Autosomal-dominant medullary cystic kidney disease type 1: Clinical and molecular findings in six large Cypriot families

Kidney International

Volumn 62, Issue 4, 2002, Pages 1385-1394

  Stavrou, Christoforos ^a,b,c,d   Koptides, Michael ^a,b,c,d,e   Tombazos, Christos ^a,b,c,d   Psara, Evlalia ^a,b,c,d   Patsias, Charalambos ^a,b,c,d   Zouvani, Ioanna ^a,b,c,d   Kyriacou, Kyriacos ^a,b,c,d   Hildebrandt, Friedhelm ^a,b,c,d   Christofides, Tasos ^a,b,c,d   Pierides, Alkis ^a,b,c,d   Deltas, C Constantinou ^a,b,c,d  

^a NICOSIA GENERAL HOSPITAL   (Cyprus)

^b Pafos General Hospital   (Cyprus)

^c UNIVERSITY OF FREIBURG   (Germany)

^d UNIVERSITY OF CYPRUS   (Cyprus)

^e INTERCOLLEGE   (Cyprus)

Author keywords

ADMCKD; Gout; Hyperuricemia; Linkage analysis; MCKD1 gene; Medullary cystic kidney disease; Nephronophthisis

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BIOCHEMISTRY; BODY SURFACE; CALCULATION; CLINICAL FEATURE; CONTROLLED STUDY; CREATININE CLEARANCE; DNA FLANKING REGION; ECHOGRAPHY; FAMILY; FEMALE; HISTOPATHOLOGY; HUMAN; HYPERTENSION; HYPERURICEMIA; KIDNEY CONCENTRATING CAPACITY; KIDNEY CYST; KIDNEY FAILURE; KIDNEY FUNCTION; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MEDULLARY SPONGE KIDNEY; PRIORITY JOURNAL; SODIUM EXCRETION;

EID: 18544388555     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2002.00581.x     Document Type: Article

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