Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 gene
Satoh, Mari, Aso, Keiko, Ogikubo, Sayaka, Yoshizawa-Ogasawara, Atsuko, Saji, Tsutomu
Published in Journal of Pediatric Endocrinology & Metabolism (01.05.2015)
Published in Journal of Pediatric Endocrinology & Metabolism (01.05.2015)
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Journal Article
Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2
Yoshizawa-Ogasawara, Atsuko, Abe, Kiyomi, Ogikubo, Sayaka, Narumi, Satoshi, Hasegawa, Tomonobu, Satoh, Mari
Published in Journal of Pediatric Endocrinology & Metabolism (01.03.2016)
Published in Journal of Pediatric Endocrinology & Metabolism (01.03.2016)
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Journal Article
SAT-295 Low Dose rFSH Prior to HCG-rFSH Therapy in Kallmann Syndrome
Yoshizawa-Ogasawara, Atsuko, Yanai, Toshihiro, Sato, Naoko
Published in Journal of the Endocrine Society (30.04.2019)
Published in Journal of the Endocrine Society (30.04.2019)
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Journal Article
Third-generation Aromatase Inhibitor Improved Adult Height in a Japanese Boy with Testotoxicosis
Yoshizawa-Ogasawara, Atsuko, Katsumata, Noriyuki, Horikawa, Reiko, Satoh, Mari, Urakami, Tatsuhiko, Tanaka, Toshiaki
Published in Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology (01.04.2014)
Published in Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology (01.04.2014)
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