نتایج جستجو برای: msa model

تعداد نتایج: 2106435  

Journal: :Archives of neurology 2007
Kenju Hara Yoshio Momose Susumu Tokiguchi Mitsuteru Shimohata Kenshi Terajima Osamu Onodera Akiyoshi Kakita Mitsunori Yamada Hitoshi Takahashi Motoyuki Hirasawa Yoshikuni Mizuno Katsuhisa Ogata Jun Goto Ichiro Kanazawa Masatoyo Nishizawa Shoji Tsuji

BACKGROUND Multiple system atrophy (MSA) has been considered a sporadic disease, without patterns of inheritance. OBJECTIVE To describe the clinical features of 4 multiplex families with MSA, including clinical genetic aspects. DESIGN Clinical and genetic study. SETTING Four departments of neurology in Japan. Patients Eight patients in 4 families with parkinsonism, cerebellar ataxia, and ...

Journal: :Circulation 2012
Hajime Imura Takashi Nitta Shun-Ichiro Sakamoto Kazuo Shimizu Masami Ochi

A 70-year-old man was admitted to our hospital for surgical treatment of mitral insufficiency. A preoperative echocardiogram revealed a prolapsed anterior mitral leaflet, membranous septal aneurysm (MSA), and unusual chordae extending from the ventricular septum to the anterior mitral leaflet (Movies I and II in the online-only Data Supplement). In surgery, the aneurysm was examined through the...

Journal: :American journal of physiology. Heart and circulatory physiology 2007
A Lipp P Sandroni J Eric Ahlskog D M Maraganore C W Shults P A Low

In multiple system atrophy (MSA), increased venous compliance with excessive venous pooling is assumed to be a major contributor to orthostatic hypotension (OH); however, venous compliance has never been assessed in MSA patients. We evaluated the severity and distribution of adrenergic, cardiovagal, and sudomotor failure in 11 patients with probable MSA, 14 age- and sex-matched control subjects...

2012
Jiing-Feng Lirng Po-Shan Wang Hung-Chieh Chen Bing-Wen Soong Wan Yuo Guo Hsiu-Mei Wu Cheng-Yen Chang

PURPOSE A broad spectrum of diseases can manifest cerebellar ataxia. In this study, we investigated whether proton magnetic resonance spectroscopy (MRS) may help differentiate spinocerebellar ataxias (SCA) from multiple systemic atrophy- cerebellar type (MSA-C). MATERIAL AND METHODS This prospective study recruited 156 patients with ataxia, including spinocerebellar ataxia (SCA) types 1, 2, 3...

2017
Yi Wang Yun Shen Kang-Ping Xiong Pei-Cheng He Cheng-Jie Mao Jie Li Fu-Yu Wang Ya-Li Wang Jun-Ying Huang Chun-Feng Liu

BACKGROUND Both Parkinson's disease (PD) and multiple system atrophy (MSA) have associated sleep disorders related to the underlying neurodegenerative pathology. Clinically, MSA with predominant parkinsonism (MSA-P) resembles PD in the manifestation of prominent parkinsonism. Whether the amount of rapid eye movement (REM) sleep without atonia could be a potential marker for differentiating MSA-...

Journal: :Brain : a journal of neurology 2005
C Kamm D G Healy N P Quinn U Wüllner J C Moller L Schols F Geser K Burk A D Børglum M T Pellecchia E Tolosa F del Sorbo C Nilsson O Bandmann M Sharma P Mayer M Gasteiger A Haworth T Ozawa A J Lees J Short P Giunti E Holinski-Feder T Illig H E Wichmann G K Wenning N W Wood T Gasser

The recent identification of fragile X-associated tremor ataxia syndrome (FXTAS) associated with premutations in the FMR1 gene and the possibility of clinical overlap with multiple system atrophy (MSA) has raised important questions, such as whether genetic testing for FXTAS should be performed routinely in MSA and whether positive cases might affect the specificity of current MSA diagnostic cr...

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...

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