Showing results (151-160 of 224) with videos related to
Sort By:
Pageof 23
American Journal of Human Genetics|April 1, 1993
De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16)J Lamb, P C Harris, A O Wilkie, et al.Alimentary Pharmacology & Therapeutics|July 2, 2015
Somatostatin analogues improve health-related quality of life in polycystic liver disease: a pooled analysis of two randomised, placebo-controlled trialsM K Neijenhuis, T J G Gevers, F Nevens, et al.Computers in Biology and Medicine|July 14, 2020
Semi-supervised labelling of the femur in a whole-body post-mortem CT database using deep learningC A Peña-Solórzano, D W Albrecht, R B Bassed, et al.Kidney International|June 1, 1987
Blood pressure determinants in living-related renal allograft donors and their recipientsV E Torres, K P Offord, C F Anderson, et al.Circulation|June 1, 1991
Pathogenesis of edema in constrictive pericarditis. Studies of body water and sodium, renal function, hemodynamics, and plasma hormones before and after pericardiectomyI S Anand, R Ferrari, G S Kalra, et al.International Journal of Cardiology|September 1, 1990
Enalapril as initial and sole treatment in severe chronic heart failure with sodium retentionI S Anand, G S Kalra, R Ferrari, et al.Circulation|August 1, 1989
Edema of cardiac origin. Studies of body water and sodium, renal function, hemodynamic indexes, and plasma hormones in untreated congestive cardiac failureI S Anand, R Ferrari, G S Kalra, et al.Human Molecular Genetics|April 1, 1995
Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletionB Peral, V Gamble, J L San Millán, et al.American Journal of Medical Genetics|October 16, 1996
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 GeneS Rossetti, E Bresin, G Restagno, et al.Molecular Cell|September 12, 1998
Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominant polycystic kidney diseaseT J Watnick, V E Torres, M A Gandolph, et al.Pageof 23