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

2. B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C)

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3. Expanded population of low-density neutrophils in juvenile idiopathic arthritis

4. Evaluation of presepsin as a diagnostic tool in newborns with risk of early-onset neonatal sepsis

5. Immunoprofiling of monocytes in STAT1 gain-of-function chronic mucocutaneous candidiasis

6. Risk Factors for Severe COVID-19 and Hospital Admission in Patients With Inborn Errors of Immunity - Results From a Multicenter Nationwide Study

7. Natural Course of Activated Phosphoinositide 3-Kinase Delta Syndrome in Childhood and Adolescence

8. Searching for COVID-19 Antibodies in Czech Children—A Needle in the Haystack

9. Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic

10. Anti-IL6 Autoantibodies in an Infant With CRP-Less Septic Shock

11. Disharmonic Inflammatory Signatures in COVID-19: Augmented Neutrophils’ but Impaired Monocytes’ and Dendritic Cells’ Responsiveness

12. CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID

14. EAACI statement on the pathogenesis, immunology, and immune-targeted management of the Multisystem Inflammatory Syndrome in Children (MIS-C) or Pediatric Inflammatory Multisystem Syndrome (PIMS)

15. Accelerated Maturation, Exhaustion, and Senescence of T cells in 22q11.2 Deletion Syndrome

16. Aberrant tolerogenic functions and proinflammatory skew of dendritic cells in STAT1 gain-of-function patients may contribute to autoimmunity and fungal susceptibility

17. Manifestations of cutaneous mycobacterial infections in patients with inborn errors of IL-12/IL-23-IFNγ immunity

18. Aberrant autophagy and skewed inflammatory and tolerogenic functions in STAT1 gain-of-function dendritic cells

19. High Prevalence of Likely Passively Acquired Anti-TPO and Anti-GAD Autoantibodies in Common Variable Immunodeficiency

20. B cells, BAFF and interferons in MIS-C

22. Impact of JAK Inhibitors in Pediatric Patients with STAT1 Gain-of-Function (GOF) Mutations – 10 Children and Review of the Literature

23. TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins

24. Risk Factors for Severe COVID-19 and Hospital Admission in Patients With Inborn Errors of Immunity - Results From a Multicenter Nationwide Study

25. Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency

26. Czech Hizentra Noninterventional Study With Rapid Push: Efficacy, Safety, Tolerability, and Convenience of Therapy With 20% Subcutaneous Immunoglobulin

27. Accelerated Maturation, Exhaustion, and Senescence of T cells in 22q11.2 Deletion Syndrome

28. Immunogenicity and Safety of COVID-19 mRNA Vaccine in STAT1 GOF Patients

29. A unique association of diaphragmatic hernia and pulmonary tuberculosis in an infant

30. Neutrophils mediate Th17 promotion in COVID‐19 patients

31. Complex Immunometabolic Profiling Reveals the Activation of Cellular Immunity and Biliary Lesions in Patients with Severe COVID-19

32. An eosinophilic papulopustular rash in a baby

33. Complex Immuno-metabolic Profiling Reveals Activation of Cellular Immunity and Biliary Lesion in Patients with Severe COVID-19

34. Bronchial Asthma and Bronchial Hyperresponsiveness and Their Characteristics in Patients with Common Variable Immunodeficiency

35. Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation

36. The prevalence, clinical relevance and origin of autoantibodies in patients with Common variable immunodeficiency on regular immunoglobulin replacement therapy – the results from a prospective observational study

37. Selective IgM Deficiency: Clinical and Laboratory Features of 17 Patients and a Review of the Literature

38. Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic

39. Otorhinolaryngological manifestations in 61 patients with mucopolysaccharidosis

40. Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

41. The role of 18F-FDG PET/CT in diagnosis and therapeutic approach in small child with MSMD

42. Follicular Helper T Cells in DiGeorge Syndrome

43. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19