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Titolo Data di pubblicazione Autore(i) File
Spinal surgery is not always essential in management of scoliosis in Duchenne muscular dystrophy 1-gen-2002 Kinali, M; Messina, Sonia; Mercuri, E; Manzur, Ay; Dubowitz, V; Muntoni, F.
Apoptosis and apoptosis-related proteins in thyroid myopathies 1-gen-2002 Monici, M. C.; Rodolico, Carmelo; Toscano, Antonio; Messina, Sonia; Benvenga, Salvatore; Messina, Corrado; Vita, Giuseppe
Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases 1-gen-2002 RODOLICO C.; TOSCANO A; AUTUNNO M; MESSINA S; NICOLOSI C; AGUENNOUZ M; LAURA M; GIRLANDA P; MESSINA C; VITA G
Gli strumenti di QoL nelle patologie neuromuscolari ed esperienze preliminari sullo sviluppo di un questionario specifico per la di un questionario specifico per la distrofia muscolare di Duchenne. 1-gen-2003 Messina, Sonia; Kinali, M; Mercuri, E; Padua, L; Main, M; Muntoni, F.
Axial myopathy in myasthenia: a misleading cause of dropped head.. 1-gen-2003 Rodolico, Carmelo; Messina, Sonia; Sinicropi, S; Toscano, Antonio; Gaeta, M; Darrigo, G; Vita, Giuseppe
Pilot trial of salbutamol in structural congenital myopathies. 1-gen-2003 Hartley, L; Messina, Sonia; Kinali, M; Mercuri, E; Main, M; Stephens, Oa; Muntoni, F.
Expression of the trascription factor NFkB in different muscular dystrophies 1-gen-2003 Aguennouz, M'Hammed; Musumeci, Olimpia; Rodolico, Carmelo; Messina, Sonia; Toscano, Antonio; Monici, Mc; Buemi, C; Ciranni, Annamaria; Vita, Giuseppe
Management of scoliosis in Duchenne muscular dystrophy: a 10 year retrospective study. 1-gen-2003 Messina, Sonia; Kinali, M; Mercuri, E; Lehovsky, J; Edge, G; Manzur, Ay; Muntoni, F.
Congenital form of distal spinal muscular atrophy affecting the lower limbs: a common condition in childhood 1-gen-2003 Mercuri, E; Messina, Sonia; Kinali, M; Cini, C; Battini, R; Cioni, G; Muntoni, F.
Bone mineral density measurement in children with Duchenne muscular dystrophy: effect of low dose intermittent prednisolone 1-gen-2003 Messina, Sonia; Kinali, M; Mercuri, E; Banks, L; Manzur, Ay; Muntoni, F.
Bone mineral density measurement in children with Duchenne muscular dystrophy: effect of low dose intermittent prednisolone.. 1-gen-2003 Kinali, M; Messina, Sonia; Mercuri, E; Stephens, Da; Jaywant, S; Manzur, Ay; Banks, L; Muntoni, F.
Muscle Magnetic Resonance Imaging in patients with congenital muscular dystrophy and Ulrich phenotype 1-gen-2003 Mercuri, E; Cini, C; Pichiecchio, A; Allsop, J; Counsell, S; Zolkipli, Z; Messina, Sonia; Kinali, M; Brown, Sc; Jimenez, C; Brockington, M; Yuva, Y; Sewry, Ca; Muntoni, F.
Hypotonia does not equal weakness: diagnostic consideration on a large cohort of neonates referred for a suspected neuromuscular condition 1-gen-2003 Vasta, I; Kinali, M; Kapellou, O; Messina, Sonia; Guzzetta, A; Manzur, Ay; Cowan, F; Muntoni, F; Mercuri, E.
Pilot trial of salbutamol in congenital myopathies 1-gen-2004 Messina, Sonia; Hartley, L; Mercuri, E; Main, M; Stephens, Oa; Muntoni, F.
Pilot trial of salbutamol in congenital myopathies 1-gen-2004 Messina, Sonia; Hartley, L; Mercuri, E; Main, M; Stephens, Oa; Muntoni, F.
Pilot trial of salbutamol in congenital myopathies 1-gen-2004 Messina, Sonia; Hartley, L; Main, M; Kinali, M; Mercuri, E; Main, M; Stephens, Oa; Muntoni, F.
Distrofie muscolari congenite 1-gen-2004 Messina, Sonia; Mercuri, E; Muntoni, F.
Hypotonia does not equal primary neuromuscular disorder: diagnostic outcomes on a large cohort of neonates referred for a suspected neuromuscular condition. 1-gen-2004 M., Kinali; I., Vasta; O., Kapellou; Messina, Sonia; A., Guzzetta; F., Cowan; Ay, Manzur; E., Mercuri; F., Muntoni
Phenylbutyrate increases SMN gene expression and motor function in spinal muscular atrophy patients 1-gen-2004 TIZIANO F., D; Vitali, T; Angelozzi, C; Messina, Sonia; Brahe, C.
Phenylbutyrate in non-ambulant SMA II/III: from an open trial to a double-blind study 1-gen-2004 Mercuri, E; Bertini, E; TIZIANO F., D; Vitali, T; Angelozzi, C; Messina, Sonia; Brahe, C.
Mostrati risultati da 1 a 20 di 342
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