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R A Kark

Showing results (1-10 of 28) with videos related to

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Neurology|January 1, 1979
Pyruvate dehydrogenase deficiency in spinocerebellar degenerationsR A Kark, M Rodriguez-Budelli
Muscle & Nerve|January 1, 1981
Multiple genotypes, multiple phenotypes, and partial defectsR A Kark, D M Becker
Neurology|July 1, 1979
Clinical correlations of partial deficiency of lipoamide dehydrogenaseR A Kark, M M Rodriguez-Budelli
Neurology|March 1, 1981
Double-blind, triple-crossover trial of low doses of oral physostigmine in inherited ataxiasR A Kark, M M Budelli, R Wachsner
Annals of Neurology|May 1, 1981
Retraction: reduced enzyme activity in hereditary ataxiaR A Kark, D M Becker, S Perlman
Journal of Neurochemistry|December 1, 1980
Effects of denervation and simple disuse on rates of oxidation and on activities of four mitochondrial enzymes in type I muscleP M Nemeth, D Meyer, R A Kark
Neurology|January 1, 1977
Physostigmine in familial ataxiasR A Kark, J P Blass, M A Spence
Neurology|April 1, 1970
The movement disorder of battery refiner's disease (elemental mercury poisoning)R A Kark, J D Bullock, D C Poskanzer
Advances in Neurology|January 1, 1978
Evidence for a primary defect of lipoamide dehydrogenase in Friedreich's ataxiaR A Kark, M Rodriguez-Budelli, J P Blass
The American Journal of Cardiology|December 1, 1979
Cardiac conduction in the Kearns-Sayre syndrome (a neuromuscular disorder associated with progressive external ophthalmoplegia and pigmentary retinopathy). Report of 2 cases and review of 17 published casesN K Roberts, J K Perloff, R A Kark
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Neurology|January 1, 1979
Pyruvate dehydrogenase deficiency in spinocerebellar degenerationsR A Kark, M Rodriguez-Budelli
Muscle & Nerve|January 1, 1981
Multiple genotypes, multiple phenotypes, and partial defectsR A Kark, D M Becker
Neurology|July 1, 1979
Clinical correlations of partial deficiency of lipoamide dehydrogenaseR A Kark, M M Rodriguez-Budelli
Neurology|March 1, 1981
Double-blind, triple-crossover trial of low doses of oral physostigmine in inherited ataxiasR A Kark, M M Budelli, R Wachsner
Annals of Neurology|May 1, 1981
Retraction: reduced enzyme activity in hereditary ataxiaR A Kark, D M Becker, S Perlman
Journal of Neurochemistry|December 1, 1980
Effects of denervation and simple disuse on rates of oxidation and on activities of four mitochondrial enzymes in type I muscleP M Nemeth, D Meyer, R A Kark
Neurology|January 1, 1977
Physostigmine in familial ataxiasR A Kark, J P Blass, M A Spence
Neurology|April 1, 1970
The movement disorder of battery refiner's disease (elemental mercury poisoning)R A Kark, J D Bullock, D C Poskanzer
Advances in Neurology|January 1, 1978
Evidence for a primary defect of lipoamide dehydrogenase in Friedreich's ataxiaR A Kark, M Rodriguez-Budelli, J P Blass
The American Journal of Cardiology|December 1, 1979
Cardiac conduction in the Kearns-Sayre syndrome (a neuromuscular disorder associated with progressive external ophthalmoplegia and pigmentary retinopathy). Report of 2 cases and review of 17 published casesN K Roberts, J K Perloff, R A Kark
Pageof 3