Showing results (541-550 of 1,194) with videos related to

Sort By:
Pageof 120
Journal of Lipid Research|December 1, 1996
A single nucleotide substitution in the promoter region of the apolipoprotein C-II gene identified in individuals with chylomicronemiaR Streicher, J Geisel, C Weisshaar, et al.
The Journal of Infectious Diseases|November 7, 1998
Herpes simplex virus shedding among human immunodeficiency virus-negative men who have sex with men: site and frequency of sheddingM R Krone, S R Tabet, M Paradise, et al.
Klinische Padiatrie|August 22, 2008
Extreme hyponatremia in an infant with congenital adrenal hypoplasia due to a novel NR0B1 (DAX-1) mutationA Holzinger, F G Riepe, N Krone, et al.
Chest|July 1, 1976
Severe coarctation of the aorta with pulmonary edema. An unusual presentation of a traumatic aortic aneurysmR D Fry, R J Krone, A S Geha, et al.
Journal of the American College of Cardiology|August 17, 2013
In-hospital outcomes of percutaneous coronary interventions in extremely obese and normal-weight patients: findings from the NCDR (National Cardiovascular Data Registry)Saeed Payvar, Sunghee Kim, Sunil V Rao, et al.
Bulletin of Mathematical Biology|January 15, 2020
The Timing and Nature of Behavioural Responses Affect the Course of an EpidemicRebecca C Tyson, Stephanie D Hamilton, Aboubakr S Lo, et al.
The Lancet. Respiratory Medicine|February 8, 2014
Immunosenescence and pneumococcal disease: an imbalance in host-pathogen interactionsCassandra L Krone, Kirsten van de Groep, Krzysztof Trzciński, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 15, 2000
Herpes simplex virus type 2 shedding in human immunodeficiency virus-negative men who have sex with men: frequency, patterns, and risk factorsM R Krone, A Wald, S R Tabet, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|May 16, 2002
Identification of a novel mutation in the arginine vasopressin-neurophysin II gene in familial central diabetes insipidusC Bullmann, J Kotzka, T Grimm, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneityFelix G Riepe, Nils Krone, Michel Morlot, et al.
Pageof 120