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2. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

3. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

4. The HyperPed-COVID international registry: Impact of age of onset, disease presentation and geographical distribution on the final outcome of MIS-C

5. Semiquantitative classification (SQC) and Oxford classifications predict poor renal outcome better than The International Study of Kidney Disease in Children (ISKDC) and Haas in patients with IgAV nephritis: a multicenter study

6. Clinical features, treatment and outcome of pediatric patients with severe cutaneous manifestations in IgA vasculitis: Multicenter international study

9. Association of Glutathione Transferase M1, T1, P1 and A1 Gene Polymorphism and Susceptibility to IgA Vasculitis.

13. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

14. HLA Polymorphisms and Clinical Manifestations in IgA Vasculitis

16. Correction to: Semiquantitative classification (SQC) and Oxford classifications predict poor renal outcome better than The International Study of Kidney Disease in Children (ISKDC) and Haas in patients with IgAV nephritis: a multicenter study

17. Comparison of EULAR/PRINTO/PReS Ankara 2008 and 2022 ACR/EULAR Classification Criteria for Granulomatosis with Polyangiitis in Children

19. Razvoj imunološkog sustava i izloženost infekcijama.

21. The characteristics of patients with COVID-19-associated pediatric vasculitis: an international, multicenter study

25. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

26. The diversity and distribution of HLA-DRB1 alleles in the population of Croatian patients with IgA vasculitis (IgAV)

27. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

29. Correction to: Semiquantitative classification (SQC) and Oxford classifications predict poor renal outcome better than The International Study of Kidney Disease in Children (ISKDC) and Haas in patients with IgAV nephritis: a multicenter study

30. Semiquantitative classification (SQC) and Oxford classifications predict poor renal outcome better than The International Study of Kidney Disease in Children (ISKDC) and Haas in patients with IgAV nephritis: a multicenter study

31. The Characteristics of Patients With COVID‐19–Associated Pediatric Vasculitis: An International, Multicenter Study.

32. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

33. Case Report: Simultaneously Developed Amyopathic Dermatomyositis and Autoimmune Sclerosing Cholangitis – a Coincidence or a Shared Immunopathogenesis?

34. Utjecaj polimorfizama gena za glutation S- transferazu (GST) u bolesnika s IgA vaskulitisom

36. The paediatric vasculitis activity score (PVAS) and proteinuria in IgAV nephritis: is there an association with different histologic findings?

37. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

38. Neonatal lupus erythematosus in non-identical twins

40. Association between glutathione S-transferase (GST) M1,T1 and A1 polymorphisms and IgA vasculitis: a pilot study

42. Software Quality Control (SQC) and Oxford classifications predict poor renal outcome better than The International Study of Kidney Disease in Children (ISKDC) and Haas in patients with IgAV nephritis: a multicenter study

43. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

48. 443 Different histological classifications for IgA vasculitis nephritis – which one has the best association with the disease outcome?

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