Yoshikuni Mizuno

发表

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism

N. Hattori, H. Yoshino, H. Miyajima, 2005, Neurology.

Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q

T. Kondo, Y. Mizuno, H. Matsumine, 1998, Neurology.

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

B. Ghetti, K. Arima, R. Uitti, 2002, Neurology.

PARK9-LINKED PARKINSONISM IN EASTERN ASIA: MUTATION DETECTION IN ATP13A2 AND CLINICAL PHENOTYPE

N. Hattori, H. Yoshino, S. Kuwabara, 2008, 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.

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease.

K. Ohno, T. Ozawa, H. Ino, 1991, Biochemical and biophysical research communications.

Iron accumulation in the substantia nigra of autosomal recessive juvenile parkinsonism (ARJP).

N. Hattori, H. Mochizuki, Y. Mizuno, 2001, Parkinsonism & related disorders.

Mitochondrial complex I and II activities of lymphocytes and platelets in Parkinson's disease

H. Yoshino, Y. Mizuno, Y. Nakagawa-Hattori, 1992, Journal of neural transmission. Parkinson's disease and dementia section.

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.

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

N. Hattori, H. Yoshino, R. Rosales, 2004, Neurology.

Progress in the clinical and molecular genetics of familial parkinsonism

S. Minoshima, N. Shimizu, N. Hattori, 2000, Neurogenetics.

Accumulation of 4-hydroxynonenal-modified proteins in hippocampal CA1 pyramidal neurons precedes delayed neuronal damage in the gerbil brain

N. Hattori, K. Uchida, Y. Yamasaki, 2000, Neuroscience.

Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation.

Y. Mizuno, S. Kuzuhara, H. Matsumine, 1998, Parkinsonism & related disorders.