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Quoted phrase not found in phrase index: "Immunodeficiency, common variable, 6"
Page 1
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. ...AREAS COVERED: This review will focus on current medical treatmen …
INTRODUCTION: Patients with common variable immunodeficiency (CVID) have a high frequency of inflammatory complications …
Systematic review of case reports of antiphospholipid syndrome following infection.
Abdel-Wahab N, Lopez-Olivo MA, Pinto-Patarroyo GP, Suarez-Almazor ME. Abdel-Wahab N, et al. Lupus. 2016 Dec;25(14):1520-1531. doi: 10.1177/0961203316640912. Epub 2016 Apr 7. Lupus. 2016. PMID: 27060064 Free PMC article. Review.
The most common preceding infection was viral (55.6%). In cases that developed thromboembolic events Human immunodeficiency and Hepatitis C viruses were the most frequently reported. ...Few patients in groups 1 and 2 had persistent antiphospholipid antibodies …
The most common preceding infection was viral (55.6%). In cases that developed thromboembolic events Human immunodeficiency …
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Lorenzini T, Fliegauf M, Klammer N, Frede N, Proietti M, Bulashevska A, Camacho-Ordonez N, Varjosalo M, Kinnunen M, de Vries E, van der Meer JWM, Ameratunga R, Roifman CM, Schejter YD, Kobbe R, Hautala T, Atschekzei F, Schmidt RE, Schröder C, Stepensky P, Shadur B, Pedroza LA, van der Flier M, Martínez-Gallo M, Gonzalez-Granado LI, Allende LM, Shcherbina A, Kuzmenko N, Zakharova V, Neves JF, Svec P, Fischer U, Ip W, Bartsch O, Barış S, Klein C, Geha R, Chou J, Alosaimi M, Weintraub L, Boztug K, Hirschmugl T, Dos Santos Vilela MM, Holzinger D, Seidl M, Lougaris V, Plebani A, Alsina L, Piquer-Gibert M, Deyà-Martínez A, Slade CA, Aghamohammadi A, Abolhassani H, Hammarström L, Kuismin O, Helminen M, Allen HL, Thaventhiran JE, Freeman AF, Cook M, Bakhtiar S, Christiansen M, Cunningham-Rundles C, Patel NC, Rae W, Niehues T, Brauer N, Syrjänen J, Seppänen MRJ, Burns SO, Tuijnenburg P, Kuijpers TW; NIHR BioResource; Warnatz K, Grimbacher B; NIHR BioResource. Lorenzini T, et al. J Allergy Clin Immunol. 2020 Oct;146(4):901-911. doi: 10.1016/j.jaci.2019.11.051. Epub 2020 Apr 9. J Allergy Clin Immunol. 2020. PMID: 32278790 Free PMC article.
Incomplete clinical penetrance (70%) and age-dependent severity of NFKB1-related phenotypes were observed. The phenotype included hypogammaglobulinemia (88.9%), reduced switched memory B cells (60.3%), and respiratory (83%) and gastrointestinal (28.6%) infections, t …
Incomplete clinical penetrance (70%) and age-dependent severity of NFKB1-related phenotypes were observed. The phenotype included hyp …
Cytomegalovirus in primary immunodeficiency.
Godsell J, Chan S, Slade C, Bryant V, Douglass JA, Sasadeusz J, Yong MK. Godsell J, et al. Curr Opin Infect Dis. 2021 Dec 1;34(6):663-671. doi: 10.1097/QCO.0000000000000797. Curr Opin Infect Dis. 2021. PMID: 34608876 Review.
PURPOSE OF REVIEW: Cytomegalovirus (CMV) infection and disease are well described in the setting of secondary immunodeficiency. Less is known about CMV in the context of primary immunodeficiencies (PIDs), where inborn errors in one or more arms of the immune system result …
PURPOSE OF REVIEW: Cytomegalovirus (CMV) infection and disease are well described in the setting of secondary immunodeficiency. Less …
Clinical Symptoms, Laboratory Parameters and Long-Term Follow-up in a National DADA2 Cohort.
