K. Yoshizawa

发表

Association between polymorphism of the cholecystokinin gene and idiopathic Parkinson's disease

S. Harada, N. Ohkoshi, C. Fujii, 1999, Clinical genetics.

Argentophilic intracytoplasmic inclusions in multiple system atrophy

I. Kanazawa, A. Mochizuki, Kiyoharu Inoue, 1992, Journal of Neurology.

Progressive supranuclear palsy presenting with pure akinesia.

I. Kanazawa, A. Mochizuki, H. Mizusawa, 1993, Advances in neurology.

Alterations in Muscarinic Cholinergic Receptors and the Second Messenger System in the Cerebral Cortex in Alzheimer-Type Dementia

I. Kanazawa, K. Mizukawa, N. Ogawa, 1990 .

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

I. Kanazawa, S. Tsuji, M. Miwa, 1997, American journal of human genetics.

Unusual Electrocardiographic Findings Associated with Type A Wolff‐Parkinson‐White Syndrome

Y. Sugishita, I. Yamaguchi, K. Kuga, 1993, Pacing and clinical electrophysiology : PACE.

Studies on neurotransmitter markers and neuronal cell density in the cerebellar system in olivopontocerebellar atrophy and cortical cerebellar atrophy

I. Kanazawa, N. Nukina, H. Mizusawa, 1985, Journal of the Neurological Sciences.

Cross-cultural traits for personality of patients with Parkinson's disease in Japan.

S. Harada, N. Ohkoshi, C. Fujii, 2000, American journal of medical genetics.

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6

T. Tsutsumi, H. Mizusawa, S. Shoji, 2004, Journal of Human Genetics.

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia

T. Yamawaki, H. Mizusawa, S. Shoji, 2000, Neurology.

Inhibitory effects of L-threo-3,4-dihydroxyphenylserine against maximal electroconvulsion and brain norepinephrine in mice

Motoaki Yoshida, T. Nakanishi, K. Yoshizawa, 1990 .

Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6)

I. Kanazawa, H. Mizusawa, S. Shoji, 1999, Journal of neurology, neurosurgery, and psychiatry.

Dysfunction of the hypothalamic-pituitary system in mitochondrial encephalomyopathies.

S. Shoji, N. Ohkoshi, A. Ishii, 1998, Journal of medicine.

Superoxide dismutases of muscle in mitochondrial encephalomyopathies

S. Shoji, K. Harada, K. Yoshizawa, 1995, Muscle & nerve.

Association between Catechol-O-Methyltransferase Gene Polymorphisms and Wearing-Off and Dyskinesia in Parkinson’s Disease

S. Shoji, S. Harada, N. Ohkoshi, 2003, Neuropsychobiology.

A case with myasthenia gravis (MG) emerging after splenectomy for idiopathic thrombocytopenic purpura (ITP): possible effects of thymectomy on autoantibodies.

A. Tamaoka, S. Matsuno, S. Shoji, 2000, Journal of medicine.

16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

H. Shimazaki, T. Amino, H. Mizusawa, 2006, Journal of the Neurological Sciences.