J Tohyama - JoVE Visualize

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Annals of Neurology|June 1, 1992

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathyY Goto, M Tojo, J Tohyama, et al.

Clinical EEG (Electroencephalography)|April 1, 1997

Epileptic seizures and event-related potentials (P300) in childhood partial epilepsiesY Naganuma, T Konishi, K Hongou, et al.

Neuroradiology|January 1, 1993

Intracranial calcification in siblings with nephrogenic diabetes insipidus: CT and MRIJ Tohyama, M Inagaki, T Koeda, et al.

American Journal of Medical Genetics|March 13, 1995

Multiple epiphyseal dysplasia with small head, congenital nystagmus, hypoplasia of corpus callosum, and leukonychia totalis: a variant of Lowry-Wood syndrome?T Yamamoto, J Tohyama, T Koeda, et al.

Nucleic Acids Research|July 10, 1981

Inhibitory effects of 3'deoxycytidine 5'-triphosphate and 3'-deoxyuridine 5'-triphosphate on DNA-dependent RNA polymerases I and II purified from Dictyostelium discoideum cellsM Saneyoshi, J Tohyama, C Nakayama, et al.

Human Genetics|April 1, 1996

Acid alpha-glucosidase deficiency: identification and expression of a missense mutation (S529V) in a Japanese adult phenotypeH Tsunoda, T Ohshima, J Tohyama, et al.

Neurology|July 1, 1992

Clinical and neuroradiologic findings of congenital hydrocephalus in infant born to mother with HTLV-I-associated myelopathyJ Tohyama, H Kawahara, M Inagaki, et al.

Brain & Development|March 1, 1997

Event-related potentials (P300) and EEG activity in childhood partial epilepsyY Naganuma, T Konishi, K Hongou, et al.

Human Molecular Genetics|June 22, 2000

Paradoxical influence of acid beta-galactosidase gene dosage on phenotype of the twitcher mouse (genetic galactosylceramidase deficiency)J Tohyama, M T Vanier, K Suzuki, et al.

Human Molecular Genetics|May 24, 2001

A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouseJ Matsuda, M T Vanier, Y Saito, et al.

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Showing results (11-20 of 40) with videos related to

Sort By:

Pageof 4

Annals of Neurology|June 1, 1992

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathyY Goto, M Tojo, J Tohyama, et al.

Clinical EEG (Electroencephalography)|April 1, 1997

Epileptic seizures and event-related potentials (P300) in childhood partial epilepsiesY Naganuma, T Konishi, K Hongou, et al.

Neuroradiology|January 1, 1993

Intracranial calcification in siblings with nephrogenic diabetes insipidus: CT and MRIJ Tohyama, M Inagaki, T Koeda, et al.

American Journal of Medical Genetics|March 13, 1995

Multiple epiphyseal dysplasia with small head, congenital nystagmus, hypoplasia of corpus callosum, and leukonychia totalis: a variant of Lowry-Wood syndrome?T Yamamoto, J Tohyama, T Koeda, et al.

Nucleic Acids Research|July 10, 1981

Inhibitory effects of 3'deoxycytidine 5'-triphosphate and 3'-deoxyuridine 5'-triphosphate on DNA-dependent RNA polymerases I and II purified from Dictyostelium discoideum cellsM Saneyoshi, J Tohyama, C Nakayama, et al.

Human Genetics|April 1, 1996

Acid alpha-glucosidase deficiency: identification and expression of a missense mutation (S529V) in a Japanese adult phenotypeH Tsunoda, T Ohshima, J Tohyama, et al.

Neurology|July 1, 1992

Clinical and neuroradiologic findings of congenital hydrocephalus in infant born to mother with HTLV-I-associated myelopathyJ Tohyama, H Kawahara, M Inagaki, et al.

Brain & Development|March 1, 1997

Event-related potentials (P300) and EEG activity in childhood partial epilepsyY Naganuma, T Konishi, K Hongou, et al.

Human Molecular Genetics|June 22, 2000

Paradoxical influence of acid beta-galactosidase gene dosage on phenotype of the twitcher mouse (genetic galactosylceramidase deficiency)J Tohyama, M T Vanier, K Suzuki, et al.

Human Molecular Genetics|May 24, 2001

A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouseJ Matsuda, M T Vanier, Y Saito, et al.

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