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1967 2
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1984 7
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1998 70
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2000 60
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2003 67
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2007 109
2008 141
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Quoted phrase not found in phrase index: "Immunodeficiency 70"
Page 1
Immune dysregulation.
Long A, Kleiner A, Looney RJ. Long A, et al. J Allergy Clin Immunol. 2023 Jan;151(1):70-80. doi: 10.1016/j.jaci.2022.11.001. J Allergy Clin Immunol. 2023. PMID: 36608984 Free article. Review.
There is increasing evidence that altered microbiome and gut barrier dysfunction contribute to systemic inflammation in patients with primary immunodeficiency and in patients with rheumatic disease. Recent research provides insight into the process of induction and maturat …
There is increasing evidence that altered microbiome and gut barrier dysfunction contribute to systemic inflammation in patients with primar …
Clinical, Immunological, and Genetic Features in Patients with Activated PI3Kδ Syndrome (APDS): a Systematic Review.
Jamee M, Moniri S, Zaki-Dizaji M, Olbrich P, Yazdani R, Jadidi-Niaragh F, Aghamahdi F, Abolhassani H, Condliffe AM, Aghamohammadi A, Azizi G. Jamee M, et al. Clin Rev Allergy Immunol. 2020 Dec;59(3):323-333. doi: 10.1007/s12016-019-08738-9. Clin Rev Allergy Immunol. 2020. PMID: 31111319
A total of 243 APDS patients were identified from 55 articles. For all patients, demographic, clinical, immunologic, and molecular data were collected. Overall, 179 APDS1 and 64 APDS2 patients were identified. ...The predominant immunologic phenotype was hyper-IgM s …
A total of 243 APDS patients were identified from 55 articles. For all patients, demographic, clinical, immunologic, and molecular da …
Defining combined immunodeficiency.
Roifman CM, Somech R, Kavadas F, Pires L, Nahum A, Dalal I, Grunebaum E. Roifman CM, et al. J Allergy Clin Immunol. 2012 Jul;130(1):177-83. doi: 10.1016/j.jaci.2012.04.029. Epub 2012 Jun 2. J Allergy Clin Immunol. 2012. PMID: 22664165
BACKGROUND: Although the extreme condition of typical profound T-cell dysfunction (TD), severe combined immunodeficiency (SCID), has been carefully defined, we are currently in the process of better defining less typical T-cell deficiencies, which tend to present with auto …
BACKGROUND: Although the extreme condition of typical profound T-cell dysfunction (TD), severe combined immunodeficiency (SCID), has …
Early Diagnosis of Primary Immunodeficiency Disease Using Clinical Data and Machine Learning.
Mayampurath A, Ajith A, Anderson-Smits C, Chang SC, Brouwer E, Johnson J, Baltasi M, Volchenboum S, Devercelli G, Ciaccio CE. Mayampurath A, et al. J Allergy Clin Immunol Pract. 2022 Nov;10(11):3002-3007.e5. doi: 10.1016/j.jaip.2022.08.041. Epub 2022 Sep 13. J Allergy Clin Immunol Pract. 2022. PMID: 36108921 Free article.
BACKGROUND: Primary immunodeficiency diseases (PIDD) are a group of immune-related disorders that have a current median delay of diagnosis between 6 and 9 years. ...Adding laboratory results, medications, and radiological orders improved discrimination (c-statistic: 0.7 …
BACKGROUND: Primary immunodeficiency diseases (PIDD) are a group of immune-related disorders that have a current median delay of diag …
Diagnostic challenges of bronchiectasis.
Suarez-Cuartin G, Chalmers JD, Sibila O. Suarez-Cuartin G, et al. Respir Med. 2016 Jul;116:70-7. doi: 10.1016/j.rmed.2016.05.014. Epub 2016 May 17. Respir Med. 2016. PMID: 27296824 Free article. Review.
Bronchiectasis related to allergic bronchopulmonary aspergillosis (ABPA), immunodeficiencies with antibody production deficiency, primary ciliary dyskinesia, cystic fibrosis and alpha-1-antitrypsin deficiency, among others, require a specific management that …
Bronchiectasis related to allergic bronchopulmonary aspergillosis (ABPA), immunodeficiencies with antibody production deficiency …
Skin manifestations of primary immune deficiency.
