Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Renata Wojtala"'
Autor:
Tomasz Gołębiowski, Jakub Kuźniar, Tomasz Porażko, Renata Wojtala, Andrzej Konieczny, Magdalena Krajewska, Marian Klinger
Publikováno v:
International Journal of Environmental Research and Public Health. 19(4):1-8
The over-secretion of monoclonal immunoglobulin light chains by clonal B cells followed by the aggregation and extracellular deposition of fibrillar deposits are responsible forthe clinical course AL amyloidosis. It is well documented that silica sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76197c0c72eeb3e3c525ecf480f74b7b
https://www.mdpi.com/1660-4601/19/4/2297
https://www.mdpi.com/1660-4601/19/4/2297
Publikováno v:
Clinical Rheumatology. 23:193-198
The aims of this study were to determine the proportion of rheumatoid arthritis (RA) patients attending hospital in whom amyloid deposits were present in abdominal fat aspiration (AFA) samples, and to assess possible risk factors for amyloid developm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1a9994e3380ac366478d887a4845a43
https://doi.org/10.1007/s10067-003-0842-y
https://doi.org/10.1007/s10067-003-0842-y
Publikováno v:
Annales Academiae Medicae Stetinensis. 58(2)
The Churg-Strauss syndrome is a necrotic eosinophilic vasculitis affecting small and medium vessels. The etiology of this disease known to have an autoimmune background remains unclear. The Churg-Strauss syndrome is progressive and may involve multip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7bb1e2719f0da8f05b6770945b6031d0
https://pubmed.ncbi.nlm.nih.gov/23767179
https://pubmed.ncbi.nlm.nih.gov/23767179
Autor:
Monika, Kosacka, Renata, Wojtala, Paweł, Piesiak, Ewa, Passowicz-Muszyńska, Renata, Jankowska
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 25(150)
Amyloidosis is a generic term for a heterogeneous group of disorders associated with deposition of protein in an abnormal fibrillar form. We report a case of kappa L-chain primary lung amyloidosis. A 44-year-old woman without symptoms. Roentgenogram
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c59eb146a5c28f482dc35632f2138af1
https://pubmed.ncbi.nlm.nih.gov/19205385
https://pubmed.ncbi.nlm.nih.gov/19205385