Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood

Kidney International

Volumn 80, Issue 7, 2011, Pages 768-776

  Faguer, Stanislas ^a,b,c   Decramer, Stéphane ^b,c,d   Chassaing, Nicolas ^c,e   Bellanné Chantelot, Christine ^f   Calvas, Patrick ^c,e   Beaufils, Sandrine ^f   Bessenay, Lucie ^g   Lengelé, Jean Philippe ^h   Dahan, Karine ^h   Ronco, Pierre ⁱ   Devuyst, Olivier ^h   Chauveau, Dominique ^a,b,c  

^a CHU RANGUEIL   (France)

^b Centre de Référence des Maladies Rénales Rares du Sud Ouest   (France)

^c University Hospital of Toulouse   (France)

^d HÔPITAL DES ENFANTS   (France)

^e CHU PURPAN   (France)

^f PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^g UNIVERSITY HOSPITAL OF CLERMONT FERRAND   (France)

^h CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

ⁱ HÔPITAL TENON   (France)

Author keywords

adult patients; HNF1Beta; hypomagnesemia; MODY5; tubulointerstitial nephropathy

Indexed keywords

ADOLESCENT; ADULT; ADULTHOOD; AGED; ARTICLE; CLINICAL ARTICLE; DISEASE COURSE; FANCONI RENOTUBULAR SYNDROME; FEMALE; GENE; GENE DELETION; GENETIC ANALYSIS; HNF1B GENE; HNF1B NEPHROPATHY; HUMAN; HYPOKALEMIA; HYPOMAGNESEMIA; INFERTILITY; KIDNEY CYST; KIDNEY DISEASE; KIDNEY FAILURE; MALE; MATURITY ONSET DIABETES MELLITUS; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; PROGNOSIS; SOLITARY KIDNEY;

EID: 80052844338     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/ki.2011.225     Document Type: Article

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