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Hiroshima Journal of Medical Sciences|March 7, 2012
Treatment of iliac artery rupture during percutaneous transluminal angioplasty: a report of three casesKatsutoshi Sato, Kazumasa Orihashi, Yoshiharu Hamanaka, et al.Congenital Anomalies|March 2, 2005
Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?Rika Kosaki, Masataka Higuchi, Norimasa Mitsui, et al.Congenital Anomalies|March 14, 2013
Patient with terminal 9 Mb deletion of chromosome 9p: refining the critical region for 9p monosomy syndrome with trigonocephalyNorimasa Mitsui, Kenji Shimizu, Hiroshi Nishimoto, et al.Journal of Cardiology Cases|June 10, 2022
A vegetation in a unique location without exposure to regurgitation or a shunt jet: A case reportKenji Masada, Hironori Ueda, Masamichi Ozawa, et al.General Thoracic and Cardiovascular Surgery|September 18, 2012
Safety of the paravertebral block in patients ineligible for epidural block undergoing pulmonary resectionTatsuya Katayama, Shinji Hirai, Rei Kobayashi, et al.Congenital Anomalies|May 21, 2005
Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2 duplicationRika Kosaki, Kenjiro Kosaki, Kazushige Matsushima, et al.American Journal of Medical Genetics. Part A|April 1, 2004
Mosaic supernumerary inv dup(15) chromosome with four copies of the P gene in a boy with pigmentary dysplasiaKeiko Akahoshi, Richard A Spritz, Kazuyoshi Fukai, et al.Annals of Thoracic and Cardiovascular Surgery : Official Journal of the Association of Thoracic and Cardiovascular Surgeons of Asia|May 19, 2011
Inflammatory pseudotumor suspected of lung cancer treated by thoracoscopic resectionShinji Hirai, Tatsuya Katayama, Naru Chatani, et al.World Journal of Emergency Surgery : WJES|August 23, 2011
Post-traumatic diaphragmatic herniation of the liver, examined by positron emission tomography: case reportKatsutoshi Sato, Kazumasa Orihashi, Yoshiharu Hamanaka, et al.American Journal of Medical Genetics. Part A|May 2, 2008
Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadismReiko Shimizu, Norimasa Mitsui, Yasuhiro Mori, et al.Pageof 4