R. Namba

发表

GM1 gangliosidosis in adults: Clinical and molecular analysis of 16 Japanese patients

Yoshiyuki Suzuki, N. Yanagisawa, Kunihiro Yoshida, 1992, Annals of neurology.

Mitochondrial encephalomyopathy (MELAS): Pathological study and successful therapy with coenzyme Q10 and idebenone

S. Kuroda, T. Shirabe, R. Namba, 1989, Journal of the Neurological Sciences.

Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.

M. Nishibori, S. Terada, Y. Tanaka, 2001, Archives of neurology.

Superoxide dismutase and free radicals in sporadic amyotrophic lateral sclerosis: relationship to clinical data

Keiko Sato, M. Kibata, A. Mori, 1995, Journal of the Neurological Sciences.

Selective colocalization of transglutaminase-like activity in ubiquitinated intranuclear inclusions of hereditary dentatorubral-pallidoluysian atrophy

M. Shoji, H. Kamada, Keiko Sato, 2002, Brain Research.

A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studies

M. Taniike, K. Inui, H. Tsukamoto, 1990, Journal of Neurology.

Variability and heterogeneity in Alzheimer's disease with cotton wool plaques: a clinicopathological study of four autopsy cases

F. Checler, T. Ishihara, S. Terada, 2003, Acta Neuropathologica.

A family of familial hypercholesterolemia with cerebral infarction and without coronary heart disease An unusual case with corneal opacity, polyneuropathy and carpal tunnel syndrome in the family: Therapy with probucol and tocopherol nicotinate

H. Mabuchi, K. Kajinami, M. Kibata, 1991, Journal of Neurological Sciences.

The influence of long-term treatment with povidone-iodine on thyroid function.

S. Kawahara, R. Namba, K. Nobukuni, 1997, Dermatology.

Free radicals, lipid peroxides and antioxidants in blood of patients with myotonic dystrophy

Keiko Sato, Jiankang Liu, S. Miyata, 1995, Journal of Neurology.

Unique cerebellar-cerebral form of autosomal recessive ataxia.

E. Matsubara, M. Shoji, I. Nagano, 2005, The Tohoku journal of experimental medicine.

Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)

S. Tsuji, E. Uyama, Hajime Tanaka, 2001, Journal of Human Genetics.

Reduction rate of body mass index predicts prognosis for survival in amyotrophic lateral sclerosis: A multicenter study in Japan

Y. Kuroiwa, Toshio Shimizu, T. Komori, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[A case of mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)--treatment with coenzyme Q10 and idebenone].

S. Kuroda, R. Namba, Y. Ihara, 1988, Rinsho shinkeigaku = Clinical neurology.

Cerebrospinal fluid corticotropin-releasing hormone in neurodegenerative diseases: reduction in spinocerebellar degeneration.

K. Urakami, K. Hashimoto, S. Suemaru, 1995, Life sciences.

Autonomic nervous disorder in motor neuron disease: a study of advanced stage patients.

K. Kashihara, K. Morimoto, R. Namba, 1995, Internal medicine.

Optic neuritis: Studies on the epidemiology and the cerebrospinal fluid

S. Otsuki, H. Fukui, R. Namba, 1977 .

[Relation between cerebral white matter damage on CT and MRI and clinical data in DRPLA (pseudo-Huntington form)].

S. Kuroda, R. Namba, K. Nobukuni, 1991, Rinshō shinkeigaku Clinical neurology.