Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fouad, Alghamdi"'
Autor:
Khloud Mubark Alotaibi, Mohannad Alsuhaibani, Khalid S. Al-Essa, Ahmed Khamis Bamaga, Amnah S. Mukhtar, Ali Mohammed Alrumaih, Huda F. Al-Hasinah, Shaikhah Aldossary, Fouad Alghamdi, Mohamad-Hani Temsah, Norah Abanmy, Monira Alwhaibi, Yousif Asiri, Yazed AlRuthia
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundSpinal muscular atrophy (SMA) is a rare debilitating condition with a significant burden for patients and society. However, little is known about how it affects Saudi Arabia's population. The socioeconomic and medical characteristics of aff
Externí odkaz:
https://doaj.org/article/93269d5213e04f6f935a604668566766
Autor:
Fouad Alghamdi, Asmaa Al-Tawari, Hadil Alrohaif, Walaa Alshuaibi, Hicham Mansour, Annemieke Aartsma-Rus, André Mégarbané
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The timely and accurate genetic diagnosis of Duchenne muscular dystrophy (DMD) enables prompt initiation of disease management and genetic counseling and optimal patient care. Despite the existence of best practice guidelines for the diagnosis of DMD
Externí odkaz:
https://doaj.org/article/2fa4eebc95d54d11a3a354a2155878dd
Autor:
Ahmed K. Bamaga, Fouad Alghamdi, Nahla Alshaikh, Waleed Altwaijri, Fahad A. Bashiri, Khalid Hundallah, Musaad Abukhaled, Osama Y. Muthaffar, Sameer Al-Mehmadi, Tahani Ahmed Jamaly, Mohammad A. Al-Muhaizea, Abdulaziz Al-Saman
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: The coronavirus disease 2019 (COVID-19) pandemic has caused overwhelming challenges in healthcare worldwide. During such an outbreak, some needs of high-risk groups who require regular follow-ups and long-term management are not met. The
Externí odkaz:
https://doaj.org/article/7afbdcab69a64029b4233f05a7e46459
Autor:
Alaa Alghamdi, Shaikhah AlDossary, Ahmed N. Othman, Wala Alabdulqader, Fawzia Amer, Mona Ali, Momen Almomen, Fouad Alghamdi
IntroductionSpinal Muscular atrophy (SMA) is an inherited, neuromuscular disease which is characterized by the deterioration of spinal motor neurons, causing progressive muscular atrophy and weakening. It is an autosomal recessive disease with the ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f52829a87a5becd778afe44b0eb4ad9
https://doi.org/10.21203/rs.3.rs-1760703/v1
https://doi.org/10.21203/rs.3.rs-1760703/v1
Autor:
Fouad, Alghamdi, Nahla, Alshaikh, Ahmed K, Bamaga, Fahad A, Bashiri, Khalid, Hundallah, Ali, Alshehri, Mohammad, Al-Muhaizea, Abdulaziz, Al-Saman
Publikováno v:
Neurosciences