Publications Syndromes hyperéosinophliques

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

C-Reactive protein as a diagnostic tool in differential diagnosis of hypereosinophilic syndrome and antineutrophil cytoplasmic antibody-negative eosinophilic granulomatosis with polyangiitis.

Premiere étude sur une large cohorte montrant la localisation tissulaire de la proliferation lymphocytaire CD3-CD4+ dans les SHE-lymphoides permettant de classer cette hémopathie comme un authentique syndrome lymphoprolifératif T indolente: CD3−CD4+ lymphoid variant of hypereosinophilic syndrome: nodal and extranodal histopathological and immunophenotypic features of a peripheral indolent clonal T-cell lymphoproliferative disorder. Haematologica August 2015 100: 1086-1095; doi:10.3324/haematol.2014.118042.

CD3-CD4+ lymphoid variant of hypereosinophilic syndrome: nodal and extranodal histopathological and immunophenotypic features of a peripheral indolent clonal T-cell lymphoproliferative disorder.
 
Successful Heart Transplantation for Unreversible Endomyocardial Fibrosis Related to FIP1L1-PDGFRA Chronic Eosinophilic Leukemia.