M. Suehara

发表

Localized scleroderma associated with progressing ischemic stroke

N. Kanzato, T. Matsuzaki, Y. Komine, 1999, Journal of the Neurological Sciences.

Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan

K. Arimura, R. Hirano, H. Takashima, 2009, Journal of Human Genetics.

The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patients.

S. Suwazono, M. Nakagawa, H. Takashima, 2018, Intractable & rare diseases research.

PS-19-8 Isaacs syndrome as a channelopathy of voltage dependent potassium channel

Masaki Kameyama, Yoshito Sonoda, Osamu Watanabe, 1995 .

Serum of Isaacs' syndrome suppresses potassium channels in PC‐12 cell lines

K. Arimura, M. Kameyama, M. Osame, 1996, Muscle & nerve.

Germline mosaicism of MPZ Gene in Dejerine-Sottas syndrome (HMSN III) associated with hereditary stomatocytosis

M. Nakagawa, S. Izumo, H. Takashima, 1999, Neuromuscular Disorders.

Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1

J. Terwilliger, M. Nakagawa, H. Takashima, 1999, Neuromuscular Disorders.

Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant Connexin 32 (GJB1)

M. Nakagawa, H. Takashima, T. Moritoyo, 2001, Journal of Human Genetics.

Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease

M. Osame, I. Higuchi, A. Saito, 2002, Muscle & nerve.

Miyoshi myopathy patients with novel 5' splicing donor site mutations showed different dysferlin immunostaining at the sarcolemma

M. Nakagawa, Toshiaki Takahashi, M. Aoki, 2002, Acta Neuropathologica.

Immunological abnormality in patients with lysinuric protein intolerance

T. Moritoyo, M. Osame, Y. Yoshida, 1995, Journal of the Neurological Sciences.

Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Osame, I. Higuchi, 2006, Muscle & nerve.

Pathological changes in skeletal muscle in HTLV-I-associated myelopathy

K. Arimura, M. Osame, I. Higuchi, 1992, Journal of the Neurological Sciences.

Histopathological analysis of four autopsy cases of HTLV-I-associated myelopathy/tropical spastic paraparesis: inflammatory changes occur simultaneously in the entire central nervous system

Y. Isashiki, T. Moritoyo, M. Osame, 2000, Acta Neuropathologica.

Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene

M. Nakagawa, H. Takashima, K. Goto, 2001, Journal of the Neurological Sciences.

Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, T. Hashiguchi, 2003, Acta Neuropathologica.

Lambert–Eaton myasthenic syndrome with ophthalmoparesis and pseudoblepharospasm

M. Motomura, N. Kanzato, M. Suehara, 1999, Muscle & nerve.

Frameshift mutation in the collagen VI gene causes Ullrich's disease

K. Arimura, M. Nakagawa, T. Hashiguchi, 2001, Annals of neurology.

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene

K. Arimura, M. Nakagawa, R. Hirano, 2006, Neurogenetics.

Persistent hiccups and vomiting with multiple cranial nerve palsy in a case of zoster sine herpete.

S. Suwazono, R. Nakachi, M. Suehara, 2014, Internal medicine.

A new type of hereditary motor and sensory neuropathy linked to chromosome 3

K. Arimura, M. Nakagawa, S. Izumo, 1997, Annals of neurology.

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, M. Osame, 2003, Neuromuscular Disorders.

Collagen VI deficiency in Ullrich's disease

K. Arimura, M. Nakagawa, M. Osame, 2001, Annals of neurology.

Association of a particular amino acid sequence of the HLA‐DR β1 chain with HTLV‐I‐associated myelopathy

T. Tabira, K. Tokunaga, M. Nishizawa, 1990, European journal of immunology.

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease

I. Maruyama, K. Arimura, M. Nakagawa, 2002, Acta Neuropathologica.

[Clinical manifestations of 5 patients with idiopathic paroxysmal kinesigenic choreoathetosis].

S. Suwazono, R. Nakachi, M. Suehara, 2016, Rinsho shinkeigaku = Clinical neurology.

INFLAMMATORY CHANGES IN HAM/TSP OCCUR SIMULTANEOUSLY IN THE ENTIRE CNS: HISTOPATHOLOGIC ANALYSIS OF FOUR AUTOPSY CASES

S. Izumo, T. Moritoyo, M. Osame, 1999 .

Antibodies to potassium channels pc12 in serum of Isaacs' syndrome: Western blot and immunohistochemical studies

I. Kitajima, K. Arimura, M. Osame, 1997, Muscle & nerve.

Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation

H. Takashima, T. Tokashiki, A. Yoshimura, 2023, Frontiers in neurology.

Three‐tesla magnetic resonance neurography of the brachial plexus in cervical radiculopathy

S. Suwazono, M. Suehara, Takeshi Yoshida, 2015, Muscle & nerve.

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects.

M. Miyata, M. Nakagawa, M. Osame, 1995, Circulation.

Epidemiology of progressive muscular dystrophy in Okinawa, Japan. Classification with molecular biological techniques.

M. Osame, K. Nakahara, I. Higuchi, 1991, Neuroepidemiology.

Gap junction protein beta 1 (GJB1) mutations and central nervous system symptoms in X‐linked Charcot–Marie–Tooth disease

K. Arimura, M. Nakagawa, H. Takashima, 2003, Acta neurologica Scandinavica.

Germanium myopathy: clinical and experimental pathological studies

M. Nakagawa, S. Izumo, M. Osame, 2004, Acta Neuropathologica.

A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths

S. Sakoda, M. Nakagawa, S. Izumo, 1999, Neurology.