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A Brice

Showing results (41-50 of 353) with videos related to

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Neuromuscular Disorders : NMD|March 29, 2000
Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsiesO 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 ataxiasC Marelli, C Cazeneuve, A Brice, et al.
Environmental Science & Technology|November 24, 2006
Trends in polycyclic aromatic hydrocarbon concentrations in the great lakes atmospherePing 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 hybridizationE Viegas-Péquignot, S Berrard, A Brice, et al.
Bulletin of Environmental Contamination and Toxicology|August 1, 1984
Automative quantification of rat duodenal rhythmic contractionE 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 COPDE A Brice, W Friedlander, E D Bateman, et al.
Dialogues in Clinical Neuroscience|October 29, 2011
Genetics of inherited human epilepsiesI 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 controlsS 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 manifestationJ Johansson, L Forsgren, O Sandgren, et al.
Pageof 36

Showing results (41-50 of 353) with videos related to

Sort By:
Pageof 36
Neuromuscular Disorders : NMD|March 29, 2000
Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsiesO 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 ataxiasC Marelli, C Cazeneuve, A Brice, et al.
Environmental Science & Technology|November 24, 2006
Trends in polycyclic aromatic hydrocarbon concentrations in the great lakes atmospherePing 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 hybridizationE Viegas-Péquignot, S Berrard, A Brice, et al.
Bulletin of Environmental Contamination and Toxicology|August 1, 1984
Automative quantification of rat duodenal rhythmic contractionE 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 COPDE A Brice, W Friedlander, E D Bateman, et al.
Dialogues in Clinical Neuroscience|October 29, 2011
Genetics of inherited human epilepsiesI 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 controlsS 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 manifestationJ Johansson, L Forsgren, O Sandgren, et al.
Pageof 36