Zobrazeno 1 - 5
of 5
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
Autor:
Shuaib, Taghreed, Al-Hashmi, Nadia, Ghaziuddin, Mohammad, Megdad, Eman, Abebe, Dejene, Al-Saif, Amr, Doubi, Alaa, Aldhalaan, Hesham, Abouzied, Mohei Eldin, Al-Owain, Mohammed
Publikováno v:
Journal of Child Neurology; Jun2012, Vol. 27 Issue 6, p799-803, 5p
Autor:
Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, Verena Peters
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or bioch
