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Autor:
Milan Profant, M Huckova, A Jovankovicova, Irina Sebova, Daniela Gasperikova, L Demesova, Lukas Varga
Publikováno v:
Bratislava Medical Journal. 120:699-702
Objectives The aim of our study is to demonstrate a causal link between two distinct diagnoses, the hereditary hearing loss, and the sudden sensorineural hearing loss. Background Sudden sensorineural hearing loss is an emergency condition in otolaryn
Autor:
Lubica Ticha, D. Virgova, Martina Surova, M Huckova, Lucia Valentinova, D. Lobotkova, Stanikova D, M. Petrasova, Juraj Stanik, Martina Skopkova, Iwar Klimes, Marian Mokan, Daniela Gasperikova
Publikováno v:
Scopus-Elsevier
The most common etiology of non-syndromic monogenic obesity are mutations in gene for the Melanocortin-4 receptor (MC485) with variable prevalence in different countries (1.2-6.3 % of obese children). The aim of our study was 1) to search for MC4R mu
Autor:
Pavel Langer, Iwar Klimes, Daniela Gasperikova, M Huckova, B Drobna, Richard Imrich, Tomas Trnovec, A Kocan, Zofia Radikova, Jozef Ukropec
Publikováno v:
Endocrine Regulations. 48:17-24
This study was aimed to evaluate possible obesogenic and diabetogenic impact of highly increased serum level of persistent organochlorinated pollutants POPs, such as polychlorinated biphenyls (PCBs), dichlorodiethyl-dichloroethylene (p,p'-DDE), and h
Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications
Autor:
Iwar Klimes, Zuzana Kabátová, Milan Profant, Ivica Masindova, Daniela Gasperikova, M Huckova, Lukas Varga
Publikováno v:
European Archives of Oto-Rhino-Laryngology. 271:1401-1407
Hereditary etiology plays an important role in bilateral profound deafness as a main indication for cochlear implantation. Mutations in DFNB1 locus account for most of the inherited deafness cases in Caucasians. To provide actual data on mutation pre
Autor:
Daniela Gasperikova, Dominika Gabcova, Iwar Klimes, M Huckova, Branislav Vohnout, Katarina Raslova
Publikováno v:
Wiener klinische Wochenschrift. 128(23-24)
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder characterized by strikingly elevated low-density lipoprotein (LDL) cholesterol levels and premature atherosclerosis. For individuals with a definite or probable diagnosis of
Autor:
K Susienkova, Zofia Radikova, M Huckova, Richard Imrich, A Kocan, Jozef Ukropec, B Drobna, Pavel Langer
Publikováno v:
Endocrine Regulations. 45:149-155
OBJECTIVE It is aimed to obtain some general information about the prevalence of certain biomarkers in highly exposed population and on the interrelations between their serum level as related to that of some major organochlorines (OCs). METHODS The l
Autor:
Tomas Trnovec, Iwar Klimes, M Huckova, Daniela Gasperikova, Elena Šeböková, Jozef Ukropec, Zofia Radikova, Beata Drobná, K Susienkova, V. Labudova, Juraj Koska, Pavel Langer, Anton Kočan
Publikováno v:
Diabetologia. 53:899-906
A heavily polluted area of Eastern Slovakia was targeted by the PCBRISK cross-sectional survey to search for possible links between environmental pollution and both prediabetes and diabetes.Associations of serum levels of five persistent organic poll
Autor:
M Huckova, Richard Imrich, Iwar Klimes, K Susienkova, Zofia Radikova, Lucia Kšinantová, Pavel Langer, B Drobna, A Kocan
Publikováno v:
Endocrine Regulations. 44:109-114
OBJECTIVE It was aimed to evaluate some fundamental correlations of 15 individual PCB congeners and their sum with serum testosterone level in highly and long-term exposed males with special respect to minimize the interfering effect of age. METHODS
Autor:
Nadežda Mišovicová, Julian C. Knight, M Huckova, Kevin Colclough, Iwar Klimes, Nicolas D. Tribble, L Barak, Jozef Michalek, Kate Wicks, B A Barrow, Sian Ellard, Daniela Gasperikova, Lucia Valentinova, Radoslav Dobránsky, Martijn van de Bunt, Eva Bereczková, Juraj Stanik, Anna L. Gloyn
Publikováno v:
Diabetes
OBJECTIVEInactivating mutations in glucokinase (GCK) cause mild fasting hyperglycemia. Identification of a GCK mutation has implications for treatment and prognosis; therefore, it is important to identify these individuals. A significant number of pa