Facultad de Medicina (FM)
Centro académico
Necker-Enfants Malades Hospital
París, FranciaPublications in collaboration with researchers from Necker-Enfants Malades Hospital (21)
2024
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Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection
Human Genetics and Genomics Advances, Vol. 5, Núm. 3
2023
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Correction: “The 5th edition of The World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms” Leukemia. 2022 Jul;36(7):1720–1748 (Leukemia, (2022), 36, 7, (1720-1748), 10.1038/s41375-022-01620-2)
Leukemia
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
2022
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The alternative RelB NF-κB subunit is a novel critical player in diffuse large B-cell lymphoma
Blood, Vol. 139, Núm. 3, pp. 384-398
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
2020
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Fenfluramine for Treatment-Resistant Seizures in Patients with Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial
JAMA Neurology, Vol. 77, Núm. 3, pp. 300-308
2019
2018
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Arterial tortuosity syndrome: 40 new families and literature review
Genetics in Medicine, Vol. 20, Núm. 10, pp. 1236-1245
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Automated database-guided expert-supervised orientation for immunophenotypic diagnosis and classification of acute leukemia
Leukemia, Vol. 32, Núm. 4, pp. 874-881
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Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency
Journal of Clinical Immunology, Vol. 38, Núm. 4, pp. 513-526
2017
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A new case of congenital malabsorptive diarrhea and diabetes secondary to mutant Neurogenin-3
Pediatrics, Vol. 140, Núm. 2
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Long-term survival of patients with CLL after allogeneic transplantation: A report from the European Society for Blood and Marrow Transplantation
Bone Marrow Transplantation, Vol. 52, Núm. 3, pp. 372-380
2015
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Current preventive strategies and management of Epstein-Barr virus-related post-transplant lymphoproliferative disease in solid organ transplantation in Europe. Results of the ESGICH Questionnaire-based Cross-sectional Survey
Clinical Microbiology and Infection, Vol. 21, Núm. 6, pp. 604.e1-604.e9
2009
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SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
Epilepsia, Vol. 50, Núm. 7, pp. 1670-1678
2008
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Survival of Patients Identified as Candidates for Intestinal Transplantation: A 3-Year Prospective Follow-Up
Gastroenterology, Vol. 135, Núm. 1, pp. 61-71
2006
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Candidates for intestinal transplantation: A multicenter survey in Europe
American Journal of Gastroenterology, Vol. 101, Núm. 7, pp. 1633-1643
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Home
Home Parenteral Nutrition (CABI Publishing), pp. 325-341
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Transcription factor TCF7L2 genetic study in the French population: Expression in human β-cells and adipose tissue and strong association with type 2 diabetes
Diabetes, Vol. 55, Núm. 10, pp. 2903-2908
2003
1999
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A novel immunodeficient mouse model - RAG2 x common cytokine receptor γ chain double mutants - Requiring exogenous cytokine administration for human hematopoietic stem cell engraftment
Journal of Interferon and Cytokine Research, Vol. 19, Núm. 5, pp. 533-541