| Year |
Citation |
Score |
| 2023 |
Eldemire R, Mestroni L, Taylor MRG. Genetics of Dilated Cardiomyopathy. Annual Review of Medicine. PMID 37788487 DOI: 10.1146/annurev-med-052422-020535 |
0.383 |
|
| 2023 |
Cannie DE, Syrris P, Protonotarios A, Bakalakos A, Pruny JF, Ditaranto R, Martinez-Veira C, Larrañaga-Moreira JM, Medo K, Bermúdez-Jiménez FJ, Ben Yaou R, Leturq F, Mezcua AR, Marini-Bettolo C, Cabrera E, ... ... Mestroni L, et al. Emery-Dreifuss Muscular Dystrophy 1 is associated with high risk of malignant ventricular arrhythmias and end-stage heart failure. European Heart Journal. PMID 37639473 DOI: 10.1093/eurheartj/ehad561 |
0.315 |
|
| 2022 |
Chen SN, Lam CK, Wan YW, Gao S, Malak OA, Zhao SR, Lombardi R, Ambardekar AV, Bristow MR, Cleveland J, Gigli M, Sinagra G, Graw S, Taylor MRG, Wu JC, ... Mestroni L, et al. Activation of PDGFRA signaling contributes to filamin C-related arrhythmogenic cardiomyopathy. Science Advances. 8: eabk0052. PMID 35196083 DOI: 10.1126/sciadv.abk0052 |
0.313 |
|
| 2021 |
Castrichini M, Eldemire R, Groves DW, Taylor MR, Miyamoto S, Mestroni L. Clinical and genetic features of arrhythmogenic cardiomyopathy: diagnosis, management and the heart failure perspective. Progress in Pediatric Cardiology. 63. PMID 34970070 DOI: 10.1016/j.ppedcard.2021.101459 |
0.331 |
|
| 2021 |
Gao S, Mumme-Monheit A, Chen SN, Spector EB, Slavov D, Baralle FE, Bristow MR, Mestroni L, Taylor MRG. An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report. American Journal of Medical Genetics. Part A. PMID 34652067 DOI: 10.1002/ajmg.a.62530 |
0.332 |
|
| 2021 |
Lachaize V, Peña B, Ciubotaru C, Cojoc D, Chen SN, Taylor MRG, Mestroni L, Sbaizero O. Compromised Biomechanical Properties, Cell-Cell Adhesion and Nanotubes Communication in Cardiac Fibroblasts Carrying the Lamin A/C D192G Mutation. International Journal of Molecular Sciences. 22. PMID 34502098 DOI: 10.3390/ijms22179193 |
0.373 |
|
| 2021 |
Eldemire R, Tharp CA, Taylor MRG, Sbaizero O, Mestroni L. The Sarcomeric Spring Protein Titin: Biophysical Properties, Molecular Mechanisms, and Genetic Mutations Associated with Heart Failure and Cardiomyopathy. Current Cardiology Reports. 23: 121. PMID 34269900 DOI: 10.1007/s11886-021-01550-y |
0.338 |
|
| 2021 |
Sanchez F, Weitz C, Gutierrez JM, Mestroni L, Hanneman K, Vargas D. Cardiac MR Imaging of Muscular Dystrophies. Current Problems in Diagnostic Radiology. PMID 33551194 DOI: 10.1067/j.cpradiol.2020.12.010 |
0.301 |
|
| 2020 |
Tharp C, Mestroni L, Taylor M. Modifications of Titin Contribute to the Progression of Cardiomyopathy and Represent a Therapeutic Target for Treatment of Heart Failure. Journal of Clinical Medicine. 9. PMID 32859027 DOI: 10.3390/Jcm9092770 |
0.422 |
|
| 2020 |
Pecorari I, Mestroni L, Sbaizero O. Current Understanding of the Role of Cytoskeletal Cross-Linkers in the Onset and Development of Cardiomyopathies. International Journal of Molecular Sciences. 21. PMID 32824180 DOI: 10.3390/Ijms21165865 |
0.366 |
|
| 2020 |
Del Favero G, Bonifacio A, Rowland TJ, Gao S, Song K, Sergo V, Adler ED, Mestroni L, Sbaizero O, Taylor MRG. Danon Disease-Associated LAMP-2 Deficiency Drives Metabolic Signature Indicative of Mitochondrial Aging and Fibrosis in Cardiac Tissue and hiPSC-Derived Cardiomyocytes. Journal of Clinical Medicine. 9. PMID 32751926 DOI: 10.3390/Jcm9082457 |
0.348 |
|
| 2020 |
Bui QM, Hong KN, Kraushaar M, Ma GS, Brambatti M, Kahn AM, Bougault C, Boynton K, Mestroni L, Taylor MRG, Adler E. Apical Sparing Strain Pattern in Danon Disease: Insights From a Global Registry. Jacc. Cardiovascular Imaging. PMID 32739374 DOI: 10.1016/J.Jcmg.2020.05.027 |
0.38 |
|
| 2020 |
Finocchiaro G, Merlo M, Sheikh N, De Angelis G, Papadakis M, Olivotto I, Rapezzi C, Carr-White G, Sharma S, Mestroni L, Sinagra G. The electrocardiogram in the diagnosis and management of patients with dilated cardiomyopathy. European Journal of Heart Failure. PMID 32243666 DOI: 10.1002/Ejhf.1815 |
0.406 |
|
| 2020 |
Borin D, Peña B, Taylor MRG, Mestroni L, Lapasin R, Sbaizero O. Viscoelastic behavior of cardiomyocytes carrying LMNA mutations. Biorheology. PMID 32083564 DOI: 10.3233/Bir-190229 |
0.447 |
|
| 2020 |
Borin D, Peña B, Chen SN, Long CS, Taylor MRG, Mestroni L, Sbaizero O. Altered microtubule structure, hemichannel localization and beating activity in cardiomyocytes expressing pathologic nuclear lamin A/C. Heliyon. 6: e03175. PMID 32021920 DOI: 10.1016/J.Heliyon.2020.E03175 |
0.375 |
|
| 2020 |
Haywood ME, Cocciolo A, Porter KF, Dobrinskikh E, Slavov D, Graw SL, Reece TB, Ambardekar AV, Bristow MR, Mestroni L, Taylor MRG. Transcriptome signature of ventricular arrhythmia in dilated cardiomyopathy reveals increased fibrosis and activated TP53. Journal of Molecular and Cellular Cardiology. PMID 31958463 DOI: 10.1016/J.Yjmcc.2019.12.010 |
0.401 |
|
| 2020 |
Brun F, Gigli M, Graw SL, Judge DP, Merlo M, Murray B, Calkins H, Sinagra G, Taylor MR, Mestroni L, James CA. truncations cause arrhythmogenic right ventricular cardiomyopathy. Journal of Medical Genetics. PMID 31924696 DOI: 10.1136/Jmedgenet-2019-106394 |
