Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ahmed Kurdi"'
Autor:
Merna Atiyah, Ahmed Kurdi, Osama Al Tuwaijry, Atif Al Sahari, Maha Al Rakaf, Inas Babic, Fahad Al Habshan, Zohair Alhalees, Khalid Al Najashi
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-6 (2020)
Abstract Background Fetal aortic stenosis may progress to hypoplastic left heart syndrome (HLHS), which carries a poor prognosis. We report two infants with fetal aortic stenosis successfully treated with fetal aortic valvuloplasty (FAV) using balloo
Externí odkaz:
https://doaj.org/article/76903bbf7d6e4d2585747d77de5787ca
Publikováno v:
Journal of Pharmaceutical Negative Results. :1985-1989
The current study aimed to reveal the evaluation of the level of liver function in infected with the parasite Entamoeba histolytica, Blood samples were collected during the period from the beginning of August 2021 until the month of April 2022. The s
Publikováno v:
Journal of Pharmaceutical Negative Results. :1990-1994
The current study aimed to reveal the evaluation of the level of some immune chemokines and liver function in infected with the parasite Entamoeba Histolytica. , Blood samples were collected during the period from the beginning of August 2021 until t
Publikováno v:
Cureus.
Autor:
Alya Alkaff, Wafaa Eyaid, Nada Alsahan, Rubina Khan, Niema Meriki, Yasser Alsaber, Saeed Al Tala, Mohamed Zain Seidahmed, Fatima Almusafri, Firdous Abdulwahab, Fowzan S. Alkuraya, Tawfeg Ben-Omran, Mariam Al Mulla, Hanan E. Shamseldin, Zeneb A. Babay, Eissa Faqeih, Ahmed Kurdi, Elham Al Mardawi, Karen El-Akouri, Ola Khalifa, Ranad Shaheen, Wesam Kurdi, Nour Ewida, Sebahattin Cirak, Eman Alobeid, Alya Qari, Zuhair Rahbeeni, Matthias Pergande, Maha Alnemer, Maha Tulbah, Bahauddin Sallout, Tarfa Alshidi, Amal Alhashem, Niema Ibrahim, Mais Hashem
Publikováno v:
Genetics in Medicine. 20:420-427
PurposeThe application of genomic sequencing to investigate unexplained death during early human development, a form of lethality likely enriched for severe Mendelian disorders, has been limited.MethodsIn this study, we employed exome sequencing as a
Autor:
Ester Garne, Mohamed Shoukri, Amal M. Hashem, Amer N. Ammari, Maha S. Al Rakaf, Muhammad A. Majeed-Saidan, Ahmed Kurdi
Publikováno v:
Preventive Medicine Reports, Vol 2, Iss C, Pp 572-576 (2015)
Preventive Medicine Reports
Al Rakaf, M S, Kurdi, A M, Ammari, A N, Al Hashem, AM, Shrouki, MM, Garne, E & Majeed-Saidan, M A 2015, ' Patterns of folic acid use in pregnant Saudi women and prevalence of neural tube defects : Results from a nested case-control study ', Preventive Medicine Reports, vol. 2, pp. 572-576 . https://doi.org/10.1016/j.pmedr.2015.06.016
Preventive Medicine Reports
Al Rakaf, M S, Kurdi, A M, Ammari, A N, Al Hashem, AM, Shrouki, MM, Garne, E & Majeed-Saidan, M A 2015, ' Patterns of folic acid use in pregnant Saudi women and prevalence of neural tube defects : Results from a nested case-control study ', Preventive Medicine Reports, vol. 2, pp. 572-576 . https://doi.org/10.1016/j.pmedr.2015.06.016
Background Although the role of folic acid (FA) in preventing neural tube defects (NTDs) is well documented, its optimal intake in pregnant women is still low in many countries. Here, we prospectively studied the prevalence of NTDs in the newborns an
Autor:
Mais Hashem, Ola Khalifa, Niema Ibrahim, Zainab A. Babay, Dalal K. Bubshait, Zuhair Rahbeeni, Firdous Abdulwahab, Wesam Kurdi, Amal M. Hashem, Fowzan S. Alkuraya, Maha Nemer, Hanan E. Shamseldin, Elham Al Mardawi, Nada Alsahan, Ahmed Kurdi, Maha Tulbah
Publikováno v:
Genome Biology
Background Identifying genetic variants that lead to discernible phenotypes is the core of Mendelian genetics. An approach that considers embryonic lethality as a bona fide Mendelian phenotype has the potential to reveal novel genetic causes, which w