All Stories

  1. Gammaplex® 5 and 10% in the treatment of primary immunodeficiency and chronic immune thrombocytopenic purpura
  2. Recombinant human hyaluronidase-facilitated subcutaneous immunoglobulin infusion in primary immunodeficiency diseases
  3. Treatment with oleic acid reduces IgE binding to peanut and cashew allergens
  4. Efficacy, safety, and tolerability of IVIG-SN in patients with primary immunodeficiency
  5. Tolerance to Allergenic Foods Following Food Oral Immunotherapy (FOIT)
  6. Single Practice Six-Year Experience Treating Food Allergy with Oral Immunotherapy
  7. Long-Term Efficacy and Safety of Recombinant Human Hyaluronidase (rHuPH20)- Facilitated Subcutaneous Infusion of Immunoglobulin G (IgG) (HyQvia; IGHy) in Patients with Primary Immunodeficiencies (PI)
  8. Pharmacokinetics of RI-002, an Investigational Igiv Preparation
  9. Subcutaneous immunoglobulin: facilitated infusion and advances in administration
  10. Hizentra for the treatment of primary immunodeficiency
  11. Decreased Immunoglobulin E (IgE) Binding to Cashew Allergens following Sodium Sulfite Treatment and Heating
  12. Overview of recombinant human hyaluronidase-facilitated subcutaneous infusion of IgG in primary immunodeficiencies
  13. A new intravenous immunoglobulin (BIVIGAM®) for primary humoral immunodeficiency
  14. Single Practice Five-Year Experience Treating Food Allergy With Oral Immunotherapy: Efficacy and Epinephrine Treated Reactions
  15. Single Practice, Five-Year Experience Treating Food Allergy With Oral Immunotherapy (FOIT): Successes and Failures
  16. Single Practice Five Year Experience Treating Food Allergy With Oral Immunotherapy (FOIT): Effect On Antigen Specific IgE (asIgE)
  17. Effect Of Oleic Acid On The Allergenic Properties Of Peanut and Cashew Allergens
  18. Retrospective Analysis Of The Clinical Utility Of Biweekly Dosing With High-Concentration Subcutaneous Immunoglobulin In 10 Patients With Primary Immunodeficiency
  19. Long-term efficacy, safety, and tolerability of Hizentra® for treatment of primary immunodeficiency disease
  20. Long-Term Tolerability and Safety Of Facilitated-Subcutaneous Infusion Of Human Immune Globulin G (IgG), 10%, and Recombinant Human Hyaluronidase (rHuPH20) (IGHy): A Phase 3 Extension Study In Patients With Primary Immunodeficiencies (PIs)
  21. Emerging Paradigm of Primary Immunodeficiency Disease: Individualizing Immunoglobulin Dose and Delivery to Enhance Outcomes
  22. Oral Immunotherapy for Peanut Allergy: Multipractice Experience With Epinephrine-treated Reactions
  23. In vitro digestion of soluble cashew proteins and characterization of surviving IgE-reactive peptides
  24. Case Studies
  25. Characterization of the Effects of Proteolysis and Reduction On Cashew Allergens
  26. Long-Term Efficacy and Tolerability of 20% Scig in the Treatment of Patients with Primary Immunodeficiency Disease
  27. C1-INH concentrate for treatment of acute hereditary angioedema: a pediatric cohort from the I.M.P.A.C.T. studies
  28. Recombinant human hyaluronidase-facilitated subcutaneous infusion of human immunoglobulins for primary immunodeficiency
  29. Per-Attack Reporting of Prodromal Symptoms Concurrent with C1-Inhibitor Treatment of Hereditary Angioedema Attacks
  30. C1-inhibitor therapy for hereditary angioedema attacks: Prospective patient assessments of health-related quality of life
  31. Progress in Gammaglobulin Therapy for Immunodeficiency: From Subcutaneous to Intravenous Infusions and Back Again
  32. Treatment response after repeated administration of C1 esterase inhibitor for successive acute hereditary angioedema attacks
  33. Discussion
  34. Introduction
  35. Safety, Efficacy and Pharmacokinetics of a New 10% Liquid Intravenous Immunoglobulin (IVIG) in Patients with Primary Immunodeficiency
  36. Safety ofL-proline as a stabilizer for immunoglobulin products
