Hirschsprung's disease

Seminars in Pediatric Surgery

Volumn 19, Issue 3, 2010, Pages 194-200

  Kenny, Simon E ^a   Tam, Paul K H ^b   Garcia Barcelo, Mercè ^b  

^a UNIVERSITY OF LIVERPOOL   (United Kingdom)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Aganglionosis; Etiology; Genetics; Hirschprungs disease

Indexed keywords

ENDOTHELIN 3; ENDOTHELIN B RECEPTOR; ENDOTHELIN CONVERTING ENZYME; GLIAL CELL LINE DERIVED NEUROTROPHIC FACTOR; NEURTURIN; PROTEIN TYROSINE KINASE; TRANSCRIPTION FACTOR SOX10; ZINC FINGER PROTEIN;

AGANGLIONOSIS; ARTICLE; CAUCASIAN; CELL DIFFERENTIATION; CELL MIGRATION; CELL SURVIVAL; CLINICAL FEATURE; DEMOGRAPHY; DOWN SYNDROME; GASTROINTESTINAL MOTILITY; HIRSCHSPRUNG DISEASE; HOMEOBOX; HUMAN; INCIDENCE; INTESTINE INNERVATION; INTESTINE OBSTRUCTION; INTESTINE SURGERY; MOLECULAR GENETICS; MULTIPLE ENDOCRINE NEOPLASIA; NERVOUS SYSTEM; NERVOUS SYSTEM DEVELOPMENT; NEURAL CREST; NEURAL CREST CELL; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ABNORMALITIES, MULTIPLE; DIGESTIVE SYSTEM ABNORMALITIES; FEMALE; FOLLOW UP; GENETIC PREDISPOSITION; GENETICS; MALE; NEWBORN; RISK ASSESSMENT; TREATMENT OUTCOME;

ABNORMALITIES, MULTIPLE; DIGESTIVE SYSTEM ABNORMALITIES; ENTERIC NERVOUS SYSTEM; FEMALE; FOLLOW-UP STUDIES; GENETIC PREDISPOSITION TO DISEASE; HIRSCHSPRUNG DISEASE; HUMANS; INCIDENCE; INFANT, NEWBORN; MALE; RISK ASSESSMENT; TREATMENT OUTCOME;

EID: 77953933416     PISSN: 10558586     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.sempedsurg.2010.03.004     Document Type: Article

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