David Hutchinson

Congenital myasthenic syndrome caused by prolonged acetylcholine receptor channel openings due to a mutation in the M2 domain of the epsilon subunit.

Kinji Ohno, David Hutchinson, Margherita Milone et al. · Proceedings of the National Academy of Sciences · 1995 · 259 citations

Life Sciences, Genetics, Molecular Genetics +17

Congential Endplate acetylocholinesterase deficiency

David Hutchinson, Timothy J. Walls, Satoshi Nakano et al. · Brain · 1993 · 120 citations

Medicine, Neurology, Neuroscience +12

Autonomic dysfunction is a major feature of cerebellar ataxia, neuropathy, vestibular areflexia 'CANVAS' syndrome

Teddy Y. Wu, Jennifer M. Taylor, Dean H. Kilfoyle et al. · Brain · 2014 · 88 citations · Full text

Medicine, Neurology, Neuroscience +16

Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: Clinical and pathological variability within a kindred

David Hutchinson, Amanda Charlton, Nigel G. Laing et al. · Neuromuscular Disorders · 2006 · 55 citations

Medicine, Genetics, Molecular Genetics +14

Implantation of the Freehand System® during initial rehabilitation using minimally invasive techniques

M.J. Mulcahey, Randal R. Betz, Scott H. Kozin et al. · Spinal Cord · 2004 · 54 citations

Medicine, Rehabilitation Medicine, Surgery +8