Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ferdos Alaa El Din"'
Autor:
Ferdos Alaa El Din, Sylvie Patri, Vincent Thoreau, Montserrat Rodriguez-Ballesteros, Eva Hamade, Sabine Bailly, Brigitte Gilbert-Dussardier, Raghida Abou Merhi, Alain Kitzis
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132111 (2015)
Hereditary Hemorrhagic Telangiectasia syndrome (HHT) or Rendu-Osler-Weber (ROW) syndrome is an autosomal dominant vascular disorder. Two most common forms of HHT, HHT1 and HHT2, have been linked to mutations in the endoglin (ENG) and activin receptor
Externí odkaz:
https://doaj.org/article/396ad9d2ea1f40a3bcdab7891357584f
Autor:
Wael Khalil, Ferdos Alaa El Din, Marwa Jaffal, Abd El Hadi Kanj, Ali Nabbouh, Mazen Kurban, Elias A Rahal, Ghassan M Matar
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7baef65c279ec2628512ae68f982955
https://doi.org/10.7759/cureus.38809
https://doi.org/10.7759/cureus.38809
Autor:
Raghida Abou Merhi, Vincent Thoreau, Brigitte Gilbert-Dussardier, Sabine Bailly, Ferdos Alaa el Din, Montserrat Rodríguez-Ballesteros, Sylvie Patri, Eva Hamade, Alain Kitzis
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 7, p e0132111 (2015)
PLoS ONE, Vol 10, Iss 7, p e0132111 (2015)
Hereditary Hemorrhagic Telangiectasia syndrome (HHT) or Rendu-Osler-Weber (ROW) syndrome is an autosomal dominant vascular disorder. Two most common forms of HHT, HHT1 and HHT2, have been linked to mutations in the endoglin (ENG) and activin receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89a8fba8a1eb552e677fb0e73a3322be
https://pubmed.ncbi.nlm.nih.gov/26176610
https://pubmed.ncbi.nlm.nih.gov/26176610