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J S O'Brien

Showing results (1-10 of 202) with videos related to

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The New England Journal of Medicine|October 31, 1974
Editorial: Synthetic defect in ganglioside metabolismJ S O'Brien
American Journal of Human Genetics|November 1, 1978
Suggestions for a nomenclature for the GM2 gangliosidoses making certain (possibly unwarrantable) assumptionsJ S O'Brien
Italian Journal of Neurological Sciences|August 1, 1981
Ganglioside storage diseases: an updated reviewJ S O'Brien
Advances in Human Genetics|January 1, 1972
Ganglioside storage diseasesJ S O'Brien
Birth Defects Original Article Series|January 1, 1975
GM1 gangliosidosis: a progress reportJ S O'Brien
Clinical Genetics|July 1, 1978
The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiencyJ S O'Brien
California Medicine|September 1, 1971
Neurology: prenatal diagnosis of inherited neurologic diseasesJ S O'Brien
Progress in Clinical and Biological Research|January 1, 1977
Pitfalls in the prenatal diagnosis of Tay-Sachs diseaseJ S O'Brien
The British Journal of Addiction to Alcohol and Other Drugs|September 1, 1972
Operant behavior of a chronic alcoholic under fixed ratio and fixed interval schedules of reinforcement using alcohol as a reinforcerJ S O'Brien
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1972
Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patientsJ S O'Brien
Pageof 21

Showing results (1-10 of 202) with videos related to

Sort By:
Pageof 21
The New England Journal of Medicine|October 31, 1974
Editorial: Synthetic defect in ganglioside metabolismJ S O'Brien
American Journal of Human Genetics|November 1, 1978
Suggestions for a nomenclature for the GM2 gangliosidoses making certain (possibly unwarrantable) assumptionsJ S O'Brien
Italian Journal of Neurological Sciences|August 1, 1981
Ganglioside storage diseases: an updated reviewJ S O'Brien
Advances in Human Genetics|January 1, 1972
Ganglioside storage diseasesJ S O'Brien
Birth Defects Original Article Series|January 1, 1975
GM1 gangliosidosis: a progress reportJ S O'Brien
Clinical Genetics|July 1, 1978
The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiencyJ S O'Brien
California Medicine|September 1, 1971
Neurology: prenatal diagnosis of inherited neurologic diseasesJ S O'Brien
Progress in Clinical and Biological Research|January 1, 1977
Pitfalls in the prenatal diagnosis of Tay-Sachs diseaseJ S O'Brien
The British Journal of Addiction to Alcohol and Other Drugs|September 1, 1972
Operant behavior of a chronic alcoholic under fixed ratio and fixed interval schedules of reinforcement using alcohol as a reinforcerJ S O'Brien
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1972
Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patientsJ S O'Brien
Pageof 21