Síndrome de Alagille: una causa de colestasis intrahepática persistente

Vázquez-Frias, Rodrigo; Worona-Dibner, Liliana; Cabrera-Muñoz, María de Lourdes; Sadowinski-Pine, Stanislaw.
Bol. méd. Hosp. Infant. Méx ; 66(2): 178-188, mar.-abr. 2009. ilus
Artículo en Español | LILACS | ID: lil-701073

Documentos relacionados

  1. Drug-Induced Vanishing Bile Duct Syndrome: From Pathogenesis to Diagnosis and Therapeutics.
  2. Use of a Comprehensive 66-Gene Cholestasis Sequencing Panel in 2171 Cholestatic Infants, Children, and Young Adults.
  3. L-carbocisteine can cause cholestasis with vanishing bile duct syndrome in children: A case report.
  4. [Cervical CUP Syndrome: Diagnosis and Therapy].
  5. Biliary atresia and other cholestatic childhood diseases: Advances and future challenges.
  6. Síndrome de Lemmel: una causa rara de obstrucción biliar no neoplásica de la vía biliar. Presentación de un caso
  7. [Diagnosis and treatment of hereditary cholestasis].
  8. Pediatric Cholestatic Diseases: Common and Unique Pathogenic Mechanisms.
  9. Cloxacillin-induced acute vanishing bile duct syndrome: A case study and literature review.
  10. Costs of pediatric liver transplantation among commercially insured and Medicaid-insured patients with cholestasis in the US.