Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS
Turner, M R, Osei-Lah, A D, Hammers, A, Al-Chalabi, A, Shaw, C E, Andersen, P M, Brooks, D J, Leigh, P N, Mills, K R
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2005)
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2005)
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Journal Article
Association of mu-opioid receptor subunit gene and idiopathic generalized epilepsy
Wilkie, H, Osei-Lah, A, Chioza, B, Nashef, L, McCormick, D, Asherson, P, Makoff, A J
Published in Neurology (10.09.2002)
Published in Neurology (10.09.2002)
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Journal Article
Something for the weak-end? Electromyography appearances of myasthenia gravis
Britton, F, Osei-Lah, A, Tighe, MP
Published in Archives of disease in childhood. Education and practice edition (01.04.2018)
Published in Archives of disease in childhood. Education and practice edition (01.04.2018)
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Journal Article
Central motor conduction abnormalities in D90A homozygous familial amyotrophic lateral sclerosis
Osei-Lah, A, Turner, M, Leigh, N, Anderson, P, Mills, K.R
Published in Clinical neurophysiology (01.05.2007)
Published in Clinical neurophysiology (01.05.2007)
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Journal Article
P02.14 Sreda in children – A report of two cases
Osei-Lah, A., Ponnusamy, A., Muthinji, P., Brunnhuber, F.
Published in Clinical neurophysiology (01.09.2006)
Published in Clinical neurophysiology (01.09.2006)
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Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy
Chioza, Barry, Osei-Lah, Abena, Nashef, Lina, Suarez-Merino, Blanca, Wilkie, Hazel, Sham, Pak, Knight, Jo, Asherson, Philip, Makoff, Andrew J
Published in European journal of human genetics : EJHG (01.12.2002)
Published in European journal of human genetics : EJHG (01.12.2002)
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