Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Jun-Suk Kang"'
Autor:
Sriramya Lapa, Inga Claus, Sarah C. Reitz, Johanna Quick‐Weller, Sonja Sauer, Sigrid Colbow, Christiane Nasari, Rainer Dziewas, Jun‐Suk Kang, Simon Baudrexel, Tobias Warnecke
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 7, Pp 1174-1180 (2020)
Abstract Objective Deep brain stimulation (DBS) of the ventral intermediate nucleus (VIM) is a mainstay treatment for severe and drug‐refractory essential tremor (ET). Although stimulation‐induced dysarthria has been extensively described, possib
Externí odkaz:
https://doaj.org/article/a6a7561c015048deb4173c4734ce2d31
Autor:
Sarah C. Reitz, Sebastian Luger, Sriramya Lapa, Michael Eibach, Natalie Filmann, Volker Seifert, Lutz Weise, Johannes C. Klein, Jun-Suk Kang, Simon Baudrexel, Johanna Quick-Weller
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Essential Tremor (ET) is a progressive neurological disorder characterized by postural and kinetic tremor most commonly affecting the hands and arms. Medically intractable ET can be treated by deep brain stimulation (DBS) of the ventral i
Externí odkaz:
https://doaj.org/article/61a3436954c6492c87e23202e0bdbf08
Publikováno v:
Journal of Neurology
Adult-onset ataxias are a genetically and clinically heterogeneous group of movement disorders. In addition to nuclear gene mutations, sequence changes have also been described in the mitochondrial genome. Here, we present findings of mutation analys
High Glucosylceramides and Low Anandamide Contribute to Sensory Loss and Pain in Parkinson's Disease
Autor:
Georg Auburger, Yannick Schreiber, Lucie Valek, Sandra Trautmann, Jun-Suk Kang, Katharina Klatt-Schreiner, Lisa Hahnefeld, Sabine Wicker, Waltraud Pfeilschifter, Dominique Thomas, Robert Gurke, Irmgard Tegeder, Jörn Lötsch, Alexander Khlebtovsky, Annett Wilken-Schmitz, Gerd Geisslinger, Ruth Djaldetti
Publikováno v:
Movement Disorders. 35:1822-1833
Background Parkinson's disease (PD) causes chronic pain in two-thirds of patients, in part originating from sensory neuropathies. The aim of the present study was to describe the phenotype of PD-associated sensory neuropathy and to evaluate its assoc
Autor:
David Prvulovic, Johannes Pantel, Monika Scheibe, Tarik Karakaya, Jun-Suk Kang, Fabian Fusser, Silke Matura, Andreas Reif, Jan Köhler, Daniel Hartmann, Felix Ehret, Christoph Mayer
Publikováno v:
Acta Neuropsychiatrica. 32:206-213
Mild cognitive impairment (MCI) often precedes Alzheimer’s Dementia (AD), and in a high proportion of individuals affected by MCI, there are already neuropathological processes ongoing that become more evident when patients progress to AD. Accordin
Autor:
Sarah Christina Reitz, Janina Lemmer-Etzrodt, Michael Eibach, Ferdinand Bohmann, Fee Keil, Nazife Dinc, Nikhil Thakur, Jun-Suk Kang, Lutz Weise, Volker Seifert, Marcus Czabanka, Simon Baudrexel, Johanna Quick-Weller
Publikováno v:
Clinical neurology and neurosurgery. 224
Deep brain stimulation (DBS) is a safe and effective treatment option for patients with movement disorders as Parkinson's disease, essential tremor and dystonia[1]. For many of these patients the need for imaging may arise in the following years afte
Autor:
