IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 21 a 40 di 343
Titolo Data di pubblicazione Autore(i) File
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.
Pilot trial of salbutamol in minicore and central core diseases. 1-gen-2004 MESSINA S.; HARTLEY L; MAIN M; KINALI M; JUNGBLUTH H; MUNTONI F; MERCURI E
NF-kB blockade reduces skeletal muscle degeneration and enhances muscle function in mdx. 1-gen-2004 Messina, Sonia; Altavilla, D; Aguennouz, M; Seminara, P; Minutoli, L; Monici, Mc; Bitto, A; Mazzeo, A; Squadrito, F; Vita, G.
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.
Axial myopathy in myasthenia: a misleading cause of dropped head 1-gen-2004 Rodolico, Carmelo; Messina, Sonia; Toscano, Antonio; Vita, Giuseppe; Gaeta, Michele
NF-kB blockade reduces skeletal muscle degeneration and enhances muscle function in mdx mice. 1-gen-2004 Messina, Sonia; Seminara, P; Aguennouz, M'Hammed; Monici, Mc; Marini, Herbert Ryan; Squadrito, Francesco; Vita, Giuseppe
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.
EFFECT OF TREATMENT WITH PDTC AND IRFI 042 ON STRENGTH AND FATIGUE IN MDX MICE 1-gen-2004 Messina, Sonia; Seminara, P; Aguennouz, M'Hammed; Monici, Mc; Marini, Herbert Ryan; Squadrito, Francesco; Vita, Giuseppe
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.
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
Congenital form of distal spinal muscular atrophy affecting the lower limbs: a common condition in childhood. 1-gen-2004 MERCURI E; MESSINA S.; KINALI M; CINI C; BATTINI R; CIONI G; MUNTONI F
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.
Dystrophin gene and SHOX gene mutations in a child with Becker muscular dystrophy and short stature 1-gen-2005 Aguennouz, M'Hammed; Messina, Maria Francesca; Rodolico, Carmelo; Messina, Sonia; Valenzise, Mariella; Crisafulli, G; Vita, Giuseppe
Effects of NF-kB blockade on muscle gene expression in mdx mice 1-gen-2005 Messina, Sonia; Aguennouz, M'Hammed; Macellani, M; Monici, Mc; Arcelli, D; Seminara, P; Volinia, S; Squadrito, F; Vita, Giuseppe
Nuovi meccanismi nelle distrofie muscolari: i difetti di glicosilazione dell’ α-distroglicano. 1-gen-2005 Mercuri, E; Pane, M; Messina, Sonia; Muntoni, F.
Quality of life outcomes following rehabilitation in knee-ankle-foot orthoses (KAFOs) in Duchenne muscular dystrophy. 1-gen-2005 Dlamini, N; Messina, Sonia; PADUA D. L., Kinali M; Main, M; Muntoni, F; Mercuri, E.
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene. 1-gen-2005 Mercuri, E; Brown, Sc; Nihoyannopoulos, P; Poulton, J; Kinali, M; Richard, P; Piercy, Rj; Messina, Sonia; Sewry, C; Burke, Mm; Mckenna, W; Bonne, G; Muntoni, F.
Can clinical signs identify newborns with neuromuscular disorders? 1-gen-2005 Vasta, I; Kinali, M; Messina, Sonia; Guzzetta, A; KAPELLOU O., MANZUR AY; Cowan, F; Muntoni, F; Mercuri, E.
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 1-gen-2005 Messina, Maria Francesca; Aguennouz, M'Hammed; Valenzise, Mariella; Rodolico, Carmelo; Messina, Sonia; Cruisafulli, G.; Vita, G.; DE LUCA, Filippo
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci 1-gen-2005 RODOLICO, C.; TOSCANO, A.; PATITUCCI, A.; MUGLIA, M.; GAETA, M.; D'ARRIGO, G.; MIGLIORATO, A.; MESSINA, S.; QUATTRONE, A.; MESSINA, C.; VITA, G.
Mostrati risultati da 21 a 40 di 343
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile