An Atypical Presentation of Alagille Syndrome
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[1] C. Pappone,et al. Novel JAG1 Deletion Variant in Patient with Atypical Alagille Syndrome , 2019, International journal of molecular sciences.
[2] H. Whyte,et al. Williams syndrome presenting with findings consistent with Alagille syndrome , 2014, Clinical case reports.
[3] V. Sundaram,et al. Atypical causes of cholestasis. , 2014, World journal of gastroenterology.
[4] N. Spinner,et al. Spectrum of JAG1 gene mutations in Polish patients with Alagille syndrome , 2014, Journal of Applied Genetics.
[5] N. Spinner,et al. Clinical utility gene card for: Alagille Syndrome (ALGS) , 2013, European Journal of Human Genetics.
[6] J. Hartley,et al. Alagille syndrome and other hereditary causes of cholestasis. , 2013, Clinics in liver disease.
[7] S. Ellard,et al. JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndrome , 2012, Clinical genetics.
[8] P. Vajro,et al. Alagille syndrome: an overview. , 2012, Clinics and research in hepatology and gastroenterology.
[9] S. Ellard,et al. Alagille syndrome: pathogenesis, diagnosis and management , 2011, European Journal of Human Genetics.
[10] I. Krantz,et al. NOTCH2 mutations in Alagille syndrome , 2011, Journal of Medical Genetics.
[11] T. Pranikoff,et al. Biliary Disease in Children , 2011, Current gastroenterology reports.
[12] C. Scudamore,et al. Choledochal cysts: part 2 of 3: Diagnosis. , 2009, Canadian journal of surgery. Journal canadien de chirurgie.
[13] Richard J. Thompson,et al. Lack of hepatocellular CD10 along bile canaliculi is physiologic in early childhood and persistent in Alagille syndrome , 2007, Laboratory Investigation.
[14] N. Spinner,et al. Interlobular Bile Duct Loss in Pediatric Cholestatic Disease is Associated with Aberrant Cytokeratin 7 Expression by Hepatocytes , 2007, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
[15] D. Piccoli,et al. Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate , 2006, Human mutation.
[16] H. Won,et al. Can MRCP replace the diagnostic role of ERCP for patients with choledochal cysts? , 2005, Gastrointestinal endoscopy.
[17] R. Sokol,et al. Proliferation to Paucity: Evolution of Bile Duct Abnormalities in a Case of Alagille Syndrome , 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
[18] I. Krantz,et al. Features of alagille syndrome in 92 patients: Frequency and relation to prognosis , 1999, Hepatology.
[19] I. Krantz,et al. Alagille syndrome. , 1997, Journal of medical genetics.
[20] E. Yunis,et al. Syndromatic paucity of interlobular bile ducts: hepatic histopathology of the early and endstage liver. , 1988, Pediatric pathology.
[21] H. Zimmerman. Hepatology: A textbook of liver disease:By D. Zakim and T. D. Boyer. 1318 pp., $95.00. W. B. Saunders Company, Philadelphia, Pennsylvania, 1982 , 1983 .
[22] M. Hadchouel,et al. Reduced ratio of portal tracts to paucity of intrahepatic bile ducts. , 1978, Archives of pathology & laboratory medicine.