Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy
Broccolini, A, Gidaro, T, Tasca, G, Morosetti, R, Rodolico, C, Ricci, E, Mirabella, M
Published in Neurology (20.07.2010)
Published in Neurology (20.07.2010)
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Journal Article
P368: Association between dysphagia and OSAS in acute stroke patients
Di Blasi, C, Della Marca, G, Broccolini, A, Pilato, F, Profice, P, Frisullo, G, Caliandro, P, Morosetti, R, Brunetti, V, Giannantoni, N.M, Testani, E, Losurdo, A, Gnoni, V, Rossini, P.M
Published in Clinical neurophysiology (01.06.2014)
Published in Clinical neurophysiology (01.06.2014)
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Journal Article
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency
Di Giovanni, S, Mirabella, M, Spinazzola, A, Crociani, P, Silvestri, G, Broccolini, A, Tonali, P, Di Mauro, S, Servidei, S
Published in Neurology (14.08.2001)
Published in Neurology (14.08.2001)
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Journal Article
NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations
Ricci, E, Broccolini, A, Gidaro, T, Morosetti, R, Gliubizzi, C, Frusciante, R, Di Lella, G M, Tonali, P A, Mirabella, M
Published in Neurology (14.03.2006)
Published in Neurology (14.03.2006)
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Journal Article
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes
Piluso, G, Politano, L, Aurino, S, Fanin, M, Ricci, E, Ventriglia, V M, Belsito, A, Totaro, A, Saccone, V, Topaloglu, H, Nascimbeni, A C, Fulizio, L, Broccolini, A, Canki-Klain, N, Comi, L I, Nigro, G, Angelini, C, Nigro, V
Published in Journal of medical genetics (01.09.2005)
Published in Journal of medical genetics (01.09.2005)
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Journal Article
Right Hemiparesis in Right Carotid Stenosis
PROFICE, P, PILATO, F, BROCCOLINI, A, SANTOLIQUIDO, A, MARCA, G. Della, DI LAZZARO, V
Published in Circulation (New York, N.Y.) (19.07.2011)
Published in Circulation (New York, N.Y.) (19.07.2011)
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Journal Article
P2.64 Muscle imaging in hereditary inclusion-body myopathy
Tasca, G, Broccolini, A, Rodolico, C, Gidaro, T, Morosetti, R, Monforte, M, Barca, E, Ricci, E, Mirabella, M
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Journal Article
P10.20 Modifications of cortical hippocampal connectivity in transient global amnesia: an EEG coherence study
Marca, G. Della, Broccolini, A, Farina, B, Vollono, C, Cianfoni, A, Dittoni, S, Frisullo, G, Pilato, F, Profice, P, Morosetti, R, Losurdo, A, Testani, E, Colicchio, S, Gnoni, V, Di Lazzaro, V
Published in Clinical neurophysiology (2011)
Published in Clinical neurophysiology (2011)
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Journal Article
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease
Traverso, M, Bruno, C, Broccolini, A, Sotgia, F, Donati, M A, Assereto, S, Gazzerro, E, Lo Monaco, M, Modoni, A, D’Amico, A, Gasperini, S, Ricci, E, Zara, F, Lisanti, M, Minetti, C
Published in Journal of neurology, neurosurgery and psychiatry (01.06.2008)
Published in Journal of neurology, neurosurgery and psychiatry (01.06.2008)
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Journal Article
Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle
Broccolini, A, Gidaro, T, Morosetti, R, Sancricca, C, Mirabella, M
Published in Acta myologica (01.10.2011)
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Published in Acta myologica (01.10.2011)
Journal Article
P2.38 Lower limb muscle MRI in a large cohort of FSHD patients
Tasca, G, Monforte, M, Iannaccone, E, Frusciante, R, Laschena, F, Ottaviani, P, Di Lella, G.M, Galluzzi, G, Tiziano, F.D, Broccolini, A, Masciullo, M, Silvestri, G, Ricci, E
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Journal Article
D.P.1.06 Gene expression analysis in MRI positive FSHD muscles
Pescatori, M, Tasca, G, Frusciante, R, Mirabella, M, Rossi, M, Iannaccone, E, Broccolini, A, Ricci, E
Published in Neuromuscular disorders : NMD (01.10.2008)
Published in Neuromuscular disorders : NMD (01.10.2008)
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Journal Article
G.P.5.05 Transient overexpression of the Rho family exchange factor GEFT stimulates myogenic differentiation of inclusion-body myositis (IBM) mesoangioblasts
Morosetti, R, Gliubizzi, C, Broccolini, A, Gidaro, T, Tonali, P.A, Liu, M, Ricci, E, Mirabella, M
Published in Neuromuscular disorders : NMD (01.10.2008)
Published in Neuromuscular disorders : NMD (01.10.2008)
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Journal Article
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene
Broccolini, A, Pescatori, M, D'Amico, A, Sabino, A, Silvestri, G, Ricci, E, Servidei, S, Tonali, P A, Mirabella, M
Published in Neurology (10.12.2002)
Published in Neurology (10.12.2002)
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G.P.13.13 Age-related abnormalities and reduced expression of the Notch ligand Delta in IBM primary muscle cultures. A clue for diminished regenerative potential of satellite cells in IBM muscle?
Gliubizzi, C, Morosetti, R, Sancricca, C, Broccolini, A, Gidaro, T, Tasca, G, Tonali, P, Ricci, E, Mirabella, M
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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Journal Article
G.P.13.14 Ex vivo treatment with TSA and IGF-1 induces myogenic differentiation of inclusion-body myositis mesoangioblasts
Morosetti, R, Gliubizzi, C, Broccolini, A, Gidaro, T, Sancricca, C, Tonali, P, Ricci, E, Cossu, G, Mirabella, M
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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G.P.17.05 Predictive role of NCAM in the identification of patients with HIBM due to GNE mutations with atypical clinical phenotype
Broccolini, A, Rodolico, C, Gidaro, T, Di Leo, R, Silvestri, G, Morosetti, R, Gliubizzi, C, Di Blasi, C, Morandi, L, Mora, M, Toscano, A, Vita, G, Ricci, E, Tonali, P, Mirabella, M
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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