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Idiopathic inflammatory myopathies: one year in review 2023.
Conticini, Edoardo; Dourado, Eduardo; Bottazzi, Francesca; Cardelli, Chiara; Bruno, Lorenza; Schmidt, Jens; Carli, Linda; Cavagna, Lorenzo; Barsotti, Simone.
Affiliation
  • Conticini E; Department of Medicine, Surgery and Neurosciences, Rheumatology Unit, University of Siena, Italy.
  • Dourado E; Rheumatology Department, Unidade Local de Saúde da Região de Aveiro; Aveiro Rheumatology Research Center, Egas Moniz Health Alliance; and Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Centro Académico de Medicina de Lisboa, Portugal.
  • Bottazzi F; Department of Internal Medicine and Therapeutics, Università di Pavia, and Division of Rheumatology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Cardelli C; Rheumatology Unit, University of Pisa, and Department of Medical Biotechnologies, University of Siena, Italy.
  • Bruno L; Rheumatology Unit, Department of Medicine and Surgery, University of Perugia, Italy.
  • Schmidt J; Department of Neurology and Pain Treatment, Immanuel Klinik Rüdersdorf, University Hospital of the Brandenburg Medical School Theodor Fontane, Rüdersdorf bei Berlin, and Department of Neurology, Neuromuscular Centre, University Medical Centre Göttingen, Germany.
  • Carli L; Rheumatology Unit, University of Pisa, Italy.
  • Cavagna L; Department of Internal Medicine and Therapeutics, Università di Pavia, and Division of Rheumatology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Barsotti S; Rheumatology Outpatient Clinic and Internal Medicine, Livorno Hospital, Italy. simone.barsotti.pisa@gmail.com.
Clin Exp Rheumatol ; 42(2): 213-224, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38488099
ABSTRACT
Idiopathic inflammatory myopathies are a group of rare, autoimmune, diseases typically involving striate muscle and also variously affecting several other systems or organs, such as joints, skin, lungs, heart and gastrointestinal tract. IIM are mainly characterised by subacute onset and chronic course and are burdened by significant morbidity and mortality. Despite the rarity of these conditions, several efforts have been undertaken in the last years to better understand their pathogenesis, as well as to achieve a more precise classification and to define the optimal therapeutic approach. The aim of this review is to provide an up-to-date digest of the most relevant studies published on this topic over the last year.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autoimmune Diseases / Myositis Limits: Humans Language: En Journal: Clin Exp Rheumatol Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autoimmune Diseases / Myositis Limits: Humans Language: En Journal: Clin Exp Rheumatol Year: 2024 Document type: Article Affiliation country: Country of publication: