Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C geneMERCURI, E; BROWN, S. C; MCKENNA, W et al.Muscle & nerve. 2005, Vol 31, Num 5, pp 602-609, issn 0148-639X, 8 p.Article

Update on the management of Duchenne muscular dystrophyMANZUR, A. Y; KINALI, M; MUNTONI, F et al.Archives of disease in childhood. 2008, Vol 93, Num 11, pp 986-990, issn 0003-9888, 5 p.Article

Muscle histology vs MRI in Duchenne muscular dystrophyKINALI, M; ARECHAVALA-GOMEZA, V; QUINLIVAN, R. M et al.Neurology. 2011, Vol 76, Num 4, pp 346-353, issn 0028-3878, 8 p.Article

Bone mineral density in a paediatric spinal muscular atrophy populationKINALI, M; BANKS, L. M; MERCURI, E et al.Neuropediatrics. 2004, Vol 35, Num 6, pp 325-328, issn 0174-304X, 4 p.Article

Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophyMERCURI, E; COUNSELL, S; ALLSOP, J et al.Neuropediatrics. 2002, Vol 33, Num 1, pp 10-14, issn 0174-304XArticle

Chronic respiratory morbidity following premature delivery : prediction by prolonged respiratory support requirement?KINALI, M; GREENOUGH, A; DIMITRIOU, G et al.European journal of pediatrics. 1999, Vol 158, Num 6, pp 493-496, issn 0340-6199Article

Physical metallurgy aspects of the austenitic nitrocarburising processBELL, T; KINALI, M; MUENSTERMANN, G et al.Heat treatment of metals. 1987, Vol 14, Num 2, pp 47-51, issn 0305-4829Conference Paper

Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expressionARECHAVALA-GOMEZA, V; KINALI, M; FENG, L et al.Neuropathology and applied neurobiology (Print). 2010, Vol 36, Num 4, pp 265-274, issn 0305-1846, 10 p.Article

Natural history of Ullrich congenital muscular dystrophyNADEAU, A; KINALI, M; MUNTONI, F et al.Neurology. 2009, Vol 73, Num 1, pp 25-31, issn 0028-3878, 7 p.Article

Pilot trial of salbutamol in central core and multi-minicore diseasesMESSINA, S; HARTLEY, L; MAIN, M et al.Neuropediatrics. 2004, Vol 35, Num 5, pp 262-266, issn 0174-304X, 5 p.Article

Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin Pre-mRNA splicing in human muscleARECHAVALA-GOMEZA, V; GRAHAM, I. R; MUNTONI, F et al.Human gene therapy. 2007, Vol 18, Num 9, pp 798-810, issn 1043-0342, 13 p.Article

Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyMERCURI, E; BERTINI, E; CINI, C et al.Neurology. 2007, Vol 68, Num 1, pp 51-55, issn 0028-3878, 5 p.Article

Cardiac tissue velocities and strain rate in the early detection of myocardial dysfunction of asymptomatic boys with Duchenne's muscular dystrophy : relationship to clinical outcomeGIATRAKOS, N; KINALI, M; STEPHENS, D et al.Heart (London 1996). 2006, Vol 92, Num 6, pp 840-842, issn 1355-6037, 3 p.Article

Congenital muscular dystrophy with short stature, proximal contractures and distal laxityMERCURI, E; LAMPE, A; BROCKINGTON, M et al.Neuropediatrics. 2004, Vol 35, Num 4, pp 224-229, issn 0174-304X, 6 p.Article

Collagen VI involvement in Ullrich syndrome: A clinical, genetic, and immunohistochemical studyMERCURI, E; YUVA, Y; BROWN, S. C et al.Neurology. 2002, Vol 58, Num 9, pp 1354-1359, issn 0028-3878, SUP6Article

Pilot trial of albuterol in spinal muscular atrophyKINALI, M; MERCURI, E; MAIN, M et al.Neurology. 2002, Vol 59, Num 4, pp 609-610, issn 0028-3878Article