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Deutsche Medizinische Wochenschrift (1946)|September 26, 2003
[Hereditary medullary thyroid carcinoma--genotype-phenotype characterization]K Frank-Raue, C Heimbach, S Rondot, et al.Pacing and Clinical Electrophysiology : PACE|May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndromeG Moennig, E Schulze-Bahr, H Wedekind, et al.The Review of Scientific Instruments|July 10, 2021
Ultrasound measurement technique for the single-turn-coil magnetsT Nomura, A Hauspurg, D I Gorbunov, et al.Journal of Chromatography. A|October 7, 2014
Modeling of the total antioxidant capacity of rooibos (Aspalathus linearis) tea infusions from chromatographic fingerprints and identification of potential antioxidant markersJoanna Orzel, Michal Daszykowski, Malgorzata Kazura, et al.Southern Medical Journal|February 3, 2007
Trigeminal trophic syndromeHedy G Setyadi, Philip R Cohen, Keith E Schulze, et al.Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|May 18, 2006
Late diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyK Müssig, S Kaltenbach, C Maser-Gluth, et al.Zeitschrift Fur Rheumatologie|April 18, 2008
[Organ-specific diagnosis in patients with systemic sclerosis: Recommendations of the German Network for Systemic Sclerosis (DNSS)]N Hunzelmann, E Genth, T Krieg, et al.Journal of Cardiovascular Pharmacology|January 1, 1986
High beta 1-selectivity and favourable pharmacokinetics as the outstanding properties of bisoprololG Haeusler, H J Schliep, P Schelling, et al.Journal of the American Geriatrics Society|February 4, 2011
An educational intervention for providers to promote bone health in high-risk older patientsMark J Simone, David H Roberts, Julie T Irish, et al.Lancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.Pageof 33