Results 71 to 80 of about 148,501 (250)

Lipids, apolipoproteins, and prognosis of amyotrophic lateral sclerosis

Neurology, 2020
Objective To determine whether lipids and apolipoproteins predict prognosis of patients with amyotrophic lateral sclerosis in a cohort study of 99 patients with amyotrophic lateral sclerosis who were diagnosed during 2015 to 2018 and followed up until ...
C. Ingre, Lin Chen, Y. Zhan, Jet D Termorshuizen, L. Yin, F. Fang   +5 more
semanticscholar   +1 more source

A Case of Amiotrophic Lateral Sclerosis Presenting with Daytime Excessive Sleepiness

Türk Uyku Tıbbı Dergisi, 2019
Amyotrophic lateral sclerosis is a neurodegenerative disease with progressive motor neuron degeneration in primary motor cortex, corticospinal pathways, brain stem and spinal cord.
Turgay Demir, Kezban Aslan, Mehmet Balal, Şebnem Bıçakcı   +3 more
doaj   +1 more source

Leukocyte-derived microparticles and scanning electron microscopic structures in two fractions of fresh cerebrospinal fluid in amyotrophic lateral sclerosis: a case report

Journal of Medical Case Reports, 2012
Introduction Amyotrophic lateral sclerosis is a progressive neurodegenerative disorder characterized by degeneration of motoneuron cells in anterior spinal horns. There is a need for early and accurate diagnosis with this condition.
Zachau Anne C, Landén Mikael, Mobarrez Fariborz, Nybom Rolf, Wallén Håkan, Wetterberg Lennart   +5 more
doaj   +1 more source

Increased in vivo glial activation in patients with amyotrophic lateral sclerosis: Assessed with [11C]-PBR28

NeuroImage: Clinical, 2015
Evidence from human post mortem, in vivo and animal model studies implicates the neuroimmune system and activated microglia in the pathology of amyotrophic lateral sclerosis.
Nicole R. Zürcher, Marco L. Loggia, Robert Lawson, Daniel B. Chonde, David Izquierdo-Garcia, Julia E. Yasek, Oluwaseun Akeju, Ciprian Catana, Bruce R. Rosen, Merit E. Cudkowicz, Jacob M. Hooker, Nazem Atassi   +11 more
doaj   +1 more source

RNA Dysregulation in Amyotrophic Lateral Sclerosis

Frontiers in Genetics, 2019
Amyotrophic lateral sclerosis (ALS) is the most common adult-onset motor neuron disease and is characterized by the degeneration of upper and lower motor neurons.
Zoé Butti, S. A. Patten
semanticscholar   +1 more source

Progressive brainstem pathology in motor neuron diseases: Imaging data from amyotrophic lateral sclerosis and primary lateral sclerosis

Data in Brief, 2020
A standardised, single-centre, longitudinal imaging protocol was used to evaluate longitudinal brainstem alterations in 100 patients with amyotrophic lateral sclerosis (ALS) with reference to 33 patients with primary lateral sclerosis (PLS), 30 patients ...
Peter Bede, Rangariroyashe H. Chipika, Eoin Finegan, Stacey Li Hi Shing, Kai Ming Chang, Mark A. Doherty, Jennifer C. Hengeveld, Alice Vajda, Siobhan Hutchinson, Colette Donaghy, Russell L. McLaughlin, Orla Hardiman   +11 more
doaj  

Etiogenic factors present in the cerebrospinal fluid from amyotrophic lateral sclerosis patients induce predominantly pro-inflammatory responses in microglia

Journal of Neuroinflammation, 2017
Background Microglial cell-associated neuroinflammation is considered as a potential contributor to the pathophysiology of sporadic amyotrophic lateral sclerosis.
Pooja-Shree Mishra, K. Vijayalakshmi, A. Nalini, T. N. Sathyaprabha, B. W. Kramer, Phalguni Anand Alladi, T. R. Raju   +6 more
doaj   +1 more source

INCIPIENT AMYOTROPHIC LATERAL SCLEROSIS, WITH RECOVERY. [PDF]

, 1902
LEO M. CRAFTS
openalex   +1 more source

INFANTILE AMYOTROPHIC LATERAL SCLEROSIS OF THE FAMILY TYPE [PDF]

, 1894
C. Brown
openalex   +1 more source

The reunification of amyotrophic lateral sclerosis [PDF]

Journal of Neurology, Neurosurgery & Psychiatry, 2018
Historically characterised as a neuromuscular disease involving progressive loss of both central and peripheral motor neurons, amyotrophic lateral sclerosis (ALS) now sits among the cerebral neurodegenerative syndromes, involving clinical, pathological and genetic overlap with frontotemporal dementia (FTD).
openaire   +2 more sources