نتایج جستجو برای: amyotrophic lateral sclerosis

تعداد نتایج: 178098  

Journal: :Brain : a journal of neurology 2015
Pinar Mesci Sakina Zaïdi Christian S Lobsiger Stéphanie Millecamps Carole Escartin Danielle Seilhean Hideyo Sato Michel Mallat Séverine Boillée

Amyotrophic lateral sclerosis is the most common adult-onset motor neuron disease and evidence from mice expressing amyotrophic lateral sclerosis-causing SOD1 mutations suggest that neurodegeneration is a non-cell autonomous process where microglial cells influence disease progression. However, microglial-derived neurotoxic factors still remain largely unidentified in amyotrophic lateral sclero...

2011
Sarah Knippenberg Thomas Brinker Stephan Steinlechner Albert Ludolph

Studies on the therapeutic potential of adult stem cells in the G93A animal model of amyotrophic lateral sclerosis (ALS) Dissertation Submitted in partial fulfillment of the requirements for the degree Significance of behavioural tests in a transgenic mouse model of amyotrophic lateral sclerosis (ALS). Behav Brain Res 213:82-87. Intraspinal injection of human umbilical cord blood-derived cells ...

Journal: :Journal of rehabilitation medicine 2007
Annet J Dallmeijer Vincent de Groot Leo D Roorda Vera P M Schepers Eline Lindeman Leonard H van den Berg Anita Beelen Joost Dekker

OBJECTIVE The aim of this study was to investigate unidimensionality and differential item functioning of the SF-36 physical functioning scale (PF10) in patients with various neurological disorders. PATIENTS PATIENTS post-stroke (n = 198), with multiple sclerosis (n = 151) and amyotrophic lateral sclerosis (n = 193) participated. METHODS Unidimensionality of the PF10 within the patient grou...

2011
Alexander Venizelos Youngsook Park Morris A Fisher

INTRODUCTION Amyotrophic lateral sclerosis is a rapidly progressive, fatal neurodegenerative disorder for which there is no effective treatment. The diagnosis is dependent on the clinical presentation and consistent electrodiagnostic studies. Typically, there is a combination of upper and lower motor neuron signs as well as electrodiagnostic studies indicative of diffuse motor axonal injury. Th...

Journal: :Journal of medical genetics 2004
A L Nishimura M Mitne-Neto H C A Silva J R M Oliveira M Vainzof M Zatz

M otor neurone disease includes a heterogeneous group of disorders with motor neurone involvement, such as amyotrophic lateral sclerosis, progressive muscular atrophy, progressive bulbar palsy, and primary lateral sclerosis. Amyotrophic lateral sclerosis is the most common adult onset form of motor neurone disease and involves the lower and upper motor neurones. It is characterised by progressi...

2004
A L Nishimura M Mitne-Neto H C A Silva J R M Oliveira M Vainzof M Zatz

M otor neurone disease includes a heterogeneous group of disorders with motor neurone involvement, such as amyotrophic lateral sclerosis, progressive muscular atrophy, progressive bulbar palsy, and primary lateral sclerosis. Amyotrophic lateral sclerosis is the most common adult onset form of motor neurone disease and involves the lower and upper motor neurones. It is characterised by progressi...

Journal: :Open access Journal of Neurology & Neurosurgery 2017

Journal: :Brain : a journal of neurology 2016
Pauline Vercruysse Jérôme Sinniger Hajer El Oussini Jelena Scekic-Zahirovic Stéphane Dieterlé Reinhard Dengler Thomas Meyer Stephan Zierz Jan Kassubek Wilhelm Fischer Jens Dreyhaupt Torsten Grehl Andreas Hermann Julian Grosskreutz Anke Witting Ludo Van Den Bosch Odile Spreux-Varoquaux Albert C Ludolph Luc Dupuis

Amyotrophic lateral sclerosis, the most common adult-onset motor neuron disease, leads to death within 3 to 5 years after onset. Beyond progressive motor impairment, patients with amyotrophic lateral sclerosis suffer from major defects in energy metabolism, such as weight loss, which are well correlated with survival. Indeed, nutritional intervention targeting weight loss might improve survival...

Journal: :Brain : a journal of neurology 2011
Vivek Swarup Daniel Phaneuf Christine Bareil Janice Robertson Guy A Rouleau Jasna Kriz Jean-Pierre Julien

Transactive response DNA-binding protein 43 ubiquitinated inclusions are a hallmark of amyotrophic lateral sclerosis and of frontotemporal lobar degeneration with ubiquitin-positive inclusions. Yet, mutations in TARDBP, the gene encoding these inclusions are associated with only 3% of sporadic and familial amyotrophic lateral sclerosis. Recent transgenic mouse studies have revealed a high degre...

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