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Transplantation, ISSN 0041-1337, 07/2018, Volume 102 Suppl 7S-1, pp. S517 - S517
INTRODUCTIONUrothelial carcinoma (UC) has the characteristic of high mutational burden and elevated degree of molecular heterogeneity compared with other solid... 
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 05/2015, Volume 30, Issue suppl_3, pp. iii572 - iii572
Journal Article
Kidney International, ISSN 0085-2538, 06/2014, Volume 85, Issue 6, pp. 1429 - 1433
Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately half of children with chronic kidney disease. CAKUT can be caused by... 
renal development | renal agenesis | genetic renal disease | CAKUT | PREVALENCE | HEPATOCYTE NUCLEAR FACTOR-1-BETA | VESICOURETERAL REFLUX | ADYSPLASIA | RENAL-COLOBOMA SYNDROME | MALFORMATIONS | UROLOGY & NEPHROLOGY | PAX2 MUTATIONS | TCF2 | HYPODYSPLASIA
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 01/2017, Volume 28, Issue 1, pp. 69 - 75
Congenital anomalies of the kidneys and urinary tract (CAKUT) are the leading cause of CKD in children, featuring a broad variety of malformations. A monogenic... 
PRIMARY HYPEROXALURIA | MALFORMATIONS | GENE | CILIOPATHIES | CLINICAL PRESENTATION | ABNORMALITIES | WOLFRAM-SYNDROME | DISEASE | RECESSIVE MUTATIONS | CYSTINOSIS | UROLOGY & NEPHROLOGY | Vesico-Ureteral Reflux - genetics | Exome - genetics | Phenotype | Humans | Mutation | Syndrome | Urogenital Abnormalities - genetics | monogenic disease | CAKUT | WES | Brief Communications
Journal Article
Journal of the American Society of Nephrology : JASN, ISSN 1046-6673, 09/2014, Volume 25, Issue 9, pp. 1917 - 1922
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 10/2013, Volume 93, Issue 4, pp. 672 - 686
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2013, Volume 93, Issue 2, pp. 336 - 345
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 04/2014, Volume 29, Issue 4, p. 695
Congenital anomalies of the kidney and urinary tract (CAKUT) cover a wide range of structural malformations that result from defects in the morphogenesis of... 
Kidneys | Gene mutations | Abnormalities | Physiological aspects | Birth defects | Genetic aspects | Research | Children | Kidney diseases | Risk factors
Journal Article
Hong Kong Journal of Nephrology, ISSN 1561-5413, 10/2015, Volume 17, Issue 2, pp. S63 - S63
Journal Article
The American Journal of the Medical Sciences, ISSN 0002-9629, 09/2018, Volume 356, Issue 3, pp. 268 - 276
BACKGROUND:Hematuria may indicate nondiabetic renal disease in diabetic chronic kidney disease (CKD). However, some studies have reported that hematuria is... 
Rapid renal progression | End-stage renal disease | Chronic kidney disease | Hematuria | MORTALITY | DIFFERENTIAL DIAGNOSTIC MODEL | OVERT PROTEINURIA | BIOPSY | CLASSIFICATION | PREVALENCE | MELLITUS | MEDICINE, GENERAL & INTERNAL | MICROSCOPIC HEMATURIA | IGA NEPHROPATHY | COHORT
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 04/2017, Volume 7, Issue 1, pp. 1236 - 9
Diabetes duration, diabetic retinopathy (DR), and a diagnostic model have been proposed as clinical parameters favoring the presence of diabetic nephropathy... 
DIAGNOSIS | ALBUMINURIA | MULTIDISCIPLINARY SCIENCES | BIOPSY | CLASSIFICATION | PREVALENCE | MELLITUS | SPECTRUM | RETINAL MICROVASCULAR ABNORMALITIES | End-stage renal disease | Diabetic retinopathy | Survival analysis | Nephropathy | Retinopathy | Diabetes mellitus | Diabetes | Kidney diseases | Proteinuria | Kidney transplantation
Journal Article
Journal Article