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B Bereznai

Showing results (1-10 of 10) with videos related to

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Neuromuscular Disorders : NMD|March 1, 1997
A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosisB Bereznai, A Winkler, G D Borasio, et al.
Annals of Neurology|July 17, 1998
Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onsetT Gasser, K Windgassen, B Bereznai, et al.
European Journal of Pharmacology|July 6, 1993
Nimodipine inhibits [3H]nitrobenzylthioinosine binding to the adenosine transporter in human brainJ Deckert, B Bereznai, A Hennemann, et al.
Deutsche Medizinische Wochenschrift (1946)|June 12, 1999
[Therapy of multiple sclerosis]B Bereznai, N Goebels, T Dang, et al.
Life Sciences|January 1, 1994
(3H)dipyridamole and (3H)nitrobenzylthioinosine binding sites at the human parietal cortex and erythrocyte adenosine transporter: a comparisonJ Deckert, A Hennemann, B Bereznai, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1996
Linkage studies in alcohol-responsive myoclonic dystoniaT Gasser, B Bereznai, B Müller, et al.
Nature Genetics|March 21, 1998
A susceptibility locus for Parkinson's disease maps to chromosome 2p13T Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Science (New York, N.Y.)|July 18, 1997
Genetic complexity and Parkinson's diseaseT Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.
Annals of Neurology|August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Vaughan, A Durr, J Tassin, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Neuromuscular Disorders : NMD|March 1, 1997
A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosisB Bereznai, A Winkler, G D Borasio, et al.
Annals of Neurology|July 17, 1998
Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onsetT Gasser, K Windgassen, B Bereznai, et al.
European Journal of Pharmacology|July 6, 1993
Nimodipine inhibits [3H]nitrobenzylthioinosine binding to the adenosine transporter in human brainJ Deckert, B Bereznai, A Hennemann, et al.
Deutsche Medizinische Wochenschrift (1946)|June 12, 1999
[Therapy of multiple sclerosis]B Bereznai, N Goebels, T Dang, et al.
Life Sciences|January 1, 1994
(3H)dipyridamole and (3H)nitrobenzylthioinosine binding sites at the human parietal cortex and erythrocyte adenosine transporter: a comparisonJ Deckert, A Hennemann, B Bereznai, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1996
Linkage studies in alcohol-responsive myoclonic dystoniaT Gasser, B Bereznai, B Müller, et al.
Nature Genetics|March 21, 1998
A susceptibility locus for Parkinson's disease maps to chromosome 2p13T Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Science (New York, N.Y.)|July 18, 1997
Genetic complexity and Parkinson's diseaseT Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.
Annals of Neurology|August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Vaughan, A Durr, J Tassin, et al.
Pageof 1