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Björn Fischler

hopital universitaire necker-enfants malades - aphp
H指数:30
被引数:4,093

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Elevated Serum Bile Acids Predict Poor Liver Outcomes in Children With Alagille Syndrome: Results From the GALA Study Group

血清胆汁酸升高可预测Alagille综合征患儿的肝脏不良结局:GALA研究小组的结果

2025-11-180
OAAI
Event-free survival of maralixibat-treated patients with Alagille syndrome compared to a real-world cohort from GALA
2023-12-2511
OAAI
△4-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid
2023-12-072
OAAI
Long-term Outcome of Asymptomatic Patients With Graft Fibrosis in Protocol Biopsies After Pediatric Liver Transplantation

小儿肝移植后无症状移植物纤维化患者的长期结果

2023-10-218
OA
Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

截断突变p.E297G和p.D482G在胆汁盐输出泵缺乏症中的基因型-表型关系

2023-02-015
OAAI
Incidence of Isolated Biliary Atresia during the COVID Lockdown in Europe: Results from a Collaborative Project by RARE-Liver

欧洲COVID封锁期间孤立性胆道闭锁的发生率: 来自RARE-Liver合作项目的结果

2023-01-185
OAAI
Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial

Odevixibat治疗进行性家族性肝内胆汁淤积症: 一项随机,安慰剂对照,3期试验

2022-09-0172
OAAI
Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency
2021-07-1328
OAAI
Genotype correlates with the natural history of severe bile salt export pump deficiency
2020-07-0180
OAAI
The natural course of FIC1 deficiency and BSEP deficiency: Initial results from the NAPPED-consortium (Natural course and Prognosis of PFIC and Effect of biliary Diversion)
2018-04-014
PREAI
De Novo Donor-Specific HLA Antibody Formation in Two Patients With Crigler-Najjar Syndrome Type I Following Human Hepatocyte Transplantation With Partial Hepatectomy Preconditioning
2016-03-0155
OAAI