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Publications by Catherine Schaffner
Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells
Journal of Clinical Investigation
Medicine
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
Genetics
Hemophagocytic Lymphohistiocytosis in 2 Patients With Underlying IFN-γ Receptor Deficiency
Journal of Allergy and Clinical Immunology
Allergy
Immunology
Munc18-2, Not Munc18-1 or Munc18-3, Regulates Platelet Exocytosis, Hemostasis, and Thrombosis
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Bone Marrow Derived Mesenchymal Stem Cells Ameliorate Inflammatory Response in an in Vitro Model of Familial Hemophagocytic Lymphohistiocytosis 2
Stem Cell Research and Therapy
Genetics
Cell Biology
Molecular Biology
Biochemistry
Medicine
Molecular Medicine
Hemophagocytic Lymphohistiocytosis
Management of Adult Onset Familial Hemophagocytic Lymphohistiocytosis (FHL): A Dilemma
Haematology International Journal
Hemophagocytic Lymphohistiocytosis in a Patient With Classical Hodgkin Lymphoma
Case Reports in Hematology
Unusual Presentation of Hemophagocytic Lymphohistiocytosis in a Kidney Transplant Patient
Case Reports in Transplantation
Hemophagocytic Lymphohistiocytosis in a Patient With Glioblastoma: A Case Report
CNS oncology
Medicine