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Cardiogenetics

ISSN: 2035--8253
Publisher: PAGEPress Publications, Pavia, Italy


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Recent advances in the genetics of atrial fibrillation: from rare and common genetic variants to microRNA signaling

Author(s): Moritz F. Sinner | Sebastian Clauss | Reza Wakili | Thomas Meitinger | Heidi Estner | Stefan Kääb
Volume: 1
Issue: 2
Year: 2011
Short QT syndrome

Author(s): Carla Giustetto | Chiara Scrocco | Daniela Giachino | Charles Antzelevitch | Fiorenzo Gaita
Volume: 1
Issue: 2
Year: 2011
DNA variation in myoMIRs of the 1, 133, and 208 families in hypertrophic cardiomyopathy

Author(s): María Palacín | Eliecer Coto | Julián R. Reguero | María Martín | César Morís | Belén Alonso | Marta Díaz | Ana I. Corao | Victoria Alvarez
Volume: 1
Issue: 2
Year: 2011
LQTS-Associated Mutation A257G in Alpha1-Syntrophin Interacts with the Intragenic Variant P74L to Modify its Biophysical Phenotype

Author(s): Jianding Cheng | David W. Van Norstrand | Argelia Medeiros-Domingo | David J. Tester | Carmen R. Valdivia | Bi-Hua Tan | Matteo Vatta | Jonathan C. Makielski | Michael J. Ackerman
Volume: 1
Issue: 2
Year: 2011
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype

Author(s): Jianding Cheng | David W. Van Norstrand | Argelia Medeiros-Domingo | David J. Tester | Carmen R. Valdivia | Bi-Hua Tan | Matteo Vatta | Jonathan C. Makielski | Michael J. Ackerman
Volume: 1
Issue: 2
Year: 2011
Long QT syndrome: from genetic basis to treatment

Author(s): Lia Crotti | Federica Dagradi | Peter J. Schwartz
Volume: 1
Issue: 2
Year: 2011
Sudden infant death syndrome and cardiac channelopathies: from mechanisms to prevention of avoidable tragedies

Author(s): Roberto Insolia | Alice Ghidoni | Cinzia Dossena | Elisa Mastantuono | Peter J. Schwartz
Volume: 1
Issue: 2
Year: 2011
Brugada syndrome

Author(s): Rachel Bastiaenen | Elijah R. Behr
Volume: 1
Issue: 2
Year: 2011
Preface

Author(s): Lia Crotti
Volume: 1
Issue: 2
Year: 2011
Ion channels and beating heart: the players and the music

Author(s): Lia Crotti | Giuseppe Limongelli | Charles Antzelevitch
Volume: 1
Issue: 2
Year: 2011
Catecholaminergic polymorphic ventricular tachycardia in 2012

Author(s): Ineke Nederend | Christian van der Werf | Arthur A.M. Wilde
Volume: 1
Issue: 2
Year: 2011
Update in cardiomyopathies and congestive heart failure

Author(s): The Heart Hospital, London, UK and Monaldi Hospital, Naples, Italy
Volume: 2
Issue: 2
Year: 2012
Molecular basis and clinical management of Pompe disease

Author(s): Giancarlo Parenti | Giuseppe Di Iorio | Simone Sampaolo | Giuseppe Fiorentino | Vincenzo Farina | Simona Fecarotta | Fabio Valente | Serena Ascione | Mario Caputi | Generoso Andria
Volume: 3
Issue: 1s
Year: 2013
Molecular basis and clinical management of Gaucher disease

Author(s): Maja Di Rocco | Andrea Loggini | Pierluigi Russo
Volume: 3
Issue: 1s
Year: 2013
Anderson-Fabry, the histrionic disease: from genetics to clinical management

Author(s): Franco Cecchi | Benedetta Tomberli | Amelia Morrone
Volume: 3
Issue: 1s
Year: 2013
Molecular basis, diagnosis and clinical management of mucopolysaccharidoses

Author(s): Rossella Parini | Francesca Bertola | Pierluigi Russo
Volume: 3
Issue: 1s
Year: 2013
Diagnosis and management of lysosomal storage disorders. Three key words: early, multidisciplinary, and network

