SCOPUS 정보 검색 플랫폼

Volumn 62, Issue 2, 2004, Pages 155-157

Late-onset primary hyperoxaluria triggered by hypothyroidism and presenting as rapidly progressive renal failure - Description of a new mutation

(5) Tintillier, M a Pochet, J M a Cosyns, J P b Delgrange, E a Donckier, J a

a UNIVERSITY HOSPITAL OF MONT GODINNE (Belgium)

b CLINIQUES UNIVERSITAIRES SAINT LUC (Belgium)

Author keywords

Liver deficiency peroxysomal alanine: Glyoxylate aminotransferase (AGT); Primary hyperoxaluria type 1 (PH1)

Indexed keywords

ACENOCOUMAROL; ALANINE AMINOTRANSFERASE; AMIODARONE; CALCIUM OXALATE; FLECAINIDE; LERCANIDIPINE;

AGED; ARTICLE; BRADYCARDIA; CASE REPORT; ENZYME ACTIVITY; FEMALE; GENE MUTATION; HEART ATRIUM FIBRILLATION; HUMAN; HYPEROXALURIA; HYPOTHYROIDISM; INTERSTITIAL NEPHRITIS; KIDNEY COLIC; KIDNEY FAILURE; LEUKOCYTURIA; PRIMARY HYPEROXALURIA TYPE 1; STROKE;

EID: 4444252990 PISSN: 03010430 EISSN: None Source Type: Journal
DOI: 10.5414/cnp62155 Document Type: Article

Times cited : (4)

References (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.