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American Journal of Human Genetics|January 1, 1995
Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathyF Muntoni, M A Melis, A Ganau, et al.Gene Therapy|June 1, 2017
Therapeutic approaches for spinal muscular atrophy (SMA)M Scoto, R S Finkel, E Mercuri, et al.Journal of Child Neurology|November 1, 1995
Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophyZ Shorer, J Philpot, F Muntoni, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2002
Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapyV Dubowitz, M Kinali, M Main, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
Velocardiofacial syndrome associated with atrophy of the shoulder girdle muscles and cervicomedullary narrowingE Bolland, A Y Manzur, T M Milward, et al.Journal of the Neurological Sciences|December 1, 1993
Muscular weakness in the mdx mouseF Muntoni, A Mateddu, F Marchei, et al.Archives of Disease in Childhood|May 20, 1999
Feeding problems in merosin deficient congenital muscular dystrophyJ Philpot, A Bagnall, C King, et al.Neuromuscular Disorders : NMD|June 1, 1997
Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?J Taylor, F Muntoni, S Robb, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
Diaphragmatic spinal muscular atrophy with bulbar weaknessE Mercuri, F Goodwin, C Sewry, et al.Neuromuscular Disorders : NMD|January 5, 2000
Expression, regulation and localisation of dystrophin isoforms in human foetal skeletal and cardiac muscleS Torelli, A Ferlini, L Obici, et al.Pageof 166