نتایج جستجو برای: sporadic amyotrophic lateral sclerosis sals

تعداد نتایج: 198646  

Journal: :Annals of neurology 2010
Han-Xiang Deng Hong Zhai Eileen H Bigio Jianhua Yan Faisal Fecto Kaouther Ajroud Manjari Mishra Senda Ajroud-Driss Scott Heller Robert Sufit Nailah Siddique Enrico Mugnaini Teepu Siddique

OBJECTIVE Amyotrophic lateral sclerosis (ALS) is a fatal disorder of motor neuron degeneration. Most cases of ALS are sporadic (SALS), but about 5 to 10% of ALS cases are familial (FALS). Recent studies have shown that mutations in FUS are causal in approximately 4 to 5% of FALS and some apparent SALS cases. The pathogenic mechanism of the mutant FUS-mediated ALS and potential roles of FUS in n...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1993

Journal: :Physiological genomics 2004
Fernando Dangond Daehee Hwang Sandra Camelo Piera Pasinelli Matthew P Frosch Gregory Stephanopoulos George Stephanopoulos Robert H Brown Steven R Gullans

Little is known about global gene expression patterns in the human neurodegenerative disease amyotrophic lateral sclerosis (ALS). To address this, we used high-density oligonucleotide microarray technology to compare expression levels of approximately 6,800 genes in postmortem spinal cord gray matter obtained from individuals with ALS as well as normal individuals. Using Fisher discriminant ana...

2013
Jin Hee Shin Jae Keun Lee

Amyotrophic lateral sclerosis (ALS) is an adult-onset neurological disorder with higher selectivity in the degeneration of the upper and lower motor neurons, which leads to progres‐ sive paralysis of voluntary muscles. Although most cases fall under sporadic ALS (sALS), 10% of cases are inherited and known as familial ALS (fALS). The etiology of most ALS cases remains unknown, but mutations of ...

2016
Myung-Jin Kim Jae-Han Bae Jeong-Min Kim Hye Ryoun Kim Byung-Nam Yoon Jung-Joon Sung Suk-Won Ahn

Amyotrophic lateral sclerosis (ALS), the most common adult onset motor neuron disease, is pathologically characterized by progressive loss of the upper and lower motor neurons. Mutations in the Cu/Zn superoxide dismutase gene (SOD1) account for about 20% of familial ALS cases and a small percentage of sporadic ALS (SALS) cases, and have revealed a validated genotype-phenotype correlation. Herei...

Journal: :medical journal of islamic republic of iran 0
mahmoud reza azarpazhooh department of neurology mashhad university of medical sciences, mashhadiran. address: no.380, sajad blvd, mashhad, iran.,سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) mohammad etemadi mashhad university of medical sciences.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) ebrahim poorakbar mashhad university of medical sciences.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) ali shoeibi mashhad university of medical sciences.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

abstract   background: amyotrophic lateral sclerosis (als) is a progressive neurological disorder with high mortality and morbidity. some risk factors have been implicated for als such as exposure to high magnetic fields, and trace elements like selenium, cadmium and lead. afew studies have been carried out throughout the world to evaluate the prevalence of als among veterans. this study was ai...

2017
Lianping Xu Danyang Tian Jiao Li Lu Chen Lu Tang Dongsheng Fan

Amyotrophic lateral sclerosis (ALS) is an ethnically heterogeneous motor neuron disease that results from the selective death of motor neurons in the brain and spinal cord. Brain-derived neurotrophic factor (BDNF) is widely distributed across the central and peripheral nervous systems and plays neurotrophic and other physiological roles in various brain regions. Alterations of neurotrophin avai...

2017
Giovanna Morello Antonio Gianmaria Spampinato Sebastiano Cavallaro

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease affecting the motor nervous system. Despite the mechanism underlying motor neuron death is not yet clarified, multiple pathogenic processes have been proposed to account for ALS. Among these, inflammatory/immune responses have recently gained particular interest, although there are conflicting reports on the role of these proces...

Journal: :Neurology 2012
Francesca L Conforti Rossella Spataro William Sproviero Rosalucia Mazzei Francesca Cavalcanti Francesca Condino Isabella L Simone Giancarlo Logroscino Alessandra Patitucci Angela Magariello Maria Muglia Carmelo Rodolico Paola Valentino Francesco Bono Tiziana Colletti Maria R Monsurrò Antonio Gambardella Vincenzo La Bella

OBJECTIVE Recent evidence suggests that intermediate-length polyglutamine (PolyQ) expansions in the ataxin-2 (ATXN-2) gene are a risk factor for amyotrophic lateral sclerosis (ALS). This work was undertaken with the aim to investigate the frequency of ataxin-1 (ATXN-1) and ATXN-2 PolyQ expansions in a cohort of patients with sporadic ALS (sALS) and patients with familial ALS (fALS) from souther...

Journal: :Journal of neuropathology and experimental neurology 2009
Yoshimi Kinoshita Hidefumi Ito Asao Hirano Kengo Fujita Reika Wate Masataka Nakamura Satoshi Kaneko Satoshi Nakano Hirofumi Kusaka

The nucleocytoplasmic transport system is essential for maintaining cell viability; transport of proteins and nucleic acids between the nucleus and the cytoplasm occurs through nuclear pore complexes (NPCs). In this study, we examined the immunohistochemical distribution of the major protein components of NPCs, Nup62, Nup88, and Nup153, in spinal cords from controls and patients with sporadic o...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید