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Physiological Research|February 2, 2012
Genetic variation screening of TNNT2 gene in a cohort of patients with hypertrophic and dilated cardiomyopathyM Jáchymová, A Muravská, T Paleček, et al.Journal of Inherited Metabolic Disease|November 11, 2008
Intravascular ultrasound assessment of coronary artery involvement in Fabry diseaseT Kovarnik, G S Mintz, D Karetova, et al.International Journal of Clinical Practice|August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome SurveyO Lidove, U Ramaswami, R Jaussaud, et al.Herz|July 11, 2019
Plasma osteopontin levels, but not its myocardial expression, reflect heart failure severity in recently diagnosed dilated cardiomyopathyJ Podzimkova, T Palecek, P Kuchynka, et al.Prague Medical Report|July 14, 2009
Thrombophilia and pulmonary endarterectomyJ Lindner, P Jansa, P Salaj, et al.Physiological Research|December 17, 2016
Disparity between two-dimensional echocardiographic and electroanatomic left and right atrial volumes in patients undergoing catheter ablation for long-standing persistent atrial fibrillationL Škňouřil, Š Havránek, V Bulková, et al.Vnitrni Lekarstvi|November 6, 2012
[Acute myocardial infarction in young patients--severe failures in the system of acute and secondary care]G Dostálová, J Bělohlávek, L Vítek, et al.European Journal of Clinical Investigation|March 18, 2004
Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome SurveyA Mehta, R Ricci, U Widmer, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 17, 2016
Gene variants at FTO, 9p21, and 2q36.3 are age-independently associated with myocardial infarction in Czech menJ A Hubacek, M Vrablik, D Dlouha, et al.Lancet (London, England)|December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry dataA Mehta, M Beck, P Elliott, et al.Pageof 11