J. Björkander

发表

IgG3 deficiency: common in obstructive lung disease. Hereditary in families with immunodeficiency and autoimmune disease.

A. Sjöholm, L. Hammarström, L. Hanson, 1986, Monographs in allergy.

Immunoglobulin prophylaxis in 350 adults with IgG subclass deficiency and recurrent respiratory tract infections: A long-term follow-up

P. Forsberg, A. Vietorisz, J. Björkander, 2007, Scandinavian journal of infectious diseases.

A validated single-cell-based strategy to identify diagnostic and therapeutic targets in complex diseases

Mika Gustafsson, Mikael Benson, Alex K. Shalek, 2019, Genome Medicine.

Immunoglobulin subclass deficiency

U. Bengtsson, A. Avanzini, J. Björkander, 1988, The Pediatric infectious disease journal.

Intravenous immunoglobulin prophylaxis causing liver damage in 16 of 77 patients with hypogammaglobulinemia or IgG subclass deficiency.

C. Cunningham-Rundles, P. Lundin, L. Hanson, 1988, The American journal of medicine.

Methodological aspects on clinical trials with inhaled corticosteroids: results of two comparisons between two steroid aerosols in patients with asthma.

E. Millqvist, S. Johansson, J. Björkander, 1982, European journal of respiratory diseases. Supplement.

Hereditary Angioedema in Swedish Adults: Report From the National Cohort.

L. Mallbris, C. Wahlgren, M. Nilsson, 2016, Acta dermato-venereologica.

Distribution of mucosal IgA and IgG subclass-producing immunocytes and alterations in various disorders.

T. Rognum, P. Brandtzaeg, L. Hanson, 1986, Monographs in allergy.

Family and linkage study of selective IgA deficiency and common variable immunodeficiency.

I. Vořechovský, L. Hammarström, C. I. Smith, 1995, Clinical immunology and immunopathology.

Fatigue Is Common in Immunoglobulin G Subclass Deficiency and Correlates With Inflammatory Response and Need for Immunoglobulin Replacement Therapy

Å. Nilsdotter-Augustinsson, C. Dahle, M. Nilsson, 2022, Frontiers in Immunology.

2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema

P. Keith, J. Bernstein, R. Schellenberg, 2010, Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology.

Impaired lung function in patients with IgA deficiency and low levels of IgG2 or IgG3.

B. Bake, L. Hanson, V. Oxelius, 1985, The New England journal of medicine.

HLA antigens in selective IgA deficiency: distribution in healthy donors and patients with recurrent respiratory tract infections.

L. Hammarström, C. I. Smith, L. Hanson, 2008, Tissue antigens.

Intravenous immunoglobulin and hepatitis C virus: the Scandinavian experience.

A. Widell, A. Fasth, J. Björkander, 1996, Clinical therapeutics.

Fcγ-receptor polymorphisms associated with clinical symptoms in patients with immunoglobulin G subclass deficiency

Å. Nilsdotter-Augustinsson, P. Söderkvist, C. Dahle, 2018, Infectious diseases.

IgG subclass deficiency with or without IgA deficiency.

P. Brandtzaeg, L. Hanson, J. Björkander, 1991, Clinical immunology and immunopathology.

Primary hypogammaglobulinaemia: impaired lung function and body growth with delayed diagnosis and inadequate treatment.

B. Bake, L. Hanson, J. Björkander, 1984, European journal of respiratory diseases.

Bronchitis in patients with hypogammaglobulinemia and other immunodeficiencies.

B. Bake, L. Hanson, J. Björkander, 1982, European journal of respiratory diseases. Supplement.

Mucociliary clearance in patients with immunoglobulin deficiency.

P. Camner, B. Mossberg, B. Afzelius, 1982, European journal of respiratory diseases.

Basophil Interleukin 4 and Interleukin 13 Production Is Suppressed during the Early Phase of Rush Immunotherapy

L. Håkansson, J. Björkander, P. Skov, 2006, International Archives of Allergy and Immunology.

Intralymphatic immunotherapy with one or two allergens renders similar clinical response in patients with allergic rhinitis due to birch and grass pollen

M. Jenmalm, P. Johansen, K. Duchén, 2022, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Intralymphatic Immunotherapy: A 3-year Randomized, Double-blind Study in 72 Patients With Allergic Rhinitis Due to Birch and Grass

M. Jenmalm, P. Johansen, B. Rolander, 2020 .

Secretory antibodies in IgA-deficient and immunosuppressed individuals

L. Hanson, J. Björkander, L. Mellander, 1986, Journal of Clinical Immunology.

Qualitative and quantitative analyses of the antibody response elicited by Haemophilus influenzae type b capsular polysaccharide–tetanus toxoid conjugates in adults with IgG subclass deficiencies and frequent infections

R. Schneerson, J. Robbins, M. Avanzini, 1994, Clinical and experimental immunology.

Intralymphatic allergen immunotherapy against pollen allergy: A 3-year open follow-up study of 10 patients.

