受强制性开放获取政策约束的文章 - philippe labrune了解详情
无法在其他位置公开访问的文章：3 篇
Molecular characterization of hepatocellular adenomas developed in patients with glycogen storage disease type I
J Calderaro, P Labrune, G Morcrette, S Rebouissou, D Franco, S Prévot, ...
Journal of Hepatology 58 (2), 350-357, 2013
强制性开放获取政策： National Institute of Health and Medical Research, France
Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France—identification of eight new mutations
A Davit-Spraul, C Costa, M Zater, D Habes, J Berthelot, P Broué, F Feillet, ...
Molecular genetics and metabolism 94 (4), 443-447, 2008
强制性开放获取政策： National Institute of Health and Medical Research, France
Narrative review of glycogen storage disorder type III with a focus on neuromuscular, cardiac and therapeutic aspects
É Berling, P Laforêt, K Wahbi, P Labrune, F Petit, G Ronzitti, A O'Brien
Journal of inherited metabolic disease 44 (3), 521-533, 2021
强制性开放获取政策： Agence Nationale de la Recherche
可在其他位置公开访问的文章：23 篇
Molecular classification of hepatocellular adenoma associates with risk factors, bleeding, and malignant transformation
JC Nault, G Couchy, C Balabaud, G Morcrette, S Caruso, JF Blanc, ...
Gastroenterology 152 (4), 880-894. e6, 2017
强制性开放获取政策： National Institute of Health and Medical Research, France, Swiss Cancer League
No perinatal HIV-1 transmission from women with effective antiretroviral therapy starting before conception
L Mandelbrot, R Tubiana, J Le Chenadec, C Dollfus, A Faye, E Pannier, ...
Clinical Infectious Diseases 61 (11), 1715-1725, 2015
强制性开放获取政策： National Institute of Health and Medical Research, France
International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up
L Welling, LE Bernstein, GT Berry, AB Burlina, F Eyskens, M Gautschi, ...
Journal of inherited metabolic disease 40, 171-176, 2017
强制性开放获取政策： Netherlands Organisation for Scientific Research
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome
CP Sentner, IJ Hoogeveen, DA Weinstein, R Santer, E Murphy, ...
Journal of inherited metabolic disease 39, 697-704, 2016
强制性开放获取政策： US National Institutes of Health
The natural history of classic galactosemia: lessons from the GalNet registry
ME Rubio-Gozalbo, M Haskovic, AM Bosch, B Burnyte, AI Coelho, ...
Orphanet journal of rare diseases 14, 1-11, 2019
强制性开放获取政策： Health Research Board, Ireland, Netherlands Organisation for Scientific Research
GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation
JC Nault, M Fabre, G Couchy, C Pilati, E Jeannot, JT Van Nhieu, ...
Journal of hepatology 56 (1), 184-191, 2012
强制性开放获取政策： National Institute of Health and Medical Research, France
Is intrapartum intravenous zidovudine for prevention of mother-to-child HIV-1 transmission still useful in the combination antiretroviral therapy era?
N Briand, J Warszawski, L Mandelbrot, C Dollfus, E Pannier, L Cravello, ...
Clinical infectious diseases 57 (6), 903-914, 2013
强制性开放获取政策： National Institute of Health and Medical Research, France
Increased risk of serious bacterial infections due to maternal immunosuppression in HIV-exposed uninfected infants in a European country
C Taron-Brocard, J Le Chenadec, A Faye, C Dollfus, T Goetghebuer, ...
Clinical Infectious Diseases 59 (9), 1332-1345, 2014
强制性开放获取政策： National Institute of Health and Medical Research, France
Prevalence and relevance of pre-existing anti-adeno-associated virus immunity in the context of gene therapy for Crigler–Najjar syndrome
SJ Aronson, P Veron, F Collaud, A Hubert, V Delahais, G Honnet, ...
Human gene therapy 30 (10), 1297-1305, 2019
强制性开放获取政策： Fondazione Telethon, Italy, European Commission, Netherlands Organisation …
Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4
N Bondurand, V Fouquet, V Baral, L Lecerf, N Loundon, M Goossens, ...
European journal of human genetics 20 (9), 990-994, 2012
强制性开放获取政策： National Institute of Health and Medical Research, France
Gene therapy in patients with the Crigler–Najjar syndrome
L D’antiga, U Beuers, G Ronzitti, N Brunetti-Pierri, U Baumann, ...
New England Journal of Medicine 389 (7), 620-631, 2023
强制性开放获取政策： Fondazione Telethon, Italy, European Commission
Galactokinase deficiency: lessons from the GalNet registry
ME Rubio-Gozalbo, B Derks, AM Das, U Meyer, D Möslinger, ML Couce, ...
Genetics in medicine 23 (1), 202-210, 2021
强制性开放获取政策： Health Research Board, Ireland, Netherlands Organisation for Scientific Research
Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment
P Laforêt, M Inoue, E Goillot, C Lefeuvre, U Cagin, N Streichenberger, ...
Acta neuropathologica communications 7, 1-16, 2019
强制性开放获取政策： Fondazione Telethon, Italy, Agence Nationale de la Recherche
Disease burden and management of Crigler‐Najjar syndrome: Report of a world registry
SJ Aronson, N Junge, M Trabelsi, W Kelmemi, A Hubert, KW Brigatti, ...
Liver International 42 (7), 1593-1604, 2022
强制性开放获取政策： European Commission, Netherlands Organisation for Health Research and …
Regenerative cell therapy for the treatment of hyperbilirubinemic Gunn rats with fresh and frozen human induced pluripotent stem cells‐derived hepatic stem cells
A Fourrier, F Delbos, S Menoret, C Collet, LT Thi Thuy, A Myara, F Petit, ...
Xenotransplantation 27 (1), e12544, 2020
强制性开放获取政策： UK Medical Research Council, National Centre for the Replacement, Refinement …
Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency
R Ben Yaou, A Hubert, I Nelson, JR Dahlqvist, D Gaist, N Streichenberger, ...
Neurology: Genetics 3 (6), e208, 2017
强制性开放获取政策： Danish Council for Independent Research, National Institute of Health and …
Correction of hyperbilirubinemia in gunn rats by surgical delivery of low doses of helper-dependent adenoviral vectors
F Schmitt, N Pastore, C Abarrategui-Pontes, M Flageul, A Myara, ...
Human gene therapy methods 25 (3), 181-186, 2014
强制性开放获取政策： Fondazione Telethon, Italy, Government of Italy
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