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Neuromuscular Disorders : NMD
|
March 29, 2000
Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies
O Dubourg, P Mouton, A Brice, et al.
Revue Neurologique
|
March 7, 2006
[Autosomal recessive cerebellar ataxias with oculomotor apraxia]
I Le Ber, S Rivaud-Péchoux, A Brice, et al.
Revue Neurologique
|
May 7, 2011
Autosomal dominant cerebellar ataxias
C Marelli, C Cazeneuve, A Brice, et al.
Environmental Science & Technology
|
November 24, 2006
Trends in polycyclic aromatic hydrocarbon concentrations in the great lakes atmosphere
Ping Sun, Pierrette Blanchard, Kenneth A Brice, et al.
Genomics
|
January 1, 1991
Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization
E Viegas-Péquignot, S Berrard, A Brice, et al.
Bulletin of Environmental Contamination and Toxicology
|
August 1, 1984
Automative quantification of rat duodenal rhythmic contraction
E R Whitcomb, A Stead, G H Ward, et al.
Chest
|
March 1, 1995
Serum angiotensin-converting enzyme activity, concentration, and specific activity in granulomatous interstitial lung disease, tuberculosis, and COPD
E A Brice, W Friedlander, E D Bateman, et al.
Dialogues in Clinical Neuroscience
|
October 29, 2011
Genetics of inherited human epilepsies
I Gourfinkel-An, S Baulac, A Brice, et al.
Journal of Medical Genetics
|
September 4, 2007
Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls
S Lesage, E Lohmann, F Tison, et al.
Human Molecular Genetics
|
March 21, 1998
Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation
J Johansson, L Forsgren, O Sandgren, et al.
Page
of 36
Search research articles
Search
Showing results (41-50 of 353) with videos related to
Sort By:
Page
of 36
Neuromuscular Disorders : NMD
|
March 29, 2000
Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies
O Dubourg, P Mouton, A Brice, et al.
Revue Neurologique
|
March 7, 2006
[Autosomal recessive cerebellar ataxias with oculomotor apraxia]
I Le Ber, S Rivaud-Péchoux, A Brice, et al.
Revue Neurologique
|
May 7, 2011
Autosomal dominant cerebellar ataxias
C Marelli, C Cazeneuve, A Brice, et al.
Environmental Science & Technology
|
November 24, 2006
Trends in polycyclic aromatic hydrocarbon concentrations in the great lakes atmosphere
Ping Sun, Pierrette Blanchard, Kenneth A Brice, et al.
Genomics
|
January 1, 1991
Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization
E Viegas-Péquignot, S Berrard, A Brice, et al.
Bulletin of Environmental Contamination and Toxicology
|
August 1, 1984
Automative quantification of rat duodenal rhythmic contraction
E R Whitcomb, A Stead, G H Ward, et al.
Chest
|
March 1, 1995
Serum angiotensin-converting enzyme activity, concentration, and specific activity in granulomatous interstitial lung disease, tuberculosis, and COPD
E A Brice, W Friedlander, E D Bateman, et al.
Dialogues in Clinical Neuroscience
|
October 29, 2011
Genetics of inherited human epilepsies
I Gourfinkel-An, S Baulac, A Brice, et al.
Journal of Medical Genetics
|
September 4, 2007
Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls
S Lesage, E Lohmann, F Tison, et al.
Human Molecular Genetics
|
March 21, 1998
Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation
J Johansson, L Forsgren, O Sandgren, et al.
Page
of 36