I. Izumi

发表

Persistent QT Prolongation in a Child with Gitelman Syndrome and SCN5A H558R Polymorphism.

H. Horigome, Takashi Murakami, Lisheng Lin, 2018, International heart journal.

Serum dipeptidyl peptidase 4 activity in children with type 1 diabetes mellitus

Atsushi Iwabuchi, M. Saito, R. Sumazaki, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Serum leptin and insulin concentrations in prepubertal lean, obese and insulin‐dependent diabetes mellitus children

T. Kamoda, A. Matsui, H. Saitoh, 1998, Clinical endocrinology.

The use of cyclosporine in a boy with a prior episode of posterior encephalopathy

N. Iwasaki, N. Hasegawa, I. Izumi, 2005, Pediatric Nephrology.

Nusinersen improved respiratory function in spinal muscular atrophy type 2

C. Kobayashi, Fujiko Fukushima, R. Tanaka, 2021, Pediatrics international : official journal of the Japan Pediatric Society.

Gianotti–Crosti syndrome associated with cytomegalovirus antigenemia after bone marrow transplantation

M. Tsuchida, K. Koike, I. Izumi, 1997, Bone Marrow Transplantation.

Characterization of the γc chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID)

T. Morio, H. Takada, K. Sugamura, 2000, Human Genetics.

Growth hormone deficiency in Dubowitz syndrome

T. Hirano, I. Izumi, ISHOU IZUMI, 1996, Acta paediatrica Japonica : Overseas edition.

FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients

Yoshihiko Saito, I. Nishino, M. Matsuo, 2021, Journal of Clinical Neuroscience.

A case of Shwachman-Diamond syndrome presenting with diabetes from early infancy.

N. Iwasaki, Takashi Saito, R. Sumazaki, 2005, Diabetes care.

Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11.

Y. Matsubara, Y. Suzuki, K. Narisawa, 1998, Biochemical and biophysical research communications.