نتایج جستجو برای: msa

تعداد نتایج: 2638  

Journal: :Journal of neurology, neurosurgery, and psychiatry 2003
R Higo N Tayama T Watanabe T Nitou S Takeuchi

BACKGROUND Vocal fold motion impairment (VFMI), especially vocal fold abductor paralysis, is frequently seen in multiple system atrophy (MSA). Since the regulation system of laryngeal function is closely related to swallowing function, swallowing function is considered to be more involved in MSA patients with VFMI than in patients that do not have VFMI. However, the relationship between dysphag...

Journal: :Pharmacological research 2015
Míriam Tarrado-Castellarnau Roldán Cortés Miriam Zanuy Josep Tarragó-Celada Ibrahim H Polat Richard Hill Teresa W M Fan Wolfgang Link Marta Cascante

Selenium supplement has been shown in clinical trials to reduce the risk of different cancers including lung carcinoma. Previous studies reported that the antiproliferative and pro-apoptotic activities of methylseleninic acid (MSA) in cancer cells could be mediated by inhibition of the PI3K pathway. A better understanding of the downstream cellular targets of MSA will provide information on its...

2016
Anna Sailer Sonja W. Scholz Michael A. Nalls Claudia Schulte Monica Federoff T. Ryan Price Andrew Lees Owen A. Ross Dennis W. Dickson Kin Mok Niccolo E. Mencacci Lucia Schottlaender Viorica Chelban Helen Ling Sean S. O'Sullivan Nicholas W. Wood Bryan J. Traynor Luigi Ferrucci Howard J. Federoff Timothy R. Mhyre Huw R. Morris Günther Deuschl Niall Quinn Hakan Widner Alberto Albanese Jon Infante Kailash P. Bhatia Werner Poewe Wolfgang Oertel Günter U. Höglinger Ullrich Wüllner Stefano Goldwurm Maria Teresa Pellecchia Joaquim Ferreira Eduardo Tolosa Bastiaan R. Bloem Olivier Rascol Wassilios G. Meissner John A. Hardy Tamas Revesz Janice L. Holton Thomas Gasser Gregor K. Wenning Andrew B. Singleton Henry Houlden

OBJECTIVE To identify genetic variants that play a role in the pathogenesis of multiple system atrophy (MSA), we undertook a genome-wide association study (GWAS). METHODS We performed a GWAS with >5 million genotyped and imputed single nucleotide polymorphisms (SNPs) in 918 patients with MSA of European ancestry and 3,864 controls. MSA cases were collected from North American and European cen...

Journal: :Clinical science 2003
David S Goldstein Courtney Holmes Nicholas Patronas Irwin J Kopin

In multiple system atrophy (MSA) and pure autonomic failure (PAF), orthostatic hypotension (OH) results from deficient noradrenaline release from sympathetic nerves during standing. Post-mortem findings have indicated loss of central noradrenergic cells in both diseases. The present study sought in vivo neurochemical evidence for central noradrenergic deficiency in patients with OH due to MSA o...

2009
Ammar Al-Chalabi Alexandra Dürr Nicholas W. Wood Michael H. Parkinson Agnes Camuzat Jean-Sébastien Hulot Karen E. Morrison Alan Renton Sigurd D. Sussmuth Bernhard G. Landwehrmeyer Albert Ludolph Yves Agid Alexis Brice P. Nigel Leigh Gilbert Bensimon

BACKGROUND Multiple system atrophy (MSA) is a progressive neurodegenerative disorder characterized by parkinsonism, cerebellar ataxia and autonomic dysfunction. Pathogenic mechanisms remain obscure but the neuropathological hallmark is the presence of alpha-synuclein-immunoreactive glial cytoplasmic inclusions. Genetic variants of the alpha-synuclein gene, SNCA, are thus strong candidates for g...

2016
C. Guevara K. Bulatova G. J. Barker G. Gonzalez N. Crossley M. J. Kempton

In multiple system atrophy (MSA) and progressive supranuclear palsy (PSP), the absence of surrogate endpoints makes clinical trials long and expensive. We aim to determine annualized whole-brain atrophy rates (a-WBAR) in idiopathic Parkinson's disease (IPD), MSA, and PSP. Ten healthy controls, 20 IPD, 12 PSP, and 8 MSA patients were studied using a volumetric MRI technique (SIENA). In controls,...

Journal: :The Journal of the Association of Physicians of India 2010
Pazhayannur V Swaminath Mona Ragothaman Suma Koshy Nagaraja Sarangmath Mohan Adhyam D K Subbakrishna Christopher J Mathias Uday B Muthane

METHODS One hundred and eighty-one parkinsonian patients were evaluated to determine if urogenital symptoms at presentation to the Neurology clinic can differentiate them as PD or MSA-P. An autonomic questionnaire was used to document urinary and genital symptoms. RESULTS Mean age at presentation and disease duration in PD and MSA-P were similar. Urinary symptoms occurred twice as frequently ...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1999
V Fetoni P Soliveri D Monza D Testa F Girotti

The objective was to determine the extent to which psychiatric disturbances (especially mood disorders) generally considered poor prognostic factors, are present in patients with striatonigral (SND) type multiple system atrophy (MSA) compared with patients with idiopathic Parkinson's disease (IPD). The Hamilton depression scale (HAM-D), brief psychiatric rating scale (BPRS), and Unified Parkins...

2014
Annamaria Vallelunga Marco Ragusa Stefania Di Mauro Tommaso Iannitti Manuela Pilleri Roberta Biundo Luca Weis Cinzia Di Pietro Angela De Iuliis Alessandra Nicoletti Mario Zappia Michele Purrello Angelo Antonini

BACKGROUND Parkinson's disease (PD) is a progressive neurodegenerative disorder which may be misdiagnosed with atypical conditions such as Multiple System Atrophy (MSA), due to overlapping clinical features. MicroRNAs (miRNAs) are small non-coding RNAs with a key role in post-transcriptional gene regulation. We hypothesized that identification of a distinct set of circulating miRNAs (cmiRNAs) c...

2013
Daniela Kuzdas Sylvia Stemberger Stefano Gaburro Nadia Stefanova Nicolas Singewald Gregor K. Wenning

Multiple system atrophy (MSA) is a fatal, rapidly progressive neurodegenerative disease with limited symptomatic treatment options. Discrimination of MSA from other degenerative disorders crucially depends on the presence of early and severe cardiovascular autonomic failure (CAF). We have previously shown that neuropathologic lesions in the central autonomic nuclei similar to the human disease ...

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