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Items: 1 to 20 of 884

1.

Everolimus Rescue Treatment for Chronic Rejection After Pediatric Living Donor Liver Transplantation: 2 Case Reports.

Ueno T, Hiwatashi S, Saka R, Yamanaka H, Takama Y, Tazuke Y, Bessho K, Okuyama H.

Transplant Proc. 2018 Mar 19. pii: S0041-1345(18)30412-3. doi: 10.1016/j.transproceed.2018.03.079. [Epub ahead of print]

PMID:
30318104
2.

Functional evidence implicating NOTCH2 missense mutations in primary ovarian insufficiency aetiology.

Patiño LC, Beau I, Morel A, Delemer B, Young J, Binart N, Laissue P.

Hum Mutat. 2018 Oct 10. doi: 10.1002/humu.23667. [Epub ahead of print]

PMID:
30304577
3.

Placebo-Controlled Randomized Trial of an Intestinal Bile Salt Transport Inhibitor for Pruritus in Alagille Syndrome.

Shneider BL, Spino C, Kamath BM, Magee JC, Bass LM, Setchell KD, Miethke A, Molleston JP, Mack CL, Squires RH, Murray KF, Loomes KM, Rosenthal P, Karpen SJ, Leung DH, Guthery SL, Thomas D, Sherker AH, Sokol RJ; Childhood Liver Disease Research Network.

Hepatol Commun. 2018 Sep 24;2(10):1184-1198. doi: 10.1002/hep4.1244. eCollection 2018 Oct.

4.

Alagille Syndrome.

Mitchell E, Gilbert M, Loomes KM.

Clin Liver Dis. 2018 Nov;22(4):625-641. doi: 10.1016/j.cld.2018.06.001. Epub 2018 Aug 22. Review.

PMID:
30266153
5.

[Biliary atresia and congenital cholestatic syndromes : Characteristics before, after and during transition].

Junge N, Dingemann J, Petersen C, Manns MP, Richter N, Klempnauer J, Baumann U, Schneider A.

Internist (Berl). 2018 Sep 27. doi: 10.1007/s00108-018-0506-2. [Epub ahead of print] Review. German.

PMID:
30264190
6.

Cholangiopathies - Towards a molecular understanding.

Tam PKH, Yiu RS, Lendahl U, Andersson ER.

EBioMedicine. 2018 Sep;35:381-393. doi: 10.1016/j.ebiom.2018.08.024. Epub 2018 Sep 17. Review. Erratum in: EBioMedicine. 2018 Oct 9;:.

7.

In-utero idiopathic ductal constriction: a prenatal manifestation of Alagille and Williams syndrome arteriopathy.

Srinivasan S, Howley LW, Cuneo BF, Chatfield KC.

J Perinatol. 2018 Sep 10. doi: 10.1038/s41372-018-0221-9. [Epub ahead of print]

PMID:
30202046
8.

From hepatocyte to cholangiocyte: the remarkable potential of transdifferentiation to treat cholestatic diseases.

Kamath B, Mack CL.

Hepatology. 2018 Sep 4. doi: 10.1002/hep.30250. [Epub ahead of print]

PMID:
30179266
9.

Successful living donor liver transplantation after stent implantation in a patient with Alagille syndrome and severe bilateral pulmonary artery stenosis.

Akagi K, Tanaka T, Baba S.

Cardiol Young. 2018 Aug 30:1-3. doi: 10.1017/S1047951118001476. [Epub ahead of print]

PMID:
30160645
10.

Increased expression and altered localization of cathepsin Z are associated with progression to jaundice stage in primary biliary cholangitis.

Aiba Y, Harada K, Ito M, Suematsu T, Aishima S, Hitomi Y, Nishida N, Kawashima M, Takatsuki M, Eguchi S, Shimoda S, Nakamura H, Komori A, Abiru S, Nagaoka S, Migita K, Yatsuhashi H, Tokunaga K, Nakamura M.

