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Publications by Astrid Cariou

Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells

Journal of Clinical Investigation

English

Related publications

Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11

American Journal of Human Genetics

English

Hemophagocytic Lymphohistiocytosis in 2 Patients With Underlying IFN-γ Receptor Deficiency

Journal of Allergy and Clinical Immunology

English

Munc18-2, Not Munc18-1 or Munc18-3, Regulates Platelet Exocytosis, Hemostasis, and Thrombosis

Journal of Biological Chemistry

Molecular Biology

English

Bone Marrow Derived Mesenchymal Stem Cells Ameliorate Inflammatory Response in an in Vitro Model of Familial Hemophagocytic Lymphohistiocytosis 2

Stem Cell Research and Therapy

Molecular Biology

Molecular Medicine

English

Hemophagocytic Lymphohistiocytosis

English

Management of Adult Onset Familial Hemophagocytic Lymphohistiocytosis (FHL): A Dilemma

Haematology International Journal

English

Hemophagocytic Lymphohistiocytosis in a Patient With Classical Hodgkin Lymphoma

Case Reports in Hematology

English

Unusual Presentation of Hemophagocytic Lymphohistiocytosis in a Kidney Transplant Patient

Case Reports in Transplantation

English

Hemophagocytic Lymphohistiocytosis in a Patient With Glioblastoma: A Case Report

English