Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Janna Krahe"'
Autor:
Jennifer Faber, David Kügler, Emad Bahrami, Lea-Sophie Heinz, Dagmar Timmann, Thomas M. Ernst, Katerina Deike-Hofmann, Thomas Klockgether, Bart van de Warrenburg, Judith van Gaalen, Kathrin Reetz, Sandro Romanzetti, Gulin Oz, James M. Joers, Jorn Diedrichsen, Martin Reuter, Paola Giunti, Hector Garcia-Moreno, Heike Jacobi, Johann Jende, Jeroen de Vries, Michal Povazan, Peter B. Barker, Katherina Marie Steiner, Janna Krahe
Publikováno v:
NeuroImage, Vol 264, Iss , Pp 119703- (2022)
Quantifying the volume of the cerebellum and its lobes is of profound interest in various neurodegenerative and acquired diseases. Especially for the most common spinocerebellar ataxias (SCA), for which the first antisense oligonculeotide-base gene s
Externí odkaz:
https://doaj.org/article/fda98a646f86424daa91258742f29642
Autor:
Alexa Haeger, Fawzi Boumezbeur, Michel Bottlaender, Cécile Rabrait-Lerman, Julien Lagarde, Shahram Mirzazade, Janna Krahe, Christian Hohenfeld, Marie Sarazin, Jörg B. Schulz, Sandro Romanzetti, Kathrin Reetz
Publikováno v:
NeuroImage: Clinical, Vol 36, Iss , Pp 103274- (2022)
Introduction: Application of MRI in clinical routine mainly addresses structural alterations. However, pathological changes at a cellular level are expected to precede the occurrence of brain atrophy clusters and of clinical symptoms. In this context
Externí odkaz:
https://doaj.org/article/1aea52441b5c4fc48bbb00427cfa6a9a
Autor:
Janna Krahe, Imis Dogan, Claire Didszun, Shahram Mirzazade, Alexa Haeger, Nadim Joni Shah, Ilaria A. Giordano, Thomas Klockgether, Guillaume Madelin, Jörg B. Schulz, Sandro Romanzetti, Kathrin Reetz
Publikováno v:
NeuroImage: Clinical, Vol 34, Iss , Pp 103025- (2022)
In patients with Friedreich ataxia, structural MRI is typically used to detect abnormalities primarily in the brainstem, cerebellum, and spinal cord. The aim of the present study was to additionally investigate possible metabolic changes in Friedreic
Externí odkaz:
https://doaj.org/article/b725dc3e59d643fb9e7f4fad6e600af1
Publikováno v:
Curr Opin Neurol
PURPOSE OF REVIEW Degenerative ataxias are rare and currently untreatable movement disorders, primarily characterized by neurodegeneration in the cerebellum and brainstem. We highlight MRI studies with the most potential for utility in pending ataxia
Autor:
Andreas Thieme, Jennifer Faber, Patricia Sulzer, Kathrin Reetz, Imis Dogan, Miriam Barkhoff, Janna Krahe, Heike Jacobi, Julia-Elisabeth Aktories, Martina Minnerop, Saskia Elben, Raquel van der Veen, Johanna Müller, Giorgi Batsikadze, Jürgen Konczak, Matthis Synofzik, Sandra Roeske, Dagmar Timmann
Publikováno v:
Journal of neurology 269(8), 4363-4374 (2022). doi:10.1007/s00415-022-11071-5
Journal of neurology 269(8), 4363-4374 (2022). doi:10.1007/s00415-022-11071-5
Published by Steinkopff, [Darmstadt]
Published by Steinkopff, [Darmstadt]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daf6229c2f0101248bee90bf3edf19c5
https://publications.rwth-aachen.de/record/862624
https://publications.rwth-aachen.de/record/862624
Autor:
Ferdinand Binkofski, Christian Hohenfeld, Imis Dogan, Nikolina Brcina, Jennifer Wojtala, Jörg B. Schulz, Anna Heidbreder, Shahram Mirzazade, Kathrin Reetz, Janna Krahe, Johannes Schiefer
Publikováno v:
Parkinsonism & related disorders 92, 76-82 (2021). doi:10.1016/j.parkreldis.2021.10.019
Introduction Altered brain activity and functional reorganization patterns during self-initiated movements have been reported in early pre-motor and motor stages of Parkinson's disease. The aim of this study was to investigate whether similar alterat
Autor:
Elisabeth Sittig, Andrea B. Maier, Wolfgang H. Oertel, Sandro Romanzetti, Kathrin Reetz, Jörg B. Schulz, Jennifer Wojtala, Annette Janzen, Anna Heidbreder, Susanne Knake, Florian Holtbernd, Imis Dogan, Janna Krahe, Johannes Schiefer
Publikováno v:
Sleep 44(3), zsaa199 (2021). doi:10.1093/sleep/zsaa199
Study Objectives Rapid eye movement sleep behavior disorder (RBD) is considered a prodromal state of Parkinson’s disease (PD). We aimed to characterize patterns of structural brain changes in RBD and PD patients using multimodal MRI. Methods A tota
Publikováno v:
Neuroscience and biobehavioral reviews. 108
Magnetic resonance spectroscopy (MRS) is applied to investigate the neurochemical profiles of degenerative hereditary ataxias. This meta-analysis provides a quantitative review and reappraisal of MRS findings in spinocerebellar ataxias (SCA) and Frie
Publikováno v:
Clinical Neurophysiology. 129:e71-e72
Background Friedreich ataxia (FRDA) is the most common autosomal recessive inherited ataxia, mainly caused by a GAA trinucleotide repeat expansion in the FRDA gene encoding the protein frataxin ( Bradley et al., 2000 ). Magnetic resonance imaging (MR