M. Jenmalm, J. Björkander, U. Nyström, 2018, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Linkage of IgA deficiency to Gm allotypes; the influence of Gm allotypes on IgA‐IgG subclass deficiency

L. Hammarström, A. Carlsson, L. Hanson, 1995, Clinical and experimental immunology.

Prospective open‐label study of pharmacokinetics, efficacy and safety of a new 10% liquid intravenous immunoglobulin in patients with hypo‐ or agammaglobulinemia

H. Ehrlich, J. Björkander, W. Engl, 2006, Vox sanguinis.

Clinical Relevance of Subclass Deficiency Diseases

L. Hanson, J. Björkander, V. Friman, 1994 .

IgG Subclass Deficiencies

R. Schneerson, L. Hanson, J. Björkander, 1986, Vox sanguinis.

Variable increases of IgG and IgM antibodies in milk of IgA deficient women

L. Padyukov, L. Hanson, J. Björkander, 1997, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

The heterogeneity of IgA deficiency

L. Hanson, J. Björkander, T. Söderström, 1988, Journal of Clinical Immunology.

IgG subclasses in selective IgA deficiency: importance of IgG2-IgA deficiency.

L. Hanson, V. Oxelius, J. Björkander, 1981, The New England journal of medicine.

Goblet cell number in the nasal mucosa relates to cell-mediated immunity in patients with antibody deficiency syndromes.

H. Hansson, L. Hanson, J. Björkander, 1985, International archives of allergy and applied immunology.

The clinical condition of IgA-deficient patients is related to the proportion of IgD- and IgM-producing cells in their nasal mucosa.

P. Brandtzaeg, L. Hanson, J. Björkander, 1987, Clinical and experimental immunology.

IgG and IgE Antibody Patterns after Immunotherapy with Monomethoxy Polyethyleneglycol Modified Honey Bee Venom

R. Einarsson, J. Björkander, S. Dreborg, 1986, Allergy.

Presence of Non-Maternal Antibodies in Newborns of Mothers with Antibody Deficiencies

A. Osterhaus, L. Hanson, J. Björkander, 1992, Pediatric Research.

Subcutaneous immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs

L. Hammarström, S. Frøland, E. Jonsson, 1995, The Lancet.

Swedish children with hereditary angioedema report good overall health and quality of life despite symptoms

L. Mallbris, Lotus Mallbris, C. Wahlgren, 2016, Acta paediatrica.

Periodontal disease and dental caries in relation to primary IgG subclass and other humoral immunodeficiencies.

G. Dahlén, L. Hanson, J. Björkander, 1993, Journal of clinical periodontology.

Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: a combined Danish and Swedish study

J. Olsen, L. Hammarström, T. Barington, 2002, Clinical and experimental immunology.

Natural killer cells in common variable immunodeficiency and selective IgA deficiency.

O. Strannegard, L. Hanson, J. Björkander, 1982, Clinical immunology and immunopathology.

Lymphoid cell populations dynamics and the mucosal immune response in humans

C. Czerkinsky, J. Holmgren, A. Svennerholm, 1990 .

Aberrant IgG2 Antibody Response to Neisseria Meningitidis Polysaccharide A After Vaccination in Frequently Infected Compared to Healthy IgA‐Deficient Individuals

L. Hanson, V. Oxelius, J. Björkander, 2004, Scandinavian journal of immunology.

Intestinal and circulating antibody‐forming cells in IgA‐deficient individuals after oral cholera vaccination

D. Ericson, C. Czerkinsky, J. Holmgren, 1994, Clinical and experimental immunology.

The nasal mucosa in immunodeficiency. Surface morphology, mucociliary function and bacteriological findings in adult patients with common variable immunodeficiency or selective IgA deficiency.

H. Hansson, J. Björkander, G. Karlsson, 1985, Acta oto-laryngologica.

B‐Cell Activation in Duodenal Mucosa after Oral Cholera Vaccination in IgA Deficient Subjects with or without IgG Subclass Deficiency

J. Holmgren, P. Brandtzaeg, L. Hanson, 1993, Scandinavian journal of immunology.

1040 Prophylactic infusions with an unmodified intravenous immunoglobulin product causing few side-effects in patients with antibody deficiency syndromes

J. Björkander, L. Hanson, C. Wadsworth, 1985, Infection.

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency

M. Triggiani, P. Schmid‐Grendelmeier, W. Aberer, 2016, Allergy.

INTRAVENOUS IMMUNOGLOBULIN IN ANTIBODY DEFICIENCY SYNDROMES

B. Bake, J. Björkander, C. Wadsworth, 1982, The Lancet.

Use of an IgA-depleted intravenous immunoglobulin in a patient with an anti-IgA antibody.

