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2005 1
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17 results

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Page 1
Relapsing polychondritis: Best Practice & Clinical Rheumatology.
Mertz P, Sparks J, Kobrin D, Ogbonnaya SA, Sevim E, Michet C, Arnaud L, Ferrada M. Mertz P, et al. Best Pract Res Clin Rheumatol. 2023 Mar;37(1):101867. doi: 10.1016/j.berh.2023.101867. Epub 2023 Oct 14. Best Pract Res Clin Rheumatol. 2023. PMID: 37839908 Review.
Lately, based on the organs involved, the disease's diverse manifestations have been categorized into specific clinical groups, based on the most likely organ involvement including auricular, nasal, pulmonary, and musculoskeletal. More recently the discovery of a ne …
Lately, based on the organs involved, the disease's diverse manifestations have been categorized into specific clinical groups, based …
VEXAS syndrome: Clinical manifestations, diagnosis, and treatment.
Loeza-Uribe MP, Hinojosa-Azaola A, Sánchez-Hernández BE, Crispín JC, Apodaca-Chávez E, Ferrada MA, Martín-Nares E. Loeza-Uribe MP, et al. Reumatol Clin (Engl Ed). 2024 Jan;20(1):47-56. doi: 10.1016/j.reumae.2023.12.004. Epub 2023 Dec 29. Reumatol Clin (Engl Ed). 2024. PMID: 38160120 Free article. Review.
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome is an adult-onset autoinflammatory syndrome characterized by somatic mutations in the UBA1 gene and is considered the prototype of hematoinflammatory diseases. Patients with VEXA …
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome is an adult-onset autoinflammatory syndrom …
Immunopathogenesis of Behcet's disease and treatment modalities.
van der Houwen TB, van Hagen PM, van Laar JAM. van der Houwen TB, et al. Semin Arthritis Rheum. 2022 Feb;52:151956. doi: 10.1016/j.semarthrit.2022.151956. Epub 2022 Jan 10. Semin Arthritis Rheum. 2022. PMID: 35038644 Free article. Review.
Increased production or responsiveness of pro-inflammatory components of the innate immune response (TLR, neutrophils, NK-cells or gammadelta T-cells) to these triggers may be a crucial step in the pathogenesis of BD. Additionally to an increased autoinflammatory response …
Increased production or responsiveness of pro-inflammatory components of the innate immune response (TLR, neutrophils, NK-cells or gammadelt …
Drug management of neutrophilic dermatoses.
Garcovich S, De Simone C, Berti E, Marzano AV. Garcovich S, et al. Expert Rev Clin Pharmacol. 2017 Oct;10(10):1119-1128. doi: 10.1080/17512433.2017.1356719. Epub 2017 Jul 27. Expert Rev Clin Pharmacol. 2017. PMID: 28715916 Review.
Neutrophilic dermatoses are a heterogenous group of chronic, cutaneous inflammatory conditions characterized by the accumulation of neutrophils in the skin and by systemic inflammation. Neutrophilic dermatoses can be idiopathic or associated with other inflammatory or syst …
Neutrophilic dermatoses are a heterogenous group of chronic, cutaneous inflammatory conditions characterized by the accumulation of neutroph …
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 autoinflammatory …
Behet disease is a multisystem inflammatory disease and variable vessel vasculitis involving primarily the oral and genital mucosa, …
Cryopyrin-associated periodic syndromes: diagnosis and management.
Miyamae T. Miyamae T. Paediatr Drugs. 2012 Apr 1;14(2):109-17. doi: 10.2165/11595040-000000000-00000. Paediatr Drugs. 2012. PMID: 22335455 Review.
Cryopyrin-associated periodic syndromes (CAPS) are a group of rare autoinflammatory disorders; many cases of CAPS are caused by mutations in the NLRP3 gene. ...CAPS include three variants, ranging in order of increasing severity from familial cold autoinflammator …
Cryopyrin-associated periodic syndromes (CAPS) are a group of rare autoinflammatory disorders; many cases of CAPS are caused b …
Diagnosis and management of autoinflammatory diseases in childhood.
Gattorno M, Federici S, Pelagatti MA, Caorsi R, Brisca G, Malattia C, Martini A. Gattorno M, et al. J Clin Immunol. 2008 May;28 Suppl 1:S73-83. doi: 10.1007/s10875-008-9178-3. Epub 2008 Mar 27. J Clin Immunol. 2008. PMID: 18368292 Review.
Cryopyrinopathies are a group of conditions associated to mutations of the gene Cryopyrin that are responsible for a spectrum of diseases (familial cold autoinflammatory syndrome, Muckle-Wells syndrome, and chronic infantile neurological cutaneous and articul …
Cryopyrinopathies are a group of conditions associated to mutations of the gene Cryopyrin that are responsible for a spectrum of diseases (f …
Pyoderma gangrenosum: a review of pathogenesis and treatment.
Ahn C, Negus D, Huang W. Ahn C, et al. Expert Rev Clin Immunol. 2018 Mar;14(3):225-233. doi: 10.1080/1744666X.2018.1438269. Epub 2018 Feb 13. Expert Rev Clin Immunol. 2018. PMID: 29406827 Review.
However, recent advances have been made in understanding the pathogenesis of this condition, and PG is now considered an autoinflammatory disease process. Areas covered: This review discusses the newest studies that further define our understanding of this disease and the …
However, recent advances have been made in understanding the pathogenesis of this condition, and PG is now considered an autoinflammatory …
Autoinflammatory skin disorders in inflammatory bowel diseases, pyoderma gangrenosum and Sweet's syndrome: a comprehensive review and disease classification criteria.
Marzano AV, Ishak RS, Saibeni S, Crosti C, Meroni PL, Cugno M. Marzano AV, et al. Clin Rev Allergy Immunol. 2013 Oct;45(2):202-10. doi: 10.1007/s12016-012-8351-x. Clin Rev Allergy Immunol. 2013. PMID: 23334898 Review.
Pyoderma gangrenosum (PG) and Sweet's syndrome (SS) are skin diseases usually presenting with recurrent ulcers and erythematous plaques, respectively. ...Treatment of PG involves a combination of wound care, topical medications, antibiotics for seconda …
Pyoderma gangrenosum (PG) and Sweet's syndrome (SS) are skin diseases usually presenting with recurrent ulcers and erythematou …
The most recent advances in pathophysiology and management of tumour necrosis factor receptor-associated periodic syndrome (TRAPS): personal experience and literature review.
Magnotti F, Vitale A, Rigante D, Lucherini OM, Cimaz R, Muscari I, Granados Afonso de Faria A, Frediani B, Galeazzi M, Cantarini L. Magnotti F, et al. Clin Exp Rheumatol. 2013 May-Jun;31(3 Suppl 77):141-9. Epub 2013 Jul 24. Clin Exp Rheumatol. 2013. PMID: 23899820 Review.
Tumour necrosis factor-receptor associated periodic syndrome (TRAPS) is a rare autosomal dominant autoinflammatory disorder characterised by recurrent episodes of long-lasting fever and inflammation in different regions of the body, as musculo-skeletal system, sk …
Tumour necrosis factor-receptor associated periodic syndrome (TRAPS) is a rare autosomal dominant autoinflammatory disorder ch …
17 results