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Journal of Cardiovascular Electrophysiology|June 19, 2001
Brugada syndrome and supraventricular tachyarrhythmias: a novel association?L Eckardt, P Kirchhof, P Loh, et al.Endocrine Research|February 1, 1995
Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylaseE Schulze, G Scharer, A Rogatzki, et al.Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndromeE Schulze-Bahr, W Haverkamp, H Wiebusch, et al.Zeitschrift Fur Kardiologie|May 16, 2000
Molecular genetics of arrhythmias--a new paradigmE Schulze-Bahr, W Haverkamp, M Borggrefe, et al.Thyroid : Official Journal of the American Thyroid Association|December 17, 2005
Primary hyperparathyroidism as the leading symptom in a patient with a Y791F RET mutationH Vierhapper, S Rondot, E Schulze, et al.Psychiatry Research|July 7, 2015
The association of non-suicidal self-injury and suicidal behavior according to DSM-5 in adolescent psychiatric inpatientsRebecca C Groschwitz, Michael Kaess, Gloria Fischer, et al.Surgical Endoscopy|August 19, 2016
Location of a biliary leak after liver resection determines success of endoscopic treatmentAnja Schaible, Peter Schemmer, Thilo Hackert, et al.Rheumatology International|January 1, 1989
IGM-containing immune complexes and antiphospholipid antibodies in patients with Sneddon's syndromeE Schulze-Lohoff, F Krapf, L Bleil, et al.Southern Medical Journal|May 31, 2007
Coincidental consort clear cell cutaneous carcinoma: facial squamous cell carcinoma in situ containing human papillomavirus and cancer cells with clear cytoplasm in an octogenarian couplePhilip R Cohen, Keith E Schulze, Peter L Rady, et al.Pageof 33