Z. Matsuyama

发表

Characteristic magnetic resonance imaging findings in spinocerebellar ataxia 6.

S. Nakamura, Y. Murata, H. Kawakami, 1998, Archives of neurology.

Spinocerebellar ataxia type 6: MRI of three Japanese patients

J. Satoh, H. Kawakami, Z. Matsuyama, 1998, Neuroradiology.

Polyglutamine repeats of spinocerebellar ataxia 6 impair the cell-death-preventing effect of CaV2.1 Ca2+ channel—loss-of-function cellular model of SCA6

J. Black, Y. Mori, T. Inuzuka, 2004, Neurobiology of Disease.

Spinocerebellar ataxia type 6 in relation to CAG repeat length

H. Kawakami, M. Nishimura, Z. Matsuyama, 1999, Acta neurologica Scandinavica.

Marked asymmetry of putaminal pathology in an MSA‐P patient with Pisa syndrome

T. Inuzuka, I. Hozumi, Z. Matsuyama, 2004, Movement disorders : official journal of the Movement Disorder Society.

The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1)

H. Kawakami, Z. Matsuyama, Y. Izumi, 1999, Journal of medical genetics.

Association between metallothionein genes polymorphisms and sporadic amyotrophic lateral sclerosis in a Japanese population

Y. Hayashi, T. Inuzuka, I. Hozumi, 2006, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

The e V ect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 ( SCA 1 )

H. Kawakami, Z. Matsuyama, Shigenobu Nakamura, 1999 .

Reduced Voltage Sensitivity of Activation of P/Q-Type Ca2+ Channels is Associated with the Ataxic Mouse MutationRolling Nagoya (tgrol )

C. Fletcher, N. Copeland, N. Jenkins, 2000, The Journal of Neuroscience.

Clinical effects of probiotic Bifidobacterium longum BB536 on immune function and intestinal microbiota in elderly patients receiving enteral tube feeding.

Z. Matsuyama, N. Iwabuchi, Jin-zhong Xiao, 2013, JPEN. Journal of parenteral and enteral nutrition.

[A case of idiopathic superficial siderosis of the central nervous system].

S. Nakamura, S. Yamaguchi, Z. Matsuyama, 1994, No to shinkei = Brain and nerve.

A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNALeu(UUR) 3254C-to-G

T. Kawarai, H. Kawakami, T. Kohriyama, 1997, Neurology.

Selective cauda equina hypertrophy with idiopathic inflammation

Y. Hayashi, Hitoshi Takahashi, T. Inuzuka, 2008, Muscle & nerve.

A novel insertion mutation of acetazolamide-responsive episodic ataxia in a Japanese family

T. Inuzuka, I. Hozumi, Z. Matsuyama, 2003, Journal of the Neurological Sciences.

Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease.

G. Sobue, I. Nishino, M. Seto, 1995, Human molecular genetics.

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).

H. Kawakami, M. Nishimura, Z. Matsuyama, 1997, Human molecular genetics.

Variation in the number of CAG repeats in the Machado–Joseph disease gene (MJD1) in the Japanese population

H. Kawakami, Z. Matsuyama, H. Maruyama, 1999, Journal of the Neurological Sciences.

Direct Alteration of the P/Q-Type Ca2+ Channel Property by Polyglutamine Expansion in Spinocerebellar Ataxia 6

Y. Mori, K. Imoto, H. Kawakami, 1999, The Journal of Neuroscience.

Characteristic magnetic resonance imaging findings in spinocerebellar ataxia 6.

T. Kohriyama, Z. Matsuyama, Y. Mimori, 1998, Archives of neurology.

Autopsy case of primary central nervous system lymphoma with subacute mental deterioration and progressive white matter lesions in an elderly man

N. Yamakita, T. Inuzuka, I. Hozumi, 2003 .