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L Ozelius

Showing results (21-30 of 32) with videos related to

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American Journal of Human Genetics|September 1, 1989
Norrie disease gene is distinct from the monoamine oxidase genesK B Sims, L Ozelius, T Corey, et al.
Annals of Neurology|September 1, 1994
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genesT Gasser, Z K Wszolek, J Trofatter, et al.
Annals of Neurology|February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34P L Kramer, D de Leon, L Ozelius, et al.
Neuron|January 1, 1989
Monoamine oxidase deficiency in males with an X chromosome deletionK B Sims, A de la Chapelle, R Norio, et al.
Molecular Biology & Medicine|December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomiaX O Breakefield, L Ozelius, M A Bothwell, et al.
American Journal of Human Genetics|January 1, 1991
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindredD J Kwiatkowski, T G Nygaard, D E Schuback, et al.
Neuron|May 1, 1989
Human gene for torsion dystonia located on chromosome 9q32-q34L Ozelius, P L Kramer, C B Moskowitz, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 15, 2005
The North American Multiple System Atrophy Study GroupS Gilman, S J May, C W Shults, et al.
Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.
Molecular Genetics and Metabolism|November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the testR Saunders-Pullman, N Blau, K Hyland, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|September 1, 1989
Norrie disease gene is distinct from the monoamine oxidase genesK B Sims, L Ozelius, T Corey, et al.
Annals of Neurology|September 1, 1994
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genesT Gasser, Z K Wszolek, J Trofatter, et al.
Annals of Neurology|February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34P L Kramer, D de Leon, L Ozelius, et al.
Neuron|January 1, 1989
Monoamine oxidase deficiency in males with an X chromosome deletionK B Sims, A de la Chapelle, R Norio, et al.
Molecular Biology & Medicine|December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomiaX O Breakefield, L Ozelius, M A Bothwell, et al.
American Journal of Human Genetics|January 1, 1991
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindredD J Kwiatkowski, T G Nygaard, D E Schuback, et al.
Neuron|May 1, 1989
Human gene for torsion dystonia located on chromosome 9q32-q34L Ozelius, P L Kramer, C B Moskowitz, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 15, 2005
The North American Multiple System Atrophy Study GroupS Gilman, S J May, C W Shults, et al.
Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.
Molecular Genetics and Metabolism|November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the testR Saunders-Pullman, N Blau, K Hyland, et al.
Pageof 4