Holger Hengel, Judith van Gaalen, Gülin Öz, Thiago Junqueira Ribeiro de Rezende, Hector Garcia-Moreno, Sandro Romanzetti, L. Schoels, Kathrin Reetz, Richard Joules, Koyak Berkan, Bart P.C. van de Warrenburg, Jon Infante, Matthis Synofzik, James M. Joers, Robin Wolz, Marcondes C. França, Heike Jacobi, Jereon J. de Vries, Tamara Schaprian, Jiang Hong, Jun Suk Kang, Matthias Schmid, Paola Giunti, Jörn Diedrichsen, Fanny Mochel, Thomas Klockgether, Alexandra Durr, Dagmar Timmann-Braun, Benjamin Bender, Weihua Liao, Jennifer Faber
Publikováno v:
Movement Disorders
Movement Disorders, In press, ⟨10.1002/mds.28610⟩
Movement Disorders, Vol. 36, No. 10, 2021
Brain and Mind Institute Researchers' Publications
Movement Disorders, Wiley, In press, ⟨10.1002/mds.28610⟩
Movement disorders 36(10), 2273-2281 (2021). doi:10.1002/mds.28610
Movement Disorders, 36(10), 2273-2281. Wiley
Movement Disorders, 36, 2273-2281
Movement Disorders, 36, 10, pp. 2273-2281
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Movement Disorders, In press, ⟨10.1002/mds.28610⟩
Movement Disorders, Vol. 36, No. 10, 2021
Brain and Mind Institute Researchers' Publications
Movement Disorders, Wiley, In press, ⟨10.1002/mds.28610⟩
Movement disorders 36(10), 2273-2281 (2021). doi:10.1002/mds.28610
Movement Disorders, 36(10), 2273-2281. Wiley
Movement Disorders, 36, 2273-2281
Movement Disorders, 36, 10, pp. 2273-2281
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Background: Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there is a need for markers that reflect disease-related alterations, in particular, in the preataxic stage, in which clinical scales are lacking sensitivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98fb0bc8e31592c86eb5cc11b47e435
https://hal.sorbonne-universite.fr/hal-03230909/document
https://hal.sorbonne-universite.fr/hal-03230909/document
Autor:
Thomas Klockgether, Wolfgang Nachbauer, Alexandra Durr, Holger Hengel, Alessandro Roca, Katrin Bürk-Gergs, Kathrin Reetz, Dagmar Timmann, Olaf Riess, Caterina Mariotti, Florian Harmuth, Sandro Romanzetti, Jörg B. Schulz, Marcella Masciullo, Carlo Casali, Lorenzo Nanetti, Alessandro Filla, Maria Rakowicz, Jun Suk Kang, Béla Melegh, Laszlo Baliko, Jon Infante, Grzegorz Makowicz, Ludger Schöls, Heike Jacobi, Marie Lorraine Monin, Sophie Tezenas du Montcel
Publikováno v:
The lancet / Neurology 19(9), 738-747 (2020). doi:10.1016/S1474-4422(20)30235-0
Summary Background Spinocerebellar ataxias (SCAs) are autosomal dominant neurodegenerative diseases. Our aim was to study the conversion to manifest ataxia among apparently healthy carriers of mutations associated with the most common SCAs (SCA1, SCA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e75b6d7f3365a7c46786ed5963148a06
http://hdl.handle.net/11573/1638827
http://hdl.handle.net/11573/1638827
Autor:
Johann Philipp Zöllner, Christian Foerch, Jun-Suk Kang, Martin Alexander Schaller, Sriramya Lapa, Helmuth Steinmetz, Marlies Wagner, Katharina Filipski
Publikováno v:
Der Nervenarzt. 90:609-615
Background Hypertrophic olivary degeneration (HOD) occurs as a result of a lesion in the anatomical functional loop of the Guillain-Mollaret triangle. Frequent causes are intracerebral hemorrhage and brain infarction. After a latent period of weeks t
Autor:
Gerhard Reichel, Christoph Kamm, Jun Suk Kang, Martina Müngersdorf, Sebastian Paus, Iris Reuter, Andrea Stenner, David Weise
Publikováno v:
Fortschritte der Neurologie · Psychiatrie. 86:368-386
Zervikale Dystonien sind die häufigsten fokalen Dystonien. Der apparativen Diagnostik müssen eine gründliche allgemeine klinische neurologische Untersuchung und eine exakte phänomenologische Bewertung voran gestellt werden. Bei der Detektion der