Classification of the biliary atresia phenotype

Pediatrics International

Volumn 52, Issue 6, 2010, Pages 897-

  Shalaby, Aly ^a   Makin, Erica ^a   Davenport, Mark ^a  

^a KING S COLLEGE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BILE DUCT ATRESIA; DISEASE CLASSIFICATION; FECES; HUMAN; HYPERBILIRUBINEMIA; LETTER; PHENOTYPE; PRIORITY JOURNAL;

AGE OF ONSET; BILIARY ATRESIA; BILIRUBIN; CHILD; DIAGNOSIS, DIFFERENTIAL; FECES; FEMALE; HEPATIC ARTERY; HUMANS; HYPERBILIRUBINEMIA; INFANT; INFANT, NEWBORN; MALE; MEDICAL HISTORY TAKING; PHENOTYPE; PREGNANCY; RETROSPECTIVE STUDIES; TAIWAN; ULTRASONOGRAPHY, PRENATAL;

EID: 78650490604     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2010.03275.x     Document Type: Letter

References (6)

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3. Davenport M, Savage M, Mowat AP, Howard ER,. Biliary atresia splenic malformation syndrome: An etiologic and prognostic subgroup. Surgery 1993; 113: 662-8.
4. Makin E, Quaglia A, Kvist N, Petersen BL, Portmann B, Davenport M,. Congenital biliary atresia: Liver injury begins at birth. J. Pediatr. Surg. 2009; 44: 630-3.
5. Caponcelli E, Knisely AS, Davenport M,. Cystic biliary atresia: An etiologic and prognostic subgroup. J. Pediatr. Surg. 2008; 43: 1619-24.
6. Livesey E, Cortina Borja M, Sharif K, et al. Epidemiology of biliary atresia in England and Wales (1999-2006). Arch. Dis. Child. Fetal Neonatal Ed. 2009; 94: F451-5.