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Quoted phrase not found in phrase index: "Autoinflammatory disease, systemic, with vasculitis"
Page 1
Interstitial lung disease in autoinflammatory disease in childhood: A systematic review of the literature.
Nayir Buyuksahin H, Basaran O, Balık Z, Bilginer Y, Ozen S, Dogru D. Nayir Buyuksahin H, et al. Pediatr Pulmonol. 2023 Feb;58(2):367-373. doi: 10.1002/ppul.26220. Epub 2022 Nov 7. Pediatr Pulmonol. 2023. PMID: 36314652
BACKGROUND/OBJECTIVES: The lung is one of the target organs in the systemic involvement of autoinflammatory disease (AID), and interstitial lung disease (ILD) is the primary phenotype of lung involvement in AID. ...
BACKGROUND/OBJECTIVES: The lung is one of the target organs in the systemic involvement of autoinflammatory disease (AI …
Association of Vasculitis and Familial Mediterranean Fever.
Abbara S, Grateau G, Ducharme-Bénard S, Saadoun D, Georgin-Lavialle S. Abbara S, et al. Front Immunol. 2019 Apr 12;10:763. doi: 10.3389/fimmu.2019.00763. eCollection 2019. Front Immunol. 2019. PMID: 31031761 Free PMC article.
We assessed the characteristics of patients with FMF and systemic vasculitis through a systematic review of the literature. Medline was searched by two independent investigators until December 2017. We screened 310 articles and selected 58 of them (IgA vasculitis …
We assessed the characteristics of patients with FMF and systemic vasculitis through a systematic review of the literature. Me …
Non-invasive biomarkers of disease activity and organ damage in ANCA-associated vasculitis: a systematic review.
Renson T, Kelly MM, Benediktsson H, Grundhoefer N, Luca N, Miettunen P, Twilt M, Grisaru S, Wade A, Banks A, Fifi-Mah A, Hamiwka L, Benseler S. Renson T, et al. RMD Open. 2024 Feb 9;10(1):e003579. doi: 10.1136/rmdopen-2023-003579. RMD Open. 2024. PMID: 38341193 Free PMC article.
BACKGROUND: In anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), histopathological assessment of affected tissue is often necessary for diagnosis and assessment of disease extent. ...Further validation of the candidate biomarkers is warranted …
BACKGROUND: In anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), histopathological assessment of affected tiss …
Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy and Elevated Temperature Syndrome: A Systemic Review.
Altom A, Khader SAE, Gad AG, Anadani R, Dang DP, Ansar F, Chaudhari J, Crespo-Quezada J, Huy NT. Altom A, et al. Am J Dermatopathol. 2023 Jun 1;45(6):355-370. doi: 10.1097/DAD.0000000000002345. Epub 2023 Feb 17. Am J Dermatopathol. 2023. PMID: 37191371
BACKGROUND: Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome is a rare, hereditary, autoinflammatory disease. However, there are few cases reported in the literature. ...The laboratories were not specific, which may be ex …
BACKGROUND: Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome is a rare, hereditary, autoinfl …
Autosomic dominant familial Behcet disease and haploinsufficiency A20: A review of the literature.
Berteau F, Rouviere B, Delluc A, Nau A, Le Berre R, Sarrabay G, Touitou I, de Moreuil C. Berteau F, et al. Autoimmun Rev. 2018 Aug;17(8):809-815. doi: 10.1016/j.autrev.2018.02.012. Epub 2018 Jun 8. Autoimmun Rev. 2018. PMID: 29890348 Review.
INTRODUCTION: Behcet disease (BD) is a systemic vasculitis involving vessels from any size with various clinical features. ...Response to colchicine is unpredictable and biotherapies like anti-TNFalpha and anti IL1 appear to be treatments of choice, like for …
INTRODUCTION: Behcet disease (BD) is a systemic vasculitis involving vessels from any size with various clinical featur …
Comparison of diagnostic spectrum between inflammation of unknown origin and fever of unknown origin: A systematic review and meta-analysis.
Betrains A, Moreel L, Mulders-Manders CM, Auwaerter PG, Torné-Cachot J, Weitzer F, Terasawa T, Ly KH, Schönau V, Blockmans D, Wright WF, Rovers C, Vanderschueren S. Betrains A, et al. Eur J Intern Med. 2024 Jun;124:115-121. doi: 10.1016/j.ejim.2024.02.021. Epub 2024 Mar 2. Eur J Intern Med. 2024. PMID: 38431500
Comparison of diagnostic subgroups revealed that IUO patients were less likely to have systemic autoinflammatory disorders (OR 0.17 [95 % CI, 0.05-0.58]; I(2) 42 %) and more likely to have vasculitis (OR 2.04 [95 % CI, 1.23-3.38]; I(2) 21 %) and rheumatoid ar …
Comparison of diagnostic subgroups revealed that IUO patients were less likely to have systemic autoinflammatory disorders (OR …
DADA2 diagnosed in adulthood versus childhood: A comparative study on 306 patients including a systematic literature review and 12 French cases.
Fayand A, Chasset F, Boutboul D, Queyrel V, Tieulié N, Guichard I, Dupin N, Franck N, Cohen P, Bessis D, Guenno GL, Koné-Paut I, Belot A, Bonhomme A, Ducharme-Bénard S, Grateau G, Sarrabay G, Touitou I, Boursier G, Georgin-Lavialle S. Fayand A, et al. Semin Arthritis Rheum. 2021 Dec;51(6):1170-1179. doi: 10.1016/j.semarthrit.2021.09.001. Epub 2021 Sep 16. Semin Arthritis Rheum. 2021. PMID: 34571400
BACKGROUND: Deficiency of adenosine deaminase 2 (DADA2) is a rare autoinflammatory disease usually presenting before the age of 10 years. ...Conversely, fewer strokes occurred in the adult group presenting with systemic vasculopathy (54% vs. 81%). Symptomatic …
BACKGROUND: Deficiency of adenosine deaminase 2 (DADA2) is a rare autoinflammatory disease usually presenting before the age o …