Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tobias Jürgen, Schmidt"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Systemic mastocytosis is a rare genetic disease characterized by aberrant proliferation and/or activation of mast cells, resulting in multi-organ, allergy-like symptoms. Mast cell activation syndrome (MCAS) is a clinically similar
Externí odkaz:
https://doaj.org/article/787af2243202486c9b0d9f2af0791d7f
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/5cabe34a3d1d48a5ac972869b25aaa0b
Background: Systemic mastocytosis is a rare genetic disease characterized by aberrant proliferation and/or activation of mast cells, resulting in multi-organ, allergy-like symptoms. Mast cell activation syndrome (MCAS) is a clinically similar, but mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61bccb4a1e24ab050e3f4c993ad3eba0
https://doi.org/10.21203/rs.3.rs-809554/v1
https://doi.org/10.21203/rs.3.rs-809554/v1
Publikováno v:
Orphanet journal of rare diseases. 17(1)
Systemic mastocytosis is a rare genetic disease characterized by aberrant proliferation and/or activation of mast cells, resulting in multi-organ, allergy-like symptoms. Mast cell activation syndrome (MCAS) is a clinically similar, but more prevalent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5833bf4dbc818f855d3e68aeb309d581
https://pubmed.ncbi.nlm.nih.gov/35906626
https://pubmed.ncbi.nlm.nih.gov/35906626