نتایج جستجو برای: msa

تعداد نتایج: 2638  

2013
David S. Tourigny Israel S. Fernández Ann C. Kelley Ramkrishna Reddy Vakiti Amit Kumar Chattopadhyay Stéphane Dorich Stephen Hanessian V. Ramakrishnan

Biosynthetically and chemically derived analogs of the antibiotic pactamycin and de-6-methylsalicylyl (MSA)-pactamycin have attracted recent interest as potential antiprotozoal and antitumor drugs. Here, we report a 3.1-Å crystal structure of de-6-MSA-pactamycin bound to its target site on the Thermus thermophilus 30S ribosomal subunit. Although de-6-MSA-pactamycin lacks the MSA moiety, it shar...

Journal: :Bioinformation 2008

2014
Yasmine T Asi Julie E Simpson Paul R Heath Stephen B Wharton Andrew J Lees Tamas Revesz Henry Houlden Janice L Holton

Multiple system atrophy (MSA) is a progressive neurodegenerative disease presenting clinically with parkinsonian, cerebellar, and autonomic features. α-Synuclein (αsyn), encoded by the gene SNCA, is the main constituent of glial cytoplasmic inclusion (GCI) found in oligodendrocytes in MSA, but the methods of its accumulation have not been established. The aim of this study is to investigate alt...

2017
Carlos Guevara Kateryna Bulatova Wendy Soruco Guido Gonzalez Gonzalo A. Farías

Objective: The absence of markers for ante-mortem diagnosis of idiopathic Parkinson's disease (IPD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP) results in these disorders being commonly mistaken for each other, particularly in the initial stages. We aimed to investigate annualized whole-brain atrophy rates (a-WBAR) in these disorders to aid in the diagnosis between ...

2013
Atsushi Umemura Tomoko Oeda Ryutaro Hayashi Satoshi Tomita Masayuki Kohsaka Kenji Yamamoto Hideyuki Sawada

BACKGROUND It is often hard to differentiate Parkinson's disease (PD) and parkinsonian variant of multiple system atrophy (MSA-P), especially in the early stages. Cardiac sympathetic denervation and putaminal rarefaction are specific findings for PD and MSA-P, respectively. PURPOSE We investigated diagnostic accuracy of putaminal apparent diffusion coefficient (ADC) test for MSA-P and (123)I-...

2012
Takayoshi Shimohata Hideaki Nakayama Masahiko Tomita Tetsutaro Ozawa Masatoyo Nishizawa

BACKGROUND The recent SLEEMSA study that evaluated excessive daytime sleepiness (EDS) in Caucasian patients with multiple system atrophy (MSA) demonstrated that EDS was more frequent in patients (28%) than in healthy subjects (2%). However, the prevalence and determinants of EDS in other ethnic populations have not been reported to date. METHODS We performed a single-hospital prospective stud...

2018
Violetta Refolo Francesco Bez Alexia Polissidis Daniela Kuzdas-Wood Edith Sturm Martina Kamaratou Werner Poewe Leonidas Stefanis M Angela Cenci Marina Romero-Ramos Gregor K Wenning Nadia Stefanova

Multiple system atrophy (MSA) is a rapidly progressive neurodegenerative disorder characterized by widespread oligodendroglial cytoplasmic inclusions of filamentous α-synuclein, and neuronal loss in autonomic centres, basal ganglia and cerebellar circuits. It has been suggested that primary oligodendroglial α-synucleinopathy may represent a trigger in the pathogenesis of MSA, but the mechanisms...

Journal: :AJNR. American journal of neuroradiology 2009
S Ito W Shirai T Hattori

BACKGROUND AND PURPOSE A hyperintense putaminal rim, putaminal hypointensity, and putaminal atrophy on T2-weighted MR images are findings suggestive of parkinsonian-dominant multiple system atrophy (MSA-P). However, putaminal hyperintensity on T1-weighted images, which has not been discussed in previous reports, is also frequently observed in patients with MSA-P. Here, we investigated whether p...

Journal: :PloS one 2016
Simon Schafferer Rimpi Khurana Violetta Refolo Serena Venezia Edith Sturm Paolo Piatti Clara Hechenberger Hubert Hackl Roman Kessler Michaela Willi Ronald Gstir Anne Krogsdam Alexandra Lusser Werner Poewe Gregor K Wenning Alexander Hüttenhofer Nadia Stefanova

Multiple system atrophy (MSA) is a fatal rapidly progressive α-synucleinopathy, characterized by α-synuclein accumulation in oligodendrocytes. It is accepted that the pathological α-synuclein accumulation in the brain of MSA patients plays a leading role in the disease process, but little is known about the events in the early stages of the disease. In this study we aimed to define potential ro...

2014
Yao Wang Wei-bo Shao Li Gao Jie Lu Hao Gu Li-hua Sun Yan Tan Ying-dong Zhang

BACKGROUND There have been limited comparative data regarding the investigations on pulmonary and respiratory muscle function in the patients with different parkinsonism disorders such as Parkinson's disease (PD) and multiple system atrophy (MSA) versus normal elderly. The present study is aiming to characterize the performance of pulmonary function and respiratory muscle strength in PD and MSA...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید