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Oncology Reports|April 17, 2002
Immunohistochemical expression of SKALP/elafin in squamous cell carcinoma of human lungNaoya Yoshida, Hiroshi Egami, Junichi Yamashita, et al.
International Journal of Cardiology|September 20, 2005
Changes in cardiac tissue characterization in carriers with gene mutations associated with hypertrophic cardiomyopathyTomoya Kaneda, Masami Shimizu, Hidekazu Ino, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|January 20, 2009
Impact of QT variables on clinical outcome of genotyped hypertrophic cardiomyopathyKatsuharu Uchiyama, Kenshi Hayashi, Noboru Fujino, et al.
American Journal of Physiology. Heart and Circulatory Physiology|October 5, 2014
Compound heterozygosity deteriorates phenotypes of hypertrophic cardiomyopathy with founder MYBPC3 mutation: evidence from patients and zebrafish modelsAkihiko Hodatsu, Tetsuo Konno, Kenshi Hayashi, et al.
Clinical Case Reports|February 5, 2024
A case of MYH7 and MYH9 genes variants with cardiomyopathy and macrothrombocytopeniaYasuhiro Ikawa, Taichi Nakamura, Noboru Fujino, et al.
Clinical Science (London, England : 1979)|February 1, 2007
Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosisTetsuo Konno, Noboru Fujino, Kenshi Hayashi, et al.
International Heart Journal|June 19, 2010
Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin I geneAkira Funada, Eiichi Masuta, Noboru Fujino, et al.
Clinical Cardiology|June 11, 2008
Assessment of QT intervals and prevalence of short QT syndrome in JapanAkira Funada, Kenshi Hayashi, Hidekazu Ino, et al.
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