Results 261 to 270 of about 164,738 (314)

Human Mutant Dynactin Subunit 1 Causes Profound Motor Neuron Disease Consistent with Possible Mechanisms Involving Axonopathy, Mitochondriopathy, Protein Nitration, and T-Cell-Mediated Cytolysis. [PDF]

Biomolecules
Xie V, Franco MC, Martin LJ.
europepmc   +1 more source

Global burden of motor neuron disease: unraveling socioeconomic disparities, aging dynamics, and divergent future trajectories (1990-2040). [PDF]

J Neurol
Liu K, Zhang K, Hu A, Li Y, Qin H, Sun W, Li X, Chen F, Liu T.   +8 more
europepmc   +1 more source

An Evaluation of the United Kingdom Motor Neuron Disease Nurses and Allied Health Professionals (UK MND NAHP) Workforce: A Census. [PDF]

PLoS One
Chau I, Stoker E, Gill J, Newton J, United Kingdom Motor Neuron Disease Nurses and Allied Health Professionals Consortium.   +4 more
europepmc   +1 more source

Mapping the Evidence for Measuring Energy Expenditure and Indicating Hypermetabolism in Motor Neuron Disease: A Scoping Review. [PDF]

Nutr Rev
Roscoe SA, Allen SP, McDermott CJ, Stavroulakis T.   +3 more
europepmc   +1 more source

Determinants and progression of stigma in amyotrophic lateral sclerosis/motor neuron disease. [PDF]

Amyotroph Lateral Scler Frontotemporal Degener
Young CA, Chaouch A, Mcdermott CJ, Al-Chalabi A, Chhetri SK, Bidder C, Edmonds E, Ellis C, Annadale J, Wilde L, Sharrack B, Malaspina A, Leach O, Mills R, Tennant A.   +14 more
europepmc   +1 more source

Identification of passive wrist-worn accelerometry outcomes for improved disease monitoring and trial design in motor neuron disease. [PDF]

EBioMedicine
Holdom CJ, Pilkar R, Guo CC, Eijk RPAV, Sethi N, Henderson RD, Ngo ST, Steyn FJ.   +7 more
europepmc   +1 more source

Fingerprinting disease-derived protein aggregates reveals unique signature of Motor Neuron Disease

Cox D, Burke M, Milani S, White MA, Waldron FM, Böken D, Lobanova E, Sreedharan J, Gregory JM, Klenerman D.   +9 more
europepmc   +1 more source

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Motor Neuron Disease

The Neurologist, 2009
In order to evaluate the prognosis and possible prognostic factors associated with a bening course, 118 cases of motor neuron disease diagnosed 1948-1975 were followed up. Survival curves, based on the actuarial method showed a survival rate of 18.7 per cent (95 per cent confidence limits: 11.4-26.0) and 7.6 per cent (95 per cent confidence limits: 2.7-
O, Kristensen, B, Melgaard
openaire   +4 more sources

Motor Neuron Disease

Physical Medicine and Rehabilitation Clinics of North America, 2001
Motor neuron disease refers to a spectrum of disorders resulting from degeneration of the upper or lower motor neurons or both. Amyotrophic lateral sclerosis is the most common form of motor neuron disease, in which patients demonstrate evidence of both anterior horn cell (lower motor neuron) and corticospinal tract (upper motor neuron) dysfunction ...
C E, Jackson, J, Rosenfeld
openaire   +2 more sources