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Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|May 17, 2016
Usefulness of Single Photon Emission Computed Tomography/Computed Tomography Fusion-Hybrid Imaging to Evaluate Coronary Artery Disorders in Patients with a History of Kawasaki DiseaseMasanori Abe, Ryuji Fukazawa, Shunichi Ogawa, et al.Brain & Development|December 8, 2021
Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorderHitomi Nishizawa, Mitsuo Motobayashi, Miwa Akahane, et al.Annals of Nuclear Medicine|July 5, 2008
Usefulness of 201TlCl/ 123I-BMIPP dual-myocardial SPECT for patients with non-ST segment elevation myocardial infarctionYoshimitsu Fukushima, Masahiro Toba, Keiichi Ishihara, et al.Rinsho Shinkeigaku = Clinical Neurology|March 26, 2013
[Current status of the predictive genetic testing for hereditary neurological diseases in Shinshu University Hospital]Keiko Tanaka, Yoshiki Sekijima, Kunihiro Yoshida, et al.Kaku Igaku. the Japanese Journal of Nuclear Medicine|February 28, 2003
[Assessment of biventricular function using gated blood pool SPECT with QBS software: comparison with planar radionuclide ventriculography]Hidenobu Nakajo, Shin-ichiro Kumita, Keiichi Cho, et al.Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine|April 4, 2017
4D Flow MR Imaging of Ophthalmic Artery Flow in Patients with Internal Carotid Artery StenosisTetsuro Sekine, Ryo Takagi, Yasuo Amano, et al.American Journal of Medical Genetics. Part A|February 5, 2003
Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: clinical course and phenotypic variations in four patientsGen Nishimura, Tomomi Honma, Takashi Shiihara, et al.Congenital Anomalies|November 30, 2004
Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFBTomohide Goto, Michihiko Aramaki, Hiroshi Yoshihashi, et al.Journal of Human Genetics|October 12, 2002
Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expressionKeiko Wakui, Atsushi Toyoda, Takeo Kubota, et al.American Journal of Medical Genetics. Part A|December 6, 2011
Myelodysplastic syndrome in a child with 15q24 deletion syndromeYoko Narumi, Masaaki Shiohara, Keiko Wakui, et al.Pageof 13