Amyotrophic lateral sclerosis definition

Amyotrophic lateral sclerosis or “ALS” means a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord.
Amyotrophic lateral sclerosis or “ALS” means a progressive
Amyotrophic lateral sclerosis means muscular weakness and atrophy, evidence of anterior horn cell dysfunction, visible muscle fasciculation, spasticity, hyperactive deep tendon reflexes and extensor plantar reflexes, evidence of corticospinal tract involvement, dysarthria and dysphagia. The diagnosis must be made by a Specialist Medical Practitioner with appropriate neuromuscular testing such as electromyogram (EMG). The disease must result in significant physical impairment (as evidenced by the Insured’s permanent irreversible inability to perform independently at least three (3) of the Activities of Daily Living).

Examples of Amyotrophic lateral sclerosis in a sentence

  • Estimated Prevalence and Incidence of Amyotrophic Lateral Sclerosis and SOD1 and C9orf72 Genetic Variants.

  • Current activities include a partnership with the Gold Coast University Hospital in Queensland, Australia This trial is exploring the effects of cannabidiol (“CBD”) oil, using CannTrust’s proprietary strain of CBD-dominant Cannatonic, in slowing the progression of Amyotrophic Lateral Sclerosis (ALS) and Motor Neuron Disease (MND).

  • The Company is targeting major central nervous system diseases including: Ischemic Spastic Paraplegia, Traumatic Spinal Cord Injury, Huntington’s disease and Amyotrophic Lateral Sclerosis (ALS), often referred to as Lou Gehrig's disease.

  • In addition to providing a valuable addition to Voyager’s intellectual property portfolio, the rights to use REGENX’s NAV vectors will position us to rapidly advance the development of breakthrough CNS gene therapies.” About Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis (ALS), also known as Xxx Xxxxxx’x disease, is a progressive, fatal neurodegenerative disease that leads to muscle weakness, loss of mobility, impaired speech, and difficulty breathing and swallowing.

  • June 2, 2014 – REGENX Biosciences, LLC and Voyager Therapeutics today announced that they have entered into a license agreement for use of REGENX’s proprietary NAV® vectors for the development and commercialization of gene therapies to treat Amyotrophic Lateral Sclerosis (ALS), Friedreich’s ataxia (FA) and Huntington’s disease (HD).

  • The validity of using a “responder analysis” and the level for which endpoint scores would be considered clinically meaningful in ALS patients was explored in a survey of 65 clinicians published in Amyotrophic Lateral Sclerosis in 2010.

  • Xxxxxxxx TITLE: Chief Executive Officer TITLE: EVP, Chief Business Officer & General Counsel Confidential SCHEDULE 1.28 Amyotrophic Lateral Sclerosis, Traumatic Brain Injury, Multiple Sclerosis, Huntington’s Disease, Epilepsy, Duchenne Muscular Dystrophy, Alzheimer’s Disease, Xxxxxxxxx’x Disease and Stroke SCHEDULE 1.49 KARYOPHARM THIRD PARTY AGREEMENTS [**] Research Agreement, made as of the 18th day of July, 2011, by and between The Multiple Myeloma Research Foundation, Inc.

  • Clinical significance in the change of decline in ALSFRS-R, Amyotrophic Lateral Sclerosis.

  • Flex Pharma Development Path ANTICIPATED TIMELINE FLX-787 Single agent TRP activator Nocturnal Leg Cramps (NLC) Multiple Sclerosis (MS) Amyotrophic Lateral Sclerosis (ALS) Phase 2B^ Human POC* Phase 3 Program Phase 2 Australia Phase 2 Australia All Studies are randomized, controlled, blinded *Study conducted under dietary supplement guidelines.

  • By harnessing advances in disease biology understanding, translational tools, and innovative modalities, Takeda is primarily focusing on rare neurology (e.g., narcolepsy, Amyotrophic Lateral Sclerosis, Huntington’s disease and other ataxias), as well as making targeted investments to potentially address well-defined segments of neurodegenerative diseases (e.g., Parkinson’s Disease).


More Definitions of Amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis means amyotrophic lateral sclerosis (ALS), as broadly defined, to include patients with mixed upper motor neuron (UMN) and lower motor neuron (LMN) pathology (classic ALS), primarily LMN disease (LMN-predominant ALS and progressive muscular atrophy) and primarily UMN disease (UMN-predominant ALS and primary lateral sclerosis).
Amyotrophic lateral sclerosis means unequivocal diagnosis by a consultant neurologist confirming well defined neurological deficit with persistent signs of involvement of the spinal nerve columns and the motor centers in the brain and with specific weakness and atrophy of the muscles of the extremities.

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