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Quoted phrase not found in phrase index: "Immunodeficiency syndrome with autoimmunity"
Page 1
Overview of Immunodeficiency Disorders.
Raje N, Dinakar C. Raje N, et al. Immunol Allergy Clin North Am. 2015 Nov;35(4):599-623. doi: 10.1016/j.iac.2015.07.001. Epub 2015 Aug 25. Immunol Allergy Clin North Am. 2015. PMID: 26454309 Free PMC article. Review.
The spectrum of primary immunodeficiency disorders (PIDs) is expanding. It includes typical disorders that primarily present with defective immunity as well as disorders that predominantly involve other systems and show few features of impaired immunity. The rapidly growin …
The spectrum of primary immunodeficiency disorders (PIDs) is expanding. It includes typical disorders that primarily present with def …
B lymphocytes: how they develop and function.
LeBien TW, Tedder TF. LeBien TW, et al. Blood. 2008 Sep 1;112(5):1570-80. doi: 10.1182/blood-2008-02-078071. Blood. 2008. PMID: 18725575 Free PMC article. Review.
The decades that followed have witnessed a continuum of unfolding complexities in B-cell development, subsets, and function that could not have been predicted. Some of the landmark discoveries that led to our current understanding of B lymphocytes as the source of protecti …
The decades that followed have witnessed a continuum of unfolding complexities in B-cell development, subsets, and function that could not h …
Selective IgA Deficiency: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management.
Yazdani R, Azizi G, Abolhassani H, Aghamohammadi A. Yazdani R, et al. Scand J Immunol. 2017 Jan;85(1):3-12. doi: 10.1111/sji.12499. Scand J Immunol. 2017. PMID: 27763681 Free article. Review.
Selective immunoglobulin A deficiency (SIgAD) is the most common primary antibody deficiency. Although more patients with SIgAD are asymptomatic, selected patients suffer from different clinical complications such as pulmonary infections, allergies, autoimmune …
Selective immunoglobulin A deficiency (SIgAD) is the most common primary antibody deficiency. Although more patients with SIgA …
The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management.
Yazdani R, Fekrvand S, Shahkarami S, Azizi G, Moazzami B, Abolhassani H, Aghamohammadi A. Yazdani R, et al. Clin Immunol. 2019 Jan;198:19-30. doi: 10.1016/j.clim.2018.11.007. Epub 2018 Nov 13. Clin Immunol. 2019. PMID: 30439505 Review.
Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by low or absent levels of serum IgG, IgA, IgE and normal or increased levels of serum IgM. ...Herein, the epidemiology, pathogenesis, clinical manifestations, diagnosis …
Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by low or absent levels of se …
Inborn Errors of Immunity and Autoimmune Disease.
Gray PE, David C. Gray PE, et al. J Allergy Clin Immunol Pract. 2023 Jun;11(6):1602-1622. doi: 10.1016/j.jaip.2023.04.018. Epub 2023 Apr 28. J Allergy Clin Immunol Pract. 2023. PMID: 37119983 Review.
Autoimmunity may be a manifestation of inborn errors of immunity, specifically as part of the subgroup of primary immunodeficiency known as primary immune regulatory disorders. ...In addition, there will be a review of autoimmunity in non-genetically defined …
Autoimmunity may be a manifestation of inborn errors of immunity, specifically as part of the subgroup of primary immunodeficiency …
Primary Immune Regulatory Disorders With an Autoimmune Lymphoproliferative Syndrome-Like Phenotype: Immunologic Evaluation, Early Diagnosis and Management.
López-Nevado M, González-Granado LI, Ruiz-García R, Pleguezuelo D, Cabrera-Marante O, Salmón N, Blanco-Lobo P, Domínguez-Pinilla N, Rodríguez-Pena R, Sebastián E, Cruz-Rojo J, Olbrich P, Ruiz-Contreras J, Paz-Artal E, Neth O, Allende LM. López-Nevado M, et al. Front Immunol. 2021 Aug 10;12:671755. doi: 10.3389/fimmu.2021.671755. eCollection 2021. Front Immunol. 2021. PMID: 34447369 Free PMC article.
