Sfoglia per Autore
Apoptosis and apoptosis-related proteins in thyroid myopathies
2002-01-01 Monici, M. C.; Rodolico, Carmelo; Toscano, Antonio; Messina, Sonia; Benvenga, Salvatore; Messina, Corrado; Vita, Giuseppe
Spinal surgery is not always essential in management of scoliosis in Duchenne muscular dystrophy
2002-01-01 Kinali, M; Messina, Sonia; Mercuri, E; Manzur, Ay; Dubowitz, V; Muntoni, F.
Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases
2002-01-01 RODOLICO C.; TOSCANO A; AUTUNNO M; MESSINA S; NICOLOSI C; AGUENNOUZ M; LAURA M; GIRLANDA P; MESSINA C; VITA G
Bone mineral density measurement in children with Duchenne muscular dystrophy: effect of low dose intermittent prednisolone
2003-01-01 Messina, Sonia; Kinali, M; Mercuri, E; Banks, L; Manzur, Ay; Muntoni, F.
Congenital form of distal spinal muscular atrophy affecting the lower limbs: a common condition in childhood
2003-01-01 Mercuri, E; Messina, Sonia; Kinali, M; Cini, C; Battini, R; Cioni, G; Muntoni, F.
Hypotonia does not equal weakness: diagnostic consideration on a large cohort of neonates referred for a suspected neuromuscular condition
2003-01-01 Vasta, I; Kinali, M; Kapellou, O; Messina, Sonia; Guzzetta, A; Manzur, Ay; Cowan, F; Muntoni, F; Mercuri, E.
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.
2003-01-01 Messina, Sonia; Kinali, M; Mercuri, E; Padua, L; Main, M; Muntoni, F.
Pilot trial of salbutamol in structural congenital myopathies.
2003-01-01 Hartley, L; Messina, Sonia; Kinali, M; Mercuri, E; Main, M; Stephens, Oa; Muntoni, F.
Expression of the trascription factor NFkB in different muscular dystrophies
2003-01-01 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.
2003-01-01 Messina, Sonia; Kinali, M; Mercuri, E; Lehovsky, J; Edge, G; Manzur, Ay; Muntoni, F.
Axial myopathy in myasthenia: a misleading cause of dropped head..
2003-01-01 Rodolico, Carmelo; Messina, Sonia; Sinicropi, S; Toscano, Antonio; Gaeta, M; Darrigo, G; Vita, Giuseppe
Muscle Magnetic Resonance Imaging in patients with congenital muscular dystrophy and Ulrich phenotype
2003-01-01 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.
Bone mineral density measurement in children with Duchenne muscular dystrophy: effect of low dose intermittent prednisolone..
2003-01-01 Kinali, M; Messina, Sonia; Mercuri, E; Stephens, Da; Jaywant, S; Manzur, Ay; Banks, L; Muntoni, F.
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.
2004-01-01 Jungbluth, H; Zhou, H; Hartley, L; Halliger Keller, B; Messina, Sonia; Longman, C; Brockington, M; Robb, Sa; Straub, V; Voit, T; Swash, M; Ferreiro, A; Bydder, G; Sewry, Ca; Muller, C; Muntoni, F.
Egen classification revisited in SMA.
2004-01-01 Steffensen, Bf; Mayhew, A; Aloysius, A; Eagle, M; Mercuri, E; Messina, Sonia
Pilot trial of phenylbutyrate in spinal muscular atrophy
2004-01-01 Mercuri, E; Bertini, E; Messina, Sonia; Pelliccioni, M; Damico, A; Colitto, F; Mirabella, M; Tiziano, Fd; Vitali, T; Angelozzi, C; Kinali, M; Main, M; Brahe, C.
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classical Emery-Dreifuss variant.
2004-01-01 MERCURI E; POPPE M; QUINLIVAN R; MESSINA S.; KINALI M; DEMAY L; BOURKE J; RICHARD P; SEWRY C; PIKE M; BONNE G; MUNTONI F; BUSHBY K
Effect of treatment with PDTC and IRFI 042 on strenght and fatigue in mdx mice
2004-01-01 Messina, Sonia; Altavilla, D; Aguennouz, M; Seminara, P; Minutoli, L; Monici, Mc; Bitto, A; Mazzeo, A; Marini, H; Squadrito, F; Vita, G.
Axial myopathy in myasthenia: a misleading cause of dropped head
2004-01-01 Rodolico, Carmelo; Messina, Sonia; Toscano, Antonio; Vita, Giuseppe; Gaeta, Michele
Magnetic resonance imaging of muscle in congenital myopathies associated with RYR 1 mutations
2004-01-01 Jungbluth, H; Davis, Mr; Muller, C; Counsell, S; Allsop, J; Chattopadhyay, A; Messina, Sonia; Mercuri, E; Laing, Ng; Sewry, Ca; Bydder, G; Muntoni, F.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
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. | |
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 | |
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. | |
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. | |
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. | |
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. | |
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. | |
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 | |
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. | |
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. | |
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. | 1-gen-2004 | Jungbluth, H; Zhou, H; Hartley, L; Halliger Keller, B; Messina, Sonia; Longman, C; Brockington, M; Robb, Sa; Straub, V; Voit, T; Swash, M; Ferreiro, A; Bydder, G; Sewry, Ca; Muller, C; Muntoni, F. | |
Egen classification revisited in SMA. | 1-gen-2004 | Steffensen, Bf; Mayhew, A; Aloysius, A; Eagle, M; Mercuri, E; Messina, Sonia | |
Pilot trial of phenylbutyrate in spinal muscular atrophy | 1-gen-2004 | Mercuri, E; Bertini, E; Messina, Sonia; Pelliccioni, M; Damico, A; Colitto, F; Mirabella, M; Tiziano, Fd; Vitali, T; Angelozzi, C; Kinali, M; Main, M; Brahe, C. | |
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classical Emery-Dreifuss variant. | 1-gen-2004 | MERCURI E; POPPE M; QUINLIVAN R; MESSINA S.; KINALI M; DEMAY L; BOURKE J; RICHARD P; SEWRY C; PIKE M; BONNE G; MUNTONI F; BUSHBY K | |
Effect of treatment with PDTC and IRFI 042 on strenght and fatigue in mdx mice | 1-gen-2004 | Messina, Sonia; Altavilla, D; Aguennouz, M; Seminara, P; Minutoli, L; Monici, Mc; Bitto, A; Mazzeo, A; Marini, H; Squadrito, F; Vita, G. | |
Axial myopathy in myasthenia: a misleading cause of dropped head | 1-gen-2004 | Rodolico, Carmelo; Messina, Sonia; Toscano, Antonio; Vita, Giuseppe; Gaeta, Michele | |
Magnetic resonance imaging of muscle in congenital myopathies associated with RYR 1 mutations | 1-gen-2004 | Jungbluth, H; Davis, Mr; Muller, C; Counsell, S; Allsop, J; Chattopadhyay, A; Messina, Sonia; Mercuri, E; Laing, Ng; Sewry, Ca; Bydder, G; Muntoni, F. |
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