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1. A unified metric of human immune health

2. Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease

5. Ancient familial Mediterranean fever mutations in human pyrin and resistance to Yersinia pestis

8. Case report: Novel variants in RELA associated with familial Behcet’s-like disease

9. Contributors

11. And Then a Miracle Occurs! Ensuring the Successful Implementation of Enterpisewide EPSS and E-Learning from Day One.

12. The Spectrum of the Deficiency of Adenosine Deaminase 2: An Observational Analysis of a 60 Patient Cohort

13. Excess Serum Interleukin‐18 Distinguishes Patients With Pathogenic Mutations inPSTPIP1

14. Performance Support for Knowledge Workers: Practical Strategies Based on Research and Practice.

15. Supplement to: Activated STING in a vascular and pulmonary syndrome.

17. Activated STING in a Vascular and Pulmonary Syndrome

18. Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2

19. An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist

20. Excess Serum Interleukin-18 Distinguishes Patients with Pathogenic Mutations in PSTPIP1

21. Systematic evaluation of nine monogenic autoinflammatory diseases reveals common and disease-specific correlations with allergy-associated features

24. Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: A cohort study to determine three- and five-year outcomes

26. Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance

27. Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease

31. A20 haploinsufficiency (HA20) : Clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease

32. A20 haploinsufficiency (HA20): Clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease

33. Dysregulated neutrophil responses and neutrophil extracellular trap formation and degradation in PAPA syndrome

34. JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies

35. Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors

36. A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease

38. Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2

40. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

41. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

42. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

43. Brief Report: Anakinra Use During Pregnancy in Patients With Cryopyrin-Associated Periodic Syndromes

49. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

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