Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Multidisciplinary care, symptom management, and cognitive/behavioral …
RG Miller, CE Jackson, EJ Kasarskis, JD England… - Neurology, 2009 - AAN Enterprises
Objective: To systematically review evidence bearing on the management of patients with
amyotrophic lateral sclerosis (ALS). Methods: The authors analyzed studies from 1998 to …
amyotrophic lateral sclerosis (ALS). Methods: The authors analyzed studies from 1998 to …
Amyotrophic lateral sclerosis
JD Mitchell, GD Borasio - The lancet, 2007 - thelancet.com
Amyotrophic lateral sclerosis (known in the UK as motor neuron disease) is a devastating
illness with uncertain pathogenesis. In this Seminar, we review its natural history, clinical …
illness with uncertain pathogenesis. In this Seminar, we review its natural history, clinical …
Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial
PH Gordon, DH Moore, RG Miller, JM Florence… - The Lancet …, 2007 - thelancet.com
Background Minocycline has anti-apoptotic and anti-inflammatory effects in vitro, and
extends survival in mouse models of some neurological conditions. Several trials are …
extends survival in mouse models of some neurological conditions. Several trials are …
Comprehensive research on past and future therapeutic strategies devoted to treatment of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a rapidly debilitating fatal neurodegenerative disorder,
causing muscle atrophy and weakness, which leads to paralysis and eventual death. ALS …
causing muscle atrophy and weakness, which leads to paralysis and eventual death. ALS …
Inflammatory processes in amyotrophic lateral sclerosis
PL McGeer, EG McGeer - Muscle & Nerve: Official Journal of …, 2002 - Wiley Online Library
Neuroinflammation is a characteristic of pathologically affected tissue in several
neurodegenerative disorders. These changes can be observed in the brainstem and spinal …
neurodegenerative disorders. These changes can be observed in the brainstem and spinal …
Pain in amyotrophic lateral sclerosis
Pain is a largely neglected symptom in patients with amyotrophic lateral sclerosis (ALS)
although it is reported by most of these patients. It occurs at all stages of the disease and can …
although it is reported by most of these patients. It occurs at all stages of the disease and can …
ALSFRS-R score and its ratio: a useful predictor for ALS-progression
K Kollewe, U Mauss, K Krampfl, S Petri… - Journal of the …, 2008 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder. To
determine predictors of survival, we studied different parameters in our ALS Database …
determine predictors of survival, we studied different parameters in our ALS Database …
The glutamate hypothesis in ALS: pathophysiology and drug development
H Blasco, S Mavel, P Corcia… - Current medicinal …, 2014 - ingentaconnect.com
Amyotrophic lateral sclerosis (ALS) is an age-related neurodegenerative disorder that is
believed to have complex genetic and environmental influences in the pathogenesis, but …
believed to have complex genetic and environmental influences in the pathogenesis, but …
A clinical trial of creatine in ALS
Background: Mitochondrial dysfunction occurs early in the course of ALS, and the
mitochondria may be an important site for therapeutic intervention. Creatine stabilizes the …
mitochondria may be an important site for therapeutic intervention. Creatine stabilizes the …
The ALSFRSr predicts survival time in an ALS clinic population
P Kaufmann, G Levy, JLP Thompson, ML Delbene… - Neurology, 2005 - AAN Enterprises
Objective: To determine whether the Amyotrophic Lateral Sclerosis Functional Rating Scale–
revised (ALSFRSr), a predictor of survival time in ALS clinical trials, predicts survival time in …
revised (ALSFRSr), a predictor of survival time in ALS clinical trials, predicts survival time in …