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Year Number of Results
2010 1
2012 1
2014 2
2015 4
2016 2
2017 4
2018 2
2019 4
2020 4
2021 1
2022 4
2023 6
2024 0

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28 results

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Page 1
Interleukin 1alpha: a comprehensive review on the role of IL-1alpha in the pathogenesis and treatment of autoimmune and inflammatory diseases.
Cavalli G, Colafrancesco S, Emmi G, Imazio M, Lopalco G, Maggio MC, Sota J, Dinarello CA. Cavalli G, et al. Autoimmun Rev. 2021 Mar;20(3):102763. doi: 10.1016/j.autrev.2021.102763. Epub 2021 Jan 20. Autoimmun Rev. 2021. PMID: 33482337 Free article. Review.
These include conditions affecting the lung and respiratory tract, dermatoses and inflammatory skin disorders, systemic sclerosis, myocarditis, pericarditis, myocardial infarction, coronary artery disease, inflammatory thrombosis, as well as complex multifactorial c …
These include conditions affecting the lung and respiratory tract, dermatoses and inflammatory skin disorders, systemic sclerosis, my …
Pediatric Behet disease: Update in diagnosis and management.
Burns E, Cooper E, Peterson R, Diaz LZ. Burns E, et al. Pediatr Dermatol. 2022 Mar;39(2):173-181. doi: 10.1111/pde.14859. Epub 2022 Jan 20. Pediatr Dermatol. 2022. PMID: 35060179 Review.
Behet disease is a multisystem inflammatory disease and variable vessel vasculitis involving primarily the oral and genital mucosa, skin, and eyes. Diagnosis is challenging due to the lack of a specific diagnostic test and overlap with other autoinflammato …
Behet disease is a multisystem inflammatory disease and variable vessel vasculitis involving primarily the oral and gen …
Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey.
Israni M, Nicholson B, Mahlaoui N, Obici L, Rossi-Semerano L, Lachmann H, Hayward G, Avramovič MZ, Guffroy A, Dalm V, Rimmer R, Solis L, Villar C, Gennery AR, Skeffington S, Nordin J, Warnatz K, Korganow AS, Antón J, Cattalini M, Amin T, Berg S, Soler-Palacin P, Burns SO, Campbell M; RITA-ERN Transition Working Group Consortium. Israni M, et al. J Clin Immunol. 2023 Jan;43(1):206-216. doi: 10.1007/s10875-022-01345-y. Epub 2022 Oct 12. J Clin Immunol. 2023. PMID: 36222999 Free PMC article.
BACKGROUND: Due to the absence of curative treatments for inborn errors of immunity (IEI), children born with IEI require long-term follow-up for disease manifestations and related complications that occur over the lifespan. ...OBJECTIVE: To understand the prevalence and p …
BACKGROUND: Due to the absence of curative treatments for inborn errors of immunity (IEI), children born with IEI require long-term follow-u …
Management of Small Vessel Vasculitides.
Lopalco G, Rigante D, Venerito V, Emmi G, Anelli MG, Lapadula G, Iannone F, Cantarini L. Lopalco G, et al. Curr Rheumatol Rep. 2016 Jun;18(6):36. doi: 10.1007/s11926-016-0580-1. Curr Rheumatol Rep. 2016. PMID: 27118389 Review.
Small vessel vasculitides (SVV) are a peculiar group of systemic disorders electively involving small intraparenchymal arteries, arterioles, capillaries, or venules and leading to different levels of vascular obstruction, tissue ischemia and risk of infarction; they …
Small vessel vasculitides (SVV) are a peculiar group of systemic disorders electively involving small intraparenchymal arterie …
Optimal management of ANCA-associated vasculitis before and during pregnancy: current perspectives.
Pecher AC, Henes M, Henes JC. Pecher AC, et al. Arch Gynecol Obstet. 2023 Aug;308(2):379-385. doi: 10.1007/s00404-022-06744-5. Epub 2022 Sep 14. Arch Gynecol Obstet. 2023. PMID: 36104505 Free PMC article. Review.
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are a group of systemic vasculitis characterized by autoantibodies against neutrophil cytoplasmic antigens (proteinase 3 PR3-ANCA and myeloperoxidase MPO-ANCA) and inflammation of small …
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are a group of systemic vasculitis characteriz …
Oral manifestations of systemic autoimmune and inflammatory diseases: diagnosis and clinical management.
