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Giorgio Tasca
Giorgio Tasca
Newcastle University, Newcastle upon Tyne, UK
Verified email at ncl.ac.uk
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Cited by
Year
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy
J Sarparanta, PH Jonson, C Golzio, S Sandell, H Luque, M Screen, ...
Nature genetics 44 (4), 450-455, 2012
2772012
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression
M Pescatori, A Broccolini, C Minetti, E Bertini, C Bruno, A D'amico, ...
The FASEB Journal 21 (4), 1210-1226, 2007
2442007
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials
K Anthony, S Cirak, S Torelli, G Tasca, L Feng, V Arechavala-Gomeza, ...
Brain 134 (12), 3547-3559, 2011
1602011
CD8+ T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI
G Frisullo, R Frusciante, V Nociti, G Tasca, R Renna, R Iorio, AK Patanella, ...
Journal of clinical immunology 31, 155-166, 2011
1412011
Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5
S Penttilä, J Palmio, T Suominen, O Raheem, A Evilä, N Muelas Gomez, ...
Neurology 78 (12), 897-903, 2012
1382012
Different impact of sex on baseline characteristics and major periprocedural outcomes of transcatheter and surgical aortic valve interventions: results of the multicenter …
F Onorati, P D’Errigo, M Barbanti, S Rosato, RD Covello, A Maraschini, ...
The Journal of thoracic and cardiovascular surgery 147 (5), 1529-1539, 2014
1202014
Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles
G Tasca, M Pescatori, M Monforte, M Mirabella, E Iannaccone, ...
PloS one 7 (6), e38779, 2012
1192012
Magnetic resonance imaging pattern recognition in sporadic inclusion‐body myositis
G Tasca, M Monforte, C De Fino, RA Kley, E Ricci, M Mirabella
Muscle & nerve 52 (6), 956-962, 2015
1142015
The genetic basis of undiagnosed muscular dystrophies and myopathies: results from 504 patients
M Savarese, G Di Fruscio, A Torella, C Fiorillo, F Magri, M Fanin, ...
Neurology 87 (1), 71-76, 2016
1092016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis
F Magri, V Nigro, C Angelini, T Mongini, M Mora, I Moroni, A Toscano, ...
Muscle & nerve 55 (1), 55-68, 2017
1062017
Magnetic resonance imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials
G Tasca, M Monforte, P Ottaviani, M Pelliccioni, R Frusciante, F Laschena, ...
Annals of neurology 79 (5), 854-864, 2016
942016
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking
RFR Schindler, C Scotton, J Zhang, C Passarelli, B Ortiz-Bonnin, ...
The Journal of clinical investigation 126 (1), 239-253, 2016
942016
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking
RFR Schindler, C Scotton, J Zhang, C Passarelli, B Ortiz-Bonnin, ...
The Journal of clinical investigation 126 (1), 239-253, 2016
942016
Prevalence of congenital muscular dystrophy in Italy: a population study
A Graziano, F Bianco, A D'Amico, I Moroni, S Messina, C Bruno, ...
Neurology 84 (9), 904-911, 2015
942015
Muscle MRI in Becker muscular dystrophy
G Tasca, E Iannaccone, M Monforte, M Masciullo, F Bianco, F Laschena, ...
Neuromuscular Disorders 22, S100-S106, 2012
932012
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients
C Fiorillo, G Astrea, M Savarese, D Cassandrini, G Brisca, F Trucco, ...
Orphanet journal of rare diseases 11, 1-14, 2016
882016
Hereditary myopathy with early respiratory failure: occurrence in various populations
J Palmio, A Evilä, F Chapon, G Tasca, F Xiang, B Brådvik, B Eymard, ...
Journal of Neurology, Neurosurgery & Psychiatry 85 (3), 345-353, 2014
882014
Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping
K Anthony, V Arechavala-Gomeza, V Ricotti, S Torelli, L Feng, N Janghra, ...
JAMA neurology 71 (1), 32-40, 2014
882014
Upper girdle imaging in facioscapulohumeral muscular dystrophy
G Tasca, M Monforte, E Iannaccone, F Laschena, P Ottaviani, E Leoncini, ...
PloS one 9 (6), e100292, 2014
862014
Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1
J Böhm, F Chevessier, C Koch, GA Peche, M Mora, L Morandi, B Pasanisi, ...
Journal of medical genetics 51 (12), 824-833, 2014
852014
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