T. Nishimura

发表

Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy

N. Hattori, H. Fujimura, K. Inui, 1999, Neuromuscular Disorders.

New mutation of the myelin Po gene in a pedigree of Charcot-Marie-Tooth neuropathy type 1

K. Hayasaka, M. Takahashi, M. Kaido, 1993 .

A clinicopathological study of a patient with familial amyotrophic lateral sclerosis associated with a two base pair deletion in the copper/zinc superoxide dismutase (SOD1) gene

N. Hattori, S. Sakoda, T. Yanagihara, 1997, Acta Neuropathologica.

Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot‐Marie‐Tooth disease type 1A

S. Sakoda, Y. Nakatsuji, K. Hayasaka, 1994, Annals of neurology.

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP

G. Sobue, H. Kiyosawa, A. Ohnishi, 1997, Human Genetics.

Accumulation of peripheral myelin protein 22 in onion bulbs and Schwann cells of biopsied nerves from patients with Charcot-Marie-Tooth disease type 1A

S. Sakoda, T. Yanagihara, H. Fujimura, 1996, Acta Neuropathologica.

Familial amyloid polyneuropathy associated with transthyretin Gly42 mutation: a quantitative light and electron microscopic study of the peripheral nervous system

T. Yanagihara, S. Yorifuji, H. Fujimura, 2004, Acta Neuropathologica.

Alzheimer-type pathology in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

T. Yanagihara, S. Yorifuji, H. Fujimura, 1996, Acta Neuropathologica.

Molecular cloning of a novel putative G protein‐coupled receptor (GPCR21) which is expressed predominantly in mouse central nervous system

Y. Saeki, H. Fujimura, Y. Nagai, 1993, FEBS letters.

Cation binding at the node of Ranvier in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies

S. Sakoda, T. Yanagihara, H. Fujimura, 1996, Acta Neuropathologica.

New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.

K. Hayasaka, M. Takahashi, M. Kaido, 1993, Biochemistry and molecular biology international.

Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex

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

Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies

K. Arimura, M. Nakagawa, S. Izumo, 1995, Journal of the Neurological Sciences.

Cloning and expression of myelin-associated oligodendrocytic basic protein. A novel basic protein constituting the central nervous system myelin.

S. Sakoda, Y. Yamamoto, T. Yanagihara, 1994, The Journal of biological chemistry.

Hereditary neuropathy with liability to pressure palsies: distinguishing clinical and electrophysiological features among patients with multiple entrapment neuropathy

J. Kimura, R. Kaji, H. Yoshikawa, 1996, Journal of the Neurological Sciences.

S. Sakoda, T. Yanagihara, H. Fujimura, 1997, Acta Neuropathologica.

A clinicopathological study of a patient with familial amyotrophic lateral sclerosis associated with a two base pair deletion in the copper/zinc superoxide dismutase (SOD1) gene.

N. Hattori, S. Sakoda, T. Yanagihara, 1997, Acta Neuropathologica.

Cumulative white matter changes in the gerbil brain under chronic cerebral hypoperfusion

T. Kudo, M. Takeda, T. Nishimura, 2004, Acta Neuropathologica.