Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Bettina Meissner"'
Autor:
Uta Heinemann, Geeske T. Bohling, Inga Zerr, Anna Krasnianski, Daniela Varges, Walter J. Schulz-Schaeffer, Andreas Reif, Bettina Meissner
Publikováno v:
Journal of Alzheimer's Disease. 59:329-337
Background The polymorphism at codon 129 of the prion protein gene (PRNP) and the PrPSc types 1 and 2 belong to a molecular classification of sporadic Creutzfeldt-Jakob disease (sCJD) that correlates well with the clinical and neuropathological pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b1aab6c837cefebd27f514297cd8f3
https://doi.org/10.3233/jad-161129
https://doi.org/10.3233/jad-161129
Autor:
Anna Krasnianski, Hans A. Kretzschmar, Uta Heinemann, Bettina Meissner, Inga Zerr, Monika Bodemer, Karin Gmitterová
Publikováno v:
Neurobiology of Aging. 30:1842-1850
Background The 14-3-3 protein is a physiological cellular protein expressed in various tissues, and its release to CSF reflects extensive neuronal damage as in Creutzfeldt–Jakob disease (CJD), but also in other neurological diseases. 14-3-3 protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c32c92f7e14c32d27f0b4a9f2c98e7f
https://doi.org/10.1016/j.neurobiolaging.2008.01.007
https://doi.org/10.1016/j.neurobiolaging.2008.01.007
Autor:
Uta Heinemann, Inga Zerr, Anna Krasnianski, Hans A. Kretzschmar, Walter J. Schulz-Schaeffer, Kai Kallenberg, Bettina Meissner
Publikováno v:
Journal of Neurosurgery. 109:735-741
Object Creutzfeldt–Jakob disease (CJD) is a rare neurodegenerative disorder with diagnostic criteria defined as a combination of clinical symptoms, electroencephalography findings, cerebrospinal fluid (CSF) analysis, and MR imaging results. Special
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11299bfbed5f91eeeccae247c201ee86
https://doi.org/10.3171/jns/2008/109/10/0735
https://doi.org/10.3171/jns/2008/109/10/0735
Autor:
Daniela Varges, Walter J. Schulz-Schaeffer, Kai Kallenberg, Bettina Meissner, I. Zerr, David Summers, Anna Krasnianski, T. Talbot, Hans A. Kretzschmar, Uta Heinemann, Robert G. Will, Donald A. Collie
Publikováno v:
European Journal of Neurology. 15:762-771
Background and purpose: To establish radiological features in the atypical MV2 subtype of sCJD compared with the classical MM1 subtype, as well as region- and sequence-dependent inter-observer correlation. Methods: MRI hyperintensity of basal ganglia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17433f204b6cbd71f325309de41dfd54
https://doi.org/10.1111/j.1468-1331.2008.02209.x
https://doi.org/10.1111/j.1468-1331.2008.02209.x
Autor:
Fabian Wagner, Inga Zerr, Uta Heinemann, Sara Friederike Gloeckner, Bettina Meissner, Felix Meyne, Anna Krasnianski
Publikováno v:
Journal of Alzheimer's Disease. 14:17-25
We carried out a quantitative analysis of transthyretin (TTR), total tau protein and amyloid-beta (Abeta) peptide (1-40 and 1-42) in the lumbar cerebrospinal fluid of 106 patients with different forms of dementia including Alzheimer's disease (AD), C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51ab80cc11cf78f2e9ed361dc21c3880
https://doi.org/10.3233/jad-2008-14102
https://doi.org/10.3233/jad-2008-14102
Autor:
Bettina Meissner, Hans A. Kretzschmar, Uta Heinemann, Anna Krasnianski, Sara Friederike Gloeckner, Inga Zerr
Publikováno v:
Veterinary Microbiology. 123:328-335
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare transmissible disease caused by accumulation of pathological prion protein (PrP(sc)) in the CNS. According to the codon 129 polymorphism (methionine or valine) and the prion protein type 1 or 2, a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbc0e93fe122da67c6ca71526bc2cc47
https://doi.org/10.1016/j.vetmic.2007.04.002
https://doi.org/10.1016/j.vetmic.2007.04.002
Autor:
Bettina Meissner, Horst Urbach, Michael Knauth, Kai Kallenberg, I. Zerr, Henriette J. Tschampa, H. A. Kretzschmar
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: High cortical signal intensity on diffusion-weighted (DW) or fluid-attenuated inversion recovery (FLAIR) images is increasingly described in sporadic Creutzfeldt-Jakob disease (sCJD). The aim of this study was to assess the ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::956b4fb725fdfd6a7d897da5493e8271
https://doi.org/10.3174/ajnr.a0496
https://doi.org/10.3174/ajnr.a0496
Autor:
I. Zerr, Daniela Varges, C. Bösenberg, Bettina Meissner, M. Bartl, Anna Krasnianski, Hans A. Kretzschmar, Walter J. Schulz-Schaeffer, Kai Kallenberg, Ingo M. Westner, Michael Knauth
Publikováno v:
Neurology. 65:1544-1550
Background: Recently, six molecular subtypes of sporadic CJD (sCJD) have been identified showing differences regarding the disease course, neuropathologic lesion patterns, and sensitivity to diagnostic tools. Only isolated cases of the rare VV1 type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c343afd8edc6f14eb3424f434fd4afd6
https://doi.org/10.1212/01.wnl.0000184674.32924.c9
https://doi.org/10.1212/01.wnl.0000184674.32924.c9
Autor:
Hans A. Kretzschmar, Kai Kallenberg, Walter J. Schulz-Schaeffer, Bettina Meissner, Uta Heinemann, Anna Krasnianski, Katharina Stoeck, M. Bartl, Daniela Varges, Inga Zerr, Otto Windl, Constanze Boesenberg
Publikováno v:
Annals of Neurology. 58:533-543
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disease with the greatest incidence occurring in patients between 60 and 70 years old. Younger patients may also be affected. In this study, we used all case material available fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec9b6c8739de8a880fcb2c2267ab695
https://doi.org/10.1002/ana.20568
https://doi.org/10.1002/ana.20568
Autor:
Bettina Meissner, Sigrid Poser, Andreas Schröter, Hans A. Kretzschmar, I. Zerr, K. Körtner, Brit Mollenhauer, K. Köhler, M. Finkenstaedt, Otto Windl, U. Jastrow, M. Bartl
Publikováno v:
Neurology. 63:450-456
Objective: To assess if clinical features, prion protein codon 129, and molecular subtype correlate with MRI basal ganglia hyperintensity in sporadic Creutzfeldt-Jakob disease (CJD). Methods: The authors studied 219 patients including 153 confirmed C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a024a47d5abe667aef326c48aa7547c
https://doi.org/10.1212/01.wnl.0000136225.80445.c9
https://doi.org/10.1212/01.wnl.0000136225.80445.c9