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American Journal of Medical Genetics. Part A|April 27, 2018
Delayed peak response of cortisol to insulin tolerance test in patients with Prader-Willi syndromeYuji Oto, Keiko Matsubara, Tadayuki Ayabe, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 2016
Pyruvate Improved Insulin Secretion Status in a Mitochondrial Diabetes Mellitus PatientTakeshi Inoue, Nobuyuki Murakami, Tadayuki Ayabe, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Two novel CAV3 gene mutations in Japanese familiesKazuma Sugie, Kumiko Murayama, Satoru Noguchi, et al.
Ayu|June 1, 2013
Effects of turmeric on Alzheimer's disease with behavioral and psychological symptoms of dementiaNozomi Hishikawa, Yoriko Takahashi, Yoshinobu Amakusa, et al.
Research in Developmental Disabilities|January 12, 2018
Aberrant, autistic, and food-related behaviors in adults with Prader-Willi syndrome. The comparison between young adults and adultsHiroyuki Ogata, Hiroshi Ihara, Masao Gito, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2021
Psychiatric behavioral effect and characteristics of type 2 diabetes mellitus on Japanese patients with Prader-Willi syndrome: a preliminary retrospective studyYuji Oto, Nobuyuki Murakami, Takeshi Inoue, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|May 3, 2011
[Surveillance study on use of over-the-counter drug and health food by school pharmacist for grade-schooler, junior high school student, and high school students]Makoto Anraku, Hisao Tomida, Eiji Sato, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2021
Growth hormone treatment and bone mineral density in pediatric patients with Prader-Willi syndromeYuji Oto, Nobuyuki Murakami, Takeshi Inoue, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 9, 2011
An autopsy case of lymphomatosis cerebri showing pathological changes of intravascular large B-cell lymphoma in visceral organsNozomi Hishikawa, Hisayoshi Niwa, Takashi Hara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 29, 2015
Differing phenotypes of Moyamoya disease in a familial case involving heterozygous c.14429G > A variant in RNF213Takeshi Inoue, Nobuyuki Murakami, Satoru Sakadume, et al.
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