Shinobu Ida - Department of Pediatric Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital

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Genetic Backgrounds and Genotype-Phenotype Relationships in Anthropometric Parameters of 116 Japanese Individuals with Noonan Syndrome

Yasuko Shoji, Ayaha Hata,Takatoshi Maeyama,Tamaki Wada,Yuiko Hasegawa,Eriko Nishi,Shinobu Ida,Yuri Etani,Tetsuya Niihori,Yoko Aoki,Nobuhiko Okamoto,Masanobu Kawai

CLINICAL PEDIATRIC ENDOCRINOLOGYno. 2 (2024): 50-58

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Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years

Tomokazu Kimizu,Masatoshi Nozaki, Yousuke Okada,Akihisa Sawada, Misaki Morisaki, Hiroshi Fujita,Akemi Irie,Keiko Matsuda,Yuiko Hasegawa,Eriko Nishi,Nobuhiko Okamoto,Masanobu Kawai,Kohsuke Imai,Yasuhiro Suzuki,Kazuko Wada,Nobuaki Mitsuda,Shinobu Ida

GENESno. 3 (2024)

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Reductions in Estimated Glomerular Filtration Rate During Puberty in GH-treated Children Born Small for Gestational Age Are Associated with Prematurity and Low Birth Weight, Not the Dosage of GH Treatment

Mikiko Koizumi,Shinobu Ida,Yuri Etani,Masanobu Kawai

Clinical pediatric endocrinologyno. 2 (2023): 98-104

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Very Young Children with Prader-Willi Syndrome Are Refractory to Growth Hormone-Associated Decreases in Free Thyroxine Levels

Ayako Konishi,Mikiko Koizumi,Yuri Etani,Shinobu Ida,Masanobu Kawai

Endocrine journal（2023）

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Newborn Screening for Spinal Muscular Atrophy in Osaka -Challenges in a Japanese Pilot Study-

Tomokazu Kimizu,Shinobu Ida,Keisuke Oki, Morimasa Shima,Shizuka Nishimoto,Ken Nakajima,Tae Ikeda,Yukiko Mogami,Keiko Yanagihara,Keiko Matsuda,Eriko Nishi,Yuiko Hasegawa,Masatoshi Nozaki, Hiroshi Fujita,Akemi Irie, Toru Katayama,Nobuhiko Okamoto,Kohsuke Imai,Hisahide Nishio,Yasuhiro Suzuki

BRAIN & DEVELOPMENTno. 7 (2023): 363-371

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Evaluations for Wilms Tumor and Late‐onset Nephrotic Syndrome in 46,XY DSD

Mikiko Koizumi,Shinobu Ida,Yuri Etani,Masanobu Kawai

Pediatrics internationalno. 1 (2023)

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Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature

Tamaki Wada,Chihiro Ichikawa,Makoto Takeuchi,Futoshi Matsui,Fumi Matsumoto,Shinobu Ida,Yuri Etani,Masanobu Kawai

CLINICAL PEDIATRIC ENDOCRINOLOGY（2022）

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Subcutaneous Adipose Tissue is a Positive Predictor for Bone Mineral Density in Prepubertal Children with Prader-Willi Syndrome Independent of Lean Mass

Masanobu Kawai,Yuri Etani,Shinobu Ida

Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism（2022）

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Clinical Guidelines for the Diagnosis and Treatment of 21-Hydroxylase Deficiency (2021 Revision)

Tomohiro Ishii,Kenichi Kashimada,Naoko Amano,Kei Takasawa,Akari Nakamura-Utsunomiya,Shuichi Yatsuga,Tokuo Mukai,Shinobu Ida,Mitsuhisa Isobe,Masaru Fukushi,Hiroyuki Satoh,Kaoru Yoshino,Michio Otsuki,Takuyuki Katabami,Toshihiro Tajima

Clinical Pediatric Endocrinologyno. 3 (2022): 116-143

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Current Status of Transition Medicine for 21-Hydroxylase Deficiency in Japan: from the Perspective of Pediatric Endocrinologists

Kei Takasawa,Akari Nakamura-Utsunomiya,Naoko Amano,Tomohiro Ishii,Tomonobu Hasegawa,Yukihiro Hasegawa,Toshihiro Tajima,Shinobu Ida

ENDOCRINE JOURNAL（2022）

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