学士（医学）

日本てんかん学会

日本小児神経学会

日本小児科学会

Expanding the KIF4A-associated phenotype.

Kalantari S, Carlston C, Alsaleh N, Abdel-Salam GMH, Alkuraya F, Kato M, Matsumoto N, Miyatake S, Yamamoto T, Fares-Taie L, Rozet JM, Chassaing N, Vincent-Delorme C, Kang-Bellin A, McWalter K, Bupp C, Palen E, Wagner MD, Niceta M, Cesario C, Milone R, Kaplan J, Wadman E, Dobyns WB, Filges I

American journal of medical genetics. Part A   2021.8

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy.

Parenti I, Lehalle D, Nava C, Torti E, Leitão E, Person R, Mizuguchi T, Matsumoto N, Kato M, Nakamura K, de Man SA, Cope H, Shashi V, Undiagnosed Diseases Network., Friedman J, Joset P, Steindl K, Rauch A, Muffels I, van Hasselt PM, Petit F, Smol T, Le Guyader G, Bilan F, Sorlin A, Vitobello A, Philippe C, van de Laar IMBH, van Slegtenhorst MA, Campeau PM, Au PYB, Nakashima M, Saitsu H, Yamamoto T, Nomura Y, Louie RJ, Lyons MJ, Dobson A, Plomp AS, Motazacker MM, Kaiser FJ, Timberlake AT, Fuchs SA, Depienne C, Mignot C

Human genetics   140 ( 7 )   1109 - 1120   2021.7

トピラマート/TRH療法併用により発作抑制された難治性West症候群の１例

花田勇

小児科臨床   2014.1

A Case of Megaloblastic Anemia that Developed after Intestinal Tube Feeding for Six Years

TANDAI Satoru, KONNO Yuki, YAMAMOTO Tatsuya, TAKAHASHI Yoshihiro, ITO Etsuro

21 ( 5 )   238 - 241   2007.12

第278回生涯教育研修会

2018.01

第1回平川地区てんかん講演会

2017.10