Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mohammed Al Muqbil"'
Autor:
Abdulaziz S. AlSaman, Fouad Al Ghamdi, Ahmed K. Bamaga, Nahla AlShaikh, Mohammed Al Muqbil, Osama Muthaffar, Fahad A. Bashiri, Baleegh Ali, Arzu Mulayim, Elena Heider, Abdullah A. Alshahrani, Mohammed A. Al Muhaizea
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Duchenne muscular dystrophy (DMD) is a rare neuromuscular disorder that is characterized by progressive muscle weakness, resulting in disability and premature death. Onset of symptoms typically occurs at 2–3 years of age, and disease progression is
Externí odkaz:
https://doaj.org/article/48f3a8dd2e8649f4b391f6da29efacd2
Autor:
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Publikováno v:
European Journal of Pediatrics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::511e5c2a73f0b1ad982ac1d0a7282bd6
https://doi.org/10.1007/s00431-023-05012-1
https://doi.org/10.1007/s00431-023-05012-1
Autor:
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Publikováno v:
European Journal of Pediatrics.
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare inherited neurometabolic disorder that can lead to severe physical and developmental impairment. This report includes 16 patients from the Middle East and is the largest series of patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d26142e1ab3d79a92f343603be745f6
https://doi.org/10.1007/s00431-023-04886-5
https://doi.org/10.1007/s00431-023-04886-5