Results 301 to 310 of about 293,569 (356)

A Case of Facial-Onset Sensory Motor Neuronopathy - A Rare Variant of Motor Neuron Disease. [PDF]

open access: yesAnn Indian Acad Neurol
Kumar SP   +8 more
europepmc   +1 more source

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

open access: yes
Cox D   +9 more
europepmc   +1 more source

Systematic Living Evidence for Clinical Trials (SyLECT): a data-driven framework for drug selection in clinical trials in motor neuron disease

open access: yes
Wong C   +15 more
europepmc   +1 more source

Motor neurone disease

BMJ, 2014
A 59 year old man initially presented with weakness in his right leg and occasional trips. He had a longstanding history of mild low back pain and had a magnetic resonance image performed under the orthopaedic team that showed some cervical spondylolisthesis sparing the spinal cord.
Saiji, Nageshwaran   +3 more
openaire   +2 more sources

Conjugal motor neuron disease

Neurology, 1982
We describe a husband and wife with motor neuron disease. The woman had been ill for 10 years with predominantly upper motor neuron signs when her husband developed progressive muscular atrophy. This is the first known report of sporadic motor neuron disease occurring in both partners of a marriage.
D, Chad   +5 more
openaire   +2 more sources

Motor neurone disease

Nursing Standard, 2016
Essential facts Motor neurone disease describes a group of related diseases, affecting the neurones in the brain and spinal cord. Progressive, incurable and life-limiting, MND is rare, with about 1,100 people developing it each year in the UK and up to 5,000 people affected at any one time.
openaire   +2 more sources

Reversible Motor Neuron Disease

European Neurology, 1993
We investigated a 69-year-old male with a clinical syndrome resembling amyotrophic lateral sclerosis characterized by fasciculation, wasting of the limb muscles and increased deep tendon reflexes in the lower limbs. Electromyographic (EMG) studies showed abundant positive sharp waves and fibrillation potentials with decreased recruitment in the limbs ...
C P, Tsai   +6 more
openaire   +2 more sources

“A” motor neuron disease

Journal of the Neurological Sciences, 2014
Allgrove syndrome is a rare autosomal recessive disorder characterised by achalasia, alacrima, adrenal insufficiency, autonomic dysfunction and amyotrophy. The syndrome has been described in childhood and adult presentation, as in our case, is very rare.
Venugopalan Y, Vishnu   +4 more
openaire   +2 more sources

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