S. Shimoda-Matsubayashi

Mitochondrial dysfunction in parkinson's disease

N. Hattori, H. Yoshino, Y. Mizuno, 1998, Annals of neurology.

Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's disease.

Y. Mizuno, H. Matsumine, Y. Nakagawa-Hattori, 1996, Biochemical and biophysical research communications.

Structural Dimorphism in the Mitochondrial Targeting Sequence in the Human Manganese Superoxide Dismutase Gene: A Predictive Evidence for Conformational Change to Influence Mitochondrial Transport and a Study of Allelic Association in Parkinson's Disease: Volume226,Number 2 (1996), pages 561–565:

Y. Mizuno, H. Matsumine, Y. Nakagawa-Hattori, 1996 .

Serum creatine kinase is elevated in patients with Parkinson's disease: a case controlled study.

Y. Mizuno, S. Shimoda-Matsubayashi, H. Takubo, 2003, Parkinsonism & related disorders.

MRI findings in the mild type of mucopolysaccharidosis II (Hunter's syndrome)

N. Hattori, H. Sumie, S. Shimoda-Matsubayashi, 2004, Neuroradiology.

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27.

A A Schäffer, Y Mizuno, Y Yamamura, 1997, American journal of human genetics.

Mn SOD activity and protein in a patient with chromosome 6-linked autosomal recessive parkinsonism in comparison with Parkinson's disease and control

M. Chiba, A. Shinohara, T. Kondo, 1997, Neurology.

Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium

S. Tsuji, A. Schaffer, Y. Mizuno, 1998, Journal of Human Genetics.