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Quoted phrase not found in phrase index: "Immunodeficiency 87 and autoimmunity"
Page 1
Advances in the diagnosis and management of pulmonary aspergillosis.
Gao Y, Soubani A. Gao Y, et al. Adv Respir Med. 2019;87(6):231-243. doi: 10.5603/ARM.2019.0061. Adv Respir Med. 2019. PMID: 31970725 Free article. Review.
Invasive pulmonaryaspergillosisoccurs primarily in patients with severe immunodeficiency. The significance of this infection has dramatically increased with growing numbers of patients with impaired immune state associated with the management of malignancy, organ transplan …
Invasive pulmonaryaspergillosisoccurs primarily in patients with severe immunodeficiency. The significance of this infection has dram …
Hypogammaglobulinemia: a diagnosis that must not be overlooked.
Pimenta FMCA, Palma SMU, Constantino-Silva RN, Grumach AS. Pimenta FMCA, et al. Braz J Med Biol Res. 2019 Oct 10;52(10):e8926. doi: 10.1590/1414-431X20198926. eCollection 2019. Braz J Med Biol Res. 2019. PMID: 31618370 Free PMC article.
Hypothyroidism was identified in 4/8 (50%) patients. Rhinitis was found in 7/8 (87.5%) and asthma in 3/8 (37.5%) patients. The tomographic findings were consolidations, atelectasis, emphysema, ground glass opacity, budding tree, bronchial thickening, and bronchiectasis. Im …
Hypothyroidism was identified in 4/8 (50%) patients. Rhinitis was found in 7/8 (87.5%) and asthma in 3/8 (37.5%) patients. The tomogr …
Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency.
Catak MC, Akcam B, Bilgic Eltan S, Babayeva R, Karakus IS, Akgun G, Baser D, Bulutoglu A, Bayram F, Kasap N, Kiykim A, Hancioglu G, Kokcu Karadag SI, Kendir Demirkol Y, Ozen S, Cekic S, Ozcan D, Edeer Karaca N, Sasihuseyinoglu AS, Cansever M, Ozek Yucel E, Tamay Z, Altintas DU, Aydogmus C, Celmeli F, Cokugras H, Gulez N, Genel F, Metin A, Guner SN, Kutukculer N, Keles S, Reisli I, Kilic SS, Yildiran A, Karakoc-Aydiner E, Lo B, Ozen A, Baris S. Catak MC, et al. Allergy. 2022 Oct;77(10):3108-3123. doi: 10.1111/all.15331. Epub 2022 May 12. Allergy. 2022. PMID: 35491430
BACKGROUND: Lipopolysaccharide-responsive beige-like anchor protein (LRBA) deficiency and cytotoxic T-lymphocyte protein-4 (CTLA-4) insufficiency are recently described disorders that present with susceptibility to infections, autoimmunity, and lymphoproliferation. …
BACKGROUND: Lipopolysaccharide-responsive beige-like anchor protein (LRBA) deficiency and cytotoxic T-lymphocyte protein-4 (CTLA-4) i …
Interstitial Lung Disease in Common Variable Immunodeficiency.
Lopes JP, Ho HE, Cunningham-Rundles C. Lopes JP, et al. Front Immunol. 2021 Mar 11;12:605945. doi: 10.3389/fimmu.2021.605945. eCollection 2021. Front Immunol. 2021. PMID: 33776995 Free PMC article.
Interstitial lung disease (ILD) is a common complication in patients with common variable immunodeficiency (CVID) and often associated with other features, such as bronchiectasis and autoimmunity. ...Lung biopsy pathology revealed granulomas in 25 patients (54.4%), …
Interstitial lung disease (ILD) is a common complication in patients with common variable immunodeficiency (CVID) and often associate …
The GAIN Registry - a New Prospective Study for Patients with Multi-organ Autoimmunity and Autoinflammation.
Staus P, Rusch S, El-Helou S, Müller G, Krausz M, Geisen U, Caballero-Oteyza A, Krüger R, Bakhtiar S, Lee-Kirsch MA, Fasshauer M, Baumann U, Hoyer BF, Farela Neves J, Borte M, Carrabba M, Hauck F, Ehl S, Bader P, von Bernuth H, Atschekzei F, Seppänen MRJ, Warnatz K, Nieters A, Kindle G, Grimbacher B. Staus P, et al. J Clin Immunol. 2023 Aug;43(6):1289-1301. doi: 10.1007/s10875-023-01472-0. Epub 2023 Apr 21. J Clin Immunol. 2023. PMID: 37084016 Free PMC article.
