Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mohamed Saleh Amoudi"'
Autor:
Muhammad Faiyaz-Ul-Haque, Moeenaldeen D. Al-Sayed, Eissa Faqeih, Masood Jamil, Anjum Saeed, Mohamed Saleh Amoudi, Namik Kaya, Halah Abalkhail, Ahmed Al-Abdullatif, Mohamed Rashed, Mohammed Al-Owain, Iskra Peltekova, Syed HE Zaidi
Publikováno v:
Annals of Saudi Medicine, Vol 34, Iss 2, Pp 107-114 (2014)
BACKGROUND AND OBJECTIVES: L-2-hydroxyglutaric aciduria is a neurometabolic disorder with autosomal recessive mode of inheritance in which patients exhibit elevated L-2-hydroxyglutaric acid in body fluids, central nervous system manifestations, and i
Externí odkaz:
https://doaj.org/article/663eafe589bb4d6eaf54b45ec34f2837
Autor:
I Peltekova, Namik Kaya, Ahmed Al-Abdullatif, Mohammed Al-Owain, Eissa Faqeih, Anjum Saeed, Mohamed S. Rashed, Mohamed Saleh Amoudi, Syed H.E. Zaidi, Muhammad Faiyaz-Ul-Haque, Masood Jamil, Halah Abalkhail, Moeenaldeen Al-Sayed
Publikováno v:
Annals of Saudi Medicine, Vol 34, Iss 2, Pp 107-114 (2014)
BACKGROUND AND OBJECTIVES: L-2-hydroxyglutaric aciduria is a neurometabolic disorder with autosomal recessive mode of inheritance in which patients exhibit elevated L-2-hydroxyglutaric acid in body fluids, central nervous system manifestations, and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8031d0e8fcc44370b7d70fc5091ea3e6
https://doi.org/10.5144/0256-4947.2014.107
https://doi.org/10.5144/0256-4947.2014.107