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Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

Circulation research, 2001-04, Vol.88 (7), p.740-745

2001

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Peopling of three Mediterranean Islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variability

American journal of physical anthropology, 2003-07, Vol.121 (3), p.270-279

2003

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FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Cell, 2003-06, Vol.113 (7), p.829-840

2003

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Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region

Human immunology, 2001-09, Vol.62 (9), p.871-884

2001

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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2001-01, Vol.103 (2), p.196-200

2001

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Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2002-07, Vol.106 (1), p.69-74

2002

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Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Annals of human genetics, 2000-09, Vol.64 (5), p.395-412

2000

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Brugada syndrome and sudden cardiac death in children

The Lancet (British edition), 2000-03, Vol.355 (9206), p.808-809

2000

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Genetic structure and affinities of the corsican population (France): Classical genetic markers analysis

American journal of human biology, 2003-03, Vol.15 (2), p.151-163

2003

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Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region

European journal of human genetics : EJHG, 2004-08, Vol.12 (8), p.613-619

2004

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Finger dermatoglyphics in the Corsican population (France)

Anthropologischer Anzeiger, 1999-12, Vol.57 (4), p.339

1999

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The polymorphism of the APOB 3' VNTR in the populations of the three largest islands of the western Mediterranean

Anthropologischer Anzeiger, 1998-09, Vol.56 (3), p.227

1998

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β-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations

Human biology, 2003-12, Vol.75 (6), p.855-871

2003

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Study on the variability of seven genetic serum protein markers in Corsica (France)

Anthropologischer Anzeiger, 1996-06, Vol.54 (2), p.97

1996

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Mitochondrial DNA sequence analysis in Sicily

American journal of human biology, 2001-09, Vol.13 (5), p.576-589

2001

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Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression

Journal of medical genetics, 1998-09, Vol.35 (9), p.778-783

1998

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A pentanucleotide repeat polymorphism (TTTTA) in the apolipoprotein (a) gene--its distribution and its association with the risk of cardiovascular disease

Collegium antropologicum, 2003-06, Vol.27 (1), p.105-115

2003

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Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

Journal of the American College of Cardiology, 2016-03, Vol.67 (9), p.1053-1058

2016

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Novel Insight Into the Natural History of Short QT Syndrome

Journal of the American College of Cardiology, 2014-04, Vol.63 (13), p.1300-1308

2014

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Balloon dilatation of anastomotic strictures secondary to surgical repair of oesophageal atresia

British journal of radiology, 2003-01, Vol.76 (901), p.26

2003

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Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers

JAMA cardiology, 2022-05, Vol.7 (5), p.504

2022

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Epidemiology and patterns of care of patients admitted to Italian Intensive Cardiac Care units: the BLITZ-3 registry

Journal of cardiovascular medicine (Hagerstown, Md.), 2010-06, Vol.11 (6), p.450

2010

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Elderly patients with acute coronary syndromes admitted to Italian intensive cardiac care units: a Blitz-3 Registry sub-analysis

Journal of cardiovascular medicine (Hagerstown, Md.), 2012-03, Vol.13 (3), p.165

2012

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Tubulovillous adenoma in the common bile duct causing obstructive jaundice

Acta gastro-enterologica belgica, 2009-10, Vol.72 (4), p.450-454

2009

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Heart failure in Italian intensive cardiac care units: data from the BLITZ-3 survey

Giornale italiano di cardiologia (2006), 2012-07, Vol.13 (7-8), p.511

2012

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Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

Peopling of three Mediterranean Islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variability

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia

Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Brugada syndrome and sudden cardiac death in children

Genetic structure and affinities of the corsican population (France): Classical genetic markers analysis

Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region

Finger dermatoglyphics in the Corsican population (France)

The polymorphism of the APOB 3' VNTR in the populations of the three largest islands of the western Mediterranean

β-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations

Study on the variability of seven genetic serum protein markers in Corsica (France)

Mitochondrial DNA sequence analysis in Sicily

Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression

A pentanucleotide repeat polymorphism (TTTTA) in the apolipoprotein (a) gene--its distribution and its association with the risk of cardiovascular disease

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

Novel Insight Into the Natural History of Short QT Syndrome

Balloon dilatation of anastomotic strictures secondary to surgical repair of oesophageal atresia

Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers

Epidemiology and patterns of care of patients admitted to Italian Intensive Cardiac Care units: the BLITZ-3 registry

Elderly patients with acute coronary syndromes admitted to Italian intensive cardiac care units: a Blitz-3 Registry sub-analysis

Tubulovillous adenoma in the common bile duct causing obstructive jaundice

Heart failure in Italian intensive cardiac care units: data from the BLITZ-3 survey

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