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Annals of Nuclear Medicine|October 8, 2017
Feasibility of combined risk stratification with coronary CT angiography and stress myocardial SPECT in patients with chronic coronary artery diseaseTomonari Kiriyama, Yoshimitsu Fukushima, Hiromitsu Hayashi, et al.The International Journal of Cardiovascular Imaging|March 21, 2018
Feasibility of myocardial flow reserve prediction without the use of dynamic data from myocardial perfusion positron emission tomographyHidenobu Hashimoto, Yoshimitsu Fukushima, Shin-Ichiro Kumita, et al.American Journal of Medical Genetics. Part A|March 11, 2006
Neonatal management of trisomy 18: clinical details of 24 patients receiving intensive treatmentTomoki Kosho, Tomohiko Nakamura, Hiroshi Kawame, et al.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.Autism Research and Treatment|August 31, 2012
Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum DisorderKumiko Yanagi, Tadashi Kaname, Keiko Wakui, et al.Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|January 15, 2014
A definitive diagnosis of mucosa-associated lymphoid tissue lymphoma made at a second biopsyTsutomu Igarashi, Akira Shimizu, Hiroki Yamaguchi, et al.American Journal of Medical Genetics. Part A|September 15, 2005
Ehlers-Danlos syndrome type VIB with characteristic facies, decreased curvatures of the spinal column, and joint contractures in two unrelated girlsTomoki Kosho, Jun Takahashi, Hirofumi Ohashi, et al.American Journal of Medical Genetics. Part A|January 6, 2005
A woman with 46,XX,dup(16)(p13.11 p13.3) and the ATR-X phenotypeKeiko Akahoshi, Hirohumi Ohashi, Yukio Hattori, et al.Journal of Human Genetics|February 25, 2006
Molecular characterization of a novel translocation t(5;14)(q21;q32) in a patient with congenital abnormalitiesShawkat Haider, Rie Matsumoto, Nobuyuki Kurosawa, et al.Genetic Testing|November 4, 2008
One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2Hirofumi Kojima, Takahito Wada, Hiroshi Seki, et al.Pageof 13