CFTR and/or pancreatitis susceptibility genes mutations as risk factors of pancreatitis in cystic fibrosis patients?
Author:
Funder
Vaincre La Mucoviscidose
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology,Endocrinology, Diabetes and Metabolism
Reference36 articles.
1. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis;Welsh;Cell,1993
2. Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice;Castellani;J Cyst Fibros,2008
3. Discussion on genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis;Dray;Gastroenterology,2003
4. The Cystic Fibrosis Genotype-Phenotype Consortium. Correlation between genotype and phenotype in patients with cystic fibrosis;NEngl J Med,1993
5. Recurrent acute pancreatitis in patients with cystic fibrosis with normal pancreatic enzymes;Shwachman;Pediatrics,1975
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1. Acute Recurrent Pancreatitis in a Child With INS-Related Monogenic Diabetes and a Heterozygous Pathogenic CFTR Mutation;Journal of the Endocrine Society;2022-12-12
2. Central role of the sentinel acute pancreatitis event (SAPE) model in understanding recurrent acute pancreatitis (RAP): Implications for precision medicine;Frontiers in Pediatrics;2022-08-15
3. International Approaches to Management of CFTR-Related Metabolic Syndrome/Cystic Fibrosis Screen Positive, Inconclusive Diagnosis;International Journal of Neonatal Screening;2022-01-11
4. Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID);Journal of Cystic Fibrosis;2021-09
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