Sci Rep. 2018 Aug 7;8(1):11808. doi: 10.1038/s41598-018-30146-w.

11.

Clinical Features and Genetic Analysis of Pediatric Patients with Alagille Syndrome Presenting Initially with Liver Function Abnormalities.

Liu Y, Wang H, Dong C, Feng JX, Huang ZH.

Curr Med Sci. 2018 Apr;38(2):304-309. doi: 10.1007/s11596-018-1879-0. Epub 2018 Apr 30.

PMID:
30074189
12.

Outcomes of Alagille syndrome following the Kasai operation: a systematic review and meta-analysis.

Fujishiro J, Suzuki K, Watanabe M, Uotani C, Takezoe T, Takamoto N, Hayashi K.

Pediatr Surg Int. 2018 Oct;34(10):1073-1077. doi: 10.1007/s00383-018-4316-3. Epub 2018 Aug 2.

PMID:
30073479
13.

Bone Density in Children with Chronic Liver Disease Correlates with Growth and Cholestasis.

Loomes KM, Spino C, Goodrich NP, Hangartner TN, Marker AE, Heubi JE, Kamath BM, Shneider BL, Rosenthal P, Hertel PM, Karpen SJ, Molleston JP, Murray KF, Schwarz KB, Squires RH, Teckman J, Turmelle YP, Alonso EM, Sherker AH, Magee JC, Sokol RJ; Childhood Liver Disease Research Network (ChiLDReN).

Hepatology. 2018 Jul 31. doi: 10.1002/hep.30196. [Epub ahead of print]

PMID:
30063078
14.

A Novel c.91dupG JAG1 Gene Mutation Is Associated with Early Onset and Severe Alagille Syndrome.

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 Jun 25;2018:1369413. doi: 10.1155/2018/1369413. eCollection 2018.

15.

A Rare Case Of a 2 year old Boy With Alagille Syndrome & Type 3 Hereditary Hemochromatosis With TFR2 Mutation.

Khayat AA, Suchi M, Vitola B.

J Pediatr Gastroenterol Nutr. 2018 Jul 6. doi: 10.1097/MPG.0000000000002078. [Epub ahead of print] No abstract available.

PMID:
29985876
16.

Surgical management of children and adolescents with upfront completely resected hepatocellular carcinoma.

D'Souza AM, Shah R, Gupta A, Towbin AJ, Alonso M, Nathan JD, Bondoc A, Tiao G, Geller JI.

Pediatr Blood Cancer. 2018 Nov;65(11):e27293. doi: 10.1002/pbc.27293. Epub 2018 Jul 3.

PMID:
29968976
17.

JAG1 loss‑of‑function mutations contributed to Alagille syndrome in two Chinese families.

Zhang E, Xu Y, Yu Y, Chen S, Yu Y, Sun K.

Mol Med Rep. 2018 Aug;18(2):2356-2364. doi: 10.3892/mmr.2018.9217. Epub 2018 Jun 25.

PMID:
29956768
18.

Alagille Syndrome.

Diaz-Frias J, Kondamudi NP.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2018 Jan-.
2018 Jun 18.

19.

Wilms Tumor After Orthotopic Liver Transplant in a Patient With Alagille Syndrome.

Carlos EC, Ajay D, Muniz-Alers S, Wechsler DS, Sushama DV, Rice HE, Madden J, Routh JC.

Urology. 2018 Jun 5. pii: S0090-4295(18)30538-7. doi: 10.1016/j.urology.2018.05.020. [Epub ahead of print]

PMID:
29879405
20.

Bile duct paucity in childhood-spectrum, profile, and outcome.

Meena BL, Khanna R, Bihari C, Rastogi A, Rawat D, Alam S.

Eur J Pediatr. 2018 Aug;177(8):1261-1269. doi: 10.1007/s00431-018-3181-3. Epub 2018 Jun 4.

PMID:
29868931

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