Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ina R. Vogt"'
Publikováno v:
European journal of neurology 30(2), 548-551 (2022). doi:10.1111/ene.15596
The Scale for Assessment and Rating of Ataxia (SARA) is a widely used clinical scale. The objective was to study the age dependence of SARA in healthy adults and to define age-specific cut-off values to differentiate healthy from ataxic individuals.D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8adf9ecd232fab37e03738342d7a0fd2
https://pub.dzne.de/record/165381
https://pub.dzne.de/record/165381
Autor:
Winfried Ilg, Björn Müller, Jennifer Faber, Judith van Gaalen, Holger Hengel, Ina R. Vogt, Guido Hennes, Bart van de Warrenburg, Thomas Klockgether, Luger Schöls, Matthis Synofzik
Measures of step variability and body sway during gait have shown to correlate with clinical ataxia severity in several cross-sectional studies. However, to serve as a valid progression biomarker, these gait measures have to prove their sensitivity t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3467a8fd0305e9cf96a01b46361f11fa
https://doi.org/10.1101/2022.03.10.22272119
https://doi.org/10.1101/2022.03.10.22272119
Autor:
René Hurlemann, Oliver Kaut, Tamara Schaprian, Thomas Klockgether, Marcus Grobe-Einsler, Ina R. Vogt
Publikováno v:
Neurodegenerative diseases 20(2-3), 104-109 (2020). doi:10.1159/000510057
Background: Rivastigmine is an acetylcholine esterase inhibitor which is commonly used as therapy for dementia in Alzheimer’s disease and Parkinson’s disease (PD). Recently, a randomized controlled trial demonstrated a positive effect of rivastig
Autor:
Ina R. Vogt, Andrew J. Lees, Bernd O. Evert, Thomas Klockgether, Ullrich Wüllner, Michael Bonin
Publikováno v:
Experimental Neurology. 199:465-478
Multiple system atrophy (MSA) and sporadic, non-mendelian Parkinson's disease (PD) are progressive neurodegenerative disorders with overlapping clinical symptoms and pathology. The etiology of both disorders is unknown, and complex combinations of mu
Autor:
Mathias M. Borst, Helmut F. Kuecherer, Wolfgang Kübler, Ina R. Vogt, Ulrike Barth, Derliz Mereles, Bart Janssen, Christine Fischer, Horst Olschewski, Ekkehard Grünig
Publikováno v:
Scopus-Elsevier
Background —Familial primary pulmonary hypertension (PPH) is an autosomal-dominant inherited disease with incomplete penetrance and poor prognosis. This study was performed to examine whether asymptomatic carriers of a mutated PPH gene can be ident
Autor:
Gerd Schulte-Körne, Sven Cichon, Markus M. Nöthen, Ina R. Vogt, Tiemo Grimm, Helmut Remschmidt, Peter Propping, Bertram Müller-Myhsok
Publikováno v:
The American Journal of Human Genetics. 63(1):279-282
We are extremely grateful to the families who participated in this work. We appreciate the assistance of Katarina Muller and Wolfgang Deimel (Marburg). This work was supported by Deutsche Forschungsgemeinschaft grants Re 471/9-1 and Schu 988/2-1//2-3
Autor:
Tobias Höller, Markus M. Nöthen, Muhammad Faiyaz ul Haque, Mahmud Ahmad, Sven Cichon, Sayedul Haque, Ina R. Vogt, Peter Propping, Michael Knapp, Marcella Rietschel, Roland Kruse, Susanne Hemmer
Publikováno v:
The American Journal of Human Genetics. 62(2):386-390
SummaryComplete or partial congenital absence of hair (congenital alopecia) may occur either in isolation or with associated defects. The majority of families with isolated congenital alopecia has been reported to follow an autosomal-recessive mode o
Publikováno v:
Spine. 25:2262-2264
Study Design Case report. Objective To report a rare case of primary lymphoma of the spinal cord and to discuss therapeutic options. Summary of Background Data Only few cases of primary spinal cord lymphomas are reported. Prognosis is often poor, and
Autor:
Bernd O. Evert, Rob A.I. de Vos, Lucia Ozimek, Thomas Klockgether, Ullrich Wüllner, Ina R. Vogt, Ewout R. Brunt, Ana Maria Menezes Vieira-Saecker
Publikováno v:
Journal of neuropathology and experimental neurology, 62(10), 1006-1018. Oxford University Press
Spinocerebellar ataxia type 3 (SCA3) is a late-onset neurodegenerative disorder caused by the expansion of a polyglutamine tract Within the gene product, ataxin-3 We have previously shown that mutant ataxin-3 causes upregulation of inflammatory genes
Autor:
Claudia Kindermann, Ina Schmitt, Rob A.I. de Vos, Ullrich Wüllner, Bernd O. Evert, Ina R. Vogt, Lucia Ozimek, Ewout R. Brunt, Thomas Klockgether
Publikováno v:
The Journal of Neuroscience, 21(15), 5389-5396. Oxford University Press
Spinocerebellar ataxia type 3 (SCA3) is a polyglutamine disorder caused by a CAG repeat expansion in the coding region of a gene encoding ataxin-3. To study putative alterations of gene expression induced by expanded ataxin-3, we performed PCR-based