Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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Catheter Ablation for Atrial Arrhythmias in Patients With Cardiac Amyloidosis.Atrial Fibrillation Associated Genetic Variants and Left Atrial Histology: Evaluation for Molecular Sub-Phenotypes.Left ventricular remodeling in hypertrophic cardiomyopathy patients with atrial fibrillation

P2860

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P2860

Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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http://www.wikidata.org/entity/Q38620899

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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name

Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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P1476

Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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P2093

Domenico Corradi

http://www.w3.org/2001/XMLSchema#string

Roberta Manuguerra

http://www.w3.org/2001/XMLSchema#string

Sergio Callegari

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P2860

Role of TBX1 in human del22q11.2 syndrome

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

Tafamidis, a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and F

HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation: Recommendations for Personnel, Policy, Procedures and Follow-Up

TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype

CMR findings in patients with hypertrophic cardiomyopathy and atrial fibrillation.

Syncope and inducible ventricular fibrillation in a woman with hemochromatosis.

P304

242-252

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scholarly article

P356

10.1111/JCE.12872

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P478

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2015-10-31T00:00:00Z

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P698

26519209

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Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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P2860

P2860

Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.

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P1433

P1476

P2093

P2860

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P1433

P1476

P2093

P2860

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P433

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P698