0.422 |
|
| 2019 |
Tharp CA, Haywood ME, Sbaizero O, Taylor MRG, Mestroni L. The Giant Protein Titin's Role in Cardiomyopathy: Genetic, Transcriptional, and Post-translational Modifications of TTN and Their Contribution to Cardiac Disease. Frontiers in Physiology. 10: 1436. PMID 31849696 DOI: 10.3389/Fphys.2019.01436 |
0.443 |
|
| 2019 |
Axelsson Raja A, Shi L, Day SM, Russell M, Zahka K, Lever H, Colan SD, Margossian R, Hall EK, Becker J, Jefferies JL, Patel AR, Choudhury L, Murphy AM, Canter C, ... ... Mestroni L, et al. Baseline Characteristics of the VANISH Cohort. Circulation. Heart Failure. 12: e006231. PMID 31813281 DOI: 10.1161/Circheartfailure.119.006231 |
0.373 |
|
| 2019 |
Chen SN, Sbaizero O, Taylor MRG, Mestroni L. Lamin A/C Cardiomyopathy: Implications for Treatment. Current Cardiology Reports. 21: 160. PMID 31773301 DOI: 10.1007/S11886-019-1224-7 |
0.405 |
|
| 2019 |
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM, Hua W, Indik JH, Ingles J, James CA, ... ... Mestroni L, et al. 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary. Heart Rhythm. 16: e373-e407. PMID 31676023 DOI: 10.1016/J.Hrthm.2019.09.019 |
0.423 |
|
| 2019 |
Corrado D, van Tintelen PJ, McKenna WJ, Hauer RNW, Anastastakis A, Asimaki A, Basso C, Bauce B, Brunckhorst C, Bucciarelli-Ducci C, Duru F, Elliott P, Hamilton RM, Haugaa KH, James CA, ... ... Mestroni L, et al. Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis. European Heart Journal. PMID 31637441 DOI: 10.1093/Eurheartj/Ehz669 |
0.301 |
|
| 2019 |
Gigli M, Merlo M, Graw SL, Barbati G, Rowland TJ, Slavov DB, Stolfo D, Haywood ME, Dal Ferro M, Altinier A, Ramani F, Brun F, Cocciolo A, Puggia I, Morea G, ... ... Mestroni L, et al. Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy. Journal of the American College of Cardiology. 74: 1480-1490. PMID 31514951 DOI: 10.1016/J.Jacc.2019.06.072 |
0.361 |
|
| 2019 |
Roberts JD, Murphy NP, Hamilton RM, Lubbers ER, James CA, Kline CF, Gollob MH, Krahn AD, Sturm AC, Musa H, El-Refaey M, Koenig S, Aneq MÅ, Hoorntje ET, Graw SL, ... ... Mestroni L, et al. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy. The Journal of Clinical Investigation. 130. PMID 31264976 DOI: 10.1172/Jci125538 |
0.35 |
|
| 2019 |
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM, Hua W, Indik JH, Ingles J, James CA, ... ... Mestroni L, et al. 2019 HRS Expert Consensus Statement on Evaluation, Risk Stratification, and Management of Arrhythmogenic Cardiomyopathy. Heart Rhythm. PMID 31078652 DOI: 10.1016/J.Hrthm.2019.05.007 |
0.417 |
|
| 2019 |
Peña B, Maldonado M, Bonham AJ, Aguado BA, Dominguez-Alfaro A, Laughter MR, Rowland TJ, Bardill JR, Farnsworth N, Alegret Ramon N, Taylor MRG, Anseth KS, Prato M, Shandas R, McKinsey TA, ... ... Mestroni L, et al. A Gold Nanoparticle Functionalized Reverse Thermal Gel for Tissue Engineering Applications. Acs Applied Materials & Interfaces. PMID 31021594 DOI: 10.1021/Acsami.9B00666 |
0.329 |
|
| 2019 |
Parikh VN, Caleshu C, Reuter C, Lazzeroni LC, Ingles J, Garcia J, McCaleb K, Adesiyun T, Sedaghat-Hamedani F, Kumar S, Graw S, Gigli M, Stolfo D, Dal Ferro M, Ing AY, ... ... Mestroni L, et al. Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy. Circulation. Heart Failure. 12: e005371. PMID 30871351 DOI: 10.1161/Circheartfailure.118.005371 |
0.464 |
|
| 2019 |
Marreddy Cheedipudi S, Matkovich SJ, Coarfa C, Hu X, Robertson MJ, Sweet ME, Taylor M, Mestroni L, Cleveland JC, Willerson JT, Gurha P, Marian AJ. Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy. Circulation Research. PMID 30739589 DOI: 10.1161/Circresaha.118.314177 |
0.383 |
|
| 2019 |
Chen SN, Lombardi R, Karmouch J, Tsai JY, Czernuszewicz GZ, Taylor M, Mestroni L, Coarfa C, Gurha P, Marian AJ. DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated with Lamin A/C Mutations. Circulation Research. PMID 30696354 DOI: 10.1161/Circresaha.118.314238 |
0.401 |
|
| 2018 |
Cortez D, Svensson A, Carlson J, Graw S, Sharma N, Brun F, Spezzacatene A, Mestroni L, Platonov PG. The S-wave angle identifies arrhythmogenic right ventricular cardiomyopathy in patients with electrocardiographically concealed disease phenotype. Journal of Electrocardiology. 51: 1003-1008. PMID 30497719 DOI: 10.1016/J.Jelectrocard.2018.08.009 |
0.317 |
|
| 2018 |
Sweet ME, Cocciolo A, Slavov D, Jones KL, Sweet JR, Graw SL, Reece TB, Ambardekar AV, Bristow MR, Mestroni L, Taylor MRG. Transcriptome analysis of human heart failure reveals dysregulated cell adhesion in dilated cardiomyopathy and activated immune pathways in ischemic heart failure. Bmc Genomics. 19: 812. PMID 30419824 DOI: 10.1186/S12864-018-5213-9 |
0.342 |
|
| 2018 |
Paldino A, Angelis GD, Merlo M, Gigli M, Ferro MD, Severini GM, Mestroni L, Sinagra G. Genetics of Dilated Cardiomyopathy: Clinical Implications. Current Cardiology Reports. 20: 83-83. PMID 30105555 DOI: 10.1007/S11886-018-1030-7 |