  37. Diagnosis and treatment of primary immunodeficiency disease: the role of the otolaryngologist
  38. Reply
  39. Pharmacokinetics of Subcutaneous IgPro20 in Patients with Primary Immunodeficiency
  40. Author Response
  41. Efficacy, Safety, and Pharmacokinetics of a 10% Liquid Immune Globulin Preparation (GAMMAGARD LIQUID, 10%) Administered Subcutaneously in Subjects with Primary Immunodeficiency Disease
  42. Prospective study of C1 esterase inhibitor in the treatment of successive acute abdominal and facial hereditary angioedema attacks
  43. Office-based oral immunotherapy for food allergy is safe and effective
  44. Hereditary angioedema: Validation of the end point time to onset of relief by correlation with symptom intensity
  45. Recurrent Granulibacter bethesdensis Infections and Chronic Granulomatous Disease
  46. Population pharmacokinetics of plasma-derived C1 esterase inhibitor concentrate used to treat acute hereditary angioedema attacks
  47. Prospective Study of Rapid Relief Provided by C1 Esterase Inhibitor in Emergency Treatment of Acute Laryngeal Attacks in Hereditary Angioedema
  48. Efficacy and Safety of a New 20% Immunoglobulin Preparation for Subcutaneous Administration, IgPro20, in Patients With Primary Immunodeficiency
  49. Use of intravenous immunoglobulin and adjunctive therapies in the treatment of primary immunodeficiencies
  50. Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks
  51. Pharmacokinetics of a new 10% intravenous immunoglobulin in patients receiving replacement therapy for primary immunodeficiency
  52. Safety and Efficacy of Privigen®, a Novel 10% Liquid Immunoglobulin Preparation for Intravenous Use, in Patients with Primary Immunodeficiencies
  53. Real-world assessment of a metered-dose inhaler with integrated dose counter
  54. Intrainfusion and postinfusion adverse events related to intravenous immunoglobulin therapy in immunodeficiency states
  55. Efficacy and safety of inhaled fluticasone propionate chlorofluorocarbon in 2- to 4-year-old patients with asthma: results of a double-blind, placebo-controlled study
  56. Efficacy, Safety and Tolerability of a New 10% Liquid Intravenous Immune Globulin [IGIV 10%] in Patients with Primary Immunodeficiency
  57. Stable Enterovirus 5′ Nontranslated Region over a 7‐Year Period in a Patient with Agammaglobulinemia and Chronic Infection
  58. Evaluating children with respiratory tract infections: the role of immunization with bacterial polysaccharide vaccine
  59. Immunodeficiencies
  60. Chronic Sinusitis as a Manifestation of Primary Immunodeficiency in Adults
  61. Antibody deficiency
  62. Sir,
  63. Polymorphisms of Immunologically Relevant Loci in Human Disease.
  64. IGG SUBCLASS DETERMINATIONS
  65. FAILURE OF ANTI-PNEUMOCOCCAL ANTIBODY FORMATION IN PATIENTS WITH COMPLETE IgA DEFICIENCY AND NORMAL IgG LEVELS
  66. HUMAN ANTI-HAPTEN ANTIBODY DIVERSITY DERIVES FROM COMBINATORIAL MECHANISMS EMPLOYING FEW VH GENES AND SEVERAL JH GENES
  67. Intravenous gamma globulin prophylaxis for newborn infants
  68. In vitro stimulation prior to fusion generates antigen-binding human-human hybridomas
  69. Ataxia-telangiectasia Associated with Sarcoidosis
  70. Reply
  71. Caustic substance injuries
  72. 1035 HUMAN HYBRIDOMA ANTIBODIES SPECIFIC FOR THE GROUP B STREPTOCOCCAL TYPE III (GBS-III) POLYSACCHARIDE
  73. Immunology for the Practicing Physician
  74. IN VITRO SENSITIZATION PRIOR TO FUSION GENERATES A HIGH FREQUENCY OF HUMAN-HUMAN HYBRIDOMAS BINSING TO GROUP B STREPTOCOCCI (GBS)
  75. Transfusion-associated cytomegalovirus infection and acquired immune deficiency syndrome in an infant
  76. Unconventional therapies for neonatal sepsis
  77. The amino acid sequence of the light chain variable region of a canine myeloma immunoglobulin: Evidence that the vk subgroups predated mammalian speciation
  78. Primary structure of the variable regions of two canine immunoglobulin heavy chains
  79. Immunoglobulins