Barbara Merico

Università Cattolica del Sacro Cuore — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

5h-index446citations9works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(6), Cardiomyopathy and Myosin Studies(4), Neurogenetic and Muscular Disorders Research(2), Cardiac Valve Diseases and Treatments(1), Cardiac electrophysiology and arrhythmias(1)

Publications9 total

When Manual Analysis of 12-Lead ECG Holter Plays a Critical Role in Discovering Unknown Patterns of Increased Arrhythmogenic Risk: A Case Report of a Patient Treated with Tamoxifen and Subsequent Pneumonia in COVID-19
Cardiovascular Toxicology·2021· 3 citedOpen Access
Isolated compression of the ulnar motor branch due to carpal joint ganglia: clinical series, surgical technique and postoperative outcomes
European Journal of Orthopaedic Surgery & Traumatology·2020· 10 citedOpen Access
Acute myopathic quadriplegia in patients with COVID-19 in the intensive care unit
Neurology·2020· 51 cited
S21.4 Sleep studies in facioscapulohumeral muscular distrophy
Clinical Neurophysiology·2011
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype
Annals of Neurology·1999· 297 cited
Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease
Neuromuscular Disorders·1999· 27 cited
Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy
The American Journal of Human Genetics·1998· 58 citedOpen Access
The impact of the molecular data on clinical practice in facio-scapulohumeral muscular dystrophy (FSHD)
Neuromuscular Disorders·1997
Mechanism of the 4q35 rearrangement in facio-scapulo-humeral muscular dystrophy (FSHD): sequence homology of 4qter and 10qter loci favors the instability of subtelomeric KpnI repeats
Neuromuscular Disorders·1997

Frequent Co-authors

Giuliana Galluzzi(5), Giancarlo Deidda(5), S. Cacurri(5), L. Felicetti(5), Enzo Ricci(4), Luca Colantoni(4), Serenella Servidei(4), N. Piazzo(3), Eliana Vigneti(3), P. Tonali(3), Gabriella Silvestri(2), Francesca Mangiola(2), Francesca Madia(2), Pietro Tonali(2), V. Pasceri(1), Massimiliano Mirabella(1), Guido Primiano(1), Salvatore Lucio Cutuli(1), Gennaro De Pascale(1), A Pachı̀(1)