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Wesam A Mokhtar

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Genes & Diseases|June 14, 2019
Maternal vitamin D level and vitamin D receptor gene polymorphism as a risk factor for congenital heart diseases in offspring; An Egyptian case-control studyWesam A Mokhtar, Amal Fawzy, Reem M Allam, et al.
Pediatric Nephrology (Berlin, Germany)|October 8, 2025
Unexpected Gaucher disease in a case of steroid-resistant nephrotic syndromeMona Hamed Gehad, Doaa Mohammed Youssef, Wesam A Mokhtar, et al.
Expert Review of Hematology|December 16, 2022
Genetic variant of endothelial protein C receptor genes and its serum level in B thalassemic childrenM Hesham, Adel S Ali, Shimaa Mahmoud Abogabela, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 10, 2017
Does implementing a regime of dexamethasone before planned cesarean section at term reduce admission with respiratory morbidity to neonatal intensive care unit? A randomized controlled trialAhmed Mohamed Nooh, Hussein Mohammed Abdeldayem, Eisa Arafa, et al.
International Journal of Pediatrics|December 9, 2020
Propionic and Methylmalonic Acidemias: Initial Clinical and Biochemical PresentationAmira Mobarak, Heba Dawoud, Wesam A Mokhtar, et al.
Paediatrics and International Child Health|April 2, 2019
Conventional intensive <i>versus</i> LED intensive phototherapy oxidative stress burden in neonatal hyperbilirubinaemia of haemolytic originWesam A Mokhtar, Laila M Sherief, Hany Elsayed, et al.
BMC Pediatrics|March 11, 2017
Premature atherosclerosis in children with beta-thalassemia major: New diagnostic markerLaila M Sherief, Osama Dawood, Adel Ali, et al.
Italian Journal of Pediatrics|September 15, 2020
Factor VIII inhibitor development in Egyptian hemophilia patients: does intron 22 inversion mutation play a role?Laila M Sherief, Osama A Gaber, Hala Mosaad Youssef, et al.
Medicine|August 16, 2021
Vitamin D status and healthy Egyptian adolescents: Where do we stand?Laila M Sherief, Adel Ali, Ahmed Gaballa, et al.
Molecular Genetics & Genomic Medicine|May 27, 2021
Genetic polymorphism of vitamin D receptors and plasminogen activator inhibitor-1 and osteonecrosis risk in childhood acute lymphoblastic leukemiaLaila M Sherief, Mohamed Beshir, Nermin Raafat, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Genes & Diseases|June 14, 2019
Maternal vitamin D level and vitamin D receptor gene polymorphism as a risk factor for congenital heart diseases in offspring; An Egyptian case-control studyWesam A Mokhtar, Amal Fawzy, Reem M Allam, et al.
Pediatric Nephrology (Berlin, Germany)|October 8, 2025
Unexpected Gaucher disease in a case of steroid-resistant nephrotic syndromeMona Hamed Gehad, Doaa Mohammed Youssef, Wesam A Mokhtar, et al.
Expert Review of Hematology|December 16, 2022
Genetic variant of endothelial protein C receptor genes and its serum level in B thalassemic childrenM Hesham, Adel S Ali, Shimaa Mahmoud Abogabela, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 10, 2017
Does implementing a regime of dexamethasone before planned cesarean section at term reduce admission with respiratory morbidity to neonatal intensive care unit? A randomized controlled trialAhmed Mohamed Nooh, Hussein Mohammed Abdeldayem, Eisa Arafa, et al.
International Journal of Pediatrics|December 9, 2020
Propionic and Methylmalonic Acidemias: Initial Clinical and Biochemical PresentationAmira Mobarak, Heba Dawoud, Wesam A Mokhtar, et al.
Paediatrics and International Child Health|April 2, 2019
Conventional intensive <i>versus</i> LED intensive phototherapy oxidative stress burden in neonatal hyperbilirubinaemia of haemolytic originWesam A Mokhtar, Laila M Sherief, Hany Elsayed, et al.
BMC Pediatrics|March 11, 2017
Premature atherosclerosis in children with beta-thalassemia major: New diagnostic markerLaila M Sherief, Osama Dawood, Adel Ali, et al.
Italian Journal of Pediatrics|September 15, 2020
Factor VIII inhibitor development in Egyptian hemophilia patients: does intron 22 inversion mutation play a role?Laila M Sherief, Osama A Gaber, Hala Mosaad Youssef, et al.
Medicine|August 16, 2021
Vitamin D status and healthy Egyptian adolescents: Where do we stand?Laila M Sherief, Adel Ali, Ahmed Gaballa, et al.
Molecular Genetics & Genomic Medicine|May 27, 2021
Genetic polymorphism of vitamin D receptors and plasminogen activator inhibitor-1 and osteonecrosis risk in childhood acute lymphoblastic leukemiaLaila M Sherief, Mohamed Beshir, Nermin Raafat, et al.
Pageof 2