0.455 |
|
| 2018 |
Begay RL, Graw SL, Sinagra G, Asimaki A, Rowland TJ, Slavov DB, Gowan K, Jones KL, Brun F, Merlo M, Miani D, Sweet M, Devaraj K, Wartchow EP, Gigli M, ... ... Mestroni L, et al. Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures. Jacc. Clinical Electrophysiology. 4: 504-514. PMID 30067491 DOI: 10.1016/J.Jacep.2017.12.003 |
0.409 |
|
| 2018 |
Peña B, Laughter M, Jett S, Rowland TJ, Taylor MRG, Mestroni L, Park D. Injectable Hydrogels for Cardiac Tissue Engineering. Macromolecular Bioscience. e1800079. PMID 29733514 DOI: 10.1002/Mabi.201800079 |
0.342 |
|
| 2018 |
Mestroni L, Sbaizero O. Arrhythmogenic Cardiomyopathy: Mechanotransduction Going Wrong. Circulation. 137: 1611-1613. PMID 29632153 DOI: 10.1161/Circulationaha.118.033558 |
0.528 |
|
| 2018 |
Sweet ME, Mestroni L, Taylor MRG. Genetic Infiltrative Cardiomyopathies. Heart Failure Clinics. 14: 215-224. PMID 29525649 DOI: 10.1016/J.Hfc.2017.12.003 |
0.483 |
|
| 2018 |
Laurini E, Martinelli V, Lanzicher T, Puzzi L, Borin D, Chen SN, Long CS, Lee P, Mestroni L, Taylor MRG, Sbaizero O, Pricl S. Biomechanical defects and rescue of cardiomyocytes expressing pathologic nuclear lamins. Cardiovascular Research. PMID 29432544 DOI: 10.1093/Cvr/Cvy040 |
0.396 |
|
| 2018 |
Marreddy SC, Gurha P, Hu H, Sweet M, Taylor M, Mestroni L, Coarfa C, Marian AJ. Abstract 499: Identification and Characterization of Lamin-Associated Domains in Cardiac Myocytes Isolated From Human Patients With Dilated Cardiomyopathy Caused by LMNA Pathogenic Variant and Their Effects on Gene Expression and DNA Methylation Circulation Research. 123. DOI: 10.1161/Res.123.Suppl_1.499 |
0.353 |
|
| 2017 |
Puzzi L, Borin D, Martinelli V, Mestroni L, Kelsell DP, Sbaizero O. Cellular biomechanics impairment in keratinocytes is associated with a C-terminal truncated desmoplakin: An atomic force microscopy investigation. Micron (Oxford, England : 1993). 106: 27-33. PMID 29291530 DOI: 10.1016/J.Micron.2017.12.005 |
0.333 |
|
| 2017 |
Chen SN, R G Taylor M, Mestroni L. Unraveling Missing Genes and Missing Inheritance in Arrhythmogenic Cardiomyopathy. Circulation. Arrhythmia and Electrophysiology. 10. PMID 29038109 DOI: 10.1161/Circep.117.005813 |
0.494 |
|
| 2017 |
Cortez D, Svensson A, Carlson J, Graw S, Sharma N, Brun F, Spezzacatene A, Mestroni L, Platonov PG. Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities. Bmc Cardiovascular Disorders. 17: 261. PMID 29029613 DOI: 10.1186/S12872-017-0696-X |
0.34 |
|
| 2017 |
McNally EM, Mestroni L. Dilated Cardiomyopathy: Genetic Determinants and Mechanisms. Circulation Research. 121: 731-748. PMID 28912180 DOI: 10.1161/Circresaha.116.309396 |
0.364 |
|
| 2017 |
D'souza RS, Mestroni L, Taylor MRG. Danon disease for the cardiologist: case report and review of the literature. Journal of Community Hospital Internal Medicine Perspectives. 7: 107-114. PMID 28638575 DOI: 10.1080/20009666.2017.1324239 |
0.441 |
|
| 2017 |
Dal Ferro M, Stolfo D, Altinier A, Gigli M, Perrieri M, Ramani F, Barbati G, Pivetta A, Brun F, Monserrat L, Giacca M, Mestroni L, Merlo M, Sinagra G. Association between mutation status and left ventricular reverse remodelling in dilated cardiomyopathy. Heart (British Cardiac Society). PMID 28416588 DOI: 10.1136/Heartjnl-2016-311017 |
0.468 |
|
| 2017 |
Gigli M, Sinagra G, Mestroni L. [Gene therapy in heart failure: the unexpected results from the CUPID 2 trial]. Giornale Italiano Di Cardiologia (2006). 18: 101-105. PMID 28398363 DOI: 10.1714/2663.27295 |
0.342 |
|
| 2017 |
Ho CY, Day SM, Colan SD, Russell MW, Towbin JA, Sherrid MV, Canter CE, Jefferies JL, Murphy AM, Cirino AL, Abraham TP, Taylor M, Mestroni L, Bluemke DA, Jarolim P, et al. The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet Study. Jama Cardiology. PMID 28241245 DOI: 10.1001/Jamacardio.2016.5670 |
0.506 |
|
| 2017 |
Te Riele AS, Agullo-Pascual E, James CA, Leo-Macias A, Cerrone M, Zhang M, Lin X, Lin B, Sobreira NL, Amat-Alarcon N, Marsman RF, Murray B, Tichnell C, van der Heijden JF, Dooijes D, ... ... Mestroni L, et al. Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis. Cardiovascular Research. 113: 102-111. PMID 28069705 DOI: 10.1093/Cvr/Cvw234 |
0.49 |
|
| 2016 |
Losurdo P, Stolfo D, Merlo M, Barbati G, Gobbo M, Gigli M, Ramani F, Pinamonti B, Zecchin M, Finocchiaro G, Mestroni L, Sinagra G. Early Arrhythmic Events in Idiopathic Dilated Cardiomyopathy. Jacc. Clinical Electrophysiology. 2: 535-543. PMID 29759572 DOI: 10.1016/J.Jacep.2016.05.002 |
0.387 |
|
| 2016 |
Begay RL, Tharp CA, Martin A, Graw SL, Sinagra G, Miani D, Sweet ME, Slavov DB, Stafford N, Zeller MJ, Alnefaie R, Rowland TJ, Brun F, Jones KL, Gowan K, ... Mestroni L, et al. FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy. Jacc. Basic to Translational Science. 1: 344-359. PMID 28008423 DOI: 10.1016/J.Jacbts.2016.05.004 |
0.441 |
|
| 2016 |
