Tsujino Seiichi

ツジノセイイチ | Tsujino Seiichi

Affiliation and department：
Job title： Section Chief

Research keywords (8)： Molcular Genetics , Metabolic disease , Inherited disease , Neurology , 分子遺伝学 , 代謝性疾患 , 遺伝性疾患 , 神経内科学

Research theme for competitive and other funds (2)：

神経内科学遺伝性疾患の分子遺伝学
Neurology Molecular genetics of inherited diseases

MISC (10)：

Nonlysosomal glyconoses, In Myology (edited by Engel A.G. & Franzini Armstrong C.), 2nd ed. McGraw-Hill, New York
Disorders of Carbohydorte metabolism: Glycogen storage disease, In the Molecular and Genetic Basis of Neurological disease (edited by Roseberb R.N., et al), 2nd ed., pp.1067-1097, 1997. Butterworth-Heinemann, Boston
Three new mutations in patients with myophosphorylase deficiency (McArdle disease). Am. J. Hum. Genet. Vol. 54, pp. 44-52, 1994
Structure of the gene encoding the muscle-specific subunit of human phosphoglycerate mutase. J. Biol. Chem. Vol. 264, pp. 15334-15337, 1989
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease). N. Engl. J. Med. Vol. 329, pp. 241-245, 1993

ｍore...

Education (2)：

Gifu University School of Medicine
Gifu University School of Medicine

Professional career (1)：

Doctor of Medicine

Association Membership(s) (4)：

Japanese Society of Inherited Metabolic Disease , Japanese Association of Neurology , Japanese Association of Internal Medicine , Japanese Association of Child Neurology

※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page