All Stories

  1. On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema
  2. SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies
  3. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency
  4. Atomic Coordination Reflects Peptide Immunogenicity
  5. The coordination of unprotonated peptide tertiary structure as a metric of pMHC–TCR functional avidity
  6. Human Cytomegalovirus variant peptides adapt by decreasing their total coordination upon binding to a T cell receptor
  7. F12-46C/T and hereditary angioedema severity
  8. The quantum chemical causality of pMHC-TCR biological avidity: Peptide atomic coordination data and the electronic state of agonist N termini
  9. Genetic polymorphisms of innate and adaptive immunity as predictors of outcome in critically ill patients
  10. Quantum chemical calculations predict biological function
  11. Hereditary angioedema: Molecular and clinical differences among European populations
  12. MBL2Genotypes and Their Associations with MBL Levels and NICU Morbidity in a Cohort of Greek Neonates
  13. Impaired degradation and aberrant phagocytosis of necrotic cell debris in the peripheral blood of patients with primary Sjögren's syndrome
  14. TACI Expression and Signaling in Chronic Lymphocytic Leukemia
  15. Hereditary Hyperferritinemia Cataract Syndrome as a Cause of Childhood Hyperferritinemia
  16. A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
  17. Hereditary Angioedema in Greece: The First Results of the Greek Hereditary Angioedema Registry
  18. Rapid detection of MYD88-L265P mutation by PCR-RFLP in B-cell lymphoproliferative disorders
  19. Reply to: “SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting”
  20. Corrigendum to: Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV [Blood Cells Mol. Dis. 40:3 (2008) 353–359]
  21. Allergy and risk of acute lymphoblastic leukemia among children: A nationwide case control study in Greece
  22. Heterozygous Alterations of TNFRSF13B/TACI in Tonsillar Hypertrophy and Sarcoidosis
  23. Liver FOXP3 and PD1/PDL1 Expression is Down-Regulated in Chronic HBV Hepatitis on Maintained Remission Related to the Degree of Inflammation
  24. C0176 Influence of common thrombophilia polymorphisms on the thrombosis risk in patients with JAK2-V617F-positive myeloproliferative neoplasms
  25. IgA antibodies against deamidated gliadin peptides in patients with chronic liver diseases
  26. Expression patterns of endothelin-1 and its receptors in colorectal cancer
  27. Neutrophil gelatinase-associated lipocalin (NGAL) in inflammatory bowel disease: association with pathophysiology of inflammation, established markers, and disease activity
  28. CLINICAL SIGNIFICANCE OF DEAMIDATED GLIADIN PEPTIDE ANTIBODIES IN PATIENTS WITH CHRONIC LIVER DISEASES
  29. SLC40A1-R178G mutation and ferroportin disease
  30. TNFRSF13B/TACI Alterations in Greek Patients with Antibody Deficiencies
  31. Survivin isoform expression patterns in CML patients correlate with resistance to imatinib and progression, but do not trigger cytolytic responses
  32. Foxp3Expression in Liver Correlates with the Degree but Not the Cause of Inflammation
  33. Toll-Like Receptor 4 Gene (TLR4), but NotTLR2, Polymorphisms Modify the Risk of Tonsillar Disease Due toStreptococcus pyogenesandHaemophilus influenzae
  34. Determinants of cancer immunotherapy success
  35. Downregulation of serum epidermal growth factor in patients with inflammatory bowel disease. Is there a link with mucosal damage?