Rowland TJ, Graw SL, Sweet ME, Gigli M, Taylor MR, Mestroni L. Obscurin Variants in Patients With Left Ventricular Noncompaction. Journal of the American College of Cardiology. 68: 2237-2238. PMID 27855815 DOI: 10.1016/J.Jacc.2016.08.052 |
0.402 |
|
| 2016 |
Gigli M, Begay RL, Morea G, Graw SL, Sinagra G, Taylor MR, Granzier H, Mestroni L. A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies. Frontiers in Cardiovascular Medicine. 3: 21. PMID 27493940 DOI: 10.3389/Fcvm.2016.00021 |
0.509 |
|
| 2016 |
Rowland TJ, Sweet ME, Mestroni L, Taylor MR. Danon disease - dysregulation of autophagy in a multisystem disorder with cardiomyopathy. Journal of Cell Science. PMID 27165304 DOI: 10.1242/Jcs.184770 |
0.365 |
|
| 2016 |
Peña B, Martinelli V, Jeong M, Bosi S, Lapasin R, Taylor MR, Long CS, Shandas R, Park D, Mestroni L. Biomimetic Polymers for Cardiac Tissue Engineering. Biomacromolecules. PMID 27073119 DOI: 10.1021/Acs.Biomac.5B01734 |
0.334 |
|
| 2016 |
Disertori M, Gulizia MM, Casolo G, Delise P, Di Lenarda A, Di Tano G, Lunati M, Mestroni L, Salerno-Uriarte J, Tavazzi L. Improving the appropriateness of sudden arrhythmic death primary prevention by implantable cardioverter-defibrillator therapy in patients with low left ventricular ejection fraction. Point of view. Journal of Cardiovascular Medicine (Hagerstown, Md.). 17: 245-55. PMID 26895401 DOI: 10.2459/Jcm.0000000000000368 |
0.34 |
|
| 2016 |
Mestroni L, Sweet ME, Taylor MR. Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms. Journal of the American College of Cardiology. 67: 526-8. PMID 26846951 DOI: 10.1016/J.Jacc.2015.11.030 |
0.307 |
|
| 2016 |
Porto AG, Brun F, Severini GM, Losurdo P, Fabris E, Taylor MR, Mestroni L, Sinagra G. Clinical Spectrum of PRKAG2 Syndrome. Circulation. Arrhythmia and Electrophysiology. 9. PMID 26729852 DOI: 10.1161/Circep.115.003121 |
0.504 |
|
| 2015 |
Sweet M, Taylor MR, Mestroni L. Diagnosis, prevalence, and screening of familial dilated cardiomyopathy. Expert Opinion On Orphan Drugs. 3: 869-876. PMID 27547593 DOI: 10.1517/21678707.2015.1057498 |
0.365 |
|
| 2015 |
Gulizia MM, Casolo G, Delise P, Di Lenarda A, Di Tano G, Lunati M, Mestroni L, Salerno-Uriarte JA, Tavazzi L. [Remarks on polyparametric assessment of sudden death risk for primary prevention ICD implantation in patients with left ventricular dysfunction of ischemic and non ischemic etiology. Italian Association of Hospital Cardiologists (ANMCO) Experts Position Paper]. Giornale Italiano Di Cardiologia (2006). 16: 651-66. PMID 26571481 DOI: 10.1714/2066.22442 |
0.343 |
|
| 2015 |
Begay RL, Graw S, Sinagra G, Merlo M, Slavov D, Gowan K, Jones KL, Barbati G, Spezzacatene A, Brun F, Di Lenarda A, Smith JE, Granzier HL, Mestroni L, Taylor M, et al. Role of Titin Missense Variants in Dilated Cardiomyopathy. Journal of the American Heart Association. 4. PMID 26567375 DOI: 10.1161/Jaha.115.002645 |
0.432 |
|
| 2015 |
Spezzacatene A, Sinagra G, Merlo M, Barbati G, Graw SL, Brun F, Slavov D, Di Lenarda A, Salcedo EE, Towbin JA, Saffitz JE, Marcus FI, Zareba W, Taylor MR, Mestroni L, et al. Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias. Journal of the American Heart Association. 4. PMID 26475296 DOI: 10.1161/Jaha.115.002149 |
0.402 |
|
| 2015 |
Lanzicher T, Martinelli V, Puzzi L, Del Favero G, Codan B, Long CS, Mestroni L, Taylor MR, Sbaizero O. The Cardiomyopathy Lamin A/C D192G Mutation Disrupts Whole-Cell Biomechanics in Cardiomyocytes as Measured by Atomic Force Microscopy Loading-Unloading Curve Analysis. Scientific Reports. 5: 13388. PMID 26323789 DOI: 10.1038/Srep13388 |
0.373 |
|
| 2015 |
Lanzicher T, Martinelli V, Long CS, Del Favero G, Puzzi L, Borelli M, Mestroni L, Taylor MR, Sbaizero O. AFM single-cell force spectroscopy links altered nuclear and cytoskeletal mechanics to defective cell adhesion in cardiac myocytes with a nuclear lamin mutation. Nucleus (Austin, Tex.). 0. PMID 26309016 DOI: 10.1080/19491034.2015.1084453 |
0.462 |
|
| 2015 |
Borne RT, Mestroni L. Wide Complex Tachycardia After Exertion: Finding The Right Cause Journal of the American College of Cardiology. 65. DOI: 10.1016/S0735-1097(15)60745-8 |
0.402 |
|
| 2014 |
Mestroni L, Brun F, Spezzacatene A, Sinagra G, Taylor MR. GENETIC CAUSES OF DILATED CARDIOMYOPATHY. Progress in Pediatric Cardiology. 37: 13-18. PMID 25584016 DOI: 10.1016/J.Ppedcard.2014.10.003 |
0.448 |
|
| 2014 |
Pinamonti B, Brun F, Mestroni L, Sinagra G. Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges. World Journal of Cardiology. 6: 1234-44. PMID 25548613 DOI: 10.4330/Wjc.V6.I12.1234 |
0.452 |
|
| 2014 |
D'souza RS, Levandowski C, Slavov D, Graw SL, Allen LA, Adler E, Mestroni L, Taylor MR. Danon disease: clinical features, evaluation, and management. Circulation. Heart Failure. 7: 843-9. PMID 25228319 DOI: 10.1161/Circheartfailure.114.001105 |
0.369 |
|
| 2014 |
Brun F, Barnes CV, Sinagra G, Slavov D, Barbati G, Zhu X, Graw SL, Spezzacatene A, Pinamonti B, Merlo M, Salcedo EE, Sauer WH, Taylor MR, Mestroni L. Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy. Journal of Medical Genetics. 51: 669-76. PMID 25157032 DOI: 10.1136/Jmedgenet-2014-102591 |
