Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hamad Alsheikh"'
Autor:
Fahad A. Bashiri, Rawan AlSheikh, Muddathir H. Hamad, Hamad Alsheikh, Rana Abdullah Alsheikh, Amal Kentab, Najd AlTheeb, Malak Alghamdi
Publikováno v:
Children, Vol 10, Iss 8, p 1334 (2023)
Background: Despite the high consanguinity rates, data on genetic epilepsy in Saudi Arabia is limited. The objective of the current study was to characterize genetic mutations associated with epilepsy in pediatric patients and describe their phenotyp
Externí odkaz:
https://doaj.org/article/680062900ff24d18a657b938f924b3be
Autor:
Malak Ali Alghamdi, Hicham Benabdelkamel, Afshan Masood, Narjes Saheb Sharif-Askari, Mahmood Y. Hachim, Hamad Alsheikh, Muddathir H. Hamad, Mustafa A. Salih, Fahad A. Bashiri, Khalid Alhasan, Tarek Kashour, Pilar Guatibonza Moreno, Sabine Schröder, Vasiliki Karageorgou, Aida M. Bertoli-Avella, Hisham Alkhalidi, Dima Z. Jamjoom, Ibrahim A. Alorainy, Assim A. Alfadda, Rabih Halwani
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Galloway-Mowat syndrome is a rare autosomal recessive disease characterized by a unique combination of renal and neurological manifestations, including early-onset steroid-resistant nephrotic syndrome, microcephaly, psychomotor delay, and gyral abnor
Externí odkaz:
https://doaj.org/article/8db6644c11c4473ea480bba4e547fa50
Autor:
Fahad A. Bashiri, Rawan AlSheikh, Rana AlSheikh, Hamad AlSheikh, Muddathir H. Hamad, Amal Kentab, Najd AlTheeb, Malak AlGhamdi
Publikováno v:
SSRN Electronic Journal.