Bjorn Fischler
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Explore the profile of Bjorn Fischler including associated specialties, affiliations and a list of published articles.
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122
Citations
1499
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Recent Articles
11.
Dona D, Bravo-Gallego L, Frauca Remacha E, Cananzi M, Gastaldi A, Canizalez J, et al.
Pediatr Transplant
. 2023 Aug;
27(7):e14589.
PMID: 37543721
Background: There is considerable variation in vaccination practices between pediatric transplant centers. This study aims to evaluate active immunization attitudes and practices among ERN-TransplantChild centers and identify potential areas of...
12.
Hartleif S, Hodson J, Lloyd C, Cousin V, Czubkowski P, DAntiga L, et al.
Transplantation
. 2023 May;
107(11):2394-2405.
PMID: 37143195
Background: The histological prevalence of allograft fibrosis in asymptomatic children after liver transplantation (LT) is well documented. However, long-term graft and patient survival remain unclear. This retrospective multicenter study aims...
13.
Gonzalez-Peralta R, Wirth S, Squires R, Mutschler F, Lang T, Pawlowska M, et al.
Hepatol Commun
. 2023 Feb;
7(3):e0031.
PMID: 36790337
Background: Approximately 3.5 million children and adolescents worldwide are chronically infected with HCV. This study uses pharmacokinetic modeling to identify pediatric doses of elbasvir/grazoprevir (EBR/GZR) that achieve plasma concentrations similar...
14.
Liliemark U, Svensson J, Fischler B
Pediatr Surg Int
. 2023 Feb;
39(1):117.
PMID: 36773050
Purpose: Patients with biliary atresia (BA) and cytomegalovirus (CMV) infection may have poorer outcomes after Kasai portoenterostomy (KPE) than uninfected patients, suggesting a rationale for antiviral treatment (AVT). We aimed...
15.
Nomden M, Alizai N, Betalli P, Bruggink J, Cananzi M, Christensen V, et al.
J Clin Med
. 2023 Feb;
12(3).
PMID: 36769422
Background: Biliary atresia (BA) is a rare cholangiopathy where one of the proposed aetiological mechanisms is an infectious viral trigger. Coronavirus disease-19 (COVID) lockdown restrictions were implemented to reduce the...
16.
Felzen A, van Wessel D, Gonzales E, Thompson R, Jankowska I, Shneider B, et al.
JHEP Rep
. 2023 Jan;
5(2):100626.
PMID: 36687469
Background & Aims: Bile salt export pump (BSEP) deficiency frequently necessitates liver transplantation in childhood. In contrast to two predicted protein truncating mutations (PPTMs), homozygous p.D482G or p.E297G mutations are...
17.
Hankeova S, Van Hul N, Laznovsky J, Verboven E, Mangold K, Hensens N, et al.
EMBO Mol Med
. 2022 Nov;
14(12):e15809.
PMID: 36345711
Spontaneous bleeds are a leading cause of death in the pediatric JAG1-related liver disease Alagille syndrome (ALGS). We asked whether there are sex differences in bleeding events in patients, whether...
18.
Stone V, Utorova R, Butrym M, Sioofy-Khojine A, Hankaniemi M, Ringqvist E, et al.
iScience
. 2022 Sep;
25(10):105070.
PMID: 36157581
Viral respiratory tract infections exacerbate airway disease and facilitate life-threatening bacterial colonization in cystic fibrosis (CF). Annual influenza vaccination is recommended and vaccines against other common respiratory viruses may further...
19.
Vandriel S, Li L, She H, Wang J, Gilbert M, Jankowska I, et al.
Hepatology
. 2022 Aug;
77(2):512-529.
PMID: 36036223
Background And Aims: Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real-world data are lacking. This study aimed...
20.
Thompson R, Arnell H, Artan R, Baumann U, Calvo P, Czubkowski P, et al.
Lancet Gastroenterol Hepatol
. 2022 Jul;
7(9):830-842.
PMID: 35780807
Background: Progressive familial intrahepatic cholestasis (PFIC) is a group of inherited paediatric liver diseases resulting from mutations in genes that impact bile secretion. We aimed to evaluate the effects of...