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Behavioural Neurology|December 4, 2015
Gender Differences in the Behavioral Symptom Severity of Prader-Willi SyndromeMasao Gito, Hiroshi Ihara, Hiroyuki Ogata, et al.American Journal of Medical Genetics. Part A|December 15, 2012
Characterization of fat distribution in Prader-Willi syndrome: relationships with adipocytokines and influence of growth hormone treatmentYuriko Tanaka, Yoshiko Abe, Yuji Oto, et al.Neuromuscular Disorders : NMD|March 16, 2013
Congenital generalized lipodystrophy type 4 with muscular dystrophy: clinical and pathological manifestations in early childhoodNobuyuki Murakami, Yukiko K Hayashi, Yuji Oto, et al.American Journal of Medical Genetics. Part A|May 16, 2012
Growth hormone secretion and its effect on height in pediatric patients with different genotypes of Prader-Willi syndromeYuji Oto, Kazuo Obata, Keiko Matsubara, et al.Cureus|October 1, 2025
Endocrine Characteristics of 246 Cases of Childhood-Onset Anorexia Nervosa in Japan: A Single-Center ExperienceYuji Oto, Takeshi Inoue, Ryoko Otani, et al.Experimental and Therapeutic Medicine|February 19, 2021
Successful treatment of Gaucher disease type 1 by enzyme replacement therapy over a 10-year duration in a Japanese pediatric patient: A case reportYuji Oto, Takeshi Inoue, So Nagai, et al.American Journal of Medical Genetics. Part A|June 9, 2012
Scoliosis in Prader-Willi syndrome: effect of growth hormone therapy and value of paravertebral muscle volume by CT in predicting scoliosis progressionNobuyuki Murakami, Kazuo Obata, Yoshiko Abe, et al.Behavioural Neurology|February 15, 2018
Autistic, Aberrant, and Food-Related Behaviors in Adolescents and Young Adults with Prader-Willi Syndrome: The Effects of Age and GenotypeAtsushi Ishii, Hiroshi Ihara, Hiroyuki Ogata, et al.Endocrine Journal|July 24, 2025
A questionnaire-based survey on hyperphagia in individuals with Prader-Willi syndrome in JapanMakiko Tachibana, Yuji Oto, Kenichi Kashimada, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|February 4, 2024
A case report of odonto-hypophosphatasia with a novel variant in the <i>ALPL</i> geneYuji Oto, Daiki Suzuki, Tsubasa Morita, et al.Pageof 4