Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Martin Wilhelm Kurz"'
Autor:
Christopher Elnan, Kvistad, Vojtech, Novotny, Martin Wilhelm, Kurz, Ole Morten, Rønning, Bente, Thommessen, Maria, Carlsson, Ulrike, Waje-Andreassen, Halvor, Næss, Lars, Thomassen, Nicola, Logallo
Publikováno v:
Stroke. 50(5)
Background and Purpose- Tenecteplase represents a promising alternative to alteplase as thrombolytic treatment in acute ischemic stroke. There are limited data on tenecteplase 0.4 mg/kg in patients with increased stroke severity. We aimed to assess s
Autor:
Jörg T. Epplen, Jan Petter Larsen, Dirk Woitalla, Gabriele Dekomien, Thomas Müller, Martin Wilhelm Kurz, Anna Melissa Schlitter
Publikováno v:
Acta Neurologica Scandinavica. 113:9-13
Objectives – Mutations in the Parkin gene can cause autosomal recessive early-onset Parkinson's disease (PD). Recently, Parkin mutations were also suggested to play a role in the commoner late-onset forms of PD. Methods – We compared a German coh
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 22:288-295
Parkinson’s disease with dementia (PDD) and dementia with Lewy bodies (DLB) are common clinical dementias characterized neuropathologically by the presence of cortical Lewy body pathology and with distinct clinical and neurobiological similarities.
Tumor necrosis factor-alpha-converting enzyme is expressed in the inflamed peripheral nervous system
Publikováno v:
Journal of the Peripheral Nervous System. 10:311-318
Tumor necrosis factor-alpha (TNF-alpha) is considered to play a critical role in the pathogenesis of immune-mediated inflammatory demyelinating disorders of the peripheral nervous system (PNS). Processing of membrane-bound inactive pro-TNF-alpha into
Publikováno v:
European Journal of Neurology. 10:159-163
Genetic factors seem to be important in the pathogenesis of Parkinson's disease (PD). It is however, still controversial whether these factors also are reflected in a familial aggregation of PD. The aim of this study was to investigate the frequency
Autor:
Silke Jörgens, Katja Biermann-Ruben, Kathinka Daehli Kurz, Rüdiger J. Seitz, Martin Wilhelm Kurz, Claudia Flügel, Christina Antke, Alfons Schnitzler, Hans-Peter Hartung
Publikováno v:
Neurocase. 14(4)
Pure word deafness is a rare disorder dramatically impairing comprehension of spoken language, while auditory functions remain relatively intact. We present a 71-year-old woman with a slowly progressive disturbance of speech perception due to pure wo
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 128(10)
Autor:
Thomas Mueller, Yvonne Klenk, Jan Petter Larsen, Gabriele Dekomien, Dag Aarsland, Anna Melissa Schlitter, Martin Wilhelm Kurz
Publikováno v:
Journal of geriatric psychiatry and neurology. 20(2)
Carriers of expanded alleles of the fragile X mental retardation ( FMR1) gene may display parkinsonism, cognitive decline, and behavioral changes. The authors screened 2 male groups of patients affected with Parkinson's disease (PD) (n = 137). One gr
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 21(12)
Dementia is common in patients with Parkinson's disease (PDD). The etiology of PDD is still unclear, but exciting advances have been made in discovering pathogenetic components in Parkinson's disease (PD), implicating the role of genetic factors. It
Autor:
Martin Wilhelm, Kurz, Anna Melissa, Schlitter, Jan Petter, Larsen, Clive, Ballard, Dag, Aarsland
Publikováno v:
Dementia and geriatric cognitive disorders. 22(4)
Parkinson's disease with dementia (PDD) and dementia with Lewy bodies (DLB) are common clinical dementias characterized neuropathologically by the presence of cortical Lewy body pathology and with distinct clinical and neurobiological similarities. I