0.396 |
|
| 2014 |
Marcus F, Mestroni L. Family members of patients with ARVC: who is at risk? At what age? When and how often should we evaluate to determine risk? Journal of the American College of Cardiology. 64: 302-3. PMID 25034068 DOI: 10.1016/J.Jacc.2014.04.046 |
0.366 |
|
| 2014 |
Mestroni L, Begay RL, Graw SL, Taylor MR. Pharmacogenetics of heart failure. Current Opinion in Cardiology. 29: 227-34. PMID 24717669 DOI: 10.1097/Hco.0000000000000056 |
0.313 |
|
| 2014 |
Feldman AM, Begay RL, Knezevic T, Myers VD, Slavov DB, Zhu W, Gowan K, Graw SL, Jones KL, Tilley DG, Coleman RC, Walinsky P, Cheung JY, Mestroni L, Khalili K, et al. Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy. Journal of Cellular Physiology. 229: 1697-702. PMID 24623017 DOI: 10.1002/Jcp.24615 |
0.456 |
|
| 2013 |
Ganesh SK, Arnett DK, Assimes TL, Assimes TL, Basson CT, Chakravarti A, Ellinor PT, Engler MB, Goldmuntz E, Herrington DM, Hershberger RE, Hong Y, Johnson JA, Kittner SJ, McDermott DA, ... ... Mestroni L, et al. Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association. Circulation. 128: 2813-51. PMID 24297835 DOI: 10.1161/01.Cir.0000437913.98912.1D |
0.415 |
|
| 2013 |
Campbell N, Sinagra G, Jones KL, Slavov D, Gowan K, Merlo M, Carniel E, Fain PR, Aragona P, Di Lenarda A, Mestroni L, Taylor MR. Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy. Plos One. 8: e78104. PMID 24205113 DOI: 10.1371/Journal.Pone.0078104 |
0.409 |
|
| 2013 |
Merlo M, Sinagra G, Carniel E, Slavov D, Zhu X, Barbati G, Spezzacatene A, Ramani F, Salcedo E, Di Lenarda A, Mestroni L, Taylor MR. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy. Clinical and Translational Science. 6: 424-8. PMID 24119082 DOI: 10.1111/Cts.12116 |
0.426 |
|
| 2013 |
Martinelli V, Cellot G, Fabbro A, Bosi S, Mestroni L, Ballerini L. Improving cardiac myocytes performance by carbon nanotubes platforms. Frontiers in Physiology. 4: 239. PMID 24027533 DOI: 10.3389/Fphys.2013.00239 |
0.301 |
|
| 2013 |
Fabris E, Brun F, Porto AG, Losurdo P, Vitali Serdoz L, Zecchin M, Severini GM, Mestroni L, Di Chiara A, Sinagra G. Cardiac hypertrophy, accessory pathway, and conduction system disease in an adolescent: the PRKAG2 cardiac syndrome. Journal of the American College of Cardiology. 62: e17. PMID 23810891 DOI: 10.1016/J.Jacc.2013.02.099 |
0.397 |
|
| 2012 |
Steckman DA, Schneider PM, Schuller JL, Aleong RG, Nguyen DT, Sinagra G, Vitrella G, Brun F, Cova MA, Pagnan L, Mestroni L, Varosy PD, Sauer WH. Utility of cardiac magnetic resonance imaging to differentiate cardiac sarcoidosis from arrhythmogenic right ventricular cardiomyopathy. The American Journal of Cardiology. 110: 575-9. PMID 22595349 DOI: 10.1016/J.Amjcard.2012.04.029 |
0.374 |
|
| 2012 |
Herman DS, Lam L, Taylor MR, Wang L, Teekakirikul P, Christodoulou D, Conner L, DePalma SR, McDonough B, Sparks E, Teodorescu DL, Cirino AL, Banner NR, Pennell DJ, Graw S, ... ... Mestroni L, et al. Truncations of titin causing dilated cardiomyopathy. The New England Journal of Medicine. 366: 619-28. PMID 22335739 DOI: 10.1056/Nejmoa1110186 |
0.493 |
|
| 2012 |
Miani D, Taylor M, Mestroni L, D'Aurizio F, Finato N, Fanin M, Brigido S, Proclemer A. Sudden death associated with danon disease in women. The American Journal of Cardiology. 109: 406-11. PMID 22074992 DOI: 10.1016/J.Amjcard.2011.09.024 |
0.443 |
|
| 2011 |
Bortot B, Athanasakis E, Brun F, Rizzotti D, Mestroni L, Sinagra G, Severini GM. High-throughput genotyping robot-assisted method for mutation detection in patients with hypertrophic cardiomyopathy. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 20: 175-9. PMID 21817903 DOI: 10.1097/Pdm.0B013E31820B34Fb |
0.391 |
|
| 2011 |
Taylor M, Graw S, Sinagra G, Barnes C, Slavov D, Brun F, Pinamonti B, Salcedo EE, Sauer W, Pyxaras S, Anderson B, Simon B, Bogomolovas J, Labeit S, Granzier H, ... Mestroni L, et al. Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes. Circulation. 124: 876-85. PMID 21810661 DOI: 10.1161/Circulationaha.110.005405 |
0.53 |
|
| 2011 |
McNair WP, Sinagra G, Taylor MR, Di Lenarda A, Ferguson DA, Salcedo EE, Slavov D, Zhu X, Caldwell JH, Mestroni L. SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism. Journal of the American College of Cardiology. 57: 2160-8. PMID 21596231 DOI: 10.1016/J.Jacc.2010.09.084 |
0.75 |
|
| 2011 |
Pinamonti B, Dragos AM, Pyxaras SA, Merlo M, Pivetta A, Barbati G, Di Lenarda A, Morgera T, Mestroni L, Sinagra G. Prognostic predictors in arrhythmogenic right ventricular cardiomyopathy: results from a 10-year registry. European Heart Journal. 32: 1105-13. PMID 21362707 DOI: 10.1093/Eurheartj/Ehr040 |
0.343 |
|
| 2011 |
Mestroni L, Merlo M, Taylor MR, Camerini F, Sinagra G. Heart failure and personalized medicine. Journal of Cardiovascular Medicine (Hagerstown, Md.). 12: 6-12. PMID 20814312 DOI: 10.2459/Jcm.0B013E32833E8B0D |
0.363 |
|
| 2010 |