Mays JW, Sarmadi M, Moutsopoulos NM. Mays JW, et al. J Evid Based Dent Pract. 2012 Sep;12(3 Suppl):265-82. doi: 10.1016/S1532-3382(12)70051-9. J Evid Based Dent Pract. 2012. PMID: 23040353 Review.
After systemic diagnosis, oral lesions benefit from specialized care by dentists in collaboration with the medical team. ...In this brief review, we aim to discuss the presentation/prevalence, diagnosis, and treatment of oral manifestations encountered in autoimmune …
After systemic diagnosis, oral lesions benefit from specialized care by dentists in collaboration with the medical team. ...In …
Treatment Strategies in Neutrophilic Dermatoses: A Comprehensive Review.
Starita-Fajardo G, Lucena-López D, Ballester-Martínez MA, Fernández-Guarino M, González-García A. Starita-Fajardo G, et al. Int J Mol Sci. 2023 Oct 26;24(21):15622. doi: 10.3390/ijms242115622. Int J Mol Sci. 2023. PMID: 37958609 Free PMC article. Review.
Neutrophilic dermatoses (NDs) are a group of noninfectious disorders characterized by the presence of a sterile neutrophilic infiltrate without vasculitis histopathology. Their physiopathology is not fully understood. The association between neutrophilic dermatoses and …
Neutrophilic dermatoses (NDs) are a group of noninfectious disorders characterized by the presence of a sterile neutrophilic infiltrate with …
Update on the Medical Management of Gastrointestinal Behcet's Disease.
Lopalco G, Rigante D, Venerito V, Fabiani C, Franceschini R, Barone M, Lapadula G, Galeazzi M, Frediani B, Iannone F, Cantarini L. Lopalco G, et al. Mediators Inflamm. 2017;2017:1460491. doi: 10.1155/2017/1460491. Epub 2017 Jan 22. Mediators Inflamm. 2017. PMID: 28210071 Free PMC article. Review.
Behcet's disease (BD) is a multisystemic disorder of unknown etiology mainly defined by recurrent oral aphthosis, genital ulcers, and chronic relapsing bilateral uveitis, all of which represent the "stigmata" of disease. However, many other organs including the vasc …
Behcet's disease (BD) is a multisystemic disorder of unknown etiology mainly defined by recurrent oral aphthosis, genital ulcers, and …
Current State of Precision Medicine in Primary Systemic Vasculitides.
Demirkaya E, Arici ZS, Romano M, Berard RA, Aksentijevich I. Demirkaya E, et al. Front Immunol. 2019 Dec 17;10:2813. doi: 10.3389/fimmu.2019.02813. eCollection 2019. Front Immunol. 2019. PMID: 31921111 Free PMC article. Review.
Here, we review the advances in practicing PM in patients with primary systemic vasculitides (PSVs). We summarize recent genetic studies and discuss current knowledge on the contribution of epigenetic factors and extracellular vesicles (EVs) in disease progre …
Here, we review the advances in practicing PM in patients with primary systemic vasculitides (PSVs). We summarize recent genet …
Unveiling the Efficacy, Safety, and Tolerability of Anti-Interleukin-1 Treatment in Monogenic and Multifactorial Autoinflammatory Diseases.
Bettiol A, Lopalco G, Emmi G, Cantarini L, Urban ML, Vitale A, Denora N, Lopalco A, Cutrignelli A, Lopedota A, Venerito V, Fornaro M, Vannacci A, Rigante D, Cimaz R, Iannone F. Bettiol A, et al. Int J Mol Sci. 2019 Apr 17;20(8):1898. doi: 10.3390/ijms20081898. Int J Mol Sci. 2019. PMID: 30999610 Free PMC article. Review.
Autoinflammatory diseases (AIDs) are heterogeneous disorders characterized by dysregulation in the inflammasome, a large intracellular multiprotein platform, leading to overproduction of interleukin-1(IL-1)beta that plays a predominant pathogenic role in such dis …
Autoinflammatory diseases (AIDs) are heterogeneous disorders characterized by dysregulation in the inflammasome, a large intra …
28 results