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Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series

Intractable & Rare Diseases Research, 2017/05/31, Vol.6(2), pp.95-101

2017

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The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution

Genes, 2022-01, Vol.13 (2), p.258

2022

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Current Views on Infective Endocarditis: Changing Epidemiology, Improving Diagnostic Tools and Centering the Patient for Up-to-Date Management

Life (Basel, Switzerland), 2023-01, Vol.13 (2), p.377

2023

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Risk of Cardiac Arrhythmias in Patients with Late-Onset Pompe Disease—Results from a Long Follow-Up in a Group of 12 Patients and Review of Literature

Cardiogenetics, 2024-02, Vol.14 (1), p.38-50

2024

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Cardiovascular Effects of Weight Loss in Obese Patients with Diabetes: Is Bariatric Surgery the Additional Arrow in the Quiver?

Life (Basel, Switzerland), 2023-07, Vol.13 (7), p.1552

2023

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Echocardiographic Features of Cardiac Involvement in Myotonic Dystrophy 1: Prevalence and Prognostic Value

Journal of clinical medicine, 2023-03, Vol.12 (5), p.1947

2023

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Low Intraocular Pressure Resulting from Ciliary Body Detachment in Patients with Myotonic Dystrophy

Ophthalmology (Rochester, Minn.), 2011-02, Vol.118 (2), p.260-264

2011

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X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers

Genes, 2019-11, Vol.10 (11), p.919

2019

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Intraocular Pressure and Corneal Biomechanical Properties in Patients with Myotonic Dystrophy

Ophthalmology (Rochester, Minn.), 2009-02, Vol.116 (2), p.231-234

2009

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Muscular Dystrophies: Key Elements for Everyday Diagnosis and Management

Cardiogenetics, 2013-12, Vol.3 (1), p.e9-e9

2013

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Cardiac involvement in laminopathies – short invited review

Family medicine & primary care review, 2015-10, Vol.4 (4), p.327-329

2015

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ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies

Trends in cardiovascular medicine, 2018-07, Vol.28 (5), p.330-337

2018

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Risk of arrhythmias in myotonic dystrophy: trial design of the RAMYD study

Journal of cardiovascular medicine (Hagerstown, Md.), 2009-01, Vol.10 (1), p.51-58

2009

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Prevalence of atrial fibrillation in myotonic dystrophy type 1: A systematic review

Neuromuscular disorders : NMD, 2021-04, Vol.31 (4), p.281-290

2021

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Beneficial effects of one-month sacubitril/valsartan treatment in a patient affected by end-stage dystrophinopathic cardiomyopathy

Acta myologica, 2020-09, Vol.39 (3), p.136-140

2020

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Children enteroparasitosis in north east Argentine urban area

Medicina (Buenos Aires), 2007, Vol.67 (3), p.238-242

2007

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Efficacy and safety of ropivacaine HCl in peribulbar anaesthesia for cataract surgery in patients with myotonic dystrophy type 1

Acta myologica, 2020-06, Vol.39 (2), p.90-93

2020

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SITUACIÓN DE SALUD BUCAL DE PACIENTES MAYORES DE 18 AÑOS. CÁTEDRA PRÁCTICA CLÍNICA PREVENTIVA I, FACULTAD DE ODONTOLOGÍA UNNE, ARGENTINA, 2010

Revista de la Facultad de Odontología Universidad de Antioquia, 2013-06, Vol.24 (2), p.214-231

2013

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Prevalence and clinical outcomes of dystrophin‐associated dilated cardiomyopathy without severe skeletal myopathy

European journal of heart failure, 2021-08, Vol.23 (8), p.1276-1286

2021

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T2-T3 sympathectomy versus sympathicotomy for essential palmar hyperhidrosis: comparison of effects on cardio-respiratory function

European journal of cardio-thoracic surgery, 2012-09, Vol.42 (3), p.454-461

2012

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Complete resolution of left atrial appendage thrombosis with oral dabigatran etexilate in a patient with Myotonic Dystrophy type 1 and atrial fibrillation

Acta myologica, 2017-12, Vol.36 (4), p.218-222

2017

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Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies

Acta myologica, 2019-06, Vol.38 (2), p.33-36

2019

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Heart transplantation in a patient with Myotonic Dystrophy type 1 and end-stage dilated cardiomyopathy: a short term follow-up

Acta myologica, 2018-12, Vol.37 (4), p.267-271

2018

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Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results

Acta myologica, 2019-03, Vol.38 (1), p.1-7

2019

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Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series

The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution

Current Views on Infective Endocarditis: Changing Epidemiology, Improving Diagnostic Tools and Centering the Patient for Up-to-Date Management

Risk of Cardiac Arrhythmias in Patients with Late-Onset Pompe Disease—Results from a Long Follow-Up in a Group of 12 Patients and Review of Literature

Cardiovascular Effects of Weight Loss in Obese Patients with Diabetes: Is Bariatric Surgery the Additional Arrow in the Quiver?

Echocardiographic Features of Cardiac Involvement in Myotonic Dystrophy 1: Prevalence and Prognostic Value

Low Intraocular Pressure Resulting from Ciliary Body Detachment in Patients with Myotonic Dystrophy

X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers

Intraocular Pressure and Corneal Biomechanical Properties in Patients with Myotonic Dystrophy

Muscular Dystrophies: Key Elements for Everyday Diagnosis and Management

Cardiac involvement in laminopathies – short invited review

ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies

Risk of arrhythmias in myotonic dystrophy: trial design of the RAMYD study

Prevalence of atrial fibrillation in myotonic dystrophy type 1: A systematic review

Beneficial effects of one-month sacubitril/valsartan treatment in a patient affected by end-stage dystrophinopathic cardiomyopathy

Children enteroparasitosis in north east Argentine urban area

Cardiac and Neuromuscular Features of Patients With LMNA -Related Cardiomyopathy

Efficacy and safety of ropivacaine HCl in peribulbar anaesthesia for cataract surgery in patients with myotonic dystrophy type 1

SITUACIÓN DE SALUD BUCAL DE PACIENTES MAYORES DE 18 AÑOS. CÁTEDRA PRÁCTICA CLÍNICA PREVENTIVA I, FACULTAD DE ODONTOLOGÍA UNNE, ARGENTINA, 2010

Prevalence and clinical outcomes of dystrophin‐associated dilated cardiomyopathy without severe skeletal myopathy

T2-T3 sympathectomy versus sympathicotomy for essential palmar hyperhidrosis: comparison of effects on cardio-respiratory function

Complete resolution of left atrial appendage thrombosis with oral dabigatran etexilate in a patient with Myotonic Dystrophy type 1 and atrial fibrillation

Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies

Heart transplantation in a patient with Myotonic Dystrophy type 1 and end-stage dilated cardiomyopathy: a short term follow-up

Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results

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