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Background: The hereditary hemorrhagic telangiectasia (HHT) or Osler-Weber-Rendu syndrome is an autosomal dominant genetic disorder affecting the small blood vessels due to mutations in specific genes that lead to angiogenesis errors. HHT represents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbf4149c1552ef4fe844f975970af0c2
https://europepmc.org/articles/PMC5788230/
https://europepmc.org/articles/PMC5788230/
Akademický článek
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Autor:
Galanou P; Anesthesia and Pain Treatment Unit, General Hospital of Rhodes, Greece, Rhodes, GRC., Tsoleridis T; Anesthesia and Pain Treatment Unit, General Hospital of Rhodes, Greece, Rhodes, GRC., Tsoleridis S; Anesthesia and Pain Treatment Unit, General Hospital of Rhodes, Greece, Rhodes, GRC.
Publikováno v:
Cureus [Cureus] 2021 Jul 26; Vol. 13 (7), pp. e16634. Date of Electronic Publication: 2021 Jul 26 (Print Publication: 2021).
Autor:
Tsoleridis T; Department of Anesthesiology and Pain Treatment, General Hospital of Rhodes, Rhodes, Greece., Galanou L; Department of Anesthesiology and Pain Treatment, General Hospital of Rhodes, Rhodes, Greece., Tsoleridis S; Department of Anesthesiology and Pain Treatment, General Hospital of Rhodes, Rhodes, Greece.
Publikováno v:
Hippokratia [Hippokratia] 2016 Oct-Dec; Vol. 20 (4), pp. 303-305.