C. Cunningham-Rundles, L. Hanson, J. Björkander, 1986, Clinical immunology and immunopathology.

131 Antibody deficiency syndromes with anti-IgA antibodies and successful immunoglobulin prophylaxis

C. Cunningham-Rundles, L. Hammarström, R. Buckley, 1985 .

Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema.

William H. Yang, P. Keith, P. Schmid‐Grendelmeier, 2010, The New England journal of medicine.

Long‐term safety of icatibant treatment of patients with angioedema in real‐world clinical practice

M. Triggiani, W. Aberer, B. Goichot, 2017, Allergy.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

Effectiveness of icatibant for treatment of hereditary angioedema attacks is not affected by body weight: findings from the Icatibant Outcome Survey, a cohort observational study

W. Aberer, B. Goichot, S. Kivity, 2018, Clinical and Translational Allergy.

Quantifying the burden of disease and perceived health state in patients with hereditary angioedema in Sweden.

L. Mallbris, C. Wahlgren, J. Björkander, 2014, Allergy and asthma proceedings.

The establishment and utility of Sweha-Reg: a Swedish population-based registry to understand hereditary angioedema

L. Mallbris, C. Wahlgren, J. Björkander, 2007, BMC dermatology.

C. Wahlgren, M. Nilsson, J. Björkander, 2017, Allergy and asthma proceedings.

[Hereditary angioedema--difficult disease with new therapeutic options].

J. Björkander, E. W. Nielsen, A. Bygum, 2012, Lakartidningen.

Lifelong treatment with gammaglobulin for primary antibody deficiencies: the patients' experiences of subcutaneous self-infusions and home therapy.

D. Ericson, L. Hammarström, S. Frøland, 1995, Journal of advanced nursing.

Successful treatment of refractory autoimmune haemolytic anaemia by plasmapheresis.

G. Westberg, L. Hanson, J. Björkander, 2009, Scandinavian journal of haematology.

Shared HLA class II-associated genetic susceptibility and resistance, related to the HLA-DQB1 gene, in IgA deficiency and common variable immunodeficiency.

L. Hammarström, C. I. Smith, J. Björkander, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Clinical and molecular analysis of patients with defects in μ heavy chain gene

Mary Ellen Conley, Lennart Hammarström, C. Pignata, 2002 .

Does the frequency of respiratory tract infections help to identify humoral immunodeficiencies in a primary health-care cohort?

Å. Nilsdotter-Augustinsson, L. Brudin, C. Dahle, 2015, Infectious diseases.

Interferon and β2-microglobulin in patients with common variable immunodeficiency or selective IgA deficiency

K. Hellstrand, A. Pacsa, L. Hanson, 1987 .

Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases

A. Oldfors, C Lindberg, L I Persson, 1994, Acta neurologica Scandinavica.

Enhanced IgG1 and IgG3 responses to pneumococcal polysaccharides in isolated IgA deficiency.

L. Hanson, J. Björkander, J. Henrichsen, 1989, Clinical and experimental immunology.

Infections of the nose and paranasal sinuses in adult patients with immunodeficiency.

L. Hanson, J. Björkander, G. Karlsson, 1985, Archives of otolaryngology.

Humoral immunity in nasal mucosa of patients with common variable immunodeficiency

P. Brandtzaeg, L. Hanson, J. Björkander, 2004, Journal of Clinical Immunology.

Sublingual immunotherapy alters expression of IL‐4 and its soluble and membrane‐bound receptors

M. Benson, J. Ernerudh, E. Dadfar, 2014, Allergy.

Production of interleukin-12 by monocytes and interferon-gamma by natural killer cells in allergic patients during rush immunotherapy.

L. Håkansson, J. Björkander, S. Rak, 2006, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

A validated gene regulatory network and GWAS identifies early regulators of T cell–associated diseases

Mika Gustafsson, Mikael Benson, Danuta R. Gawel, 2015, Science Translational Medicine.

Lack of IgA in Cμ-deficient patients

L. Hammarström, M. Conley, J. Björkander, 2002, Nature Immunology.

Lack of IgA in C(mu)-deficient patients.

L. Hammarström, M. Conley, J. Björkander, 2002, Nature immunology.

Immunoglobulin prophylaxis in patients with antibody deficiency syndromes and anti-IgA antibodies

C. Cunningham-Rundles, L. Hammarström, C. I. Smith, 2004, Journal of Clinical Immunology.

Intralymphatic immunotherapy with birch and grass pollen extracts. A randomized double‐blind placebo‐controlled clinical trial

M. Jenmalm, K. Duchén, D. Govindaraj, 2023, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Symptoms in patients with lowered levels of IgG subclasses, with or without IgA deficiency, and effects of immunoglobulin prophylaxis.

U. Bengtsson, L. Hanson, V. Oxelius, 1986, Monographs in allergy.