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Publikováno v:
Romanian Journal of Neurology, Vol 17, Iss 4, Pp 200-203 (2018)
Fabry disease is a rare genetic disease involving a deficiency of an enzyme. A decrease in the enzyme activity leads to a selective suffering of specific anatomic and functional structures resulting in heteromorphic clinical signs that increase the d
Externí odkaz:
https://doaj.org/article/fa1763a888124ae495407378bfa1e136
Autor:
Madalina Valeanu, Vitalie Văcăraș, Angela Cozma, Lucia Maria Procopciuc, Nicoleta Decea, Ioana Simina Barac, Dafin Fior Mureșanu
Publikováno v:
In Vivo
Background Multiple sclerosis (MS) is one of the most debilitating neurological diseases of young adults. The presence of a single nucleotide polymorphism in the promoter regions of the interleukin 27 gene (IL27 T4730C, rs181206) may alter the transc
Publikováno v:
Česká a slovenská neurologie a neurochirurgie. :368-374