Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Essa Sabi"'
Autor:
Jacqueline Stockley, Shaista P Nisar, Vincenzo C Leo, Essa Sabi, Margaret R Cunningham, Jeroen C Eikenboom, Stefan Lethagen, Reinhard Schneppenheim, Anne C Goodeve, Steve P Watson, Stuart J Mundell, Martina E Daly, GAPP Study in Collaboration with the MCMDM-1VWD Study Group
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0143913 (2015)
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other mild bleeding diatheses. We previously showed that mutations in the platelet P2Y12 ADP receptor gene (P2RY12) could contribute to the bleeding phenoty
Externí odkaz:
https://doaj.org/article/11d6dee9ef184a37a4aee9385245570a
Autor:
Michel Laguerre, Essa Sabi, Martina Daly, Jacqueline Stockley, Paquita Nurden, Xavier Pillois, Alan T Nurden
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e78683 (2013)
Mutations in ITGA2B and ITGB3 cause Glanzmann thrombasthenia, an inherited bleeding disorder in which platelets fail to aggregate when stimulated. Whereas an absence of expression or qualitative defects of αIIbβ3 mainly affect platelets and megakar
Externí odkaz:
https://doaj.org/article/c8887d68a1e741e1bb1070cdc0e2e72c
Autor:
Ahmed Mujamammi, Essa Sabi, Abdulaziz Dakhil, Ali Alammari, Saleh Almoaiqel, Zeyad Alkhenizan, Abdulaziz Almuhanna
Publikováno v:
International Journal of Medicine in Developing Countries. :557-562
Objectives: To estimate the level of knowledge and practice in type-2 diabetic patients, regarding the effect of lifestyle habits. Also, to estimate the knowledge of diabetic smokers toward smoking cessation benefits and its relation in decreasing di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82b87095687cc0ade720326715bfc6cd
https://doi.org/10.24911/ijmdc.51-1672144103
https://doi.org/10.24911/ijmdc.51-1672144103
Autor:
Ahmed Mujamammi, Essa Sabi, Abdulaziz Aldrgam, Faisal Alsaif, Abduljabbar Alyamani, Fahad Alfaiz, Mohammed BinMayouf, Abduelah Aldossari
Publikováno v:
International Journal of Medicine in Developing Countries. :784-790
Background: Genetic testing has become an invaluable tool for the fight against cancer. Yet the general population of Saudi Arabia shows a lack of awareness and utilization of this tool. This study aimed at assessing the knowledge, attitudes, and pra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd503059d330c484f186e6176b30c390
https://doi.org/10.24911/ijmdc.51-1673005474
https://doi.org/10.24911/ijmdc.51-1673005474
Autor:
Xavier Pillois, Paquita Nurden, Martina E. Daly, Essa Sabi, Alan T. Nurden, Michel Laguerre, Jacqueline Stockley
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e78683 (2013)
PLoS ONE
PLoS ONE
Mutations in ITGA2B and ITGB3 cause Glanzmann thrombasthenia, an inherited bleeding disorder in which platelets fail to aggregate when stimulated. Whereas an absence of expression or qualitative defects of αIIbβ3 mainly affect platelets and megakar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8249cf46006d5d519980d135cbf0c4f
https://doi.org/10.1371/journal.pone.0078683
https://doi.org/10.1371/journal.pone.0078683