Andriessen MVE, Legger GE, Bredius RGM, van Gijn ME, Hak AE, Muller PCEH, Kamphuis S, Klouwer FCC, Kuijpers TW, Leavis HL, Nierkens S, Rutgers A, van der Veken LT, van Well GTJ, Mulders-Manders CM, van Montfrans JM. Andriessen MVE, et al. J Clin Immunol. 2023 Oct;43(7):1581-1596. doi: 10.1007/s10875-023-01521-8. Epub 2023 Jun 5. J Clin Immunol. 2023. PMID: 37277582 Free PMC article. Review.
All patients had biallelic pathogenic variants in the ADA2 gene. The most common clinical findings included cutaneous involvement (79.3%), (hepato)splenomegaly (70.8%) and recurrent infections (58.6%). ...Patients presented most often with a mixed phenotype involvin …
All patients had biallelic pathogenic variants in the ADA2 gene. The most common clinical findings included cutaneous involvement (79 …
Clinical features and predictors of osteoarticular manifestations in common variable immunodeficiency.
Ben Khaled M, Merdassi A, Rekaya S, Fraj IB, Lamouchi T, Zaiter I, Kouki R, Bejaoui M, Mellouli F, Ouederni M. Ben Khaled M, et al. Clin Rheumatol. 2023 Nov;42(11):3123-3129. doi: 10.1007/s10067-023-06722-5. Epub 2023 Jul 28. Clin Rheumatol. 2023. PMID: 37505303
INTRODUCTION: This study aimed to assess osteoarticular manifestations in patients with common variable immunodeficiency (CIVD) and to identify the predictive factors. ...The cumulative incidence of infectious complications was 17%. In multivariate ana …
INTRODUCTION: This study aimed to assess osteoarticular manifestations in patients with common variable immunodeficiency …
Cryptosporidiosis in perspective.
Tzipori S. Tzipori S. Adv Parasitol. 1988;27:63-129. doi: 10.1016/s0065-308x(08)60353-x. Adv Parasitol. 1988. PMID: 3289331 Free PMC article. Review.
Cryptosporidiosis seems to cause diarrhoea in young ruminants, less frequently in pets. In birds the parasite has been observed in the gastrointestinal tract, without ill effect, and in the respiratory tract, in which clinical symptoms of variable severity have been …
Cryptosporidiosis seems to cause diarrhoea in young ruminants, less frequently in pets. In birds the parasite has been observed in th …
Neurologic Manifestations of Common Variable Immunodeficiency: Impact on Quality of Life.
De Almeida BI, Smith TL, Delic A, Esquibel L, Galli J, Millsap L, Paz Soldán MM, Cortez MM, Rose J, Greenlee JE, Gundlapalli AV, Hill HR, Wong KH, Clardy SL. De Almeida BI, et al. Neurol Neuroimmunol Neuroinflamm. 2023 Feb 16;10(3):e200088. doi: 10.1212/NXI.0000000000200088. Print 2023 May. Neurol Neuroimmunol Neuroinflamm. 2023. PMID: 36797058 Free PMC article.
BACKGROUND AND OBJECTIVES: Common variable immunodeficiency is a systemic disease and not solely a disease of humoral immunity. Neurologic symptoms associated with common variable immunodeficiency are underrecognized and warrant further s …
BACKGROUND AND OBJECTIVES: Common variable immunodeficiency is a systemic disease and not solely a disease of humoral i …
Dysregulated Lymphocyte Antigen Receptor Signaling in Common Variable Immunodeficiency with Granulomatous Lymphocytic Interstitial Lung Disease.
Lui VG, Ghosh T, Rymaszewski A, Chen S, Baxter RM, Kong DS, Ghosh D, Routes JM, Verbsky JW, Hsieh EWY. Lui VG, et al. J Clin Immunol. 2023 Aug;43(6):1311-1325. doi: 10.1007/s10875-023-01485-9. Epub 2023 Apr 24. J Clin Immunol. 2023. PMID: 37093407 Free PMC article.
PURPOSE: A subset of common variable immunodeficiency (CVID) patients either presents with or develops autoimmune and lymphoproliferative complications, such as granulomatous lymphocytic interstitial lung disease (GLILD), a major cause of morbidity and mortal …
PURPOSE: A subset of common variable immunodeficiency (CVID) patients either presents with or develops autoimmune and l …
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. ...OBJECTIVE: To develop a machine learning model using elements within the electronic health record dat …
BACKGROUND: Primary immunodeficiency diseases (PIDD) are a group of immune-related disorders that have a current median delay of diag …
245 results