Moretti M, Merlo M, Barbati G, Di Lenarda A, Brun F, Pinamonti B, Gregori D, Mestroni L, Sinagra G. Prognostic impact of familial screening in dilated cardiomyopathy. European Journal of Heart Failure. 12: 922-7. PMID 20525703 DOI: 10.1093/Eurjhf/Hfq093 |
0.325 |
|
| 2010 |
Merlo M, Moretti M, Barbati G, Gregori D, Lenarda AD, Mestroni L, Sinagra G. Prognostic Value Of A Systematic Familial Screening In Idiopathic Dilated Cardiomyopathy. The Experience Of Trieste Heart Muscle Disease Journal of the American College of Cardiology. 55. DOI: 10.1016/S0735-1097(10)61224-7 |
0.354 |
|
| 2010 |
Mestroni L, McNair W, Sinagra G, Di Lenarda A, Ferguson D, Salcedo EE, Slavov D, Slavov D, Zhu X, Caldwell J, Taylor MR. SCN5A MUTATIONS ASSOCIATED WITH DILATED CARDIOMYOPATHY COMMONLY LOCALIZE TO THE VOLTAGE-SENSING MECHANISM Journal of the American College of Cardiology. 55: A35.E336. DOI: 10.1016/S0735-1097(10)60337-3 |
0.725 |
|
| 2010 |
Mestroni L, Merlo M, Carniel E, Slavov D, Zhu X, Ferguson D, Salcedo EE, Cavanaugh J, Lenarda AD, Sinagra G, Taylor MRG. Mutation Screening Of Sarcomere Genes Myh7, Mybpc3, Ldb3, And Tnnt2 In A Large Cohort Of Dilated Cardiomyopathy Families Journal of the American College of Cardiology. 55. DOI: 10.1016/S0735-1097(10)60294-X |
0.447 |
|
| 2009 |
Mestroni L. Phenotypic heterogeneity of sarcomeric gene mutations: a matter of gain and loss? Journal of the American College of Cardiology. 54: 343-5. PMID 19608032 DOI: 10.1016/J.Jacc.2009.04.029 |
0.417 |
|
| 2009 |
Taylor MR, Slavov D, Humphrey K, Zhao L, Cockroft J, Zhu X, Lavori P, Bristow MR, Mestroni L, Lazzeroni LC. Pharmacogenetic effect of an endothelin-1 haplotype on response to bucindolol therapy in chronic heart failure. Pharmacogenetics and Genomics. 19: 35-43. PMID 18953265 DOI: 10.1097/Fpc.0B013E328317Cc57 |
0.306 |
|
| 2008 |
Sinagra G, Di Lenarda A, Moretti M, Mestroni L, Pinamonti B, Perkan A, Salvi A, Pyxaras S, Bussani R, Silvestri F, Camerini F. The challenge of cardiomyopathies in 2007. Journal of Cardiovascular Medicine (Hagerstown, Md.). 9: 545-54. PMID 18475121 DOI: 10.2459/Jcm.0B013E3282F2C9F9 |
0.439 |
|
| 2008 |
Amat di San Filippo C, Taylor MR, Mestroni L, Botto LD, Longo N. Cardiomyopathy and carnitine deficiency. Molecular Genetics and Metabolism. 94: 162-6. PMID 18337137 DOI: 10.1016/J.Ymgme.2008.02.002 |
0.383 |
|
| 2008 |
Zecchin M, Di Lenarda A, Gregori D, Merlo M, Pivetta A, Vitrella G, Sabbadini G, Mestroni L, Sinagra G. Are nonsustained ventricular tachycardias predictive of major arrhythmias in patients with dilated cardiomyopathy on optimal medical treatment? Pacing and Clinical Electrophysiology : Pace. 31: 290-9. PMID 18307623 DOI: 10.1111/J.1540-8159.2008.00988.X |
0.308 |
|
| 2007 |
Taylor MR, Ku L, Slavov D, Cavanaugh J, Boucek M, Zhu X, Graw S, Carniel E, Barnes C, Quan D, Prall R, Lovell MA, Mierau G, Ruegg P, Mandava N, ... ... Mestroni L, et al. Danon disease presenting with dilated cardiomyopathy and a complex phenotype. Journal of Human Genetics. 52: 830-5. PMID 17899313 DOI: 10.1007/S10038-007-0184-8 |
0.508 |
|
| 2007 |
Taylor MR, Slavov D, Ku L, Di Lenarda A, Sinagra G, Carniel E, Haubold K, Boucek MM, Ferguson D, Graw SL, Zhu X, Cavanaugh J, Sucharov CC, Long CS, Bristow MR, ... ... Mestroni L, et al. Prevalence of desmin mutations in dilated cardiomyopathy. Circulation. 115: 1244-51. PMID 17325244 DOI: 10.1161/Circulationaha.106.646778 |
0.448 |
|
| 2007 |
Mestroni L, Miyamoto SD, Taylor MRG. Genetics of dilated cardiomyopathy conduction disease Progress in Pediatric Cardiology. 24: 3-13. DOI: 10.1016/J.Ppedcard.2007.08.003 |
0.523 |
|
| 2006 |
Taylor MR, Carniel E, Mestroni L. Cardiomyopathy, familial dilated. Orphanet Journal of Rare Diseases. 1: 27. PMID 16839424 DOI: 10.1186/1750-1172-1-27 |
0.478 |
|
| 2005 |
Taylor MR, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PR, Carniel E, Di Lenarda A, Sinagra G, Boucek MM, Cavanaugh J, Graw SL, Ruegg P, Feiger J, Zhu X, ... ... Mestroni L, et al. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy. Human Mutation. 26: 566-74. PMID 16247757 DOI: 10.1002/Humu.20250 |
0.491 |
|
| 2005 |
Carniel E, Taylor MR, Sinagra G, Di Lenarda A, Ku L, Fain PR, Boucek MM, Cavanaugh J, Miocic S, Slavov D, Graw SL, Feiger J, Zhu XZ, Dao D, Ferguson DA, ... ... Mestroni L, et al. Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy. Circulation. 112: 54-9. PMID 15998695 DOI: 10.1161/Circulationaha.104.507699 |
0.474 |
|
| 2004 |
Taylor MR, Robinson ML, Mestroni L. Analysis of genetic variations of lamin A/C gene (LMNA) by denaturing high-performance liquid chromatography. Journal of Biomolecular Screening. 9: 625-8. PMID 15475483 DOI: 10.1177/1087057104266393 |
0.451 |
|
| 2004 |
McNair WP, Ku L, Taylor MR, Fain PR, Dao D, Wolfel E, Mestroni L. SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. Circulation. 110: 2163-7. PMID 15466643 DOI: 10.1161/01.Cir.0000144458.58660.Bb |
0.745 |
|
| 2004 |
