Search Results - "Masindová, I"

Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications by Varga, L., Mašindová, I., Hučková, M., Kabátová, Z., Gašperíková, D., Klimeš, I., Profant, M.

“…Hereditary etiology plays an important role in bilateral profound deafness as a main indication for cochlear implantation. Mutations in DFNB1 locus account for…”
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Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report by Stanik, J, Kusekova, M, Huckova, M, Valentinova, L, Masindova, I, Stanikova, D, Ferenczova, J, Gasperikova, D, Klimes, I

“…Glucokinase (GCK) diabetes is a mild form of the monogenic diabetes characterized by the fasting hyperglycemia without signs of metabolic syndrome and very low…”
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Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies by Masindova, I, Varga, L, Stanik, J, Valentinova, L, Profant, M, Klimes, I, Gasperikova, D

“…Hearing loss is one of the most widespread sensory disorders. The incidence of deafness in general population is 1:1000 newborns. About one half of the cases…”
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Genetics of monogenic forms of diabetes by Staník, J, Hucková, M, Staníková, D, Masindová, I, Valentínová, L, Gasperíková, D, Klimes, I

“…Monogenic diabetes mellitus is a type of diabetes, where genetics without any other factors is strong enough to cause the disease. According to the clinical…”
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