Medicina
Fakultät
Assistance Publique -Hopitaux De Paris
París, FranciaPublikationen in Zusammenarbeit mit Forschern von Assistance Publique -Hopitaux De Paris (121)
2024
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Moderators of Loneliness Trajectories in People with Systemic Sclerosis During the COVID-19 Pandemic: A SPIN COVID-19 Cohort Longitudinal Study
International Journal of Behavioral Medicine
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The science of micronutrients in clinical practice – Report on the ESPEN symposium
Clinical Nutrition
2023
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A Simple Procedure to Measure the Tidal Volume Delivered by Mechanical Ventilators: A Tool for Bedside Verification and Quality Control
Archivos de Bronconeumologia, Vol. 59, Núm. 1, pp. 61-62
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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 4, pp. 984-996.e10
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Acute respiratory distress syndrome after SARS-CoV-2 infection on young adult population: International observational federated study based on electronic health records through the 4CE consortium
PLoS ONE, Vol. 18, Núm. 1 January
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Clinical outcomes by supplemental oxygen use in remdesivir-treated, hospitalised adults with COVID-19
Infectious Diseases Now, Vol. 53, Núm. 7
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Correction to: Improving clinical paediatric research and learning from COVID-19: recommendations by the Conect4Children expert advice group (Pediatric Research, (2022), 91, 5, (1069-1077), 10.1038/s41390-021-01587-3)
Pediatric Research
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Correction: Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY (Leukemia, (2023), 37, 2, (339-347), 10.1038/s41375-022-01802-y)
Leukemia
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Depression, anxiety, and suicidal ideation in a population-based cohort of young adults before and during the first 12 months of the COVID-19 pandemic in Canada
Canadian Journal of Public Health, Vol. 114, Núm. 3, pp. 368-377
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Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY
Leukemia, Vol. 37, Núm. 2, pp. 339-347
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External multicentre validation of pseudomyxoma peritonei PSOGI-Ki67 classification
European Journal of Surgical Oncology, Vol. 49, Núm. 8, pp. 1481-1488
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Invasive Bacterial Infections in Children With Sickle Cell Disease: 2014–2019
Pediatrics, Vol. 152, Núm. 4
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Patterns of patient-reported symptoms and association with sociodemographic and systemic sclerosis disease characteristics: a scleroderma Patient-centered Intervention Network (SPIN) Cohort cross-sectional study
eClinicalMedicine, Vol. 62
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Potential pitfalls in the use of real-world data for studying long COVID
Nature Medicine
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Prognostic Models for Global Functional Outcome and Post-Concussion Symptoms Following Mild Traumatic Brain Injury: A Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) Study
Journal of Neurotrauma, Vol. 40, Núm. 15-16, pp. 1651-1670
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Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations
Nature genetics, Vol. 55, Núm. 3, pp. 369-376
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Sex influence on outcomes of patients with systemic sclerosis-associated interstitial lung disease: A EUSTAR database analysis
Rheumatology (United Kingdom), Vol. 62, Núm. 7, pp. 2483-2491
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Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective
The Lancet. Haematology, Vol. 10, Núm. 8, pp. e687-e694
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The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study
Social Psychiatry and Psychiatric Epidemiology, Vol. 58, Núm. 10, pp. 1573-1580
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The value of the CHAP model for prediction of the bleeding risk in patients with unprovoked venous thromboembolism: Findings from the RIETE registry
Thrombosis Research