  36. Cord blood as a source of non-senescent lymphocytes for tumor immunotherapy
  37. Naturally occurring tumor-specific CD8+ T-cell precursors in individuals with and without cancer
  38. Cytolytic T-cell response against Epstein-Barr virus in lung cancer patients and healthy subjects
  39. Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene
  40. Hereditary angioedema in Greek families caused by novel and recurrent mutations
  41. Anti-survivin antibody responses in lung cancer
  42. TLR2 and TLR4 polymorphisms in familial Mediterranean fever
  43. Clinical, functional and biochemical changes during recovery from COPD exacerbations
  44. Association of TLR4-T399I Polymorphism with Chronic Obstructive Pulmonary Disease in Smokers
  45. Imbalance of tissue inhibitors of metalloproteinases (TIMP) – 1 and – 4 serum levels, in patients with inflammatory bowel disease
  46. Baseline levels of CD8+ T cells against survivin and survivin-2B in the blood of lung cancer patients and cancer-free individuals
  47. Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV
  48. Co-expression patterns of tumor-associated antigen genes by non-small cell lung carcinomas: Implications for immunotherapy
  49. Adiponectin: A New Independent Predictor of Liver Steatosis and Response to IFN-α Treatment in Chronic Hepatitis C
  50. Anti-cyclic citrullinated peptide-2 (CCP2) autoantibodies and extra-articular manifestations in Greek patients with rheumatoid arthritis
  51. TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders
  52. Immunological features of visceral leishmaniasis may mimic systemic lupus erythematosus
  53. Foxp3 expression in human cancer cells
  54. Prevalence of coeliac disease in the adult population of central Greece
  55. Tumor immune escape mediated by indoleamine 2,3-dioxygenase
  56. Indoleamine 2,3-dioxygenase (IDO) expression in lung cancer
  57. Acute phase markers for the differentiation of infectious and malignant pleural effusions
  58. Diagnostic value of anti-cyclic citrullinated peptide antibodies in Greek patients with rheumatoid arthritis
  59. DHLAS: A web-based information system for statistical genetic analysis of HLA population data
  60. A Brief Exposure to Moderate Passive Smoke Increases Metabolism and Thyroid Hormone Secretion
  61. Diagnostic value of anticyclic citrullinated peptide antibodies in Greek patients with rheumatoid arthritis: association with extra-articular manifestations
  62. Immunoepigenetics: the unseen side of cancer immunoediting
  63. Alterations of leptin during IFN-α therapy in patients with chronic viral hepatitis
  64. Cytokine levels in the sera of patients with idiopathic pulmonary fibrosis
  65. Performance of Antibodies against Tissue Transglutaminase for the Diagnosis of Celiac Disease: Meta-Analysis
  66. Morning Levels of C-Reactive Protein in Children with Obstructive Sleep-disordered Breathing
  67. Complement: An Inflammatory Pathway Fulfilling Multiple Roles at the Interface of Innate Immunity and Development
  68. Circulating adhesion molecules levels in type 2 diabetes mellitus and hypertension
  69. Morning levels of fibrinogen in children with sleep-disordered breathing
  70. Soluble adhesion molecules are not involved in the development of retinopathy in type 2 diabetic patients
  71. Evaluation of a Microsphere‐Based Flow Cytometric Assay for Diagnosis of Celiac Disease
  72. IN VIVO EFFECT OF rhGM-CSF AND rhG-CSF ON MONOCYTE HLA-DR EXPRESSION OF SEPTIC NEONATES
  73. STL3/433: IATROTEK On-line: The Hellenic medical literature retrieval system
  74. Nationwide collaborative study of HLA class II associations with distinct types of juvenile chronic arthritis (JCA) in Greece
  75. Beyond the Ingelfinger Rule: the intellectual property ethics after the end of biomedical journals' monopoly
  76. Non-indexed medical journals in the Web: new perspectives in the medical literature
  77. THE IMMUNOMODULATORY EFFECT OF LEFLUNOMIDE IN RAT CARDIAC ALLOTRANSPLANTATION
  78. Kinetics of heat-damaged homologous erythrocytes
  79. Function of reticuloendothelial system in splenectomised thalassemics
  80. C3 Polymorphism in Greece
  81. Plasma fibronectin (Fn) study in homozygous ?-thalassemia: Relation to splenectomy and transfusion
  82. Group-Specific Component and Haptoglobin Phenotypes in Multiple Myeloma
  83. Serum Alpha-1-Antitrypsin Study in Beta-Thalassaemic Patients