Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Khalifa, Ola A."'
Autor:
Al-Hassnan, Zuhair N., Khalifa, Ola A., Bubshait, Dalal K., Tulbah, Sahar, Alkorashy, Maarab, Alzaidan, Hamad, Alowain, Mohammed, Rahbeeni, Zuhair, Al-Sayed, Moeen
Publikováno v:
In Molecular Genetics and Metabolism Reports June 2018 15:50-54
Autor:
Shamseldin, Hanan E., Kurdi, Wesam, Almusafri, Fatima, Alnemer, Maha, Alkaff, Alya, Babay, Zeneb, Alhashem, Amal, Tulbah, Maha, Alsahan, Nada, Khan, Rubina, Sallout, Bahauddin, Al Mardawi, Elham, Seidahmed, Mohamed Zain, Meriki, Niema, Alsaber, Yasser, Qari, Alya, Khalifa, Ola, Eyaid, Wafaa, Rahbeeni, Zuhair, Kurdi, Ahmed, Hashem, Mais, Alshidi, Tarfa, Al-Obeid, Eman, Abdulwahab, Firdous, Ibrahim, Niema, Ewida, Nour, El-Akouri, Karen, Al Mulla, Mariam, Ben-Omran, Tawfeg, Pergande, Matthias, Cirak, Sebahattin, Al Tala, Saeed, Shaheen, Ranad, Faqeih, Eissa, Alkuraya, Fowzan S.
Publikováno v:
In Genetics in Medicine April 2018 20(4):420-427
Autor:
Khalifa, Ola, Al-Sahlawi, Zahra, Imtiaz, Faiqa, Ramzan, Khushnooda, Allam, Rabab, Al-Mostafa, Abeer, Abdel-Fattah, Maaly, Abuharb, Gheid, Nester, Michael, Verloes, Alain, Al-Zaidan, Hamad
Publikováno v:
In European Journal of Medical Genetics May 2015 58(5):293-299
Autor:
AlOwain, Mohammed1,2 (AUTHOR), Khalifa, Ola Ali3 (AUTHOR), Al Sahlawi, Zahra4 (AUTHOR), Hussein, Maged H5 (AUTHOR), Sulaiman, Raashda A1,2 (AUTHOR), Al-Sayed, Moeen1,2 (AUTHOR), Rahbeeni, Zuhair1,2 (AUTHOR), Al-Hassnan, Zuhair1,2 (AUTHOR), Al-Zaidan, Hamad1,2 (AUTHOR), Nezzar, Hachemi6,7 (AUTHOR), Al Homoud, Iftetah8 (AUTHOR), Eldali, Abdelmoneim9 (AUTHOR), Altonen, Brian10 (AUTHOR), Handoom, Bedour S11 (AUTHOR), Mbekeani, Joyce N12,13 (AUTHOR) jnanjinga888@gmail.com
Publikováno v:
Ophthalmic Genetics. Aug2019, Vol. 40 Issue 4, p313-322. 10p.
Publikováno v:
Journal of Medicine & Life; Feb2023, Vol. 16 Issue 2, p215-219, 5p
Publikováno v:
QJM: An International Journal of Medicine; 2024 Supplement, Vol. 117, pii136-ii136, 1p
Akademický článek
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Autor:
Zayed, Hatem, El Khayat, Hamed, Tomoum, Hoda, Khalifa, Ola, Siddiq, Ehab, Mohammad, Shaimaa A, Gamal, Radwa, Shi, Zumin, Mosailhy, Ahmed, Zaki, Osama K
Glutaric acidemia type 1 (GA1) is an inherited metabolic autosomal recessive disorder that is caused by a deficiency in glutaryl-CoA dehydrogenase (GCDH). Untreated patients suffer primarily from severe striatal damage. More than 250 variants in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1664::d10c9bd28399b9a82c8920b0ec2d8953
https://hdl.handle.net/10576/11606
https://hdl.handle.net/10576/11606
Autor:
Khalifa, Ola1, Imtiaz, Faiqa2, Al-Sakati, Nadia3, Al-Manea, Khalid4, Verloes, Alain5, Al-Owain, Mohammed1 alowain@kfshrc.edu.sa
Publikováno v:
European Journal of Pediatrics. Jan2011, Vol. 170 Issue 1, p121-126. 6p. 1 Color Photograph, 2 Black and White Photographs, 1 Chart, 1 Graph.
Autor:
Assar, Effat Hussein1, Rachwan, Maha M. Taher2, Khalifa, Ola Abd Elmonem1 olakhalifa4568@gmail.com, Ahmed, Marwa Elsayed1
Publikováno v:
Egyptian Journal of Hospital Medicine. Jan2023, Vol. 90 Issue 2, p2695-2700. 6p.