Publications in collaboration with researchers from Necker-Enfants Malades Hospital (25)

2024

  1. Development and external validation of the 'Global Surgical-Site Infection' (GloSSI) predictive model in adult patients undergoing gastrointestinal surgery

    British Journal of Surgery, Vol. 111, Núm. 6

  2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

    Human Genetics and Genomics Advances, Vol. 5, Núm. 3

2023

  1. 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

  2. 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

  1. Genomic profiling for clinical decision making in lymphoid neoplasms

    Blood

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

  2. Tapering Canakinumab Monotherapy in Patients With Systemic Juvenile Idiopathic Arthritis in Clinical Remission: Results From a Phase IIIb/IV Open-Label, Randomized Study

    Arthritis and Rheumatology, Vol. 73, Núm. 2, pp. 336-346

2020

  1. 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

  1. Correction: Arterial tortuosity syndrome: 40 new families and literature review (Genetics in Medicine, (2018), 20, 10, (1236-1245), 10.1038/gim.2017.253)

    Genetics in Medicine

2018

  1. Arterial tortuosity syndrome: 40 new families and literature review

    Genetics in Medicine, Vol. 20, Núm. 10, pp. 1236-1245

  2. Automated database-guided expert-supervised orientation for immunophenotypic diagnosis and classification of acute leukemia

    Leukemia, Vol. 32, Núm. 4, pp. 874-881

  3. Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency

    Journal of Clinical Immunology, Vol. 38, Núm. 4, pp. 513-526

2017

  1. A new case of congenital malabsorptive diarrhea and diabetes secondary to mutant Neurogenin-3

    Pediatrics, Vol. 140, Núm. 2

  2. 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

2016

  1. Mortality of emergency abdominal surgery in high-, middle- and low-income countries

    British Journal of Surgery, Vol. 103, Núm. 8, pp. 971-988

2015

  1. 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

  1. SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

    Epilepsia, Vol. 50, Núm. 7, pp. 1670-1678

2008

  1. Survival of Patients Identified as Candidates for Intestinal Transplantation: A 3-Year Prospective Follow-Up

    Gastroenterology, Vol. 135, Núm. 1, pp. 61-71

2006

  1. Candidates for intestinal transplantation: A multicenter survey in Europe

    American Journal of Gastroenterology, Vol. 101, Núm. 7, pp. 1633-1643

  2. Home

    Home Parenteral Nutrition (CABI Publishing), pp. 325-341