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Your search keyword '"Martelius, Timi"' showing total 45 results

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45 results on '"Martelius, Timi"'

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1. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

2. Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis

3. Clinical and functional spectrum of RAC2-related immunodeficiency

4. PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants

5. 49 Early-Onset Common Variable Immunodeficiency in a Patient with Heterozygous Variants in Interferon Response-Associated Genes TRAF3 and IRF4

6. Hybrid Immunity Improves the Immune Response after the Fourth COVID-19 Vaccine Dose in Individuals with Medical Conditions Predisposing to Severe COVID-19

7. Hybrid immunity improves the immune response after fourth Covid-19 vaccine dose in individuals with medical conditions predisposing to severe Covid-19

11. Analysis of novel RAC2 variants associated with neutrophil dysfunction, lymphopenia, and primary immunodeficiency

12. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

15. Long-term follow up of families with pathogenic NFKB1 variants reveals incomplete penetrance and frequent inflammatory sequelae

16. Editorial : Updates on the pathogenesis of common variable immunodeficiency (CVID)

17. Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes

24. Clinical characteristics of patients with Epstein Barr virus in cerebrospinal fluid

25. Somatic Mutations in T Cells As Possible Regulators of Immunodeficiency

26. Mononukleoosi

27. ADA2 deficiency: Clonal lymphoproliferation in a subset of patients

28. Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland

30. Dominant NFKB1 Mutations Cause Antibody Deficiency and Autoinflammatory Episodes

32. Nosocomial bloodstream infections caused by Escherichia coli and Klebsiella pneumoniae resistant to third-generation cephalosporins, Finland, 1999–2013: Trends, patient characteristics and mortality.

41. Additional file 2: of Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

42. Additional file 2: of Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

44. Somatic mutations and T-cell clonality in patients with immunodeficiency.

45. [Whipple's disease--a rare and severe systemic infection].

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