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Showing page 1 of results 1 - 10 of about 10 pages

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Relationship Between Chloride Infusion and Base Excess in Initial Treatment of Pediatric Diabetic Ketoacidosis | ESPE2019
Kentaro Sawano; Fusa Nagamatsu; Kazuhiro Shimura; Yuki Abe; Yukie Izumita; Yohei Ogawa; Nagisa Komatsu; Shigeru Takishima; Akie
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-54
Published: 2019-08-22

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Imprinting Defects and Copy Number Variations in Short Children Born Small for Gestational Age | ESPE2019
Masayo Kagami; Akie Nakamura; Takanobu Inoue; Sayaka Kawashima; Kaori Hara; Tomoko Fuke; Keiko Mastubara; Maki Fukami; Tsutomu O
http://abstracts.eurospe.org/hrp/0092/hrp0092RFC12.3
Published: 2019-08-22

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Relationship Between Chloride Infusion and Base Excess in Initial Treatment of Pediatric Diabetic Ketoacidosis | ESPE2019
Kentaro Sawano; Fusa Nagamatsu; Kazuhiro Shimura; Yuki Abe; Yukie Izumita; Yohei Ogawa; Nagisa Komatsu; Shigeru Takishima; Akie
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-54.html
Published: 2019-08-22

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Imprinting Defects and Copy Number Variations in Short Children Born Small for Gestational Age | ESPE2019
Masayo Kagami; Akie Nakamura; Takanobu Inoue; Sayaka Kawashima; Kaori Hara; Tomoko Fuke; Keiko Mastubara; Maki Fukami; Tsutomu O
http://abstracts.eurospe.org/hrp/0092/hrp0092rfc12.3.html
Published: 2019-08-22

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Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Six Patients | ESPE2018
Sayaka Kawashima; Akie Nakamura; Takanobu Inoue; Keiko Matsubara; Reiko Horikawa; Keiko Wakui; Kyoko Takano; Yoshimitsu Fukushim
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p186.htm
Published: 2018-08-28

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Molecular and Clinical Analyses of Two UPD(16)mat Patients Detected by Screening of 94 Silver-Russell Syndrome Patients without Known Etiology | ESPE2018
Takanobu Inoue; Hideaki Yagasaki; Junko Nishioka; Akie Nakamura; Keiko Matsubara; Satoshi Narumi; Kazuhiko Nakabayashi; Kazuki Y
http://abstracts.eurospe.org/hrp/0089/hrp0089rfc15.2.htm
Published: 2018-08-28

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NR0B1 Frameshift Mutation in a Boy with Precocious Puberty and Normal Adrenal Function | ESPE2016
Hirohito Shima; Shuichi Yatsuga; Akie Nakamura; Shinichiro Sano; Takako Sasaki; Noriyuki Katsumata; Erina Suzuki; Tsutomu Ogata;
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc15.2.htm
Published: 2016-08-19

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Various Imprinting Disorders Underlying Silver-Russell Syndrome-Compatible Phenotype | ESPE2015
Masayo Kagami; Keiko Matsubara; Shinichiro Sano; Akie Nakamura; Seiji Mizuno; Naoki Hamajima; Atsuhiro Yanagisawa; Miyuki Hashim
http://abstracts.eurospe.org/hrp/0084/hrp0084p1-95.htm
Published: 2015-08-26

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A 26-Day-Old Japanese Girl with Aldosterone Synthase Deficiency Caused by a Novel Mutation in the CYP11B2 Gene | ESPE2014
Satomi Koyama; Tatsuo Tsuboi; Naoto Shimura; Akie Nakamura; Toshihiro Tajima; Osamu Arisaka
http://abstracts.eurospe.org/hrp/0082/hrp0082p2-d2-280.htm
Published: 2014-08-28

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A Novel Mutation of wfs1 Gene in a Japanese Infant of Diabetes Mellitus, Deafness, and Congenital Cataract | ESPE2014
Shuntaro Morikawa; Akie Nakamura; Katsura Ishizu; Satoru Kumaki; Toshihiro Tajima
http://abstracts.eurospe.org/hrp/0082/hrp0082p1-d2-73.htm
Published: 2014-08-28

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