Between November 2019 and July 2022, twelve centers from Europe have registered 419 patients with multi-organ autoimmunity or autoinflammation. The median age at onset of symptoms was 13 years (IQR 3-28) and the median delay from onset to diagnosis was 5 years (IQR 1-14). …
Between November 2019 and July 2022, twelve centers from Europe have registered 419 patients with multi-organ autoimmunity or autoinf …
Systematic review of mortality and survival rates for APDS.
Hanson J, Bonnen PE. Hanson J, et al. Clin Exp Med. 2024 Jan 27;24(1):17. doi: 10.1007/s10238-023-01259-y. Clin Exp Med. 2024. PMID: 38280023 Free PMC article.
Activated phosphoinositide 3-kinase delta syndrome (APDS) is a rare genetic disorder that presents clinically as a primary immunodeficiency. Clinical presentation of APDS includes severe, recurrent infections, lymphoproliferation, lymphoma, and other cancers, autoimmuni …
Activated phosphoinositide 3-kinase delta syndrome (APDS) is a rare genetic disorder that presents clinically as a primary immunodeficien …
Characterization of infectious and non-infectious gastrointestinal disease in common variable immunodeficiency: analysis of 114 patient cohort.
Sanchez DA, Rotella K, Toribio C, Hernandez M, Cunningham-Rundles C. Sanchez DA, et al. Front Immunol. 2023 Aug 30;14:1209570. doi: 10.3389/fimmu.2023.1209570. eCollection 2023. Front Immunol. 2023. PMID: 37711607 Free PMC article.
Common Variable Immunodeficiency (CVID), a complex primary immunodeficiency syndrome defined by defective B cell responses to infection and vaccination, has heterogeneous clinical manifestations. ...CVID enteropathy was the most encountered GI diagnosis based on end …
Common Variable Immunodeficiency (CVID), a complex primary immunodeficiency syndrome defined by defective B cell responses to …
Serum anti-tissue transglutaminase IgA and prediction of duodenal villous atrophy in adults with suspected coeliac disease without IgA deficiency (Bi.A.CeD): a multicentre, prospective cohort study.
Ciacci C, Bai JC, Holmes G, Al-Toma A, Biagi F, Carroccio A, Ciccocioppo R, Di Sabatino A, Gingold-Belfer R, Jinga M, Makharia G, Niveloni S, Norman GL, Rostami K, Sanders DS, Smecuol E, Villanacci V, Vivas S, Zingone F; Bi.A.CeD study group. Ciacci C, et al. Lancet Gastroenterol Hepatol. 2023 Nov;8(11):1005-1014. doi: 10.1016/S2468-1253(23)00205-4. Epub 2023 Sep 9. Lancet Gastroenterol Hepatol. 2023. PMID: 37696284
The AUC for serum tTG-IgA for the prediction of duodenal villous atrophy was 0.87 (95% CI 0.81-0.92) when applying the categorical definition of serum tTG-IgA (positive [>1 ULN] vs negative [1 ULN]), and 0.93 (0.89-0.96) when applying the numerical definition of serum t …
The AUC for serum tTG-IgA for the prediction of duodenal villous atrophy was 0.87 (95% CI 0.81-0.92) when applying the categorical de …
Prevalence and factors associated with latent autoimmune diabetes in adults (LADA): a cross-sectional study.
Manisha AM, Shangali AR, Mfinanga SG, Mbugi EV. Manisha AM, et al. BMC Endocr Disord. 2022 Jul 8;22(1):175. doi: 10.1186/s12902-022-01089-1. BMC Endocr Disord. 2022. PMID: 35804315 Free PMC article.
BACKGROUND: The Latent Autoimmune Diabetes in Adults (LADA) is a slowly progressive Type 1 diabetes subgroup with onset during middle age. ...The parameters such as mean age, family history of diabetes mellitus status, Fasting Blood Glucose, clinical characteristics, and c …
BACKGROUND: The Latent Autoimmune Diabetes in Adults (LADA) is a slowly progressive Type 1 diabetes subgroup with onset during middle …
Prognostic markers for immunodeficiency-associated primary central nervous system lymphoma.
Kaulen LD, Galluzzo D, Hui P, Barbiero F, Karschnia P, Huttner A, Fulbright R, Baehring JM. Kaulen LD, et al. J Neurooncol. 2019 Aug;144(1):107-115. doi: 10.1007/s11060-019-03208-w. Epub 2019 Jun 13. J Neurooncol. 2019. PMID: 31190317
We aimed to define clinical and imaging features and determine prognostic factors for immunodeficiency-associated PCNSL. METHODS: All PCNSL cases seen at Yale-New Haven Hospital between 2002 and 2017 were retrospectively screened for immunodeficiency. ...Predictors …
We aimed to define clinical and imaging features and determine prognostic factors for immunodeficiency-associated PCNSL. METHODS: All …
55 results