> (Немає відомостей про примірники) Шифр: N3/2014/29/1 Журнал 2014р. Vol. 29 N 1 McIntyre, Ch. W. Cardiovascular benefits of daily haemodialysis: peeling the onion / Ch.W. McIntyre. - P.1-4 Wang, C. J. Implications of predonation GFR to recipient and donor outcomes / C.J. Wang, J.B. Wetmore, B.L. Kasiske. - P.5-9 : табл. Lemley, K. V. LMX1B mutations with nails and kneecaps: a new paradigm? / K.V. Lemley. - P.9-12 : il Kovesdy, C. P. Do FGF23 levels change over time and if yes, what do such changes mean / C.P. Kovesdy. - P.12-14 Floege, J. The ERA-EDTA database on recurrent glomerulonephritis following renal transplantation / J. Floege, H. Regele, L. Gesualdo. - P.15-21 : табл. Desir, G. V. Renalase in hypertension and kidney disease / G.V. Desir, A.J. Peixoto. - P.22-28 : цв.ил Haemostasis in chronic kidney disease . - P.29-40 : цв.ил Lorenz, G. Canonical and non-canonical effects of the NLRP3 inflammasome in kidney inflammation and fibrosis / G. Lorenz, M.N. Darisipudi, H.-J. Anders. - P.41-48 : цв.ил The role of heparanase and the endothelial glycocalyx in the development of proteinuria. - P.49-55 : табл. p-Cresyl sulphate has pro-inflammatory and cytotoxic actions on human proximal tubular epithelial cells. - P.56-64 : граф. Fluid flow shear stress over podocytes is increased in the solitary kidney. - P.65-72 : граф. Repulsive guidance cue semaphorin 3A in urine predicts the progression of acute kidney injury in adult patients from a mixed intensive care unit. - P.73-80 : табл. LMX1B mutation with residual trancriptional activity as a cause of isolated glomerulopathy. - P.81-88 : цв.ил Time-averaged level of fibriblast growth factor-23 and clinical events in chronic kidney disease. - P.88-97 : табл. The effect of cholecalciferol for lowering albuminuria in chronic kidney disease: a prospective controlled study. - P.97-109 : табл. Renal prognosis a long time after renal biopsy on patients with diabetic nephropathy. - P.109-118 : табл. Postprandial responses of incretin and pancreatic hormones in non-diabetic patients with end-stage renal disease. - P.119-127 : табл. Serum and adipose tissue fatty acid composition as biomarkers of habitual dietary fat intake in elderly men with chronic kidney disease. - P.128-136 : табл. Determination of uromodulin in human urine: influence of storage and processing. - P.136-145 : il Increased bone fractures among elderly United States hemodialysis patients . - P.146-151 : табл. Sevelamer carbonate lowers serum phosphorus effectively in haemodialysis patients: a randomized, double-blind, placebo-controlled, dose-titration study . - P.152-160 : табл. Efficacy and safety of radiofrequency catheter ablation for atrial fibrillation in chronic hemodialysis patients. - P.160-167 : табл. Effects of daily hemodialysis on heart rate variability: results from the Frequent Hemodialysis Network (FHN) Daily Trial. - P.168-178 : табл. Should current criteria for detecting and repairing arteriovenous fistula stenosis be reconsidered? Interim analysis of a randomized controlled trial . - P.179-187 : табл. Living kidney donor estimated glomerular filtration rate and recipient graft survival . - P.188-195 : табл. Longitudinal changes in body mass index following renal transplantation in UK children. - P.196-203 : табл. The prognostic value of time needed on dialysis in patients with delayed graft function. - P.203-208 : табл. Calcineurin inhibitors in HLA-identical living related donor kidney transplantation. - P.209-218 : табл. Немає відомостей про примірники |
Lemley, K. V. LMX1B mutations with nails and kneecaps: a new paradigm? [Text] / K.V. Lemley> // NEPHROLOGY DIALYSIS TRANSPLANTATION . - 2014. - Vol. 29, N1. - P9-12 : il. - 16 16 ref. . - ISSN 1753-0784 Рубрики: ГЕНЕТИЧЕСКИЕ БОЛЕЗНИ ВРОЖДЕННЫЕ--GENETIC DISEASES, INBORN NAIL-PATELLA СИНДРОМ--NAIL-PATELLA SYNDROME МУТАЦИЯ--MUTATION Экз-ры: |
Lemley, K. V. LMX1B mutations with nails and kneecaps: a new paradigm? [Text] / K.V. Lemley> // NEPHROLOGY, DIALYSIS, TRANSPLANTATION. - 2014. - Vol.29, N1. - P9-12 : il. - 16 ref. . - ISSN 0931-0509 Рубрики: ГЕНЕТИЧЕСКИЕ БОЛЕЗНИ ВРОЖДЕННЫЕ--GENETIC DISEASES, INBORN NAIL-PATELLA СИНДРОМ--NAIL-PATELLA SYNDROME МУТАЦИЯ--MUTATION Экз-ры: |