学士（医学）, 琉球大学

Postnatal intracerebral hemorrhage with hereditary hemorrhagic telangiectasia
Miyosawa Y, Kamiya M, Nakamura C, Yamaguchi T, Koshyo T.
Pediatr International, 64(1), 2022, Refereed

Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome
Daisuke Matsuoka, Shunsuke Noda, Motoko Kamiya, Yoshihiko Hidaka, Hisashi Shimojo, Yasushi Yamada, Tsutomu Miyamoto, Kandai Nozu, Kazumoto Iijima and Hiroyasu Tsukaguchi
BMC NEPHROLOGY, 21(362), 2020

A novel homozygous missense SLC25A20 mutation in three CACT-deficient patients
Yasutsugu Chinen, Kumiko Yanagi, Sadao Nakamura, Noriko Nakayama, Motoko Kamiya, Mami Nakayashiro, Tadashi Kaname, Kenji Naritomi and Koichi Nakanishi
Human Genome Variation, 7(11), 2020, Refereed

在宅高流量鼻カニュラで在宅移行した先天性筋無力症候群の乳児例
酒井慧、稲葉雄二、斎間陽子、山内翔子、中嶋英子、福山哲広、三澤由佳、塚原孝典、神谷素子、古庄知己
日本小児科学会雑誌, 123(8), 1255-1260, Aug. 2019, Refereed

Decreased Circulating Insulin-Like Growth Factor 1 Levels Are Associated with Cardiac Diastolic Dysfunction in Small for Gestational Age Infants.
Akazawa Y, Yamazaki S, Obinata H, Hachiya A, Kamiya M, Motoki N, Nakamura T
Am J Perinatol, 35(12), 1178-1185, 2018, Refereed

Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter
Hirokazu Morokawa, Motoko Kamiya, Keiko Wakui, Mikiko Kobayashi, Takashi Kurata, Kazuyuki Matsuda,Rie Kawamura, Hiroyuki Kanno, Yoshimitsu Fukushima, Yozo Nakazawa1 and Tomoki Kosho
Human Genome Variation, 5(6), 2018, Refereed
Lead, Last

超早産児の予後向上のための戦略【2】　NICU入院中の管理　慢性期呼吸管理　全身管理
神谷素子、中村友彦
周産期医学, 47(8), 1033-1035, 2017
Lead, Last

Decreased Aortic Elasticity in Children With Marfan Syndrome or Loeys-Dietz Syndrome.
Akazawa Y, Motoki N, Tada A, Yamazaki S, Hachiya A, Matsuzaki S, Kamiya M, Nakamura T, Kosho T, Inaba Y.
CIRCULATION JOURNAL, 80(11), 2369-2375, 2016, Refereed