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Items: 1 to 20 of 470

1.

Spectrum of genomic variations in Indian patients with progressive familial intrahepatic cholestasis.

Sharma A, Poddar U, Agnihotry S, Phadke SR, Yachha SK, Aggarwal R.

BMC Gastroenterol. 2018 Jul 4;18(1):107. doi: 10.1186/s12876-018-0835-6.

2.

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 Jul 3:e27293. doi: 10.1002/pbc.27293. [Epub ahead of print]

PMID:
29968976
3.

Allogeneic hematopoietic stem cell transplantation eliminates alloreactive inhibitory antibodies after liver transplantation for bile salt export pump deficiency.

Brinkert F, Pukite I, Krebs-Schmitt D, Briem-Richter A, Stindt J, Häussinger D, Keitel V, Müller I, Grabhorn E.

J Hepatol. 2018 Jun 20. pii: S0168-8278(18)32156-1. doi: 10.1016/j.jhep.2018.06.003. [Epub ahead of print]

PMID:
29935200
4.

Histological changes of the intestinal mucosa in complications following a living donor liver transplantation for progressive familial intrahepatic cholestasis type 1.

Stephanie M, Irie R, Sasaki K, Hirata Y, Narumoto S, Fukuda A, Sakamoto S, Arai K, Yoshioka T, Kasahara M.

Pathol Int. 2018 Jun 22. doi: 10.1111/pin.12686. [Epub ahead of print] No abstract available.

PMID:
29935008
5.

Long-term outcome after cholecystocolostomy for progressive familial intrahepatic cholestasis.

Chen L, Xiao H, Ren XH, Li L.

Hepatol Res. 2018 Jun 22. doi: 10.1111/hepr.13222. [Epub ahead of print]

PMID:
29934967
6.

[Non-transplant surgical intervention in progressive familial intrahepatic cholestasis].

Li XF, Gong JY, Wang JS.

Zhonghua Er Ke Za Zhi. 2018 May 2;56(5):392-395. doi: 10.3760/cma.j.issn.0578-1310.2018.05.021. Chinese. No abstract available.

PMID:
29783833
7.

Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies.

Bull LN, Pawlikowska L, Strautnieks S, Jankowska I, Czubkowski P, Dodge JL, Emerick K, Wanty C, Wali S, Blanchard S, Lacaille F, Byrne JA, van Eerde AM, Kolho KL, Houwen R, Lobritto S, Hupertz V, McClean P, Mieli-Vergani G, Sokal E, Rosenthal P, Whitington PF, Pawlowska J, Thompson RJ.

Hepatol Commun. 2018 Mar 30;2(5):515-528. doi: 10.1002/hep4.1168. eCollection 2018 May.

8.

Phenotypic spectrum and diagnostic pitfalls of ABCB4 deficiency depending on age of onset.

Schatz SB, Jüngst C, Keitel-Anselmo V, Kubitz R, Becker C, Gerner P, Pfister ED, Goldschmidt I, Junge N, Wenning D, Gehring S, Arens S, Bretschneider D, Grothues D, Engelmann G, Lammert F, Baumann U.

Hepatol Commun. 2018 Mar 22;2(5):504-514. doi: 10.1002/hep4.1149. eCollection 2018 May.

9.

Surgical outcomes in Alagille syndrome and PFIC: A single institution's 20-year experience.

Flores CD, Yu YR, Miloh TA, Goss J, Brandt ML.

J Pediatr Surg. 2018 May;53(5):976-979. doi: 10.1016/j.jpedsurg.2018.02.026. Epub 2018 Feb 9.

PMID:
29729773
10.

Xenobiotic Nuclear Receptor Signaling Determines Molecular Pathogenesis of Progressive Familial Intrahepatic Cholestasis.

Kim KH, Choi JM, Li F, Arizpe A, Wooton-Kee CR, Anakk S, Jung SY, Finegold MJ, Moore DD.

Endocrinology. 2018 Jun 1;159(6):2435-2446. doi: 10.1210/en.2018-00110.

PMID:
29718219
11.

Variants Associated with Infantile Cholestatic Syndromes Detected in Extrahepatic Biliary Atresia by Whole Exome Studies: A 20-Case Series from Thailand.

Sangkhathat S, Laochareonsuk W, Maneechay W, Kayasut K, Chiengkriwate P.

J Pediatr Genet. 2018 Jun;7(2):67-73. doi: 10.1055/s-0038-1632395. Epub 2018 Feb 16.

PMID:
29707407
12.

Giant Right Atrial Aneurysm Accompanying Intrahepatic Cholestasis.

Sulu A, Baspinar O, Kervancıoglu S, Hizli S.

Case Rep Cardiol. 2018 Feb 28;2018:9025907. doi: 10.1155/2018/9025907. eCollection 2018.

13.

Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasis.

Imagawa K, Hayashi H, Sabu Y, Tanikawa K, Fujishiro J, Kajikawa D, Wada H, Kudo T, Kage M, Kusuhara H, Sumazaki R.

J Hum Genet. 2018 May;63(5):569-577. doi: 10.1038/s10038-018-0431-1. Epub 2018 Mar 5.

PMID:
29507376
14.

Liver transplantation for decompensated liver cirrhosis caused by progressive familial intrahepatic cholestasis type 3: A case report.

Xiang D, He J, Wang H, Xiong F, Cheng H, Ai J, Shan R, Wan R, Zhang L, Shi J.

Medicine (Baltimore). 2017 Dec;96(50):e9158. doi: 10.1097/MD.0000000000009158.

15.

Well Preserved Renal Function in Children With Untreated Chronic Liver Disease.

Berg UB, Németh A.

J Pediatr Gastroenterol Nutr. 2018 Apr;66(4):575-580. doi: 10.1097/MPG.0000000000001862.

PMID:
29240010
16.

Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.

Vitale G, Gitto S, Raimondi F, Mattiaccio A, Mantovani V, Vukotic R, D'Errico A, Seri M, Russell RB, Andreone P.

J Gastroenterol. 2018 Aug;53(8):945-958. doi: 10.1007/s00535-017-1423-1. Epub 2017 Dec 13.

PMID:
29238877
17.

Long-term outcomes of six patients after partial internal biliary diversion for progressive familial intrahepatic cholestasis.

Erginel B, Soysal FG, Durmaz O, Celik A, Salman T.

J Pediatr Surg. 2018 Mar;53(3):468-471. doi: 10.1016/j.jpedsurg.2017.10.055. Epub 2017 Nov 23.

PMID:
29174177
18.
19.

Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages.

Hayashi H, Naoi S, Togawa T, Hirose Y, Kondou H, Hasegawa Y, Abukawa D, Sasaki M, Muroya K, Watanabe S, Nakano S, Minowa K, Inui A, Fukuda A, Kasahara M, Nagasaka H, Bessho K, Suzuki M, Kusuhara H.

EBioMedicine. 2018 Jan;27:187-199. doi: 10.1016/j.ebiom.2017.10.007. Epub 2017 Oct 7.

20.

Zebrafish abcb11b mutant reveals strategies to restore bile excretion impaired by bile salt export pump deficiency.

Ellis JL, Bove KE, Schuetz EG, Leino D, Valencia CA, Schuetz JD, Miethke A, Yin C.

Hepatology. 2018 Apr;67(4):1531-1545. doi: 10.1002/hep.29632. Epub 2018 Feb 23.

PMID:
29091294

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