• A promising treatment to optimize delivery management in a pregnant woman with inherited thrombocytopenia: thrombopoietin-receptor agonist administration
• Adolescents and young adults with newly diagnosed primary immune thrombocytopenia
• ANKRD26 is a new regulator of type I cytokine receptor signaling in normal and pathological hematopoiesis
• Autoimmune cytopenia and Kabuki syndrome in paediatrics: Insights in 11 patients
• Case report: <em>ETS1</em> gene deletion associated with a low number of recent thymic emigrants in three patients with Jacobsen syndrome
• Case report: ETS1 gene deletion associated with a low number of recent thymic emigrants in three patients with Jacobsen syndrome
• Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome
• Determinants of long-term outcomes of splenectomy in pediatric autoimmune cytopenias
• Endothelial Loss of ETS1 Impairs Coronary Vascular Development and Leads to Ventricular Non-Compaction
• Germline <em>RUNX1</em> variants in paediatric patients in a French specialised centre
• Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupus
• Hematological abnormalities in Jacobsen syndrome: cytopenia of varying severities and morphological abnormalities in peripheral blood and bone marrow
• Impact of age at diagnosis, sex, and immunopathological manifestations in 886 patients with pediatric chronic immune thrombocytopenia
• Jacobsen Syndrome in a Patient with Combined Immunodeficiency, Thrombocytopenia, and Lymphoma
• NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells
• Patients with Chromosome 11q Deletions Are Characterized by Inborn Errors of Immunity Involving both B and T Lymphocytes
• Pediatric refractory chronic immune thrombocytopenia: Identification, patients' characteristics, and outcome
• Prenatal Identification and Confirmation of Jacobsen Syndrome: A Series of Four Cases
• Renal vein thrombosis in neonates: a case series of diagnosis, treatment and childhood kidney function follow-up
• Reply to "Jacobsen Syndrome in a Patient with Combined Immunodeficiency, Thrombocytopenia, and Lymphoma"
• Severe neonatal thrombocytopenia due to anti-HPA-4b alloantibodies: Third report described in a Caucasian mother
• The role and evolution of partial splenic embolization over three decades: A multicentric retrospective single cohort study of 90 patients from French nationwide experience