Search Results - "Dillmann, U"

Striatal FP-CIT uptake differs in the subtypes of early Parkinson's disease by Spiegel, J, Hellwig, D, Samnick, S, Jost, W, Möllers, M-O, Fassbender, K, Kirsch, C-M, Dillmann, U

“…In idiopathic Parkinson's disease (PD), a tremor-dominant type (TDT), an akinetic-rigid type (ART), and a mixed type (MT) are distinguished. We compared…”
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Facial emotion recognition in Parkinson's disease: Association with age and olfaction by Kalampokini, S., Lyros, E., Luley, M., Schöpe, J., Spiegel, J., Bürmann, J., Dillmann, U., Fassbender, K., Unger, M. M

“…Objective: The ability to recognize facial emotion expressions has been reported to be impaired in Parkinson's disease (PD), yet previous studies showed…”
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Hyperechogenicity of the substantia nigra in healthy controls is related to MRI changes and to neuronal loss as determined by F-Dopa PET by Behnke, S., Schroeder, U., Dillmann, U., Buchholz, H.G., Schreckenberger, M., Fuss, G., Reith, W., Berg, D., Krick, C.M.

“…Transcranial ultrasound (TCS) has been shown to reveal hyperechogenicity of the substantia nigra (SN) in Parkinsonian patients and in about 10% of healthy…”
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Nicotinic α4β2 acetylcholine receptors and cognitive function in Parkinson's disease by Lorenz, R., Samnick, S., Dillmann, U., Schiller, M., Ong, M. F., Faßbender, K., Buck, A., Spiegel, J.

“…Background Idiopathic Parkinson's disease (IPD) is characterized by the clinical motor symptoms of hypokinesia, rigidity, and tremor. Apart from these motor…”
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P191. The starch-iodine test in the topodiagnosis of Horner’s syndrome with heat hypohidrosis and gustatory sweating by Bürmann, J, Devlioti, A, Manitz, M, Bialas, P, Faßbender, K, Dillmann, U

“…Background and purpose Horner’s syndrome may result from a variety of central or peripheral lesions of the sympatho-excitatory pathway. Associated symptoms…”
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P44. Facial onset sensory motor neuronopathy (FOSMN) syndrome – Evidence for an oligogenic entity, though no evidence of a genetic link to ALS by Prudlo, J, Bürmann, J, Weis, J, Biskup, S, Krüger, S, Dillmann, U

“…Facial onset sensory motor neuronopathy (FOSMN) syndrome is a rare sporadic entity which has only recently been described ( Vucic et al., 2006 ). It is…”
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Mutations in the Gene Encoding Peroxisomal Sterol Carrier Protein X (SCPx) Cause Leukencephalopathy with Dystonia and Motor Neuropathy by Ferdinandusse, S., Kostopoulos, P., Denis, S., Rusch, H., Overmars, H., Dillmann, U., Reith, W., Haas, D., Wanders, R.J.A., Duran, M., Marziniak, M.

“…In this report, we describe the first known patient with a deficiency of sterol carrier protein X (SCPx), a peroxisomal enzyme with thiolase activity, which is…”
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A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy by Jonckheere, A I, Hogeveen, M, Nijtmans, L G J, van den Brand, M A M, Janssen, A J M, Diepstra, J H S, van den Brandt, F C A, van den Heuvel, L P, Hol, F A, Hofste, T G J, Kapusta, L, Dillmann, U, Shamdeen, M G, Smeitink, J A M, Rodenburg, R J T

“…To identify the biochemical and molecular genetic defect in a 16-year-old patient presenting with apical hypertrophic cardiomyopathy and neuropathy suspected…”
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ADULT MANIFESTATION OF L-2-HYDROXYGLUTARATE DEHYDROGENASE DEFICIENCY BY A NOVEL MUTATION by SÜHS, Kw, ERDMANN, P, SHAMDEEN, M. G, PAPANAGIOTOU, P, DILLMANN, U

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Impact of different stimulation types on orthostatic tremor by Spiegel, J, Fuß, G, Krick, C, Dillmann, U

“…Objective: Primary orthostatic tremor (OT) is thought to be generated by a unique supraspinal tremor generator. Here we studied the effect of ipsi- and…”
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Cardiovascular autonomic dysregulation and fatigue in multiple sclerosis by Merkelbach, S., Dillmann, U., Kölmel, C., Holz, J., Müller, M.

“…Both cardiovascular disturbances and fatigue are frequent in multiple sclerosis (MS). We investigated their relationship in 84 MS patients (mean age 39.9 +/-…”
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Neurological manifestations of AGel amyloidosis (Meretoja's syndrome) in a German family by Bürmann, J, Fassbender, K, Henn, W, Lohse, P, Holzhoffer, C, Dillmann, U

“…AGel amyloidosis is an autosomal dominantly inherited systemic amyloidosis which is most commonly observed in Finland. The clinical manifestation is…”
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Orthostatic tremor during modification of standing by Spiegel, J, Krick, C, Fuss, G, Becker, G, Dillmann, U

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Cardiovascular autonomic dysregulation and fatigue in multiple sclerosis by Merkelbach, S, Dillmann, U, Kölmel, C, Holz, J, Müller, M

“…Both cardiovascular disturbances and fatigue are frequent in multiple sclerosis (MS). We investigated their relationship in 84 MS patients (mean age 39.9+8.9…”
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141. Transcranial magnetic stimulation of the facial nerve in acute isolated peripheral facial palsy by Dillmann, U, Spiegel, J, Marziniak, M, Koenig, J, Chelius, C, Heide, G, Krick, C, Fassbender, K

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122. Cerebral and extracranial neurodegeneration are strongly coupled in Parkinson’s disease by Spiegel, J, Hellwig, D, Jost, W.H, Farmakis, G, Samnick, S, Fassbender, K, Kirsch, C.M, Dillmann, U

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Echogenic substantia nigra in patients with orthostatic tremor by Spiegel, J, Behnke, S, Fuss, G, Becker, G, Dillmann, U

“…Previous studies suggest that the nigrostriatal dopaminergic transmission is impaired in patients with primary orthostatic tremor. We used transcranial…”
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P-91 Factors influencing gait stability in healthy older adults by Röll, F., Seipelt, A., Rubly, M., Fassbender, K., Dillmann, U.

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Early deep brain stimulation for Parkinson's disease by Schnitzler, A, Fuchs, G, Baas, H, Dillmann, U, Hilker, R, Oechsner, M

“…Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is a powerful treatment for advanced Parkinson's disease with levodopa-induced motor…”
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Comparison of IPX066, a Novel Carbidopa-Levodopa (CD-LD) Extended-Release Formulation, and CD-LD-Entacapone (CLE) in Advanced Parkinson's Disease (ASCEND-PD Trial) (S02.005) by Stocchi, F., Dillmann, U., Ellenbogen, A., Hsu, A., Khanna, S., Rubens, R., Liang, G., Gupta, S.

“…Abstract only…”
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