsworth, C F Bolton, et al.
Human Genetics
|
October 6, 1998
Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene
P J Ainsworth, C F Bolton, B C Murphy, et al.
Neurology
|
January 26, 2005
Rigid spine muscular dystrophy due to SEPN1 mutation presenting as cor pulmonale
S L Venance, W J Koopman, B A Miskie, et al.
Page
of 8