230 results on '"Hautala, Timo"'
Search Results
2. Germline HAVCR2/TIM-3 Checkpoint Inhibitor Receptor Deficiency in Recurrent Autoinflammatory Myocarditis
3. Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis
4. Inflammation and Neutrophil Oxidative Burst in a Family with NFKB1 p.R157X LOF and Sterile Necrotizing Fasciitis
5. PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants
6. CD40LG Triplication Associates with Immune Dysregulation and Exhaustion
7. XMEN disease caused by the novel MAGT1 p.(Trp136*) mutation may present with neuropsychiatric symptoms
8. Low and high serum IgG associates with respiratory infections in a young and working age population
9. Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma
10. Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis
11. A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment
12. Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation
13. Tonsillar granuloma associated with hypogammaglobulinemia
14. Long-term follow up of families with pathogenic NFKB1 variants reveals incomplete penetrance and frequent inflammatory sequelae
15. Fatal Puumala Hantavirus Disease: Involvement of Complement Activation and Vascular Leakage in the Pathobiology
16. Heterozygous premature termination in zinc-finger domain of Krüppel-like factor 2 gene associates with dysregulated immunity
17. Nitazoxanide May Modify the Course of Progressive Multifocal Leukoencephalopathy
18. Inhibition of rubella virus replication by the broad-spectrum drug nitazoxanide in cell culture and in a patient with a primary immune deficiency
19. Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes
20. 52-year follow-up of a birth cohort reveals a high pneumonia incidence among young men
21. A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment
22. Effect of first-line antifungal treatment on ocular complication risk in Candida or yeast blood stream infection
23. Long-term hormonal follow-up after human Puumala hantavirus infection
24. Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction
25. Central Nervous System and Ocular Manifestations in Puumala Hantavirus Infection
26. Clinical characteristics and evaluation of the incidence of cryptococcosis in Finland 2004–2018
27. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
28. Hypophyseal hemorrhage and panhypopituitarism during Puumala virus infection: magnetic resonance imaging and detection of viral antigen in the hypophysis. (Brief Report)
29. IL-2 may possess neuroprotective properties in glaucomatous optic neuropathy
30. Late-presenting vascular graft infection caused by Aspergillus in an immunocompetent patient
31. Prospective study on ocular findings in acute Puumala hantavirus infection in hospitalised patients
32. Prevalence, incidence and epidemiology of childhood uveitis
33. Adaptive or maladaptive response to adenoviral adrenomedullin gene transfer is context-dependent in the heart
34. Adrenomedullin gene transfer induces neointimal apoptosis and inhibits neointimal hyperplasia in injured rat artery
35. Adenoviral Gene Transfer Restores Lysyl Hydroxylase Activity in Type VI Ehlers−Danlos Syndrome
36. Prevalence, incidence and epidemiology of childhood uveitis.
37. Aetiology of posterior uveitis in a tertiary centre in Finland
38. Primary Immunodeficiency, a Possible Cause of Neutrophilic Necrotizing Dermatosis
39. Young male patients are at elevated risk of developing serious central nervous system complications during acute Puumala hantavirus infection
40. Haploinsufficiency of A20 impairs protein–protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation
41. A cluster of Candida krusei infections in a haematological unit
42. Endostatin inhibits VEGF-A induced osteoclastic bone resorption in vitro
43. Adenoviral Gene Transfer Restores Lysyl Hydroxylase Activity in Type VI Ehlers-Danlos Syndrome
44. Rubella persistence in epidermal keratinocytes and granuloma M2 macrophages in patients with primary immunodeficiencies
45. ADA2 deficiency: Clonal lymphoproliferation in a subset of patients
46. Nitazoxanide May Modify the Course of Progressive Multifocal Leukoencephalopathy
47. Combined immunodeficiency and hypoglycemia associated with mutations in hypoxia upregulated 1
48. Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland
49. Large Granular Lymphocyte Infiltration in the Bone Marrow in Children and Young Adults May Suggest Primary Immune Deficiency
50. Long‐term hormonal follow‐up after human Puumala hantavirus infection
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.