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R Sakuta

Showing results (21-30 of 43) with videos related to

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Psychiatry and Clinical Neurosciences|June 1, 1995
Changes in the lymphocyte subsets during high dose immunoglobulin therapy for intractable childhood epilepsyH Shiihara, N Michihiro, R Sakuta, et al.
No to Hattatsu = Brain and Development|August 3, 1999
[Frequent convulsions in the post-eruptive stage of exanthem subitum]K Ojima, R Sakuta, A Kagaya, et al.
Internal Medicine (Tokyo, Japan)|September 1, 1994
A MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) mtDNA mutation that induces subacute dementia which mimicks Creutzfeldt-Jakob diseaseK Isozumi, Y Fukuuchi, K Tanaka, et al.
Journal of Child Neurology|April 1, 1993
A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndromeH Yoshinaga, T Ogino, S Ohtahara, et al.
The Japanese Journal of Psychiatry and Neurology|June 1, 1993
Studies of mitochondria DNA in progressive myoclonus epilepsy (PME) and a case of atypical MELAST Onuma, N Adachi, M Katoh, et al.
Neuromuscular Disorders : NMD|November 1, 1995
The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findingsM Ozawa, Y Goto, R Sakuta, et al.
No to Hattatsu = Brain and Development|March 1, 1990
[Immunoglobulin class and light chain type of oligoclonal bands in CSF in children with CNS infectious diseases]R Sakuta, K Hiyoshi, K Yanagida, et al.
No to Hattatsu = Brain and Development|February 24, 2001
[A novel allelic variation of serotonin transporter gene polymorphism in anorexia nervosa]M Narita, N Narita, M Tazoe, et al.
Pediatric Neurology|March 1, 1993
Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficienciesT Nagai, Y Tuchiya, Y Taguchi, et al.
Journal of the Neurological Sciences|August 1, 1994
Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)Y Hattori, Y Goto, R Sakuta, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Psychiatry and Clinical Neurosciences|June 1, 1995
Changes in the lymphocyte subsets during high dose immunoglobulin therapy for intractable childhood epilepsyH Shiihara, N Michihiro, R Sakuta, et al.
No to Hattatsu = Brain and Development|August 3, 1999
[Frequent convulsions in the post-eruptive stage of exanthem subitum]K Ojima, R Sakuta, A Kagaya, et al.
Internal Medicine (Tokyo, Japan)|September 1, 1994
A MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) mtDNA mutation that induces subacute dementia which mimicks Creutzfeldt-Jakob diseaseK Isozumi, Y Fukuuchi, K Tanaka, et al.
Journal of Child Neurology|April 1, 1993
A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndromeH Yoshinaga, T Ogino, S Ohtahara, et al.
The Japanese Journal of Psychiatry and Neurology|June 1, 1993
Studies of mitochondria DNA in progressive myoclonus epilepsy (PME) and a case of atypical MELAST Onuma, N Adachi, M Katoh, et al.
Neuromuscular Disorders : NMD|November 1, 1995
The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findingsM Ozawa, Y Goto, R Sakuta, et al.
No to Hattatsu = Brain and Development|March 1, 1990
[Immunoglobulin class and light chain type of oligoclonal bands in CSF in children with CNS infectious diseases]R Sakuta, K Hiyoshi, K Yanagida, et al.
No to Hattatsu = Brain and Development|February 24, 2001
[A novel allelic variation of serotonin transporter gene polymorphism in anorexia nervosa]M Narita, N Narita, M Tazoe, et al.
Pediatric Neurology|March 1, 1993
Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficienciesT Nagai, Y Tuchiya, Y Taguchi, et al.
Journal of the Neurological Sciences|August 1, 1994
Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)Y Hattori, Y Goto, R Sakuta, et al.
Pageof 5