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Biological Trace Element Research|July 8, 2010
Reversible hypomagnesaemia-induced subacute cerebellar syndromeSaam Sedehizadeh, Michael Keogh, Adrian J WillsThe Cochrane Database of Systematic Reviews|February 18, 2011
Treatment for Lambert-Eaton myasthenic syndromeMichael Keogh, Saam Sedehizadeh, Paul MaddisonClinical Neuropharmacology|July 19, 2012
The use of aminopyridines in neurological disordersSaam Sedehizadeh, Michael Keogh, Paul MaddisonBMJ Case Reports|June 28, 2012
Horner's syndrome with an ipsilateral X nerve palsy following presumed shinglesSaam Sedehizadeh, John BowenNeuromuscular Disorders : NMD|January 14, 2017
Body composition and clinical outcome measures in patients with myotonic dystrophy type 1Saam Sedehizadeh, J David Brook, Paul MaddisonInternational Journal of Molecular Sciences|September 11, 2019
An Overview of Circular RNAs and Their Implications in Myotonic DystrophyKarol Czubak, Saam Sedehizadeh, Piotr Kozlowski, et al.Human Genetics|December 15, 2021
Differential fates of introns in gene expression due to global alternative splicingAnjani Kumari, Saam Sedehizadeh, John David Brook, et al.Journal of Neurology|July 30, 2024
Pre-thymectomy disease severity predicts outcome in acetylcholine receptor antibody-positive generalised myasthenia gravisAthanasios Papathanasiou, Chris R Tench, Philip A Ambrose, et al.The Lancet. Neurology|March 22, 2005
Assessment of professional development of neurology trainees: a UK perspectiveAdrian J WillsPageof 3