Taylor MR, Carniel E, Mestroni L. Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing. Expert Review of Molecular Diagnostics. 4: 99-113. PMID 14711353 DOI: 10.1586/14737159.4.1.99 |
0.504 |
|
| 2003 |
Ku L, Feiger J, Taylor M, Mestroni L. Cardiology patient page. Familial dilated cardiomyopathy. Circulation. 108: e118-21. PMID 14581388 DOI: 10.1161/01.Cir.0000097493.70422.50 |
0.341 |
|
| 2003 |
Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, Carniel E, Di Lenarda A, Bohlmeyer TJ, Ferguson DA, Brodsky GL, Boucek MM, Lascor J, Moss AC, Li WL, Stetler GL, ... ... Mestroni L, et al. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. Journal of the American College of Cardiology. 41: 771-80. PMID 12628721 DOI: 10.1016/S0735-1097(02)02954-6 |
0.43 |
|
| 2002 |
Startari U, Taylor MR, Sinagra G, Di Lenarda A, Mestroni L. [Dilated cardiomyopathy: etiology, clinical criteria for diagnosis and screening of the familial form]. Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology. 3: 378-85. PMID 12025380 |
0.311 |
|
| 2002 |
Zolty R, Passarino G, Taylor M, Moss A, Mestroni L, Bristow M. Molecular epidemiology of cardiac actin gene mutations in dilated cardiomyopathy Journal of the American College of Cardiology. 39: 178. DOI: 10.1016/S0735-1097(02)80789-6 |
0.488 |
|
| 2002 |
Lenarda AD, Carniel E, Sabbadini G, Driussi M, Rakar S, Chiara CD, Zanchi C, Sinagra G, Mestroni L. Natural history of familial dilated cardiomyopathy: the heart muscle disease registry of trieste Journal of the American College of Cardiology. 39: 149. DOI: 10.1016/S0735-1097(02)80658-1 |
0.368 |
|
| 2001 |
Gregori D, Rocco C, Miocic S, Mestroni L. Estimating the frequency of familial dilated cardiomyopathy in the presence of misclassification errors Journal of Applied Statistics. 28: 53-62. DOI: 10.1080/02664760120011590 |
0.324 |
|
| 2000 |
Brodsky GL, Muntoni F, Miocic S, Sinagra G, Sewry C, Mestroni L. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement. Circulation. 101: 473-476. PMID 10662742 DOI: 10.1161/01.Cir.101.5.473 |
0.449 |
|
| 1999 |
Ku L, Feiger J, Taylor M, Mestroni L. Familial Dilated Cardiomyopathy Circulation. 100: 181-190. PMID 10534480 DOI: 10.1161/01.Cir.100.17.E87 |
0.435 |
|
| 1999 |
Mestroni L, Rocco C, Gregori D, Sinagra G, Di Lenarda A, Miocic S, Vatta M, Pinamonti B, Muntoni F, Caforio AL, McKenna WJ, Falaschi A, Giacca M. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. Journal of the American College of Cardiology. 34: 181-90. PMID 10400009 DOI: 10.1016/S0735-1097(99)00172-2 |
0.403 |
|
| 1999 |
Lenarda AD, Sabbadini G, Salvatore L, Sinagra G, Mestroni L, Pinamonti B, Gregori D, Ciani F, Muzzi A, Klugmann S, Camerini F. Long-term effects of carvedilol in idiopathic dilated cardiomyopathy with persistent left ventricular dysfunction despite chronic metoprolol Journal of the American College of Cardiology. 33: 1926-1934. PMID 10362195 DOI: 10.1016/S0735-1097(99)00134-5 |
0.307 |
|
| 1999 |
Mestroni L, Maisch B, McKenna WJ, Schwartz K, Charron P, Rocco C, Tesson F, Richter A, Wilke A, Komajda M. Guidelines for the study of familial dilated cardiomyopathies European Heart Journal. 20: 93-102. PMID 10099905 DOI: 10.1053/Euhj.1998.1145 |
0.333 |
|
| 1999 |
Lenarda AD, Pinamonti b, Salvatore L, Sabbadini G, Gregori D, Chiara CD, Mestroni L, Sinagra G. Effect of carvedilol on left ventricular geometry in patients with dilated cardiomyopathy poor responders to chronic metoprolol Journal of Cardiac Failure. 5: 50. DOI: 10.1016/S1071-9164(99)91532-4 |
0.327 |
|
| 1999 |
Lenarda AD, Sabbadini G, Gregori D, Mestroni L, Pinamonti B, Zanchi C, Sinagra G. Additive effects of carvedilol in idiopathic dilated cardiomyopathy with persistent left ventricular dysfunction in spite of chronic metoprolol Journal of Cardiac Failure. 5: 43. DOI: 10.1016/S1071-9164(99)91502-6 |
0.343 |
|
| 1999 |
Mestroni L, Rocco C, Gregori D, Sinagra G, Di Lenarda A, Miocic S, Vatta M, Pinamonti B, Muntoni F, Caforio AL, McKenna WJ, Falaschi A, Giacca M, Camerini F. Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity Journal of Cardiac Failure. 5: 29. DOI: 10.1016/S1071-9164(99)91449-5 |
0.375 |
|
| 1999 |
Mestroni L, Maish B, McKenna WJ, Schwartz K, Charron P, Rocco C, Tesson F, Wilke A, Komajda M. Familial dilated cardiomyopathy: Criteria for diagnosis and for family studies Journal of Cardiac Failure. 5: 27. DOI: 10.1016/S1071-9164(99)91443-4 |
0.324 |
|
| 1999 |
Zolty R, Brodsky GL, Benjamin Perryman M, Bristow MR, Mestroni L. Epidemiology of cardiac actin gene mutations in dilated cardiomyopathy Journal of Cardiac Failure. 5: 23. DOI: 10.1016/S1071-9164(99)91426-4 |
0.493 |
|
| 1998 |
Mestroni L, Rocco C, Vatta M, Miocic S, Giacca M. Advances In Molecular Genetics Of Dilated Cardiomyopathy Cardiology Clinics. 16: 611-621. PMID 9891591 DOI: 10.1016/S0733-8651(05)70038-2 |
0.446 |
|
| 1998 |
