Showing results (21-30 of 80) with videos related to
Sort By:
Pageof 8
Japanese Journal of Clinical Oncology|May 23, 2006
Novel 14 base-pair deletion of the MEN1 gene in a patient with recurrent primary hyperparathyroidismMiyuki Katai, Akihiro Sakurai, Shinya Uchino, et al.Human Genome Variation|January 21, 2026
Updated analysis of pathogenic variants in BRCA1/BRCA2 among the general Japanese populationTasuku Mariya, Masashi Idogawa, Tsuyoshi Saito, et al.Endocrine Journal|May 12, 2015
Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutationYusuke Shibata, Masanori Yamazaki, Masahiro Takei, et al.Fertility and Sterility|April 12, 2005
Fitz-Hugh and Curtis syndrome-like diaphragmatic endometriosisHiroyuki Takeuchi, Mari Kitade, Akihiro Sakurai, et al.The Journal of Physiology|September 9, 2009
Genetic basis of inter-individual variability in the effects of exercise on the alleviation of lifestyle-related diseasesMasayuki Mori, Keiichi Higuchi, Akihiro Sakurai, et al.Endocrine Journal|October 17, 2014
A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinomaMasanori Yamazaki, Toru Hanamura, Ken-ichi Ito, et al.Endocrine Journal|March 24, 2007
Long-term follow-up of patients with multiple endocrine neoplasia type 1Akihiro Sakurai, Miyuki Katai, Koh Yamashita, et al.Journal of Human Genetics|July 6, 2007
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in JapanKunihiro Yoshida, Takahito Wada, Akihiro Sakurai, et al.European Journal of Endocrinology|February 19, 2013
High penetrance of pheochromocytoma in multiple endocrine neoplasia 2 caused by germ line RET codon 634 mutation in Japanese patientsTsuneo Imai, Shinya Uchino, Takahiro Okamoto, et al.Human Genome Variation|August 11, 2016
A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorderKenichi Takano, Noriko Ogasawara, Tatsuo Matsunaga, et al.Pageof 8