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Publications by Brigitte Kasper
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
Related publications
Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells
Journal of Clinical Investigation
Medicine
Management of Adult Onset Familial Hemophagocytic Lymphohistiocytosis (FHL): A Dilemma
Haematology International Journal
Spectrum and Clinical Implications of Syntaxin 11 Gene Mutations in Familial Haemophagocytic Lymphohistiocytosis: Association With Disease-Free Remissions and Haematopoietic Malignancies
Journal of Medical Genetics
Genetics
Deletion of Inflammasome Components Is Not Sufficient to Prevent Fatal Inflammation in Models of Familial Hemophagocytic Lymphohistiocytosis
Journal of Immunology
Allergy
Immunology
Hemophagocytic Lymphohistiocytosis
Enzymatic Activity of 2′–5′-Oligoadenylate Synthetase Is Impaired by Specific Mutations That Affect Oligomerization of the Protein
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Family Hemophagocytic Lymphohistiocytosis: (2 Clinical Cases in One Family)
Jurnal Infektologii
Infectious Diseases
A Novel Compound Heterozygous Stxbp2 Mutation in a Case With Familial Hemophagocytic Lymphohistiocytosis
Turkish Journal of Pediatric Disease
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