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Pediatric Nephrology

Volumn 20, Issue 6, 2005, Pages 824-827

Clinico-pathologic findings in medullary cystic kidney disease type 2

(6) Bleyer, Anthony J a Hart, Thomas C b Willingham, Mark C a Iskandar, Samy S a Gorry, Michael C c Trachtman, Howard d

a WAKE FOREST SCHOOL OF MEDICINE (United States)

b NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH (United States)

c UNIVERSITY OF PITTSBURGH (United States)

d SCHNEIDER CHILDREN'S HOSPITAL (United States)

Author keywords

Familialjuvenile hyperuricemic nephropathy; Tamm Horsfall protein; Uromodulin; Uromodulin associated kidney disease

Indexed keywords

ALANINE; ALLOPURINOL; COLCHICINE; CYSTEINE; GLYCINE; TAMM HORSFALL GLYCOPROTEIN; TYROSINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; EXON; FAMILY HISTORY; FEMALE; FOLLOW UP; GENE MUTATION; GENETIC ANALYSIS; GLOMERULOSCLEROSIS; GOUT; HISTOPATHOLOGY; HUMAN; HYPERURICEMIA; IMMUNOHISTOCHEMISTRY; INTERSTITIAL NEPHRITIS; KIDNEY BIOPSY; KIDNEY FAILURE; KIDNEY FIBROSIS; KIDNEY TUBULE CELL; MALE; MEDULLARY SPONGE KIDNEY; OTITIS MEDIA; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SCHOOL CHILD; UREMIA;

ADENINE; CHILD; GUANINE; HUMANS; IMMUNOHISTOCHEMISTRY; KIDNEY; MALE; MUCOPROTEINS; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; POLYMORPHISM, SINGLE NUCLEOTIDE; STAINING AND LABELING;

EID: 18644384361 PISSN: 0931041X EISSN: None Source Type: Journal
DOI: 10.1007/s00467-004-1719-2 Document Type: Article

Times cited : (24)

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