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Quoted phrase not found in phrase index: "Immunodeficiency, common variable, 3"
Page 1
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. Parvovirus B19 was the most common in cases that developed antibodies withou …
The most common preceding infection was viral (55.6%). In cases that developed thromboembolic events Human immunodeficiency an …
Autoimmunity in common variable immunodeficiency: a systematic review and meta-analysis.
Rizvi FS, Zainaldain H, Rafiemanesh H, Jamee M, Hossein-Khannazer N, Hamedifar H, Sabzevari A, Yazdani R, Abolhassani H, Aghamohammadi A, Azizi G. Rizvi FS, et al. Expert Rev Clin Immunol. 2020 Dec;16(12):1227-1235. doi: 10.1080/1744666X.2021.1850272. Epub 2020 Dec 7. Expert Rev Clin Immunol. 2020. PMID: 33203275
Objectives: Common variable immunodeficiency (CVID) is the most common symptomatic inborn error of immunity characterized by variable clinical manifestations. ...Results: The overall prevalence of autoimmunity was 29.8% (95% CI: 26.4-33.3 …
Objectives: Common variable immunodeficiency (CVID) is the most common symptomatic inborn error of immunity char …
Malignancy in common variable immunodeficiency: a systematic review and meta-analysis.
Kiaee F, Azizi G, Rafiemanesh H, Zainaldain H, Sadaat Rizvi F, Alizadeh M, Jamee M, Mohammadi S, Habibi S, Sharifi L, Jadidi-Niaragh F, Haghi S, Yazdani R, Abolhassani H, Aghamohammadi A. Kiaee F, et al. Expert Rev Clin Immunol. 2019 Oct;15(10):1105-1113. doi: 10.1080/1744666X.2019.1658523. Epub 2019 Sep 15. Expert Rev Clin Immunol. 2019. PMID: 31452405
Background: Common variable immunodeficiency (CVID) is the most common clinically significant primary immunodeficiency (PID) disorder characterized by variable clinical manifestations including recurrent infections, autoimmune disorders, …
Background: Common variable immunodeficiency (CVID) is the most common clinically significant primary immunod …
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
Crider K, Williams J, Qi YP, Gutman J, Yeung L, Mai C, Finkelstain J, Mehta S, Pons-Duran C, Menéndez C, Moraleda C, Rogers L, Daniels K, Green P. Crider K, et al. Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217. Cochrane Database Syst Rev. 2022. PMID: 36321557 Free PMC article.
The WHO has highlighted the limited evidence available and has indicated the need for further research on biomarkers of folate status, particularly interactions between RBC folate concentrations and tuberculosis, human immunodeficiency virus (HIV), and antifolate antimalar …
The WHO has highlighted the limited evidence available and has indicated the need for further research on biomarkers of folate status, parti …
Alcohol use and its determinants among adults living with HIV/AIDS in Ethiopia: a systematic review and meta-analysis.
Mekuriaw B, Belayneh Z, Molla A, Mehare T. Mekuriaw B, et al. Harm Reduct J. 2021 May 17;18(1):55. doi: 10.1186/s12954-021-00503-6. Harm Reduct J. 2021. PMID: 34001138 Free PMC article. Review.
BACKGROUND: Alcohol use is a common practice of almost all communities worldwide and it is more common among persons with HIV infection. ...The pooled prevalence of lifetime, current and hazardous alcohol use among HIV patients in Ethiopia were 36.42% [95% CI (19.96 …
BACKGROUND: Alcohol use is a common practice of almost all communities worldwide and it is more common among persons with HIV …
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. ...A Kaplan-Meier survival analysis for APDS showed the conditional survival rate at the age of 20 years was 87%, age of 30 y …
Activated phosphoinositide 3-kinase delta syndrome (APDS) is a rare genetic disorder that presents clinically as a primary immunod …
Clinical, Immunologic and Molecular Spectrum of Patients with Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome: A Systematic Review.
Kiaee F, Zaki-Dizaji M, Hafezi N, Almasi-Hashiani A, Hamedifar H, Sabzevari A, Shirkani A, Zian Z, Jadidi-Niaragh F, Aghamahdi F, Goudarzvand M, Yazdani R, Abolhassani H, Aghamohammadi A, Azizi G. Kiaee F, et al. Endocr Metab Immune Disord Drug Targets. 2021;21(4):664-672. doi: 10.2174/1871530320666200613204426. Endocr Metab Immune Disord Drug Targets. 2021. PMID: 32533820
The ICF type 1, type 2, type 3 and type 4 are characterized by mutations in DNMT3B, ZBTB24, CDCA7 or HELLS gene, respectively. ...Among these patients, 60% reported with ICF-1, 30% with ICF-2, 4% with ICF-3, and 6% with ICF-4. The four most common symptoms re …
The ICF type 1, type 2, type 3 and type 4 are characterized by mutations in DNMT3B, ZBTB24, CDCA7 or HELLS gene, respectively. ...Amo …
What Works When Treating Granulomatous Disease in Genetically Undefined CVID? A Systematic Review.
van Stigt AC, Dik WA, Kamphuis LSJ, Smits BM, van Montfrans JM, van Hagen PM, Dalm VASH, IJspeert H. van Stigt AC, et al. Front Immunol. 2020 Dec 17;11:606389. doi: 10.3389/fimmu.2020.606389. eCollection 2020. Front Immunol. 2020. PMID: 33391274 Free PMC article.
BACKGROUND: Granulomatous disease is reported in at least 8-20% of patients with common variable immunodeficiency (CVID). Granulomatous disease mainly affects the lungs, and is associated with significantly higher morbidity and mortality. ...Inclusion criteri …
BACKGROUND: Granulomatous disease is reported in at least 8-20% of patients with common variable immunodeficiency (CVID …
Profound symptomatic hypogammaglobulinemia: a rare late complication after rituximab treatment for immune thrombocytopenia. Report of 3 cases and systematic review of the literature.
Levy R, Mahévas M, Galicier L, Boutboul D, Moroch J, Loustau V, Guillaud C, Languille L, Fain O, Bierling P, Khellaf M, Michel M, Oksenhendler E, Godeau B. Levy R, et al. Autoimmun Rev. 2014 Oct;13(10):1055-63. doi: 10.1016/j.autrev.2014.08.036. Epub 2014 Aug 27. Autoimmun Rev. 2014. PMID: 25183241 Review.
All 3 presented recurrent severe infections. In 2, the outcome suggested common variable immunodeficiency. In patient 3, the peripheral blood lacked CD19(+)CD20(+) B cells and the bone-marrow B-cell precursor level was impaired. ...
All 3 presented recurrent severe infections. In 2, the outcome suggested common variable immunodeficiency. In pa …
A Systematic Review on Predisposition to Lymphoid (B and T cell) Neoplasias in Patients With Primary Immunodeficiencies and Immune Dysregulatory Disorders (Inborn Errors of Immunity).
Riaz IB, Faridi W, Patnaik MM, Abraham RS. Riaz IB, et al. Front Immunol. 2019 Apr 16;10:777. doi: 10.3389/fimmu.2019.00777. eCollection 2019. Front Immunol. 2019. PMID: 31057537 Free PMC article.
As would be expected, higher susceptibility to malignancies are typically reported in patients with Common Variable Immunodeficiency (CVID), combined immunodeficiencies affecting cellular immunity, in particular, DNA repair defects, or in the context of impai …
As would be expected, higher susceptibility to malignancies are typically reported in patients with Common Variable Immunod …
12 results