Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Eman Megdad"'
Autor:
Ruqaiah Altassan, Raashda A. Sulaiman, Abdullah Alfalah, Waad Alwagiat, Eman Megdad, Dana Alqasabi, Bedour Handoom, Munirah Almesned, Hassan Al-Amri, Zuhair Alhassnan, Moeen-aldeen Alsayed, Hamad Alzaidan, Zuhair Rahbeeni, Nada Derar, Mohammed Al-Owain, Esam Albanyan
Publikováno v:
European journal of medical genetics. 65(11)
Patients with certain inherited metabolic disorders (IMD) are at high risk for metabolic decompensation with exposure to infections. The COVID-19 pandemic has been particularly challenging for health care providers dealing with IMD patients, in view
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4912b4a6a3c47c8c4385a181bacea259
https://pubmed.ncbi.nlm.nih.gov/36049607
https://pubmed.ncbi.nlm.nih.gov/36049607
Autor:
Munirah Al Mesned, Bedour S Handoom, Eman Megdad, Zuhair N. Al-Hassnan, Samir Al-Nufiee, Dana Al-Qasabi, Moeenaldeen Al-Sayed, Abdelmoneim Eldali, Reem Hawary
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 5, Iss 2, Pp 60-68 (2018)
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics & Adolescent Medicine
Background: In Saudi Arabia, a diet for life policy has been adopted in the management of amino acid metabolism disorders for years. However, the specially designed low protein products/medical foods - which are one of the important treatment tools -
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2b08ee5eea8794f55c1f2ba55b578f8
http://www.sciencedirect.com/science/article/pii/S2352646718300322
http://www.sciencedirect.com/science/article/pii/S2352646718300322
Autor:
Mohammed Al-Owain, Amr Al-Saif, Mohei Eldin Abouzied, Dejene Abebe, Eman Megdad, Nadia Al-Hashmi, Taghreed Shuaib, Hesham Aldhalaan, Mohammad Ghaziuddin, Alaa Doubi
Publikováno v:
Journal of child neurology. 27(6)
Propionic acidemia, an autosomal recessive disorder, is a common form of organic aciduria resulting from the deficiency of propionyl-CoA carboxylase. It is characterized by frequent and potentially lethal episodes of metabolic acidosis often accompan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74b94bfd855a70fa36cfba891d1a8f27
https://pubmed.ncbi.nlm.nih.gov/22156789
https://pubmed.ncbi.nlm.nih.gov/22156789