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Antonella Taglia

Observed names: A. Taglia, TAGLIA A, Taglia A, Taglia, A.
OpenAlex ID: A5078601279
Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients.
2012 · Luigia Passamano, Antonella Taglia, et al. · Europe PMC (PubMed Central) · 326
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
2012 · Luca Bello, Luisa Piva, et al. · Neurology · 81
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Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
2015 · Andrea Barp, Luca Bello, et al. · PLoS ONE · 75
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Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy
2016 · Craig M. McDonald, Thomas Meier, et al. · Neuromuscular Disorders · 62
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Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy
2017 · Thomas Meier, Christian Rummey, et al. · Neuromuscular Disorders · 57
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Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene.
2015 · Antonella Taglia, Roberta Petillo, et al. · Europe PMC (PubMed Central) · 47
Cardiac involvement in patients with spinal muscular atrophies.
2011 · Alberto Palladino, Luigia Passamano, et al. · Europe PMC (PubMed Central) · 32
Novel mutations in LMNA A/C gene and associated phenotypes.
2015 · Roberta Petillo, Paola D'Ambrosio, et al. · PubMed Central · 22
On a case of respiratory failure due to diaphragmatic paralysis and dilated cardiomyopathy in a patient with nemaline myopathy.
2012 · Antonella Taglia, Paola D'Ambrosio, et al. · Europe PMC (PubMed Central) · 11
Genetic counseling in Pompe disease.
2011 · Antonella Taglia, Esther Picillo, et al. · Europe PMC (PubMed Central) · 11
G.P.223
2014 · M. Scutifero, A. Taglia, et al. · Neuromuscular Disorders
G.P.228
2014 · P. D’Ambrosio, E. Picillo, et al. · Neuromuscular Disorders
Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients
2012 · PASSAMANO L, TAGLIA A, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
X chromosome inactivation pattern in Duchenne muscular dystrophy carriers
2012 · Viggiano E, Picillo E, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
A novel mutation in CPT2 gene in two unrelated patients from Campania region
2012 · Taglia A, Picillo E, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
Earlier cardiomyopathy onset in DMD patients carrying the TT genotype at SPP1 rs28357094.
2012 · Barp A, Bello L, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
Germline mosaicism and muscular dystrophies
2012 · Tedeschi S, Torella A, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
P-12Becker patients with isolated deletionof exon 48 in dystrophin gene presentwith a mild phenotype and seem to escapecardiomyopathy
2011 · Antonella Taglia, Emanuela Viggiano, et al. · Europe PMC (PubMed Central)
Genetic counseling in Pompe disease.
2011 · Taglia A, Picillo E, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
Becker patients with isolated deletion of exon 48 in dystrophin gene present with a mild phenotype and seem to escape cardiomyopathy
2011 · Taglia A, Viggiano E, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
Beneficial effects of angiotensin-converting enzyme inhibitors in Dystrophinopathic Cardiomyopathy
2010 · POLITANO, Luisa, Palladino A, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
Improvement of survival in Duchenne muscular dystrophy
2010 · Passamano L, Cecio MR, et al. · Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli"
Works count: 25
Citation count: 724
H-index: 10
I10-index: 10
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