Publications by authors named "Saori Kinjo"

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Epidemiology of moderate-to-severe respiratory syncytial virus infections in children in subtropical Okinawa, Japan: a 4-year retrospective study.
Kahoru Fukuoka-Araki, Kotaro Araki, Hiromi Fukuoka, Yoshiaki Cho, Kei Matayoshi, Saori Kinjo

Trop Med Health· November 2025

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Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 Patients.
Hiromune Narusawa, Tomoe Ogawa, Hideaki Yagasaki, Keisuke Nagasaki, Tatsuki Urakawa, Saori Kinjo

J Clin Endocrinol Metab· March 2025

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Genotype-Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects.
Kanako Tanase-Nakao, Megumi Iwahashi-Odano, Chiho Sugisawa, Kiyomi Abe, Koji Muroya, Saori Kinjo

J Clin Endocrinol Metab· August 2024

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5-Aminosalicylic acid-induced pericarditis in pediatric Crohn's disease.
Yuki Toguchi, Kahoru Fukuoka-Araki, Kei Matayoshi, Saori Kinjo, Toshifumi Yodoshi

Pediatr Int· January 2022

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Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997-2017.
Rie Matsushita, Keisuke Nagasaki, Tadayuki Ayabe, Yoko Miyoshi, Saori Kinjo

J Pediatr Endocrinol Metab· June 2019

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Utility of point-of-care Gram stain by physicians for urinary tract infection in children ≤36 months.
Toshifumi Yodoshi, Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo

Medicine (Baltimore)· April 2019

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SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.
Satoshi Narumi, Naoko Amano, Tomohiro Ishii, Noriyuki Katsumata, Koji Muroya, Saori Kinjo, Tadamune Kinjo

Nat Genet· July 2016

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Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
Shino Shimada, Keiko Shimojima, Noriko Sangu, Ai Hoshino, Yasuo Hachiya, Saori Kinjo

Brain Dev· November 2015

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Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism.
Yoko Izumi, Erina Suzuki, Susumu Kanzaki, Shuichi Yatsuga, Saori Kinjo

Fertil Steril· October 2014

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Vitamin D deficiency rickets caused by improper lifestyle in Japanese children.
Kenichi Miyako, Saori Kinjo, Hitoshi Kohno

Pediatr Int· April 2005

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Two cases of Allgrove syndrome with mutations in the AAAS gene.
Saori Kinjo, Megumi Takemoto, Kenichi Miyako, Hitoshi Kohno, Toshiaki Tanaka

Endocr J· October 2004

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