Y. Yamada

发表

Lack of association between neuroleptic malignant syndrome and polymorphisms in the 5-HT1A and 5-HT2A receptor genes.

T. Hanihara, K. Kosaka, C. Kawanishi, 1998, The American journal of psychiatry.

6‐Pyruvoyl‐tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms: A clinical and molecular study

T. Hanihara, H. Osaka, K. Kosaka, 1997, Movement disorders : official journal of the Movement Disorder Society.

Mutations in the Proteolipid Protein Gene in Japanese Families with Pelizaeus-Merzbacher Disease

H. Osaka, K. Kosaka, C. Kawanishi, 1997, Neurology.

A duplicated PLP gene causing Pelizaeus-Merzbacher disease detected by comparative multiplex PCR.

H. Osaka, K. Kosaka, C. Kawanishi, 1996, American journal of human genetics.

Novel acceptor splice site mutation in the invariant AG of intron 6 of alpha-galactosidase A gene, causing Fabry disease. Mutations in brief no. 146. Online.

H. Osaka, K. Kosaka, C. Kawanishi, 1998, Human mutation.

Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river.

K. Kosaka, C. Kawanishi, E. Iseki, 1998, Neurological research.

Effects of metallic detergents on the antioxidant and antiwear properties of zinc dialkyldithiophosphates

J. Igarashi, K. Inoue, Y. Yamada, 1992 .

Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males.

H. Osaka, K. Kosaka, C. Kawanishi, 1995, Biochemical and biophysical research communications.

A new restriction-site polymorphism in the human proteolipid protein gene.

H. Osaka, K. Kosaka, C. Kawanishi, 2008, Clinical genetics.

Pelizaeus‐Merzbacher disease: A novel mutation in the 5′‐untranslated region of the proteolipid protein gene

H. Osaka, Kyoko Suzuki, K. Kosaka, 1996, Human mutation.

New point mutation (R301X) of the alpha-galactosidase A gene causing Fabry disease.

T. Hanihara, H. Osaka, C. Kawanishi, 1995, Human mutation.

Oxidation stability of synthetic lubricants

Y. Yamada, H. Nakanishi, K. Onodera, 1997 .

Neuroleptic malignant syndrome and hydroxylase gene mutations: no association with CYP2D6A or CYP2D6B

T. Hanihara, K. Kosaka, C. Kawanishi, 1997, Psychiatric genetics.

[MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].

T. Hanihara, H. Osaka, S. Kawamoto, 1992, No to shinkei = Brain and nerve.

Clinical and genetic evaluation of Japanese autosomal dominant cerebellar ataxias; is Machado-Joseph disease common in the Japanese?

T. Hanihara, K. Kosaka, K. Iwabuchi, 1996, Journal of neurology, neurosurgery, and psychiatry.