Masanori Nakagawa

发表

Mitochondrial myopathy and familial thiamine deficiency

E. Naito, M. Osame, I. Higuchi, 2000, Muscle & nerve.

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13–15

H. Utsumi, H. Takashima, Hajime Tanaka, 2000, Annals of neurology.

An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy

K. Arimura, M. Osame, I. Higuchi, 2000, Muscle & nerve.

Caveolin‐3 and sarcoglycans in the vacuolar myopathies and centronuclear myopathy

M. Osame, I. Higuchi, M. Inose, 1999, Muscle & nerve.

Immunohistochemistry of the monkey retina with a monoclonal antibody against subunit V of cytochrome c oxidase

I. Higuchi, Masanori Nakagawa, Yasushi Isashiki, 1991, Acta ophthalmologica.

Detection of HTLV‐I provirus by in situ polymerase chain reaction in mononuclear inflammatory cells in skeletal muscle of viral carriers with polymyositis

K. Arimura, M. Nakagawa, S. Izumo, 1995, Muscle & nerve.

A case of paternally inherited congenital myotonic dystrophy.

T. Miki, M. Nakagawa, T. Miki, 1994, Journal of medical genetics.

HTLV-I-associated myelopathy (HAM)/tropical spastic paraparesis (TSP) with amyotrophic lateral sclerosis-like manifestations.

S. Akiba, K. Arimura, M. Nakagawa, 2000, Journal of neurovirology.

Nationwide survey of neurologic manifestations of acquired immunodeficiency syndrome in Japan.

M. Nakagawa, M. Osame, H. Sugita, 1997, Internal medicine.

A hemophiliac with human immunodeficiency virus (HIV)-1-associated dementia complex.

K. Arimura, M. Osame, Y. Maruyama, 1995, Internal medicine.

HTLV-I-associated myelopathy: analysis of 213 patients based on clinical features and laboratory findings.

K. Arimura, M. Nakagawa, S. Izumo, 1995, Journal of neurovirology.

Phylogenetic subgroups of human T cell lymphotropic virus (HTLV) type I in the tax gene and their association with different risks for HTLV-I-associated myelopathy/tropical spastic paraparesis.

M. Nakagawa, M. Yamashita, S. Izumo, 2000, The Journal of infectious diseases.

Interferon-alpha is effective in HTLV-I-associated myelopathy

Y. Itoyama, M. Nakagawa, S. Izumo, 1996, Neurology.

Therapeutic trials in 200 patients with HTLV-I-associated myelopathy/ tropical spastic paraparesis.

K. Arimura, M. Nakagawa, S. Izumo, 1996, Journal of neurovirology.

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.

Familial mitochondrial encephalomyopathy with deaf‐mutism, ophthalmoplegia and leukodvstrophy.

Y. Isashiki, M. Osame, I. Higuchi, 1995, Acta neurologica Scandinavica.

Diagnostic significance of tau protein in cerebrospinal fluid from patients with corticobasal degeneration or progressive supranuclear palsy

K. Nakashima, H. Arai, K. Wada, 2001, Journal of the Neurological Sciences.

HAM/TSP: recent perspectives in Japan.

K. Arimura, M. Nakagawa, S. Izumo, 1996, Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association.

Germanium myopathy: clinical and experimental pathological studies

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

Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.

M. Nakagawa, N. Ohba, Y. Isashiki, 1998, Acta ophthalmologica Scandinavica.

Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.

K. Arimura, M. Nakagawa, M. Osame, 1997, Internal medicine.

SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma

M Nakagawa, J. Lupski, C. Boerkoel, 2004, Neurology.

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

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

Recent studies on the epidemiology, clinical features and pathogenic mechanisms of HTLV-I associated myelopathy (HAM/TSP) and other diseases associated to HTLV.

K. Arimura, M. Nakagawa, S. Izumo, 1997, Journal of neurovirology.

Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex

M. Nakagawa, H. Yoshikawa, S. Izumo, 2004, Acta Neuropathologica.

Identification of a novel mutation (Tyr1081Ter) in sisters with hereditary component C3 deficiency and SLE‐like symptoms

H. Takashima, M. Osame, W. Matsuyama, 2001, Human mutation.