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Volumn 35, Issue 1, 2002, Pages 44-50

Niemann-Pick disease type C in neonatal cholestasis at a North American Center

Author keywords

Biliary atresia; Idiopathic neonatal hepatitis; Lipid storage disease

Indexed keywords

ADOLESCENT; ARTICLE; CHOLESTASIS; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; ELECTRON MICROSCOPY; ETHNIC GROUP; FEMALE; GENE MUTATION; HEPATOSPLENOMEGALY; HUMAN; INFANT; LIPID ANALYSIS; LIVER CIRRHOSIS; MALE; NEWBORN; NEWBORN HEPATITIS; NIEMANN PICK DISEASE; ONSET AGE; PRIORITY JOURNAL; SPLENOMEGALY;

EID: 0036068897     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005176-200207000-00011     Document Type: Article
Times cited : (87)

References (23)
  • 8
    • 0033361755 scopus 로고    scopus 로고
    • Niemann-Pick CI disease: The I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype
    • (1999) Am J Hum Genet , vol.65 , pp. 1321-1329
    • Millat, G.1    Marcais, C.2    Rafi, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.