Muntoni F, Di Lenarda A, Porcu M, Sinagra G, Mateddu A, Marrosu G, Ferlini A, Cau M, Milasin J, Melis MA, Marrosu MG, Cianchetti C, Sanna A, Falaschi A, Camerini F, ... ... Mestroni L, et al. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy. Heart (British Cardiac Society). 78: 608-12. PMID 9470882 DOI: 10.1136/Hrt.78.6.608 |
0.428 |
|
| 1998 |
Zorjal T, Vatta M, Gregori D, Recco C, Miocic S, Matulic M, Giacca M, Mestroni L. Genetic polymorphisms of the renin-angiotensin system in familial dilated cardiomyopathy Journal of the American College of Cardiology. 31: 350. DOI: 10.1016/S0735-1097(98)82161-X |
0.334 |
|
| 1997 |
Mestroni L, Giacca M. Molecular genetics of dilated cardiomyopathy. Current Opinion in Cardiology. 12: 303-9. PMID 9243088 DOI: 10.1097/00001573-199705000-00012 |
0.437 |
|
| 1997 |
Severini GM, Krajinovic M, Pinamonti B, Sinagra G, Fioretti P, Brunazzi MC, Falaschi A, Camerini F, Giacca M, Mestroni L. A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14. Genomics. 31: 193-200. PMID 8824801 DOI: 10.1006/Geno.1996.0031 |
0.379 |
|
| 1996 |
Milasin J, Muntoni F, Severini GM, Bartoloni L, Vatta M, Krajinovic M, Mateddu A, Angelini C, Camerini F, Falaschi A, Mestroni L, Giacca M. A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy. Human Molecular Genetics. 5: 73-9. PMID 8789442 DOI: 10.1093/Hmg/5.1.73 |
0.422 |
|
| 1996 |
Mestroni L, Krajinovic M, Severini GM, Milasin J, Pinamonti B, Rocco C, Vatta M, Falaschi A, Giacca M, Camerini F. Molecular genetics of dilated cardiomyopathies. European Heart Journal. 5-9. PMID 8682101 DOI: 10.1093/Eurheartj/16.Suppl_O.5 |
0.452 |
|
| 1996 |
Milasin J, Muntoni F, Severini GM, Bartoloni L, Vatta M, Krajinovic M, Angelini C, Mateddu A, Camerini F, Falaschi A, Mestroni L, Giacca M. A point mutation in the 5′ splice site of the first intron of the dystrophin gene responsible for X-linked dilated cardiomyopathy Journal of the American College of Cardiology. 27: 226. DOI: 10.1016/S0735-1097(96)81776-1 |
0.383 |
|
| 1996 |
Krajinovic M, Pinamonti B, Sinagra G, Vatta M, Severini GM, Milasin J, Falaschi A, Camerini F, Giacca M, Mestroni L. Linkage of autosomal dominant familial dilated cardiomyopathy to chromosome 9 Journal of the American College of Cardiology. 27: 226. DOI: 10.1016/S0735-1097(96)81775-X |
0.324 |
|
| 1995 |
Mestroni L, Krajinovic M, Severini GM, Pinamonti B, Di Lenarda A, Giacca M, Falaschi A, Camerini F. Familial dilated cardiomyopathy. British Heart Journal. 72: S35-41. PMID 7873323 DOI: 10.1136/Hrt.72.6_Suppl.S35 |
0.47 |
|
| 1995 |
Krajinovic M, Mestroni L, Severini GM, Pinamonti B, Camerini F, Falaschi A, Giacca M. Absence of linkage between idiopathic dilated cardiomyopathy and candidate genes involved in the immune function in a large Italian pedigree. Journal of Medical Genetics. 31: 766-71. PMID 7837253 DOI: 10.1136/Jmg.31.10.766 |
0.359 |
|
| 1995 |
Muntoni F, Wilson L, Marrosu G, Marrosu MG, Cianchetti C, Mestroni L, Ganau A, Dubowitz V, Sewry C. A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart. The Journal of Clinical Investigation. 96: 693-9. PMID 7635962 DOI: 10.1172/Jci118112 |
0.411 |
|
| 1994 |
Caforio ALP, Keeling PJ, McKenna WJ, Mann JM, Bottazzo GF, Zachara E, Mestroni L, Camerini F. Evidence from family studies for autoimmunity in dilated cardiomyopathy The Lancet. 344: 773-777. PMID 7916071 DOI: 10.1016/S0140-6736(94)92339-6 |
0.37 |
|
| 1992 |
Bristow MR, Minobe W, Rasmussen R, Larrabee P, Skerl L, Klein JW, Anderson FL, Murray J, Mestroni L, Karwande SV. Beta-adrenergic neuroeffector abnormalities in the failing human heart are produced by local rather than systemic mechanisms. The Journal of Clinical Investigation. 89: 803-15. PMID 1311717 DOI: 10.1172/Jci115659 |
0.324 |
|
| 1991 |
Camerini F, Bussani R, Lenarda D, Lardieri G, Mestroni L, Miani D, Pinamonti B, Salvi A, Silvestri F, Sinagra G. Clinical aspects and haemodynamics in the follow-up of dilated cardiomyopathy and myocarditis. European Heart Journal. 12: 193-196. PMID 1915452 DOI: 10.1093/Eurheartj/12.Suppl_D.193 |
0.359 |
|
| 1990 |
Mestroni L, Miani D, Lenarda AD, Silvestri F, Bussani R, Filippi G, Camerini F. Clinical and pathologic study of familial dilated cardiomyopathy American Journal of Cardiology. 65: 1449-1453. PMID 2353650 DOI: 10.1016/0002-9149(90)91353-8 |
0.401 |
|
| 1989 |
Tanganelli P, Lenarda AD, Bianciardi G, Salvi A, Silvestri F, Mestroni L, Camerini F. Correlation between histomorphometric findings on endomyocardial biopsy and clinical findings in idiopathic dilated cardiomyopathy. American Journal of Cardiology. 64: 504-506. PMID 2773794 DOI: 10.1016/0002-9149(89)90429-3 |
0.33 |
|
| 1987 |
Neri R, Mestroni L, Salvi A, Pandullo C, Camerini F. Ventricular arrhythmias in dilated cardiomyopathy: efficacy of amiodarone. American Heart Journal. 113: 707-715. PMID 3825860 DOI: 10.1016/0002-8703(87)90711-3 |
0.349 |
|
| 1986 |
Neri R, Mestroni L, Salvi A, Camerini F. Arrhythmias in dilated cardiomyopathy. Postgraduate Medical Journal. 62: 593-597. PMID 3774699 DOI: 10.1136/Pgmj.62.728.593 |
0.376 |
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