Author(s): Generoso Andria | Giuseppe Limongelli
Volume: 3
Issue: 1s
Year: 2013
Ion channels and beating heart: the players and the music

Author(s): Lia Crotti | Giuseppe Limongelli | Charles Antzelevitch
Volume: 1
Issue: 1s
Year: 2011
Recent advances in the genetics of atrial fibrillation: from rare and common genetic variants to microRNA signaling

Author(s): Moritz F. Sinner | Sebastian Clauss | Reza Wakili | Thomas Meitinger | Heidi Estner | Stefan Kääb
Volume: 1
Issue: 1s
Year: 2011
Sudden infant death syndrome and cardiac channelopathies: from mechanisms to prevention of avoidable tragedies

Author(s): Roberto Insolia | Alice Ghidoni | Cinzia Dossena | Elisa Mastantuono | Peter J. Schwartz
Volume: 1
Issue: 1s
Year: 2011
Short QT syndrome

Author(s): Carla Giustetto | Chiara Scrocco | Daniela Giachino | Charles Antzelevitch | Fiorenzo Gaita
Volume: 1
Issue: 1s
Year: 2011
Catecholaminergic polymorphic ventricular tachycardia in 2012

Author(s): Ineke Nederend | Christian van der Werf | Arthur A.M. Wilde
Volume: 1
Issue: 1s
Year: 2011
Brugada syndrome

Author(s): Rachel Bastiaenen | Elijah R. Behr
Volume: 1
Issue: 1s
Year: 2011
Preface

Author(s): Lia Crotti
Volume: 1
Issue: 1s
Year: 2011
Long QT syndrome: from genetic basis to treatment

Author(s): Lia Crotti | Federica Dagradi | Peter J. Schwartz
Volume: 1
Issue: 1s
Year: 2011
Update in cardiomyopathies and congestive heart failure

Author(s): The Heart Hospital, London, UK and Monaldi Hospital, Naples, Italy
Volume: 2
Issue: 1S
Year: 2012
Atrial fibrillation is poorly tolerated by patients with hypertrophic concentric cardiomyopathy caused by mitochondrial tRNALeu (UUR) mutations

Author(s): Tiina M. Heliö | Alexandra Götz | Janne Rapola | Sari Kiuru-Enari | Sari Kivistö | Terttu Heikinheimo | Anu Suomalainen
Volume: 3
Issue: 1
Year: 2013
Echocardiography in Fabry disease

Author(s): Markus Niemann | Frank Weidemann
Volume: 3
Issue: 1
Year: 2013
Cost-effectiveness of genetic studies in inherited heart diseases

Author(s): María Sabater-Molina | Esperanza García-Molina | Isabel Tovar | Francisco Ruiz-Espejo | Juan Ramón Gimeno | Mariano Valdés
Volume: 3
Issue: 1
Year: 2013
Myocardial deformation imaging and rare cardiomyopathies with hypertrophic phenotype: a review focused on Fabry disease, Friedreich ataxia and amyloidosis

Author(s): Bahaa Fadel | Luca Baldini | Valeria Pergola | Ziad Al Bulbul | Giovanni Di Salvo
Volume: 3
Issue: 1
Year: 2013
J wave syndromes as a cause of sudden arrhythmic death

Author(s): Charles Antzelevitch
Volume: 3
Issue: 1
Year: 2013
Cost-effectiveness of genetic studies in Inherited Heart Diseases

Author(s): Maria Sabater-Molina | Esperanza García-Molina | Isabel Tovar | Francisco Ruiz Espejo | Juan Ramón Gimeno | M. Valdés
Volume: 3
Issue: 1
Year: 2013
Lamin A/C mutation affecting primarily the right side of the heart

Author(s): Laura Ollila | Johanna Kuusisto | Keijo Peuhkurinen | Satu Kärkkäinen | Petri Tuomainen | Maija Kaartinen | Olayinka Raheem | Bjarne Udd | Jarkko Magga | Janne Rapola | Annukka M. Lahtinen | Eero Lehtonen | Miia Holmström | Sari Kivistö | Elisabeth Widén | Markku Saksa | Tiina Heliö
Volume: 3
Issue: 1
Year: 2013
The novel role of epigenetics in primary prevention of cardiovascular diseases

