Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Karin Mente"'
Autor:
Hyun Joo Cho, Rebecca Waugh, Tianxia Wu, Pattamon Panyakaew, Karin Mente, Demelio Urbano, Mark Hallett, Silvina G. Horovitz
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Sensory trick is a characteristic feature of cervical dystonia (CD), where a light touch on the area adjacent to the dystonia temporarily improves symptoms. Clinical benefit from sensory tricks can be observed before tactile contact is made
Externí odkaz:
https://doaj.org/article/738616abdcb24d078bd6f4a247c271d3
Autor:
Traian Popa, Laurel S. Morris, Rachel Hunt, Zhi-De Deng, Silvina Horovitz, Karin Mente, Hitoshi Shitara, Kwangyeol Baek, Mark Hallett, Valerie Voon
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Background: The mesial prefrontal cortex, cingulate cortex, and the ventral striatum are key nodes of the human mesial fronto-striatal circuit involved in decision-making and executive function and pathological disorders. Here we ask whether deep wid
Externí odkaz:
https://doaj.org/article/542eb12b556d4014b99b9297ce470555
Autor:
Daniel B. Free, Ian Syndergaard, Adam C. Pigg, Silvia Muceli, Johanna Thompson-Westra, Karin Mente, Carine W. Maurer, Dietrich Haubenberger, Mark Hallett, Dario Farina, Steven K. Charles
Publikováno v:
Journal of Neurophysiology. 129:524-540
We characterized the relationships in tremor-band activity between the 15 major superficial upper limb muscles of persons with essential tremor by quantifying the proportion of shared activity (coherence) in the tremor band and by characterizing phas
Autor:
Carine W. Maurer, Karin Mente, Johanna Thompson-Westra, Steven K. Charles, Dietrich Haubenberger, Adam C. Pigg, Mark Hallett
Publikováno v:
Clin Neurophysiol
Objective Although Essential Tremor is one of the most common movement disorders, we do not currently know which muscles are most responsible for tremor. Determining this requires multiple steps, one of which is characterizing the distribution of tre
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 77:346-352
Prion diseases comprise a group of transmissible degenerative encephalopathies resulting from propagation of a misfolded cellular protein of uncertain function. As is generally the case with rare diseases, lack of institutional experience compromises
Autor:
Edson Amaro, Mark Hallett, Eduardo Joaquim Lopes Alho, D Iacono, Nancy A. Edwards, Demelio Urbano, Ana Tereza Di Lorenzo Alho, Abhik Ray-Chaudhury, Karin Mente, Silvina G. Horovitz
Publikováno v:
Movement Disorders. 33:827-834
Background The etiology of cervical dystonia is unknown. Cholinergic abnormalities have been identified in dystonia animal models and human imaging studies. Some animal models have cholinergic neuronal loss in the striatum and increased acetylcholine
Autor:
Jeffrey J. Kim, Hesham Abboud, Ashhar Ali, Karin Mente, Meagan D. Seay, Mary A. Willis, Robert A. Bermel
Publikováno v:
International Journal of MS Care. 19:290-296
Background:Patients with multiple sclerosis (MS) present to the emergency department (ED) for various reasons. Although true relapse is rarely the underlying culprit, ED visits commonly result in new magnetic resonance imaging (MRI) and neurology adm
Autor:
John F. Crary, Christopher Grunseich, Karin Mente, Marco M. Hefti, Adrian Danek, Ruth H. Walker, Barbara I. Karp, Sun A Kim
Publikováno v:
Neuropathology and Applied Neurobiology. 43:542-546
Chorea-acanthocytosis (ChAc) is an autosomal recessive neurodegenerative disease associated with mutations in VPS13A that encodes the protein chorein. ChAc is characterized by progressive chorea, dystonia, and psychiatric symptoms, developing in youn
Autor:
James K. O’Donnell, Mark L. Cohen, Stephen E. Jones, Brian S. Appleby, Jiri G. Safar, Alberto Bizzi, Pierluigi Gambetti, Nicolas R. Thompson, Karin Mente
Publikováno v:
Alzheimer disease and associated disorders. 31(1)
Creutzfeldt-Jakob disease (CJD) and other prion diseases are rapidly progressive spongiform encephalopathies that are invariably fatal. Clinical features and magnetic resonance imaging, electroencephalogram, and cerebrospinal fluid abnormalities may
Publikováno v:
Neurology. Clinical practice. 6(5)
Background: Antibodies against voltage-gated potassium channel (VGKC)–complex are implicated in the pathogenesis of acquired neuromyotonia, limbic encephalitis, faciobrachial dystonic seizure, and Morvan syndrome. Outside these entities, the clinic