T. Taga

Two novel heterozygous variants in ATP1A3 cause movement disorders

H. Saitsu, M. Nakashima, Kazuo Kubota, 2022, Human Genome Variation.

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis

Masahiro Ito, Wang-Tso Lee, T. Fujita, 2013, Brain and Development.

Sweet’s syndrome in a neonate with non-B54 types of human leukocyte antigen

N. Kondo, Z. Kato, K. Omoya, 2012, World Journal of Pediatrics.

Cerebral infarction in incontinentia pigmenti: the first report of a case evaluated by single photon emission computed tomography

E. Matsui, T. Nishida, T. Taga, 1997, Acta paediatrica.

Restriction Fragment Length Polymorphism Analysis in Healthy Japanese Individuals and Japanese Families with Gaucher Disease

M. Masuno, T. Orii, T. Taga, 1989, Acta paediatrica Japonica : Overseas edition.

Bacterial meningitis and septicemia of neonate due to Lactococcus lactis

N. Kondo, H. Morita, T. Taga, 2011, Pediatrics international : official journal of the Japan Pediatric Society.

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis

Wang-Tso Lee, T. Fujita, S. Yasumoto, 2013, Brain and Development.