Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mohammad Al Muhaizea"'
Autor:
Fadie D. Altuame, Gretchen Foskett, Paldeep S. Atwal, Sarah Endemann, Mark Midei, Peter Milner, Mustafa A. Salih, Muddathir Hamad, Mohammad Al-Muhaizea, Mais Hashem, Fowzan S. Alkuraya
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Infantile neuroaxonal dystrophy (INAD) is a rapidly progressive neurodegenerative disorder of early onset causing premature death. It results from biallelic pathogenic variants in PLA2G6, which encodes a calcium-independent phosph
Externí odkaz:
https://doaj.org/article/38b21d6aee494db4baefdb793f62873e
Autor:
Cristina Skrypnyk, Abubaker Al Madani, Mohammed Jan, André Mégarbané, Khalid Al Thihli, Ali Al Shehri, Abdulaziz Al Saman, Mohammad Al Muhaizea, Waseem Fathalla, Andoni Urtizberea, Gholamreza Zamani, Sylvie Tuffery-Giraud, Carlos Ignacio Ortez González, Pawan Kashyape, Ahmed Al Rumayyan, Edward Cupler, Laila Bastaki, Mohammed Al Jumah, Gururaj Aithala Kodavooru
Publikováno v:
Neurodegenerative Disease Management
Aim: Duchenne muscular dystrophy (DMD) is a severe and rare X-linked neuromuscular childhood disorder that results in functional decline, loss of ambulation and early death due to cardiac or respiratory failure. The objective of this paper is to addr
Autor:
Fouad, Alghamdi, Nahla, Alshaikh, Ahmed K, Bamaga, Fahad A, Bashiri, Khalid, Hundallah, Ali, Alshehri, Mohammad, Al-Muhaizea, Abdulaziz, Al-Saman
Publikováno v:
Neurosciences