Y
Yahia Aktham
Researcher at Genzyme
Publications - 10
Citations - 36
Yahia Aktham is an academic researcher from Genzyme. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 1, co-authored 4 publications receiving 11 citations. Previous affiliations of Yahia Aktham include University of New South Wales.
Papers
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Journal ArticleDOI
The find of COVID-19 vaccine: Challenges and opportunities
Marwan ElBagoury,Mahmoud M. Tolba,Hebatallah A. Nasser,Abdul Jabbar,Ahmed M. Elagouz,Yahia Aktham,Amy Hutchinson +6 more
TL;DR: Wang et al. as mentioned in this paper presented a comprehensive visualization about SARS-CoV-2 to tackle the current pandemic and concluded that vaccines formulation within exceptional no time in this pandemic is highly recommended.
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Promise of Real-World Evidence for Patient Centricity in Gulf Cooperation Council Countries: Call to Action
Mohamed Nasr Farghaly,Ibrahim Sulaiman Mas'oud Al Ghaithi,Wael Abdel Rahman Mahamid,Abdallah A. Adlan,Saleh M Alghamdi,Thamir M Al Shammari,Nasser Alqahtani,Suliman A Al Ghnam,Marie Sleiman Awad Ibrahim,Hajer Al Mudaiheem,Mohamed Zahir Chouikrat,Yahia Aktham,Marwan Essam El Bagoury,Arun Jayarame Gowda,Khalid Al Moaikel,Nancy Syed Awad Abdallah +15 more
TL;DR: In this paper , the authors present their views and recommended key action points for the generation of robust realworld data and leveraging real-world evidence in the countries of the Gulf Cooperation Council (GCC).
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Management of Mucopolysaccharidosis Type I in Saudi Arabia: Insights from Saudi Arabia
Sulaiman M. Al-Mayouf,Rawdah Al-Sunbul,Abdul Aziz Al-Twaim,Bassam Bin-Abbas,Marwan ElBagoury,Maha Faden,Omar M. Hussein,Mohammed Olfat,Taghreed Shuaib,Yahia Aktham +9 more
TL;DR: The first management of MPS type I advisory board meeting was held in Riyadh on May 2, 2019, to reflect the expert opinions regarding different aspects of different MPS types and develop this manuscript; eight consultants from different specialties (medical genetics, pediatric rheumatology, and pediatric endocrinology), representing six Saudi institutions, in addition to a global expert in genetics participated in the meeting as discussed by the authors.
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A review of the frequency of the D409H mutation in the acid β-gluc osidase gene among Gaucher disease patients from the Gulf region -
TL;DR: The increased rate of consanguinity among Arabs, ranging from 10% to 70%, contributes to a high rate of genetic diseases, including GD, but with its associated gene mutation, GD, D409H, remains an area for further exploration in the Gulf area.
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From a Neglected Pathogen to a Public Health Emergency: Connecting the Dots in Monkeypox Emergence
TL;DR: The recent unprecedented emergence of the monkeypox outbreak rang an alarm bell creating a burden on global health and recommendations for the containment of the virus are highlighted.