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1. A unified metric of human immune health

2. Venous and arterial thrombosis in patients with VEXAS syndrome

4. Hematopoiesis under telomere attrition at the single-cell resolution

6. Early activation of inflammatory pathways in UBA1-mutated hematopoietic stem and progenitor cells in VEXAS

7. Spectrum of clonal hematopoiesis in VEXAS syndrome

8. Differential diagnosis of bone marrow failure syndromes guided by machine learning

11. Anti-COX-2 autoantibody is a novel biomarker of immune aplastic anemia

12. Single-cell genotype-phenotype mapping identifies therapeutic vulnerabilities in VEXAS syndrome

13. Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis

19. Opportunistic Infections, Mortality Risk, and Prevention Strategies in Patients With Vacuoles, E1 Enzyme, X-Linked, Autoinflammatory, Somatic (VEXAS) Syndrome.

20. Ahemolytic PNH (white cell PNH): Clinical features and implications of a distinct phenotype of paroxysmal nocturnal haemoglobinuria

21. Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1

30. Granulocyte transfusions in severe aplastic anemia

31. Clonal haematopoiesis across the age spectrum of vasculitis patients with Takayasu’s arteritis, ANCA-associated vasculitis and giant cell arteritis

38. S176: FUNCTIONAL AND ANTIGEN-SPECIFIC CHARACTERIZATION OF IMMUNE CELLS AT THE SINGLE-CELL LEVEL REVEALS CONVERGENCE OF ADAPTIVE AND INNATE IMMUNITY IN IMMUNE APLASTIC ANEMIA

42. Pathogenic TERT promoter variants in telomere diseases

48. Conditional survival and standardized mortality ratios of patients with severe aplastic anemia surviving at least one year after hematopoietic cell transplantation or immunosuppressive therapy

49. What causes aplastic anaemia?

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