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Pediatric Rehabilitation|November 23, 2006
UK physicians' attitudes and practices in long-term non-invasive ventilation of Duchenne Muscular DystrophyM Kinali, A Y Manzur, E Mercuri, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
An unusual case of hyperekplexiaH Jungbluth, M I Rees, A Y Manzur, et al.Neuropediatrics|February 1, 1991
Acute onset spinal muscular atrophy in siblingsS A Robb, M A McShane, J Wilson, et al.Developmental Medicine and Child Neurology|October 1, 1992
Does computed tomography have a role in the evaluation of complicated acute bacterial meningitis in childhood?R S Heyderman, S A Robb, B E Kendall, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 7, 2015
The value of cardiac MRI versus echocardiography in the pre-operative assessment of patients with Duchenne muscular dystrophyA Brunklaus, E Parish, F Muntoni, et al.Journal of Neuromuscular Diseases|November 19, 2016
A Large Deletion Affecting TPM3, Causing Severe Nemaline MyopathyK Kiiski, V-L Lehtokari, A Y Manzur, et al.Clinical and Experimental Dermatology|October 1, 2013
Homozygous variegate porphyria presenting with developmental and language delay in childhoodV A E Pinder, S T Holden, C Deshpande, et al.Neuromuscular Disorders : NMD|September 8, 2004
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic AtaxiaM Kinali, H Jungbluth, L H Eunson, et al.Annals of Neurology|September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nucleiJ M Wilmshurst, S Lillis, H Zhou, et al.Pageof 275