Cystic Fibrosis Presenting with Neonatal Cholestasis Simulating Biliary Atresia in a Patient with a Novel Mutation

No abstract is available for this paper.

• Publication year

  2013

• Venue

  Indian Journal of Pediatrics

• Publication date

  2013-06-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s12098-012-0842-5PMID 22798282
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Epidemiology of liver disease in cystic fibrosis: a longitudinal study.

  2004cited by this paper
• Liver disease in cystic fibrosis: A prospective study on incidence, risk factors, and outcome

  2002cited by this paper
• Retrospective review of cystic fibrosis presenting as infantile liver disease

  1999cited by this paper
• Clinical and Genetic Risk Factors for Cystic Fibrosis-related Liver Disease

  1999cited by this paper
• Natural history of liver disease in cystic fibrosis

  1999cited by this paper
• Neonatal cholestasis as the presenting feature in cystic fibrosis.

  1996cited by this paper
• Hepatobiliary Disease in Cystic Fibrosis

  1994cited by this paper
• Analysis of risk factors for the development of liver disease associated with cystic fibrosis.

  1994cited by this paper
• Cystic Fibrosis Mistaken for Idiopathic Biliary Atresia

  1985cited by this paper
• Prolonged Neonatal Jaundice in Cystic Fibrosis

  1971cited by this paper

• Afectarea hepatică în mucoviscidoză

  2023cites this paper
• Biliary Atresia and Rare Concurrent Cystic Fibrosis Variant: Case Report and Management Considerations

  2023cites this paper
• Biliary atresia and its mimics

  2022cites this paper
• Biliary Atresia: A Complex Hepatobiliary Disease with Variable Gene Involvement, Diagnostic Procedures, and Prognosis

  2022cites this paper
• [Clinical characteristics and gene variants of patients with infantile intrahepatic cholestasis].

  2021cites this paper
• Recent advances in the early treatment of cystic fibrosis: Bridging the gap to highly effective modulator therapy

  2021cites this paper
• A Proposed Diagnostic Algorithm for Inborn Errors of Metabolism Presenting With Movements Disorders

  2020cites this paper
• Neonatale Cholestase

  2020cites this paper
• Acholic stools and a small gallbladder: Not always a case of biliary atresia

  2020cites this paper
• Unusual Cystic Fibrosis Transmembrane Conductance Regulator Mutations and Liver Disease: A Case Series and Review of the Literature.

  2019cites this paper
• Neonatal cholestasis: recent insights

  2019cites this paper
• Evaluation of Etiologic and Clinical Symptoms in Intrahepatic Bile Duct Diseases: A Single Centre Study

  2019cites this paper
• Cystic Fibrosis: Clinical Phenotypes in Children and Adolescents

  2018cites this paper
• Gastrointestinal, Pancreatic, and Hepatobiliary Manifestations of Cystic Fibrosis.

  2016cites this paper
• Cystic Fibrosis Related Liver Disease—Another Black Box in Hepatology

  2014cites this paper
• Heritable disorders in the metabolism of the dolichols: A bridge from sterol biosynthesis to molecular glycosylation

  2012cites this paper