نتایج جستجو برای: als

تعداد نتایج: 27090  

Journal: :Neurology 2007
H Mitsumoto A M Ulug S L Pullman C L Gooch S Chan M-X Tang X Mao A P Hays A G Floyd V Battista J Montes S Hayes S Dashnaw P Kaufmann P H Gordon J Hirsch B Levin L P Rowland D C Shungu

OBJECTIVE To investigate the value of objective biomarkers for upper (UMN) and lower (LMN) motor neuron involvement in ALS. METHODS We prospectively studied 64 patients with ALS and its subsets using clinical measures, proton MR spectroscopic imaging ((1)H MRSI), diffusion tensor imaging, transcranial magnetic stimulation, and the motor unit number estimation (MUNE) at baseline and every 3 mo...

2012
Henny Nachmany Shane Wald Michal Abekasis Shlomo Bulvik Miguel Weil

Amyotrophic lateral sclerosis (ALS) is a fatal, neurodegenerative disorder caused by degeneration of motor neurons. The cause for most cases of ALS is multi-factorial,this enhances the need to characterize and isolate specific biomarkers found in biological samples from ALS patients. To this end we use human mesenchymal stem cells (hMSC) derived from the bone marrow of six ALS patients (ALS hMS...

2017
Da-Wei Li Mingsheng Liu Bo Cui Jia Fang Yu-Zhou Guan Qingyun Ding Xiaoguang Li Liying Cui

OBJECTIVES The accurate and early diagnosis of amyotrophic lateral sclerosis (ALS) is important for extending the life expectancy of patients. However, previous studies that have assessed the diagnostic sensitivities of the Awaji criteria (AC) and the revised El Escorial criteria (rEEC) in patients with ALS have been inconsistent, most of them were consensual regarding the advantage of Awaji ov...

2017
Philip Van Damme Wim Robberecht Ludo Van Den Bosch

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that primarily affects the motor system and presents with progressive muscle weakness. Most patients survive for only 2-5 years after disease onset, often due to failure of the respiratory muscles. ALS is a familial disease in ∼10% of patients, with the remaining 90% developing sporadic ALS. Over the past decade, major advances...

Journal: :trauma monthly 0
mehrdad hosseinpour trauma research center, kashan university of medical sciences, kashan, ir iran mahdi mohammadzadeh trauma research center, kashan university of medical sciences, kashan, ir iran mohammad paravar trauma research center, kashan university of medical sciences, kashan, ir iran azadeh sadat mirzadeh trauma research center, kashan university of medical sciences, kashan, ir iran

introduction this study determines the effect of prehospital time and advanced trauma life support interventions for trauma patients transported to an our trauma center. materials and methods this study was a retrospective study of trauma victims presenting to a trauma center in central iran by emergency medical services (ems) and hospitalized for more than 24 hours. demographic and injury char...

Journal: :Pest management science 2012
Heping Han Qin Yu Edison Purba Mei Li Michael Walsh Shane Friesen Stephen B Powles

BACKGROUND Wild radish, a problem weed worldwide, is a severe dicotyledonous weed in crops. In Australia, sustained reliance on ALS-inhibiting herbicides to control this species has led to the evolution of many resistant populations endowed by any of several ALS mutations. The molecular basis of ALS-inhibiting herbicide resistance in a novel resistant population was studied. RESULTS ALS gene ...

2016
Delphine Lefeuvre Marie-Christine Delmas Christophe Marguet Pierre Chauvin Stéphanie Vandentorren

INTRODUCTION Asthma remains poorly studied in homeless children. We sought to estimate the prevalence of asthma-like symptoms (ALS) and to identify the factors associated with ALS and healthcare service utilisation. MATERIALS AND METHODS A cross-sectional survey of a random sample of sheltered homeless families was conducted by interviewing 801 parents of children (0-12 years) in 17 languages...

2018
Jan Kassubek Hans-Peter Müller Kelly Del Tredici Dorothée Lulé Martin Gorges Heiko Braak Albert C Ludolph

OBJECTIVE Neuropathological studies in amyotrophic lateral sclerosis (ALS) have shown a dissemination in a regional sequence in four anatomically defined patterns. The aim of this retrospective study was to see whether longitudinal diffusion tensor imaging (DTI) data support the pathological findings. METHODS The application of DTI analysis to fibre structures that are prone to be involved at...

2015
Caroline Seer Stefanie Fürkötter Maj-Britt Vogts Florian Lange Susanne Abdulla Reinhard Dengler Susanne Petri Bruno Kopp

A growing body of evidence implies psychological disturbances in amyotrophic lateral sclerosis (ALS). Specifically, executive dysfunctions occur in up to 50% of ALS patients. The recently shown presence of cytoplasmic aggregates (TDP-43) in ALS patients and in patients with behavioral variants of frontotemporal dementia suggests that these two disease entities form the extremes of a spectrum. T...

2012
Ryu Katsumata Shinsuke Ishigaki Masahisa Katsuno Kaori Kawai Jun Sone Zhe Huang Hiroaki Adachi Fumiaki Tanaka Fumihiko Urano Gen Sobue

BACKGROUND Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive death of motor neurons. Although the pathogenesis of ALS remains unclear, several cellular processes are known to be involved, including apoptosis. A previous study revealed the apoptosis-related gene c-Abl to be upregulated in sporadic ALS motor neurons. METHODOLOGY/FINDINGS We in...

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