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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease: Masterclass Event Summary
8
Mins
March 2024
A masterclass initiated, organised, and funded by UCB, sought to advance understanding and expertise of myelin oligodendrocyte…
Read more
8
Mins
2nd February 2017
New Developments for Parkinson’s Therapy with COMT Inhibitors
Parkinson’s disease (PD) is a long-term degenerative disorder of the central nervous system that mainly affects the motor system. There are currently…
13th December 2016
Clinical Management of Drug-Induced Dyskinesia in Parkinson’s Disease: Why Current Approaches May Need to Be Changed to Optimise Quality of Life
Parkinson’s disease is a complex, progressive neurodegenerative disorder associated with both motor and non-motor symptoms. Current treatment strategies…
3
Mins
22nd November 2016
Delaying School Start Times to Boost Adolescent Academic Performance
Sleep is becoming an increasingly scarce commodity, especially among adolescents. For a teenager to perform at maximum cognitive levels, sleep…
3
Mins
12th July 2016
A Call from a Patient to Openly Discuss Body Image in the Treatment of Type 1 Diabetes
Diabetes is a non-communicable disease (NCD) meaning that it often cannot be seen. After 20 years of living with Type 1 diabetes I am lucky to have no…
12th July 2016
Brain Health: Translating Scientific Evidence Into Clinical Practice in Multiple Sclerosis
Brain volume loss (BVL) progresses more rapidly in patients with multiple sclerosis (MS) than in healthy individuals, and brain atrophy begins early in…
12th July 2016
Editor’s Pick: Clinical Significance of Apathy in Parkinson’s Disease
Apathy, or lack of motivation, is increasingly recognised as a major factor affecting quality of life and prognosis in Parkinson’s disease (PD)…
12th July 2016
Development and Translation of Therapies for Spinal Muscular Atrophy
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterised by widespread loss of lower motor neurons from the spinal…
12th July 2016
Wilson’s Disease: An Inherited, Silent, Copper Intoxication Disease
Wilson’s disease is a rare, autosomal recessive, genetic, copper overload disease, which evokes multiple motor or neuropsychiatric symptoms and liver…
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