Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hanaa Midhat Abdel Gader Hussein"'
Autor:
Ahmed S. Ibrahim, Hanaa Midhat Abdel Gader Hussein, Fatma S E Ebeid, Mohsen Saleh Elalfy, Ghada Samir Ibrahim, Hend Galal Eldeen Mohammed
Publikováno v:
European Journal of Pediatrics. 180:2677-2686
Children with sickle cell disease (SCD) are at a high risk for neurocognitive impairment. We aim to quantitatively measure cerebral tissue R2* to investigate the brain iron deposition in children and young adults with SCD in comparison to beta thalas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::045f5b799296557ff34f1244a9b5117d
https://doi.org/10.1007/s00431-021-04189-7
https://doi.org/10.1007/s00431-021-04189-7
Autor:
Hanaa Midhat Abdel Gader Hussein, Fatma S E Ebeid, Mohsen Saleh Elalfy, Mohammed Ahmed Samir Ibrahim
Publikováno v:
QJM: An International Journal of Medicine. 114
Background Sickle cell disease (SCD) is considered the most prevalent monogenic diseases worldwide. Iron overload is one of the major complications in those patients, especially who in need for frequent transfusion, affecting many organs including th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aee226eb74f5755c94b483fd90bd590d
https://doi.org/10.1093/qjmed/hcab113.026
https://doi.org/10.1093/qjmed/hcab113.026
Brain Iron Content in Egyptian Patients with Sickle Cell Disease: Impact on Neurocognitive Functions
Autor:
Ghada M Samir, Hanaa Midhat Abdel Gader Hussein, Hend A. Mohammed, Mohsen Saleh Elalfy, Fatma Soliman Elsayed Ebeid, Ahmed Smair
Publikováno v:
Blood. 136:37-37
Background:Children with sickle cell disease (SCD) are at a high risk for neurocognitive impairment which may be due to iron overload in brain tissue or hemoglobin polymerization and endothelial dysfunction.Primary objectivewas measuring brain iron c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93afd1231c078451374e2e6363661249
https://doi.org/10.1182/blood-2020-139168
https://doi.org/10.1182/blood-2020-139168