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Respiratory Medicine and Research|April 23, 2023
French recommendations for the diagnosis and management of lymphangioleiomyomatosisVincent Cottin, Elodie Blanchard, Mallorie Kerjouan, et al.
Haematologica|June 15, 2023
Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosisMarine Delamare, Amandine Le Roy, Mathilde Pacault, et al.
Leukemia|November 14, 2022
Gilteritinib activity in refractory or relapsed FLT3-mutated acute myeloid leukemia patients previously treated by intensive chemotherapy and midostaurin: a study from the French AML Intergroup ALFA/FILOPierre-Yves Dumas, Emmanuel Raffoux, Emilie Bérard, et al.
American Journal of Hematology|April 2, 2024
Involvement of the JAK-STAT pathway in the molecular landscape of tyrosine kinase fusion-negative hypereosinophilic syndromes: A nationwide CEREO studyMatthieu Groh, Laurène Fenwarth, Mathilde Labro, et al.
The European Respiratory Journal|April 4, 2024
High risk of lung cancer in surfactant-related gene variant carriersAlexandre Brudon, Marie Legendre, Arthur Mageau, et al.
Blood Advances|March 5, 2021
Genomic analysis of primary and secondary myelofibrosis redefines the prognostic impact of ASXL1 mutations: a FIM studyDamien Luque Paz, Jérémie Riou, Emmanuelle Verger, et al.
The European Respiratory Journal|May 13, 2017
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosisPierre-Antoine Juge, Raphaël Borie, Caroline Kannengiesser, et al.
Haematologica|May 28, 2021
Characteristics and outcome of patients with low-/intermediate-risk acute promyelocytic leukemia treated with arsenic trioxide: an international collaborative studySabine Kayser, Richard F Schlenk, Delphine Lebon, et al.
Seminars in Arthritis and Rheumatism|August 19, 2021
MUC5B promoter variant rs35705950 and rheumatoid arthritis associated interstitial lung disease survival and progressionPierre-Antoine Juge, Joshua J Solomon, Coline H M van Moorsel, et al.
Hepatology (Baltimore, Md.)|November 7, 2023
Liver disease in germline mutations of telomere-related genes: Prevalence, clinical, radiological, pathological features, outcome, and risk factorsSabrina Sidali, Raphaël Borie, Flore Sicre de Fontbrune, et al.
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