227 related articles for article (PubMed ID: 28090565)
21. Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification.
Gilbert MA; Bauer RC; Rajagopalan R; Grochowski CM; Chao G; McEldrew D; Nassur JA; Rand EB; Krock BL; Kamath BM; Krantz ID; Piccoli DA; Loomes KM; Spinner NB
Hum Mutat; 2019 Dec; 40(12):2197-2220. PubMed ID: 31343788
[TBL] [Abstract][Full Text] [Related]
22. Alagille Syndrome and the Liver: Current Insights.
P Singh S; K Pati G
Euroasian J Hepatogastroenterol; 2018; 8(2):140-147. PubMed ID: 30828556
[TBL] [Abstract][Full Text] [Related]
23. Novel Heterozygous Mutations in
Brennan A; Kesavan A
Case Rep Pediatr; 2017; 2017():1368189. PubMed ID: 28465853
[TBL] [Abstract][Full Text] [Related]
24. Alagille Syndrome: Diagnostic Challenges and Advances in Management.
Ayoub MD; Kamath BM
Diagnostics (Basel); 2020 Nov; 10(11):. PubMed ID: 33172025
[TBL] [Abstract][Full Text] [Related]
25. Alagille Syndrome.
Mitchell E; Gilbert M; Loomes KM
Clin Liver Dis; 2018 Nov; 22(4):625-641. PubMed ID: 30266153
[TBL] [Abstract][Full Text] [Related]
26. Human Jagged 1 mutants cause liver defect in Alagille syndrome by overexpression of hepatocyte growth factor.
Yuan ZR; Kobayashi N; Kohsaka T
J Mol Biol; 2006 Feb; 356(3):559-68. PubMed ID: 16403414
[TBL] [Abstract][Full Text] [Related]
27. Alagille syndrome: understanding the genotype-phenotype relationship and its potential therapeutic impact.
Halma J; Lin HC
Expert Rev Gastroenterol Hepatol; 2023; 17(9):883-892. PubMed ID: 37668532
[TBL] [Abstract][Full Text] [Related]
28. Clinical and genetic analysis in Chinese children with Alagille syndrome.
Chen Y; Sun M; Teng X
BMC Pediatr; 2022 Nov; 22(1):688. PubMed ID: 36447191
[TBL] [Abstract][Full Text] [Related]
29. Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome.
Ohashi K; Togawa T; Sugiura T; Ito K; Endo T; Aoyama K; Negishi Y; Kudo T; Ito R; Saitoh S
Acta Paediatr; 2017 Nov; 106(11):1817-1824. PubMed ID: 28695677
[TBL] [Abstract][Full Text] [Related]
30. Alagille Syndrome: A Novel Mutation in
Fischetto R; Palmieri VV; Tripaldi ME; Gaeta A; Michelucci A; Delvecchio M; Francavilla R; Giordano P
Front Pediatr; 2019; 7():199. PubMed ID: 31157196
[TBL] [Abstract][Full Text] [Related]
31. Alagille-like syndrome with surprising karyotype: a case report.
Amimoto S; Ishii M; Tanaka K; Araki S; Kuwamura M; Suga S; Kondo E; Shibata E; Kusuhara K; Yoshino K
J Med Case Rep; 2023 Apr; 17(1):186. PubMed ID: 37101309
[TBL] [Abstract][Full Text] [Related]
32. Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes.
Schindler EA; Gilbert MA; Piccoli DA; Spinner NB; Krantz ID; Loomes KM
Am J Med Genet A; 2021 Mar; 185(3):719-731. PubMed ID: 33369123
[TBL] [Abstract][Full Text] [Related]
33. Case Report: Novel JAG1 gene mutations in two infants with alagille syndrome characterized by cholestasis.
Han Y; Zhu K; Wu H; Chen B; Hu S; Lai D; Tou J
Front Pediatr; 2022; 10():1017647. PubMed ID: 36340723
[TBL] [Abstract][Full Text] [Related]
34. [From gene to disease: arteriohepatic dysplasia or Alagille syndrome].
Brooks AS; Dooijes D
Ned Tijdschr Geneeskd; 2003 Jun; 147(25):1213-5. PubMed ID: 12848056
[TBL] [Abstract][Full Text] [Related]
35. The role of Notch receptor expression in bile duct development and disease.
Flynn DM; Nijjar S; Hubscher SG; de Goyet Jde V; Kelly DA; Strain AJ; Crosby HA
J Pathol; 2004 Sep; 204(1):55-64. PubMed ID: 15307138
[TBL] [Abstract][Full Text] [Related]
36. [Advances in the diagnosis and treatment of Alagille syndrome].
Ma YL; Song YZ
Zhongguo Dang Dai Er Ke Za Zhi; 2014 Nov; 16(11):1188-92. PubMed ID: 25406571
[TBL] [Abstract][Full Text] [Related]
37. Bile Ducts in Regenerative Liver Nodules of Alagille Patients Are Not the Result of Genetic Mosaicism.
Rougemont AL; Alvarez F; McLin VA; Guiochon-Mantel A; Bouligand J; Clément S; Tonson La Tour A; Wildhaber BE; Rubbia-Brandt L; Sartelet H
J Pediatr Gastroenterol Nutr; 2015 Jul; 61(1):91-3. PubMed ID: 25643021
[TBL] [Abstract][Full Text] [Related]
38. A Novel c.91dupG
Reyes-de la Rosa ADP; Varela-Fascinetto G; García-Delgado C; Vázquez-Martínez ER; Valencia-Mayoral P; Cerbón M; Morán-Barroso VF
Case Rep Genet; 2018; 2018():1369413. PubMed ID: 30046498
[TBL] [Abstract][Full Text] [Related]
39.
Almes M; Gardin A; Davit-Spraul A; Bouligand J; Habes D; Jacquemin E
JPGN Rep; 2023 Aug; 4(3):e338. PubMed ID: 37600608
[No Abstract] [Full Text] [Related]
40. Identification of Bile Duct Paucity in Alagille Syndrome: Using CK7 and EMA Immunohistochemistry as a Reliable Panel for Accurate Diagnosis.
Herman HK; Abramowsky CR; Caltharp S; Metry D; Cundiff CA; Romero R; Gillespie SE; Shehata BM
Pediatr Dev Pathol; 2016; 19(1):47-50. PubMed ID: 26366614
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
