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Volumn 27, Issue 3, 2007, Pages 319-323

Bile duct paucity in infancy

Author keywords

[No Author keywords available]

Indexed keywords

ALAGILLE SYNDROME; ALPHA 1 ANTITRYPSIN DEFICIENCY; ARTICLE; ASPLENIA; BILE DUCT ATRESIA; CASE REPORT; CONGENITAL INFECTION; CYSTIC FIBROSIS; DISEASE COURSE; GRAFT VERSUS HOST REACTION; HISTOPATHOLOGY; HUMAN; HYPERBILIRUBINEMIA; INFANT; LIVER FUNCTION TEST; MALE; MALFORMATION SYNDROME; NIEMANN PICK DISEASE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SCLEROSING CHOLANGITIS; TRISOMY 21; WILLIAMS BEUREN SYNDROME; ZELLWEGER SYNDROME;

EID: 34548131078     PISSN: 02728087     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-985076     Document Type: Article
Times cited : (15)

References (14)
  • 1
    • 0023148932 scopus 로고
    • Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
    • Alagille D, Estrada A, Hadchouel M, Gautier M, Odievre M, Dommergues JP. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases. J Pediatr 1987;110:195-200
    • (1987) J Pediatr , vol.110 , pp. 195-200
    • Alagille, D.1    Estrada, A.2    Hadchouel, M.3    Gautier, M.4    Odievre, M.5    Dommergues, J.P.6
  • 2
    • 0024339022 scopus 로고
    • Human ontogeny of the bile duct to portal space ratio
    • Kahn E, Markowitz J, Aiges H, Daum F. Human ontogeny of the bile duct to portal space ratio. Hepatology 1989;10:21-23
    • (1989) Hepatology , vol.10 , pp. 21-23
    • Kahn, E.1    Markowitz, J.2    Aiges, H.3    Daum, F.4
  • 3
    • 0016439420 scopus 로고
    • Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur
    • Alagille D, Odievre M, Gautier M, Dommergues JP. Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr 1975;86:63-71
    • (1975) J Pediatr , vol.86 , pp. 63-71
    • Alagille, D.1    Odievre, M.2    Gautier, M.3    Dommergues, J.P.4
  • 6
    • 0026037503 scopus 로고
    • Paucity of interlobular bile ducts: Arteriohepatic dysplasia and nonsyndromic duct paucity
    • Kahn E. Paucity of interlobular bile ducts: arteriohepatic dysplasia and nonsyndromic duct paucity. Perspect Pediatr Pathol 1991;14:168-215
    • (1991) Perspect Pediatr Pathol , vol.14 , pp. 168-215
    • Kahn, E.1
  • 7
    • 0023551346 scopus 로고
    • Syndromic paucity of the intrahepatic bile ducts: Diagnostic difficulty; severe morbidity throughout early childhood
    • Deprettere A, Portmann B, Mowat AP. Syndromic paucity of the intrahepatic bile ducts: diagnostic difficulty; severe morbidity throughout early childhood. J Pediatr Gastroenterol Nutr 1987;6:865-871
    • (1987) J Pediatr Gastroenterol Nutr , vol.6 , pp. 865-871
    • Deprettere, A.1    Portmann, B.2    Mowat, A.P.3
  • 10
    • 16444386224 scopus 로고    scopus 로고
    • Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6
    • Metcalfe K, Simeonov E, Beckett W, Donnai D, Tassabehji M. Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6. Clin Dysmorphol 2005;14:61-65
    • (2005) Clin Dysmorphol , vol.14 , pp. 61-65
    • Metcalfe, K.1    Simeonov, E.2    Beckett, W.3    Donnai, D.4    Tassabehji, M.5
  • 14
    • 0029015848 scopus 로고
    • Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: Evaluation of 235 patients
    • Lowery MC, Morris CA, Ewart A, et al. Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients. Am J Hum Genet 1995;57:49-53
    • (1995) Am J Hum Genet , vol.57 , pp. 49-53
    • Lowery, M.C.1    Morris, C.A.2    Ewart, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.