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Neuromuscular Disorders : NMD|December 1, 1996
Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophyE Mercuri, J Pennock, F Goodwin, et al.
Neurology|March 1, 1993
HLA-DQA1 and -DQB1 associations with multiple sclerosis in Sardinia and French Canada: evidence for immunogenetically distinct patient groupsD G Haegert, F Muntoni, M R Murru, et al.
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.
Neuromuscular Disorders : NMD|March 1, 2025
Mortality of symptomatic children with spinal muscular atrophy in the era of disease-modifying therapiesR Finnegan, A M Rohwer, M Scoto, et al.
American Journal of Medical Genetics|April 1, 1992
X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-XpterC Cianchetti, F Muntoni, A M Falchi, et al.
Developmental Medicine and Child Neurology|January 1, 1993
Diagnosis of DMD carrier status in a family with no known affected malesF Muntoni, A Mateddu, M Cau, et al.
Neuropathology and Applied Neurobiology|December 17, 2009
Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expressionV Arechavala-Gomeza, M Kinali, L Feng, et al.
Archives of Disease in Childhood|October 16, 1999
Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1AE Mercuri, J Poulton, J Buck, et al.
Neuromuscular Disorders : NMD|December 14, 2011
X-linked myotubular myopathy due to a complex rearrangement involving a duplication of MTM1 exon 10N Trump, T Cullup, J B G M Verheij, et al.
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