Pages that link to "Q83022873"

The following pages link to Platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) (Q83022873):

Displaying 12 items.

• Platelet secretion and hemostasis require syntaxin-binding protein STXBP5. (Q34311741) (← links)
• How I treat hemophagocytic lymphohistiocytosis (Q35483540) (← links)
• Syntaxin-11, but not syntaxin-2 or syntaxin-4, is required for platelet secretion. (Q36250943) (← links)
• Munc18b/STXBP2 is required for platelet secretion. (Q36250947) (← links)
• Graded defects in cytotoxicity determine severity of hemophagocytic lymphohistiocytosis in humans and mice (Q37394923) (← links)
• Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning (Q37719014) (← links)
• Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations. (Q38696809) (← links)
• Hemophagocytic Lymphohistiocytosis Masquerading as Acute Liver Failure: A Single Center Experience. (Q41925890) (← links)
• Blood platelets and biological response to 'danger' signals and subsequent inflammation: towards a new paradigm? (Q45059688) (← links)
• Hemophagocytic lymphohistiocytosis in an adult kidney transplant recipient successfully treated by plasmapheresis: A case report and review of the literature (Q47547112) (← links)
• Type 5 Familial Hemophagocytic Lymphohistiocytosis in a Seven-year-old Girl Post Second Bone Marrow Transplantation with Failure to Thrive: STXBP2 Novel Mutation (Q91740614) (← links)
• Cytokines and related molecules, and adverse reactions related to platelet concentrate transfusions (Q92055790) (← links)