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Publications Medullar aplasia/Paroxysmal nocturnal hemoglobinuria/Fanconi’s anemia

Hematopoietic stem cell transplantation for patients with paroxysmal nocturnal hemoglobinuria previously treated with eculizumab: a retrospective study of 21 patients...

Publications Histiocytosis

Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study. Response to trametinib of histiocytosis with an...

Publications Autoimmune cytopenias (ITP/AHAI/Evans)

Synergistic convergence of microbiota-specific systemic IgG and secretory IgA Immune/microbial interface perturbation in human IgA deficiency. Microbial ecology perturbation in...

Publications Blackfan-Diamond Anemia

Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1. Rio S , Gastou M, Karboul N, Derman R, Suriyun T, Manceau H, Leblanc T, El Benna J, Schmitt...

Publications Kinin angioedema

Elderly versus younger patients with hereditary angioedema type I/II: patient characteristics and safety analysis from the Icatibant Outcome Survey. Hereditary...

Publications Hypereosinophilic syndromes

French Eosinophil Network. Abnormal T-cell phenotype in episodic angioedema with hypereosinophilia (Gleich’s syndrome): frequency, clinical implication and prognosis. J Am...

Publications AL amyloidosis and other monoclonal immunoglobulin diseases

Heavy Chain Fibrillary Glomerulonephritis: A Case Report. Monoclonal gammopathy of clinical significance: a novel concept with therapeutic implications The evaluation...

Publications Chronic neutropenia

EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome. Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic Neutropenia....

Publications Thrombotic microangiopathies

Prognostic and Long-term Survival of Immune Thrombotic Thrombocytopenic Purpura in older patients. Caplacizumab: a change in the paradigm of thrombotic...

Publications Inherited immune deficiencies

Daratumumab in life-threatening autoimmunehemolytic anemia following hematopoietic stem cell transplantation. T cell defects in patients with ARPC1B germline mutations account...

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