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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 Clinical Investigation, ISSN 0021-9738, 08/2013, Volume 123, Issue 8, pp. 3243 - 3253
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 05/2011, Volume 121, Issue 5, pp. 2013 - 2024
Steroid-resistant nephrotic syndrome (SRNS) is a frequent cause of end-stage renal failure. Identification of single-gene causes of SRNS has generated some... 
MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | GENE | COENZYME-Q BIOSYNTHESIS | DIPHOSPHATE SYNTHASE SUBUNIT-2 | NPHS2 | GLOMERULAR PROTEIN | UBIQUINONE BIOSYNTHESIS | COQ DEFICIENCY | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | SACCHAROMYCES-CEREVISIAE | Deafness | Gene mutations | Genetic aspects | Nephrotic syndrome | Research | Health aspects | Risk factors
Journal Article
The Pediatric Infectious Disease Journal, ISSN 0891-3668, 11/2019, p. 1
BACKGROUND:Urinary tract infection (UTI) is a common cause of fever in children. Despite the increasing numbers of extended-spectrum beta-lactamase-producing... 
Journal Article
Kidney International, ISSN 0085-2538, 04/2014, Volume 85, Issue 4, pp. 880 - 887
Journal Article
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 09/2010, Volume 5, Issue 9, pp. 1655 - 1662
Journal Article
世界胃肠病学杂志:英文版, ISSN 1007-9327, 2016, Issue 26, pp. 6089 - 6094
Henoch-Sch?nlein purpura(HSP) is generally a selflimited vasculitis disease and has a good prognosis. We report a 4-year-old Thai boy who presented with... 
purpura;Corticosteroids;Vasculitis;Intestinal | ischemia;Peritoniti | Henoch-Sch?nlein | perforation;Bowel
Journal Article
Journal of the American Society of Nephrology : JASN, ISSN 1046-6673, 09/2014, Volume 25, Issue 9, pp. 1917 - 1922
Journal Article
World Journal of Gastroenterology, ISSN 1007-9327, 07/2016, Volume 22, Issue 26, pp. 6089 - 6094
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 10/2011, Volume 22, Issue 10, pp. 1815 - 1820
In two siblings of consanguineous parents with intermittent nephrotic-range proteinuria, we identified a homozygous deleterious frameshift mutation in the gene... 
UROLOGY & NEPHROLOGY | LINKAGE ANALYSIS | IMERSLUND-GRASBECK-SYNDROME | NEPHROTIC SYNDROME | NEPHROPATHY | CAPTURE | DEFICIENCY | Exome | Homozygote | Frameshift Mutation | Humans | Proteinuria - genetics | Genes, Recessive | Receptors, Cell Surface - genetics | Brief Communications
Journal Article
Journal Article