Author(s): Claudio Napoli | Amelia Casamassimi | Vincenzo Grimaldi | Concetta Schiano | Teresa Infante | Alberto Zullo | Maria Lourdes Montesano | Laura Auriemma | Francesco Paolo De Luca | Gustavo De Iorio | Louis J. Ignarro | Francesco Paolo Mancini
Volume: 2
Issue: 1
Year: 2012
Compound heterozygous SCN5A gene mutations in asymptomatic Brugada syndrome child

Author(s): Elena Sommariva | Matteo Vatta | Yutao Xi | Simone Sala | Tomohiko Ai | Jie Cheng | Carlo Pappone | Maurizio Ferrari | Sara Benedetti
Volume: 2
Issue: 1
Year: 2012
Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype

Author(s): Juan Pablo Kaski | Elena Biagini | Massimo Lorenzini | Claudio Rapezzi | Perry Elliott
Volume: 2
Issue: 1
Year: 2012
Recent advances in cardiovascular research: systems biology

Author(s): Raffaella D'Alessandro | Joseph Sepe
Volume: 2
Issue: 1
Year: 2012
Compound heterozygous SCN5A gene mutations in asymptomatic Brugada syndrome child

Author(s): Elena Sommariva | Matteo Vatta | Yutao Xi | Simone Sala | Tomohiko Ai | Jie Cheng | Carlo Pappone | Maurizio Ferrari | Sara Benedetti
Volume: 2
Issue: 1
Year: 2012
An unusual case of familial hypertrophic cardiomyopathy with left ventricular systolic dysfunction: a still unsolved diagnosis

Author(s): Elena Biagini | Chiara Pazzi | Stefania Rosmini | Ornella Leone | Domenico A. Coviello | Claudio Rapezzi
Volume: 2
Issue: 1
Year: 2012
Inherited cardiac disease

Author(s): Philippe Charron
Volume: 2
Issue: 1
Year: 2012
Targeted capture and massively parallel sequencing in pediatric cardiomyopathy: development of novel diagnostics

Author(s): Muhammad Tariq | Thanh-Tam Le | Patrick Putnam | Steven Kindel | Mehdi Keddache | Stephanie M. Ware
Volume: 2
Issue: 1
Year: 2012
Transcriptional regulation of cardiac genes balance pro- and anti-hypertrophic mechanisms in hypertrophic cardiomyopathy

Author(s): Nina Gennebäck | Gerhard Wikström | Urban Hellman | Jane-Lise Samuel | Anders Waldenström | Stellan Mörner
Volume: 2
Issue: 1
Year: 2012
Combined use of in silico and in vitro splicing assays for interpretation of genomic variants of unknown significance in cardiomyopathies and channelopathies

Author(s): Hervé Crehalet | Gilles Millat | Juliette Albuisson | Véronique Bonnet | Isabelle Rouvet | Robert Rousson | Dominique Bozon
Volume: 2
Issue: 1
Year: 2012
Idiopathic restrictive cardiomyopathy - perspectives from genetics studies. Is it time to redefine these disorders?

Author(s): Ajay Bahl | Uma Nahar Saikia | Madhu Khullar
Volume: 2
Issue: 1
Year: 2012
Targeted capture and massively parallel sequencing in pediatric cardiomyopathy: development of novel diagnostics

Author(s): Muhammad Tariq | Thanh-Tam Le | Patrick Putnam | Steven Kindel | Mehdi Keddache | Stephanie M. Ware
Volume: 2
Issue: 1
Year: 2012
22q11.2 deletion (DiGeorge) syndrome: a mother’s open letter

Author(s): Antonio Baldini | Maria Cristina Digilio | Bruno Marino
Volume: 1
Issue: 1
Year: 2011
Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes

