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Journal of Pediatric Endocrinology & Metabolism : JPEM|April 9, 2026
A case of Alström syndrome with growth hormone deficiency and dyslipidemia: a novel homozygous frameshift variant of ALMS1 c.5763delTakeshi Goda, Hisakazu Nakajima, Yasuhiro Kawabe, et al.
Human Mutation|May 11, 2017
De novo IGF2 mutation on the paternal allele in a patient with Silver-Russell syndrome and ectrodactylyKaori Yamoto, Hirotomo Saitsu, Norio Nakagawa, et al.
Pediatric Diabetes|February 21, 2014
Relapsing 6q24-related transient neonatal diabetes mellitus successfully treated with a dipeptidyl peptidase-4 inhibitor: a case reportTohru Yorifuji, Yukiko Hashimoto, Rie Kawakita, et al.
Children (Basel, Switzerland)|October 27, 2022
Association of Type 2 Deiodinase Thr92Ala Polymorphism with Pediatric Obesity in Japanese Children: A Case-Control StudyTakeshi Ota, Jun Mori, Yasuhiro Kawabe, et al.
Endocrine Journal|September 6, 2019
Pituitary apoplexy after cardiac surgery in a 14-year-old girl with Carney complex: a case reportYuki Naito, Jun Mori, Jun Tazoe, et al.
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