Search Results - "Andrich, J"

Topography of cerebral atrophy in early Huntington’s disease: a voxel based morphometric MRI study by Kassubek, J, Juengling, F D, Kioschies, T, Henkel, K, Karitzky, J, Kramer, B, Ecker, D, Andrich, J, Saft, C, Kraus, P, Aschoff, A J, Ludolph, A C, Landwehrmeyer, G B

“…Objectives: To analyse grey matter changes in early stages of Huntington’s disease using magnetic resonance imaging (MRI) and the technique of voxel based…”
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Apolipoprotein E genotypes do not influence the age of onset in Huntington’s disease by Saft, C, Andrich, J E, Brune, N, Gencik, M, Kraus, P H, Przuntek, H, Epplen, J T

“…Objective: The ε4 allele of the apolipoprotein E (ApoE) gene has been defined as a critical factor for early onset neurodegeneration in Pick’s, Parkinson’s,…”
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Autonomic nervous system function in Huntington's disease by Andrich, J, Schmitz, T, Saft, C, Postert, T, Kraus, P, Epplen, J T, Przuntek, H, Agelink, M W

“…Objective: To investigate whether Huntington's disease (HD) affects autonomic nervous system (ANS) functioning. Methods: Twenty patients with HD who had…”
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Cardiovagal modulation upon postural change is altered in Huntington's disease by Bär, K. J., Boettger, M. K., Andrich, J., Epplen, J. T., Fischer, F., Cordes, J., Koschke, M., Agelink, M. W.

“…Background:  Cardiac autonomic nervous system (ANS) dysfunction in Huntington’s disease (HD) might affect both the sympathetic and parasympathetic branch of…”
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Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype by Bauer, P, Laccone, F, Rolfs, A, Wüllner, U, Bösch, S, Peters, H, Liebscher, S, Scheible, M, Epplen, J T, Weber, B H F, Holinski-Feder, E, Weirich-Schwaiger, H, Morris-Rosendahl, D J, Andrich, J, Riess, O

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Sonographic detection of bilateral striopallidodentate calcinosis by Krogias, Ch, Meves, S., Schoellhammer, M., Gold, R., Andrich, J.

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NR2A and NR2B receptor gene variations modify age at onset in Huntington disease by ARNING, Larissa, KRAUS, Peter H, VALENTIN, Sandra, SAFT, Carsten, ANDRICH, Jürgen, EPPLEN, Jörg T

“…N -Methyl-d-aspartate (NMDA) receptor-mediated excitotoxicity has been proposed to play a role in the pathogenesis of Huntington disease (HD), an autosomal…”
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Relation between electroconvulsive therapy, cognitive side effects, neuron specific enolase, and protein S-100 by Agelink, M W, Andrich, J, Postert, T, Würzinger, U, Zeit, T, Klotz, P, Przuntek, H

“…OBJECTIVE To investigate whether electroconvulsive therapy (ECT) induces brain tissue damage expressed as an increase in neuron specific enolase and protein…”
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69. Voluntary movement execution in Huntington’s disease – a combined neurophysiological and morphometric magnetic resonance imaging study by Beste, C, Konrad, C, Saft, C, Andrich, J, Gold, R, Pfleiderer, B, Hausmann, M, Falkenstein, M

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Basal ganglia alterations and brain atrophy in Huntington’s disease depicted by transcranial real time sonography by Postert, Th, Lack, B, Kuhn, W, Jergas, M, Andrich, J, Braun, B, Przuntek, H, Sprengelmeyer, R, Agelink, M, Büttner, Th

“…OBJECTIVES AND METHODS Transcranial real time sonography (TCS) was applied to 49 patients with Huntington’s disease and 39 control subjects to visualise…”
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Chronic subdural haematoma in patients with Huntington's disease by Pechlivanis, I., Andrich, J., Scholz, M., Harders, A., Saft, C., Schmieder, K.

“…We studied the frequency of patients who had chronic subdural haematomas (CSDH) and Huntington's disease (HD) in a 1-year study period. In our department a…”
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Asymmetric anhidrosis in MSA by Saft, C, Andrich, J, Stücker, M, Przuntek, H, Müller, T

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Coenzyme Q10 serum levels in Huntington's disease by Andrich, J, Saft, C, Gerlach, M, Schneider, B, Arz, A, Kuhn, W, Müller, Th

“…Mitochondrial dysfunction contributes to the neurodegenerative process in Huntington's disease (HD). Coenzyme Q10 (CoQ10) enhances mitochondrial complex I…”
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Methyltetrahydrofolate reductase polymorphism influences onset of Huntington's disease by Brune, N, Andrich, J, Gencik, M, Saft, C, Müller, Th, Valentin, S, Przuntek, H, Epplen, J T

“…Onset of Huntington's disease (HD) negatively correlates with CAG repeat length of the HD gene, which encodes the protein huntingtin. This protein interacts…”
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Relationship between major depression and heart rate variability.: Clinical consequences and implications for antidepressive treatment by Agelink, Marcus W, Boz, Cavit, Ullrich, Heiko, Andrich, Jürgen

“…A high sympathetic and/or a low cardiovagal activity in patients with major depression (MD) may contribute to the higher cardiac morbidity and mortality of MD…”
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Congruent deterioration of complex and simple movements in patients with Huntington's disease by Saft, C, Andrich, J, Meisel, N M, Przuntek, H, Müller, Th

“…Rating scales and assessment of simple and complex movements may reflect severity of Huntington's disease (HD). Objectives of our study were to compare scored…”
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Morbus Huntington - a human genetic model disease by Epplen, J T, Gencik, M, Epplen, A, Andrich, J, Saft, C, Przuntek, H

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Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease by Saft, Carsten, Zange, Jochen, Andrich, Jürgen, Müller, Klaus, Lindenberg, Katrin, Landwehrmeyer, Bernhard, Vorgerd, Matthias, Kraus, Peter H., Przuntek, Horst, Schöls, Ludger

“…Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by a CAG repeat expansion in the IT‐15 gene; however, it…”
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High Cholesterol Feeding in C57/Blc6 Mice Alters Expression within The VEGF Receptor-Ligand Family in Corporal Tissue by Xie, Donghua, Hazarika, Surovi, Andrich, Amy J., Padgett, Mike E., Kontos, Christopher D., Donatucci, Craig F., Annex, Brian H.

“…Angiogenesis, the growth and proliferation of blood vessels from existing vascular structures, is mediated by many cytokine growth factors and receptors, among…”
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NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner by ARNING, Larissa, SAFT, Carsten, WIECZOREK, Stefan, ANDRICH, Jürgen, KRAUS, Peter H, EPPLEN, Jörg T

“…In addition to the pathogenetic CAG repeat expansion other genetic factors play a significant role in determining age at onset (AO) in Huntington disease (HD),…”
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