Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Margarida Lucas, Rocha"'
Publikováno v:
BMJ case reports. 15(11)
Werner syndrome (WS), also known as adult progeria, is a rare autosomal recessive inherited progeroid syndrome characterised by multiple features consistent with accelerated ageing. This disease is associated with several rheumatic conditions such as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::672e7934eb4b122b423de6896cfa30f7
https://pubmed.ncbi.nlm.nih.gov/36396328
https://pubmed.ncbi.nlm.nih.gov/36396328
Publikováno v:
ARP rheumatology. 1(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::50672627409f643f0e24355832f8117c
https://pubmed.ncbi.nlm.nih.gov/36242592
https://pubmed.ncbi.nlm.nih.gov/36242592
Autor:
Margarida, Lucas Rocha, Laura, Gago, Alexandre, Sepriano, Tiago, Saldanha, Ana Filipa, Mourão, Manuela, Costa, Sandra, André, Jaime, C Branco
Publikováno v:
ARP rheumatology. 1
Clinically amyopathic dermatomyositis (CADM) is a rare condition characterized by dermatomyositis skin lesions without clinically apparent muscle involvement. Respiratory involvement is common, occurring in about half of the cases. Spontaneous pneumo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94764b9a670278080b2ade528e3a3292
https://pubmed.ncbi.nlm.nih.gov/36057086
https://pubmed.ncbi.nlm.nih.gov/36057086