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Yaeko Ichikawa

Showing results (11-20 of 38) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 15, 2026
Eye-hand coordination patterns of progressive and consistent micrographia in Parkinson's disease: neurophysiological correlatesNaoki Kotsuki, Shin-Ichi Tokushige, Satomi Inomata-Terada, et al.
Neurogenetics|January 27, 2011
Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1Hiroyuki Ishiura, Yoko Fukuda, Jun Mitsui, et al.
Human Molecular Genetics|December 3, 2003
Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activityYutaka Ohsawa, Haruhiro Toko, Masashi Katsura, et al.
Internal Medicine (Tokyo, Japan)|June 11, 2019
Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich AtaxiaHiroya Naruse, Yuji Takahashi, Hiroyuki Ishiura, et al.
Internal Medicine (Tokyo, Japan)|January 17, 2012
Culture-negative brain abscess with Streptococcus intermedius infection with diagnosis established by direct nucleotide sequence analysis of the 16s ribosomal RNA geneNaoko Saito, Ayumi Hida, Yuri Koide, et al.
Internal Medicine (Tokyo, Japan)|January 12, 2018
CV2/CRMP5-antibody-related Paraneoplastic Optic Neuropathy Associated with Small-cell Lung CancerMasanori Nakajima, Ayumi Uchibori, Yuki Ogawa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlationsAkatsuki Kubota, Ayumi Hida, Yaeko Ichikawa, et al.
Journal of the Neurological Sciences|June 22, 2013
Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1Yaeko Ichikawa, Hiroyuki Ishiura, Jun Mitsui, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Novel SIL1 mutations and exclusion of functional candidate genes in Marinesco-Sjögren syndromeAnna-Kaisa Anttonen, Eija Siintola, Lisbeth Tranebjaerg, et al.
Bioinformatics (Oxford, England)|November 12, 2013
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencingKoichiro Doi, Taku Monjo, Pham H Hoang, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 15, 2026
Eye-hand coordination patterns of progressive and consistent micrographia in Parkinson's disease: neurophysiological correlatesNaoki Kotsuki, Shin-Ichi Tokushige, Satomi Inomata-Terada, et al.
Neurogenetics|January 27, 2011
Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1Hiroyuki Ishiura, Yoko Fukuda, Jun Mitsui, et al.
Human Molecular Genetics|December 3, 2003
Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activityYutaka Ohsawa, Haruhiro Toko, Masashi Katsura, et al.
Internal Medicine (Tokyo, Japan)|June 11, 2019
Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich AtaxiaHiroya Naruse, Yuji Takahashi, Hiroyuki Ishiura, et al.
Internal Medicine (Tokyo, Japan)|January 17, 2012
Culture-negative brain abscess with Streptococcus intermedius infection with diagnosis established by direct nucleotide sequence analysis of the 16s ribosomal RNA geneNaoko Saito, Ayumi Hida, Yuri Koide, et al.
Internal Medicine (Tokyo, Japan)|January 12, 2018
CV2/CRMP5-antibody-related Paraneoplastic Optic Neuropathy Associated with Small-cell Lung CancerMasanori Nakajima, Ayumi Uchibori, Yuki Ogawa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlationsAkatsuki Kubota, Ayumi Hida, Yaeko Ichikawa, et al.
Journal of the Neurological Sciences|June 22, 2013
Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1Yaeko Ichikawa, Hiroyuki Ishiura, Jun Mitsui, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Novel SIL1 mutations and exclusion of functional candidate genes in Marinesco-Sjögren syndromeAnna-Kaisa Anttonen, Eija Siintola, Lisbeth Tranebjaerg, et al.
Bioinformatics (Oxford, England)|November 12, 2013
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencingKoichiro Doi, Taku Monjo, Pham H Hoang, et al.
Pageof 4