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Journal of the Neurological Sciences
|
December 27, 2016
An AOA2 patient with a novel compound heterozygous SETX frame shift mutations
Emi Motokura, Toru Yamashita, Yoshiaki Takahashi, et al.
Neuromuscular Disorders : NMD
|
May 8, 2012
Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study
Yukie Inamori, Itsuro Higuchi, Teruhiko Inoue, et al.
Muscle & Nerve
|
November 1, 2005
Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency
Keiko Higashi, Itsuro Higuchi, Takahito Niiyama, et al.
BMC Neurology
|
September 2, 2018
Peripheral neuropathy in a case with CADASIL: a case report
Yusuke Sakiyama, Eiji Matsuura, Yoshimitsu Maki, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 12, 2012
Inflammatory radiculoneuropathy in an ALS4 patient with a novel SETX mutation
Toru Saiga, Takahisa Tateishi, Takako Torii, et al.
Brain & Development
|
September 5, 2018
X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illness
Noriko Nishikura, Takanori Yamagata, Takao Morimune, et al.
Multiple Sclerosis and Related Disorders
|
April 2, 2025
Visual evoked potential in myelin oligodendrocyte glycoprotein antibody-associated disease
Chikashi Yano, Eiji Matsuura, Tomonori Nakamura, et al.
Journal of Neurology
|
February 24, 2021
Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan
Rino Inada, Makito Hirano, Nobuyuki Oka, et al.
Frontiers in Neurology
|
September 5, 2022
Multi-type <i>RFC1</i> repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy
Jun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Journal of Human Genetics
|
December 8, 2025
Respiratory complex I deficiency caused by a novel multi-exonic PUS1 deletion
Jun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 101) with videos related to
Sort By:
Page
of 11
Journal of the Neurological Sciences
|
December 27, 2016
An AOA2 patient with a novel compound heterozygous SETX frame shift mutations
Emi Motokura, Toru Yamashita, Yoshiaki Takahashi, et al.
Neuromuscular Disorders : NMD
|
May 8, 2012
Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study
Yukie Inamori, Itsuro Higuchi, Teruhiko Inoue, et al.
Muscle & Nerve
|
November 1, 2005
Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency
Keiko Higashi, Itsuro Higuchi, Takahito Niiyama, et al.
BMC Neurology
|
September 2, 2018
Peripheral neuropathy in a case with CADASIL: a case report
Yusuke Sakiyama, Eiji Matsuura, Yoshimitsu Maki, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 12, 2012
Inflammatory radiculoneuropathy in an ALS4 patient with a novel SETX mutation
Toru Saiga, Takahisa Tateishi, Takako Torii, et al.
Brain & Development
|
September 5, 2018
X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illness
Noriko Nishikura, Takanori Yamagata, Takao Morimune, et al.
Multiple Sclerosis and Related Disorders
|
April 2, 2025
Visual evoked potential in myelin oligodendrocyte glycoprotein antibody-associated disease
Chikashi Yano, Eiji Matsuura, Tomonori Nakamura, et al.
Journal of Neurology
|
February 24, 2021
Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan
Rino Inada, Makito Hirano, Nobuyuki Oka, et al.
Frontiers in Neurology
|
September 5, 2022
Multi-type <i>RFC1</i> repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy
Jun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Journal of Human Genetics
|
December 8, 2025
Respiratory complex I deficiency caused by a novel multi-exonic PUS1 deletion
Jun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Page
of 11