Search Results - "Uhrová, Tereza"

Preoperative cognitive profile predictive of cognitive decline after subthalamic deep brain stimulation in Parkinson's disease by Mana, Josef, Bezdicek, Ondrej, Růžička, Filip, Lasica, Andrej, Šmídová, Anna, Klempířová, Olga, Nikolai, Tomáš, Uhrová, Tereza, Růžička, Evžen, Urgošík, Dušan, Jech, Robert

“…Cognitive decline represents a severe non‐motor symptom of Parkinson's disease (PD) that can significantly reduce the benefits of subthalamic deep brain…”
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The Instrumental Activities of Daily Living in Parkinson’s Disease Patients Treated by Subthalamic Deep Brain Stimulation by Bezdicek, Ondrej, Mana, Josef, Růžička, Filip, Havlik, Filip, Fečíková, Anna, Uhrová, Tereza, Růžička, Evžen, Urgošík, Dušan, Jech, Robert

“…Background Everyday functioning and instrumental activities of daily living (IADL) play a vital role in preserving the quality of life in patients with…”
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Mixed anxiety-depressive disorder in Parkinson's disease associated with worse resting state functional response to deep brain stimulation of subthalamic nucleus by Filip, Pavel, Lasica, Andrej, Uhrová, Tereza, Mana, Josef, Růžička, Filip, Keller, Jiří, Mueller, Karsten, Burdová, Kristína, Kiakou, Dimitra, Jech, Robert

“…Parkinson's disease (PD), even though generally perceived as a dominantly motor disorder, is associated with a wide range of non-motor symptoms, including…”
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The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease by Klempíř, Jiří, Židovská, Jana, Štochl, Jan, Ing, Věra Kebrdlová, Uhrová, Tereza, Roth, Jan

“…Huntington's disease (HD) is caused by the expansion of the number of CAG repeats on the chromosome 4p16.3, which results in elongated glutamine tract of…”
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Importance of psychiatric examination in predictive genetic testing for Huntington disease by Uhrová, Tereza, Zidovská, Jana, Koblihová, Jana, Klempíř, Jiří, Majerová, Veronika, Roth, Jan

“…Huntington disease (HD) is an au-tosomal dominant hereditary neurodegenerative disease with multiplication of CAG triplet in the short arm of chromoso-me 4,…”
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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study by Moss, Davina J Hensman, MBBS, Pardiñas, Antonio F, PhD, Langbehn, Douglas, Prof, Lo, Kitty, PhD, Leavitt, Blair R, Prof, Roos, Raymund, Prof, Durr, Alexandra, Prof, Mead, Simon, Prof, Holmans, Peter, Prof, Jones, Lesley, Prof, Tabrizi, Sarah J, Prof

“…Summary Background Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT . Age at onset has been used as a quantitative…”
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H53 Does the risperidone influence weight in huntington’s disease? by Konvalinkova, Romana, Dusek, Pavel, Doleckova, Kristyna, Uhrova, Tereza, Roth, Jan, Klempir, Jiri

“…Unintended weight loss is a negative prognostic factor in Huntington’s disease (HD). Exact mechanism of weight loss and influence of therapeutic intervention…”
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Clinical manifestations of intermediate allele carriers in Huntington disease by Cubo, Esther, Ramos-Arroyo, María A, Martinez-Horta, Saul, Martínez-Descalls, Asunción, Calvo, Sara, Gil-Polo, Cecilia

“…OBJECTIVE:There is controversy about the clinical consequences of intermediate alleles (IAs) in Huntington disease (HD). The main objective of this study was…”
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Clinical and genetic characteristics of late-onset Huntington's disease by Oosterloo, Mayke, Bijlsma, Emilia K., van Kuijk, Sander MJ, Minkels, Floor, de Die-Smulders, Christine EM

“…The frequency of late-onset Huntington's disease (>59 years) is assumed to be low and the clinical course milder. However, previous literature on late-onset…”
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Identification of symbol digit modality test score extremes in Huntington's disease by Braisch, Ulrike, Muche, Rainer, Rothenbacher, Dietrich, Landwehrmeyer, Georg Bernhard, Long, Jeffrey D., Orth, Michael

“…Studying individuals with extreme phenotypes could facilitate the understanding of disease modification by genetic or environmental factors. Our aim was to…”
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Caudate nucleus atrophy in Huntington's disease and its relationship with clinical and genetic parameters by Roth, Jan, Klempìi, Jirí, Jech, Robert, Zidovská, Jana, Uhrová, Tereza, Doubek, Pavel, Ulmanová, Olga, Brozová, Hana, Volfová, Markéta, Serranová, Tereza, Ruzicka, Evzen

“…We analysed clinical data in 80 genetically confirmed Huntington?s disease (HD) patients and measured the severity of the head of the caudate nucleus (HCN)…”
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Assessment of the Performance of a Modified Motor Scale as Applied to Juvenile Onset Huntington's Disease by Horton, Mike C, Nopoulos, Peggy, Nance, Martha, Landwehrmyer, G Bernhard, Barker, Roger A, Squitieri, Ferdinando, Burgunder, Jean-Marc, Quarrell, Oliver

“…Huntington's disease can present at almost any age but traditionally, those with an onset ≤20 years are described as having juvenile onset Huntington's disease…”
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