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Publications by E Rudd
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
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Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
Frontiers in Pediatrics
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Perinatology
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
Fludarabine in the Treatment of an Active Phase of a Familial Haemophagocytic Lymphohistiocytosis
Archives of Disease in Childhood
Child Health
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Perinatology
Haemophagocytic Lymphohistiocytosis and Silvery Hair in Griscelli Syndrome
British Journal of Haematology
Hematology
HAX1 Mutation Positive Children Presenting With Haemophagocytic Lymphohistiocytosis
British Journal of Haematology
Hematology
P345 an Unusual Presentation of Haemophagocytic Lymphohistiocytosis
How I Treat Primary Haemophagocytic Lymphohistiocytosis
British Journal of Haematology
Hematology
Spectrum of Mutations in the Batten Disease Gene, CLN3
American Journal of Human Genetics
Genetics
Characterisation of Diverse PRF1 Mutations Leading to Decreased Natural Killer Cell Activity in North American Families With Haemophagocytic Lymphohistiocytosis
Journal of Medical Genetics
Genetics