Lehman H. Lehman H. Clin Rev Allergy Immunol. 2014 Apr;46(2):112-9. doi: 10.1007/s12016-013-8377-8. Clin Rev Allergy Immunol. 2014. PMID: 23760761 Review.
Cutaneous manifestations are common in primary immune deficiency diseases, affecting between 40 % and 70 % of patients with diagnosed primary immune deficiency. ...The skin manifestations of primary immune deficiency diseases are often early or heraldi …
Cutaneous manifestations are common in primary immune deficiency diseases, affecting between 40 % and 70 % of patients with di …
Skin manifestations of immunodeficiencies in children.
Torchia D, Connelly EA. Torchia D, et al. G Ital Dermatol Venereol. 2010 Apr;145(2):269-87. G Ital Dermatol Venereol. 2010. PMID: 20467400 Review.
More than 140 distinct genes have been identified, which abnormalities account for more than 200 different forms of primary immunodeficiencies. The skin may be one of the organs involved in immunodeficiencies and in a number of primary immunodeficiency syn …
More than 140 distinct genes have been identified, which abnormalities account for more than 200 different forms of primary immunodeficie …
Flow Cytometry Contributions for the Diagnosis and Immunopathological Characterization of Primary Immunodeficiency Diseases With Immune Dysregulation.
Cabral-Marques O, Schimke LF, de Oliveira EB Jr, El Khawanky N, Ramos RN, Al-Ramadi BK, Segundo GRS, Ochs HD, Condino-Neto A. Cabral-Marques O, et al. Front Immunol. 2019 Nov 26;10:2742. doi: 10.3389/fimmu.2019.02742. eCollection 2019. Front Immunol. 2019. PMID: 31849949 Free PMC article. Review.
Almost 70 years after establishing the concept of primary immunodeficiency disorders (PIDs), more than 320 monogenic inborn errors of immunity have been identified thanks to the remarkable contribution of high-throughput genetic screening in the last decade. ...Loss …
Almost 70 years after establishing the concept of primary immunodeficiency disorders (PIDs), more than 320 monogenic inborn er …
Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.
Karaatmaca B, Cagdas D, Esenboga S, Erman B, Tan C, Turul Ozgur T, Boztug K, van der Burg M, Sanal O, Tezcan I. Karaatmaca B, et al. Clin Exp Immunol. 2024 Feb 7;215(2):160-176. doi: 10.1093/cei/uxad110. Clin Exp Immunol. 2024. PMID: 37724703 Free PMC article.
Recombination activating genes (RAG)1 and RAG2 deficiency leads to combined T/B-cell deficiency with varying clinical presentations. This study aimed to define the clinical/laboratory spectrum of RAG1 and RAG2 deficiency. We retrospectively reviewed the clini …
Recombination activating genes (RAG)1 and RAG2 deficiency leads to combined T/B-cell deficiency with varying clinical presenta …
In-depth blood immune profiling of Good syndrome patients.
Torres-Valle A, Aragon L, Silva SL, Serrano C, Marcos M, Melero J, Bonroy C, Arenas-Caro PP, Casado DM, Olaizola PMR, Neirinck J, Hofmans M, de Arriba S, Jara M, Prieto C, Sousa AE, Prada Á, van Dongen JJM, Pérez-Andrés M, Orfao A. Torres-Valle A, et al. Front Immunol. 2023 Nov 15;14:1285088. doi: 10.3389/fimmu.2023.1285088. eCollection 2023. Front Immunol. 2023. PMID: 38035080 Free PMC article.
INTRODUCTION: Good syndrome (GS) is a rare adult-onset immunodeficiency first described in 1954. It is characterized by the coexistence of a thymoma and hypogammaglobulinemia, associated with an increased susceptibility to infections and autoimmunity. The classification an …
INTRODUCTION: Good syndrome (GS) is a rare adult-onset immunodeficiency first described in 1954. It is characterized by the coexisten …
4,687 results