148 related articles for article (PubMed ID: 28465853)
1. Novel Heterozygous Mutations in
Brennan A; Kesavan A
Case Rep Pediatr; 2017; 2017():1368189. PubMed ID: 28465853
[TBL] [Abstract][Full Text] [Related]
2. Pathogenic Novel Heterozygous Variant c.1076c>T p. (Ser359Phe) chr1: 120512166 in NOTCH2 Gene, Type 2 Alagille Syndrome Causing Neonatal Cholestasis: A Case Report.
Uddin MS; Al Fulayyih S; Al Denaini FF; Al Hatlani MM
Am J Case Rep; 2022 Oct; 23():e935840. PubMed ID: 36201396
[TBL] [Abstract][Full Text] [Related]
3. Two Novel Mutations in the
Prochazková D; Borská R; Fajkusová L; Konečná P; Hloušková E; Pavlovský Z; Slabý O; Pospíšilová Š
Diagnostics (Basel); 2021 May; 11(6):. PubMed ID: 34071626
[TBL] [Abstract][Full Text] [Related]
4. Alagille syndrome: an uncommon cause of intrahepatic cholestasis in adults.
Zhang W; Zhao X; Huang J; Ou X; Jia J
Rev Esp Enferm Dig; 2019 Apr; 111(4):323-326. PubMed ID: 30746957
[TBL] [Abstract][Full Text] [Related]
5. Not only Alagille syndrome. Syndromic paucity of interlobular bile ducts secondary to HNF1β deficiency: a case report and literature review.
Pinon M; Carboni M; Colavito D; Cisarò F; Peruzzi L; Pizzol A; Calosso G; David E; Calvo PL
Ital J Pediatr; 2019 Feb; 45(1):27. PubMed ID: 30791938
[TBL] [Abstract][Full Text] [Related]
6. Alagille syndrome and non-syndromic paucity of the intrahepatic bile ducts.
Gilbert MA; Loomes KM
Transl Gastroenterol Hepatol; 2021; 6():22. PubMed ID: 33824926
[TBL] [Abstract][Full Text] [Related]
7.
Tsai EA; Gilbert MA; Grochowski CM; Underkoffler LA; Meng H; Zhang X; Wang MM; Shitaye H; Hankenson KD; Piccoli D; Lin H; Kamath BM; Devoto M; Spinner NB; Loomes KM
Cell Mol Gastroenterol Hepatol; 2016 Sep; 2(5):663-675.e2. PubMed ID: 28090565
[TBL] [Abstract][Full Text] [Related]
8. Alagille syndrome caused by NOTCH2 mutation presented atypical pathological changes.
ShenTu Y; Mi X; Tang D; Jiang Y; Gao L; Ma X; Zhou B; Yang W; Shi J; Lan D; Chen G; Gong L
Clin Chim Acta; 2021 Oct; 521():258-263. PubMed ID: 34332988
[TBL] [Abstract][Full Text] [Related]
9. Alagille syndrome associated with total anomalous pulmonary venous connection and severe xanthomas: A case report.
Zeng HS; Zhang ZH; Hu Y; Zheng GL; Wang J; Zhang JW; Guo YX
World J Clin Cases; 2022 Sep; 10(25):8932-8938. PubMed ID: 36157644
[TBL] [Abstract][Full Text] [Related]
10. NOTCH2 mutations in Alagille syndrome.
Kamath BM; Bauer RC; Loomes KM; Chao G; Gerfen J; Hutchinson A; Hardikar W; Hirschfield G; Jara P; Krantz ID; Lapunzina P; Leonard L; Ling S; Ng VL; Hoang PL; Piccoli DA; Spinner NB
J Med Genet; 2012 Feb; 49(2):138-44. PubMed ID: 22209762
[TBL] [Abstract][Full Text] [Related]
11. Clinical, Laboratory, Radiological, and Genetic Characteristics of Pediatric Patients with Alagille Syndrome.
Isa HM; Alahmed FA
Adv Biomed Res; 2023; 12():155. PubMed ID: 37564457
[TBL] [Abstract][Full Text] [Related]
12. Novel mutations in
Shaul E; Kogan-Liberman D; Schuckalo S; Jan D; Ewart M; Nguyen T; Martinez M; Ovchinsky N
Pediatr Rep; 2019 Sep; 11(3):8206. PubMed ID: 31595186
[TBL] [Abstract][Full Text] [Related]
13. A case of Alagille syndrome presenting with chronic cholestasis in an adult.
Kim J; Yang B; Paik N; Choe YH; Paik YH
Clin Mol Hepatol; 2017 Sep; 23(3):260-264. PubMed ID: 28683534
[TBL] [Abstract][Full Text] [Related]
14. Clinical features, outcomes, and genetic analysis in Korean children with Alagille syndrome.
Cho JM; Oh SH; Kim HJ; Kim JS; Kim KM; Kim GH; Yu E; Lee BH; Yoo HW
Pediatr Int; 2015 Aug; 57(4):552-7. PubMed ID: 25676721
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene.
Hatim O; Pavlinov I; Xu M; Linask K; Beers J; Liu C; Baumgärtel K; Gilbert M; Spinner N; Chen C; Zou J; Zheng W
Stem Cell Res; 2023 Dec; 73():103231. PubMed ID: 37890331
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Outcomes of liver transplantation for Alagille syndrome after Kasai portoenterostomy: Alagille Syndrome with agenesis of extrahepatic bile ducts at porta hepatis.
Gunadi ; Kaneshiro M; Okamoto T; Sonoda M; Ogawa E; Okajima H; Uemoto S
J Pediatr Surg; 2019 Nov; 54(11):2387-2391. PubMed ID: 31104835
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