Autoimmune lymphoproliferative syndrome (ALPS) is a PIRD due to an apoptotic defect in Fas-FasL pathway and characterized by benign and chronic lymphoproliferation, autoimmunity and increased risk of lymphoma. ...Following the Preferred Reporting Items for Sy …
Autoimmune lymphoproliferative syndrome (ALPS) is a PIRD due to an apoptotic defect in Fas-FasL pathway and characterized by b …
Reappraisal of Idiopathic CD4 Lymphocytopenia at 30 Years.
Lisco A, Ortega-Villa AM, Mystakelis H, Anderson MV, Mateja A, Laidlaw E, Manion M, Roby G, Higgins J, Kuriakose S, Walkiewicz MA, Similuk M, Leiding JW, Freeman AF, Sheikh V, Sereti I. Lisco A, et al. N Engl J Med. 2023 May 4;388(18):1680-1691. doi: 10.1056/NEJMoa2202348. N Engl J Med. 2023. PMID: 37133586 Free PMC article.
BACKGROUND: Idiopathic CD4 lymphocytopenia (ICL) is a clinical syndrome that is defined by CD4 lymphopenia of less than 300 cells per cubic millimeter in the absence of any primary or acquired cause of immunodeficiency. ...METHODS: We evaluated the clinical, genetic …
BACKGROUND: Idiopathic CD4 lymphocytopenia (ICL) is a clinical syndrome that is defined by CD4 lymphopenia of less than 300 cells per …
Treatment of inflammatory complications in common variable immunodeficiency (CVID): current concepts and future perspectives.
Fevang B. Fevang B. Expert Rev Clin Immunol. 2023 Jun;19(6):627-638. doi: 10.1080/1744666X.2023.2198208. Epub 2023 Apr 6. Expert Rev Clin Immunol. 2023. PMID: 36996348 Review.
INTRODUCTION: Patients with common variable immunodeficiency (CVID) have a high frequency of inflammatory complications like autoimmune cytopenias, interstitial lung disease and enteropathy. These patients have poor prognosis and effective, timely, and safe t …
INTRODUCTION: Patients with common variable immunodeficiency (CVID) have a high frequency of inflammatory complications like autoi …
Combined immunodeficiencies.
Aranda CS, Guimarães RR, de Gouveia-Pereira Pimentel M. Aranda CS, et al. J Pediatr (Rio J). 2021 Mar-Apr;97 Suppl 1(Suppl 1):S39-S48. doi: 10.1016/j.jped.2020.10.014. Epub 2020 Dec 17. J Pediatr (Rio J). 2021. PMID: 33340461 Free PMC article. Review.
The main clinical manifestations comprise increased susceptibility to infections, autoimmunity, inflammation, allergies and malignancies. The aim of this article is to review the literature on combined immunodeficiencies (CIDs) focusing on the diagnosis and treatment and t …
The main clinical manifestations comprise increased susceptibility to infections, autoimmunity, inflammation, allergies and malignanc …
Update in Primary Immunodeficiencies.
Leonardi L, Rivalta B, Cancrini C, Chiappini E, Cravidi C, Caffarelli C, Manti S, Calvani M, Martelli A, Miraglia Del Giudice M, Duse M, Marseglia GL, Cardinale F. Leonardi L, et al. Acta Biomed. 2020 Sep 15;91(11-S):e2020010. doi: 10.23750/abm.v91i11-S.10314. Acta Biomed. 2020. PMID: 33004780 Free PMC article. Review.
More specifi- cally, immune dysregulation is very often described in novel characterized PIDs and can lead to multiple autoimmune diseases, lymphoproliferation and malignancies. If not promptly diagnosed, these could negatively impact patient's prognosis. ...Finding …
More specifi- cally, immune dysregulation is very often described in novel characterized PIDs and can lead to multiple autoimmune dis …
890 results