Author(s): M. Cristina Digilio | Paolo Versacci | Francesca Lepri | Anwar Baban | Bruno Dallapiccola | Bruno Marino
Volume: 1
Issue: 1
Year: 2011
The interpretation of genetic tests in inherited cardiovascular diseases

Author(s): Lorenzo Monserrat | Andrea Mazzanti | Martin Ortiz-Genga | Roberto Barriales-Villa | Diego Garcia-Giustiniani | Juan Ramon Gimeno-Blanes
Volume: 1
Issue: 1
Year: 2011
Matrix metalloproteinase 9 polymorphism and outcome after myocardial infarction

Author(s): Sophie Rodius | Guillermo Mulliert | Francisco Azuaje | Yvan Devaux | Daniel R. Wagner
Volume: 1
Issue: 1
Year: 2011
A new era in cardiogenetics

Author(s): Giuseppe Limongelli
Volume: 1
Issue: 1
Year: 2011
Phenotypic spectrum of mutations in cardiolaminopathies

Author(s): Ali J. Marian
Volume: 1
Issue: 1
Year: 2011
Tafazzin gene mutations are uncommon causes of dilated cardiomyopathy in adults

Author(s): Matthew Taylor | Dobromir Slavov | Ernesto Salcedo | Xiao Zhu | Deborah Ferguson | Jean Jirikowic | Andrea Di Lenarda | Gianfranco Sinagra | Luisa Mestroni
Volume: 1
Issue: 1
Year: 2011
Time for education in cardiogenetics

Author(s): Philippe Charron | Perry Elliott
Volume: 1
Issue: 1
Year: 2011
Genetic testing for hypertrophic cardiomyopathy: ongoing voyage from exploration to clinical exploitation

Author(s): Iacopo Olivotto | Heba Sh. Kassem | Francesca Girolami
Volume: 1
Issue: 1
Year: 2011
Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant

Author(s): Quinn S. Wells | Natalie L. Ausborn | Birgit H. Funke | Jean P. Pfotenhauer | Joseph L. Fredi | Samantha Baxter | Thomas G. DiSalvo | Charles C. Hong
Volume: 1
Issue: 1
Year: 2011
Genetics of cardiomyopathies in children

Author(s): Matteo Vatta | Jeffrey A. Towbin
Volume: 1
Issue: 1
Year: 2011
A new understanding of endurance exercise

Author(s): Joseph Sepe | Raffaella D'Alessandro
Volume: 1
Issue: 1
Year: 2011
DNA variation in myoMIRs of the 1, 133, and 208 families in hypertrophic cardiomyopathy

Author(s): María Palacín | Eliecer Coto | Julián R. Reguero | María Martín | César Morís | Belén Alonso | Marta Díaz | Ana I. Corao | Victoria Alvarez
Volume: 1
Issue: 1
Year: 2011
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype

Author(s): Jianding Cheng | David W. Van Norstrand | Argelia Medeiros-Domingo | David J. Tester | Carmen R. Valdivia | Bi-Hua Tan | Matteo Vatta | Jonathan C. Makielski | Michael J. Ackerman
Volume: 1
Issue: 1
Year: 2011
A new clonal chromosomal aberration (47, XY, +21) in atrial myxoma from an elderly male patient

Author(s): Ewa Stępień | Grzegorz Grudzień | Marek Andres | Małgorzata Jakóbczyk | Dorota Czapczak | Przemysław Kapusta | Wiesław Frasik | Tomasz Myrdko | Jerzy Sadowski
Volume: 2
Issue: 1
Year: 2012
Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies

Author(s): Richard J. Czosek | Paula Goldenberg | Erin M. Miller | Robert Spicer | Jeffrey A. Towbin | Stephanie M. Ware
Volume: 2
Issue: 1
Year: 2012
Novel SCN5A mutation associated with idiopathic ventricular fibrillation due to subclinical Brugada syndrome

Author(s): Juan Jiménez-Jáimez | Miguel Álvarez-López | Luis Tercedor-Sánchez | Pablo Santiago | Maria Algarra | Rocio Peñas | Francisca Valverde | Rafael Melgares-Moreno
Volume: 2
Issue: 1
Year: 2012
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