SCOPUS 정보 검색 플랫폼

Volumn 21, Issue 6, 2006, Pages 864-866

Neonatal nephrotic presentation of a child with heterozygous NPHS1 mutation

a STANFORD UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

Angiotensin converting enzyme inhibitor; Compound heterozygote; Finnish congenital nephrotic syndrome; NPHS2; Prenatal diagnosis

Indexed keywords

CAPTOPRIL; ENALAPRIL; INDOMETACIN; NEPHRIN; PODOCIN;

ARTICLE; CASE REPORT; CONGENITAL NEPHROTIC SYNDROME; DOSE RESPONSE; DRUG EFFICACY; FOLLOW UP; GENE MUTATION; GENE STRUCTURE; HETEROZYGOSITY; HUMAN; LOW DRUG DOSE; MALE; NEWBORN; PRENATAL SCREENING; PRIORITY JOURNAL;

ADULT; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; FEMALE; HETEROZYGOTE; HUMANS; INFANT, NEWBORN; MALE; MEMBRANE PROTEINS; MUTATION; NEPHROTIC SYNDROME; PRENATAL DIAGNOSIS;

EID: 33646680937 PISSN: 0931041X EISSN: None Source Type: Journal
DOI: 10.1007/s00467-006-0095-5 Document Type: Article

Times cited : (6)

References (7)

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4
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7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.