Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Loiy Obeidat"'
Autor:
Raida Khalil, Eman Albsoul, Nesrin Mwafi, Arwa Alsaraireh, Ibrahim Al Sbou, Dema Ali, Loiy Obeidat
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2021 (2021)
BioMed Research International, Vol 2021 (2021)
Background. Metabolic disorder alkaptonuria is an autosomal recessive disorder caused by mutations in the HGD gene, and a deficiency HGD enzyme activity results in an accumulation of homogentisic acid (HGA), ochronosis, and destruction of connective
Autor:
Wajdy Al-Awaida, Farah Al Madhoon, Yazun Jarrar, Hamzeh J Al-Ameer, Raida Khalil, Rand Qawadri, Loiy Obeidat, Amer Imraish, Omar Al bawareed
Publikováno v:
Endocrine, metabolicimmune disorders drug targets. 21(10)
Background: Fibromyalgia syndrome (FMS) is a chronic disease characterized by widespread body pain, weakness in certain parts of the body (critical points), low pain tolerance, sleep disturbances, and fatigue. This syndrome is considered rare in Jord