Works by Kinoshita, Eiichi

Results: 12

Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 7, p. 3359, doi. 10.1210/jc.2003-032091

By:

YOSHIDA, RIE;
HASEGAWA, TOMONOBU;
HASEGAWA, YUKIHIRO;
NAGAI, TOSHIRO;
KINOSHITA, EIICHI;
TANAKA, YOKO;
KANEGANE, HIROKAZU;
OHYAMA, KENJI;
ONISHI, TOSHIKAZU;
HANEW, KUNIHIKO;
OKUYAMA, TORAYUKI;
HORIKAWA, REIKO;
TANAKA, TOSHIAKI;
OGATA, TSUTOMU

Publication type:

Article

Genetic background of hyperphenylalaninemia in Nagasaki, Japan.

Published in:

Pediatrics International, 2016, v. 58, n. 5, p. 431, doi. 10.1111/ped.12924

By:

Dateki, Sumito;
Watanabe, Satoshi;
Nakatomi, Akiko;
Kinoshita, Eiichi;
Matsumoto, Tadashi;
Yoshiura, Koh‐ichiro;
Moriuchi, Hiroyuki

Publication type:

Article

Usefulness of renal ultrasonography for assessment of severity and course of acute tubular necrosis.

Published in:

1984

By:

Nomura, Gakuji;
Kinoshita, Eiichi;
Yamagata, Yuji;
Koga, Nobuhiko;
Nomura, G;
Kinoshita, E;
Yamagata, Y;
Koga, N

Publication type:

journal article

The Jewish-type Cohen syndrome complicated with refractory bronchial asthma and depression.

Published in:

Pediatrics International, 2005, v. 47, n. 6, p. 691, doi. 10.1111/j.1442-200x.2005.02127.x

By:

Naganuma, Masako;
Kondoh, Tatsuro;
Tashiro, Kasumi;
Gohda, Yuji;
Nakane, Hideyuki;
Kinoshita, Eiichi;
Matsumoto, Tadashi;
Moriuchi, Hiroyuki

Publication type:

Article

Patient Report Renal tubular dysgenesis complicated with severe cranium hypoplasia.

Published in:

Pediatrics International, 2004, v. 46, n. 1, p. 88, doi. 10.1111/j.1442-200X.2004.01830.x

By:

Shirakawa, Toshihiko;
Kondoh, Tatsuro;
Takahashi, Ritsuko;
Nakayama, Masahiro;
Kusumoto, Takashi;
Matsudaira, Munenori;
Nakashima, Yumiko;
Nazneen, Arifa;
Taguchi, Takashi;
Moriuchi, Hiroyuki;
Kinoshita, Eiichi;
Miyamoto, Masashi;
Masuzaki, Hideaki;
Uetania, Masataka

Publication type:

Article

A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia.

Published in:

Pediatrics International, 2000, v. 42, n. 5, p. 564, doi. 10.1046/j.1442-200x.2000.01263.x

By:

Imamura, Yoshihiko;
Kondoh, Tatsuro;
Kamei, Tsutomu;
Tsuru, Akira;
Shimasaki, Yukiharu;
Kinoshita, Eiichi;
Matsumoto, Tadashi

Publication type:

Article

A Case of Farber Disease.

Published in:

Pediatrics International, 1992, v. 34, n. 1, p. 72, doi. 10.1111/j.1442-200X.1992.tb00928.x

By:

Fujiwaki, Takehisa;
Hamanaka, Sumiko;
Koga, Mayumi;
Ishihara, Tokuhiro;
Nishikomori, Ryuuta;
Kinoshita, Eiichi;
Furusho, Kenshi

Publication type:

Article

Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency: Identification of a Single Patient with LHX4 Deletion.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 8, p. 4043, doi. 10.1210/jc.2010-0150

By:

Sumito Dateki;
Maki Fukami;
Ayumi Uematsu;
Masayuki Kaji;
Manami Iso;
Makoto Ono;
Michiyo Mizota;
Susumu Yokoya;
Katsuaki Motomura;
Eiichi Kinoshita;
Hiroyuki Moriuchi;
Tsutomu Ogata

Publication type:

Article

Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 2, p. 756, doi. 10.1210/jc.2009-1334

By:

Sumito Dateki;
Kitaro Kosaka;
Kosei Hasegawa;
Hiroyuki Tanaka;
Noriyuki Azuma;
Susumu Yokoya;
Koji Muroya;
Masanori Adachi;
Toshihiro Tajima;
Katsuaki Motomura;
Eiichi Kinoshita;
Hiroyuki Moriuchi;
Naoko Sato;
Maki Fukami;
Tsutomu Ogata

Publication type:

Article

The Boy:Girl Ratio of Children Diagnosed with Growth Hormone Deficiency-Induced Short Stature Is Associated with the Boy:Girl Ratio of Children Visiting Short Stature Clinics.

Published in:

Hormone Research in Paediatrics, 2021, v. 94, n. 5/6, p. 211, doi. 10.1159/000518995

By:

Tanaka, Toshiaki;
Soneda, Shun;
Sato, Naoko;
Kishi, Kentaro;
Noda, Masahiro;
Ogasawara, Atsuko;
Nose, Osamu;
Nakano, Yukiko;
Kinoshita, Eiichi;
Mochizuki, Takahiro;
Konda, Susumu;
Murashita, Mari;
Tanizawa, Takakuni;
Nozue, Hiroki;
Tokuda, Masakuni;
Kubota, Kazuoki;
Araki, Kumiko;
Kitanaka, Sachiko;
Inomata, Hiroaki;
Miyagi, Chuken

Publication type:

Article

Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.

Published in:

Endocrine Journal, 2013, v. 60, n. 8, p. 1013, doi. 10.1507/endocrj.ej13-0023

By:

Maki Fukami;
Manami Iso;
Naoko Sato;
Maki Igarashi;
Misuzu Seo;
Itsuro Kazukawa;
Eiichi Kinoshita;
Sumito Dateki;
Tsutomu Ogata

Publication type:

Article

Mutations in intron 3 of GH-1 gene associated with isolated GH deficiency type II in three Japanese families.

Published in:

Clinical Endocrinology, 1999, v. 51, n. 3, p. 355, doi. 10.1046/j.1365-2265.1999.00798.x

By:

Kamijo, Takashi;
Hayashi, Yoshitaka;
Shimatsu, Akira;
Kinoshita, Eiichi;
Yoshimoto, Masaaki;
Ogawa, Masamichi;
Seo, Hisao

Publication type:

Article