المؤلفون: Giuseppe Di Stolfo, Sandra Mastroianno, Nicolò Soldato, Raimondo Salvatore Massaro, Giovanni De Luca, Davide Seripa, Maria Urbano, Carolina Gravina, Antonio Greco, Paola Siena, Marco Matteo Ciccone, Andrea Igoren Guaricci, Cinzia Forleo, Massimo Carella, Domenico Rosario Potenza

المصدر: Journal of Clinical Medicine, Vol 13, Iss 11, p 3177 (2024)

مصطلحات موضوعية: TOMM40, rs2075650, left bundle branch block, cardiac conduction disease, cardiac electronic device, cardiovascular death, Medicine

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2077-0383/13/11/3177Test; https://doaj.org/toc/2077-0383Test

الوصول الحر: https://doaj.org/article/bb1b4972a21d4f76aa36dfe57b77923dTest

المؤلفون: Maoxiang Zhao, Jingli Gao, Shuohua Chen, Siyu Yao, Miao Wang, Chi Wang, Sijin Zhang, Zekun Feng, Lu Tian, Yanjie Li, Yang Liu, Shouling Wu, Hao Xue

المصدر: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 24 (2023)

مصطلحات موضوعية: atrioventricular block, cardiac conduction disease, left bundle‐branch block, right bundle‐branch block, type 2 diabetes, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2047-9980Test

الوصول الحر: https://doaj.org/article/60096fa4153c433e8adf5e12326e23d5Test

المؤلفون: Lv Xuejiao, Sun Yuxin, Tan Wenxi, Liu Yang, Wen Naiyan, Fu Shuang, Yu Lanying, Liu Tiantian, Qi Xiaocui, Shu Nanqi, Du Yanwei, Zhang Wenfeng, Meng Yan

المصدر: Open Life Sciences, Vol 16, Iss 1, Pp 1240-1251 (2021)

مصطلحات موضوعية: cardiac conduction disease, lncrna, mrna, co-expression, cerna, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2391-5412Test

الوصول الحر: https://doaj.org/article/bea64f78578f488fb43cb938916e82f6Test

المؤلفون: Reddy, Sathineni Ashwin, Nethercott, Sarah L, Teh, Wen, De Bie, Eckart Mdd, Pepke-Zaba, Joanna, Toshner, Mark R, Martin, Claire A

مصطلحات موضوعية: cardiac conduction disease, pacing and electrophysiology, pulmonary vascular disease, quality of life, Familial Primary Pulmonary Hypertension, Heart, Humans, Male, Prevalence, Prognosis, Prospective Studies, Pulmonary Arterial Hypertension

وصف الملف: application/msword

العلاقة: https://www.repository.cam.ac.uk/handle/1810/353671Test; https://doi.org/10.17863/CAM.99749Test

الإتاحة: https://doi.org/10.17863/CAM.99749Test
https://www.repository.cam.ac.uk/handle/1810/353671Test

المؤلفون: Laia Brunet Garcia, Ankita Hajra, Ella Field, Joseph Wacher, Helen Walsh, Gabrielle Norrish, Adnan Manzur, Francesco Muntoni, Pinki Munot, Stephanie Robb, Rosaline Quinlivan, Mariacristina Scoto, Giovanni Baranello, Anna Sarkozy, Luke Starling, Juan Pablo Kaski, Elena Cervi

المصدر: Frontiers in Pediatrics, Vol 10 (2022)

مصطلحات موضوعية: myotonic dystrophy (DM1), congenital myotonic dystrophy, pediatric population, neuromuscular disorder, cardiac conduction disease, electrocardiographic abnormalities, Pediatrics, RJ1-570

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2022.910660/fullTest; https://doaj.org/toc/2296-2360Test

الوصول الحر: https://doaj.org/article/3fb4b718270d4f3b9aae0d632cd63a13Test

المؤلفون: Sejpal, Manasi, Asghar, Moneeb, Bonaguro, Anne Marie, Runnoe, Hannah, Hussain, Sheraz, Naqvi, Amir, Raghuvir, Rashmi

المصدر: Advocate GME

مصطلحات موضوعية: Progressive cardiac conduction disease, PCCD, Lenegre's disease, His-Purkinje system, Advocate Cardiovascular Disease Fellows - Christ Medical Center, Advocate Cardiovascular Disease Faculty - Advocate Christ Medical Center, Cardiology

العلاقة: https://institutionalrepository.aah.org/advocategme/522Test; https://libkey.io/libraries/1712/10.1016/S0735-1097Test(24)04948-9

الإتاحة: https://doi.org/10.1016/S0735-1097Test(24)04948-9
https://institutionalrepository.aah.org/advocategme/522Test

المؤلفون: E. B. Polyakova, N. V. Shcherbakova, M. A. Shkolnikova, Е. Б. Полякова, Н. В. Щербакова, М. А. Школьникова

المصدر: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 67, № 3 (2022); 117-121 ; Российский вестник перинатологии и педиатрии; Том 67, № 3 (2022); 117-121 ; 2500-2228 ; 1027-4065

مصطلحات موضوعية: врожденное нарушение проводимости, bradyarrhythmias, familial sick sinus syndrome, familial atrioventricular block, cardiac conduction disease, брадиаритмии, наследственный синдром слабости синусного узла, наследственная атриовентрикулярная блокада

وصف الملف: application/pdf

العلاقة: https://www.ped-perinatology.ru/jour/article/view/1662/1254Test; Ackerman M.J., Priori S.G., Willems S., Berul C., Brugada R., Calkins H. et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies. Heart Rhythm 2011; 8:1308–1339. DOI:10.1016/j.hrthm.2011.05.020; Celestino-Soper P.B., Doytchinova A., Steiner H.A., Uradu A., Lynnes T.C., Groh W.J. et al. Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel. PLoS One 2015; 10(12):e 0143588. DOI:10.1371%2Fjournal.pone.0143588; Campuzano O., Sarquella-Brugada G., Brugada R., Brugada J. Genetics of channelopathies associated with sudden cardiac death. Glob Cardiol Sci Pract 2015; 3:39. DOI:10.5339/gcsp.2015.39; 2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society. J Am Coll Cardiol 2019; 74(7): 1016–1018. DOI:10.1161/CIR.0000000000000628; Cheng L., Li X., Zhao L., Wang Z., Zhang J, Liang Z., Wu Y. Reevaluating the mutation classification in genetic studies of bradycardia using ACMG/AMP variant classification Framework. Int J Genomics 2020; 2415850. DOI:10.1155/2020/2415850; Rezazadeh S., Duff H.J. Genetic determiants of hereditary bradyarrhythmias: A contemporary review of a diverse group of disorders. Can J Cardiol 2017; 33(6): 758–767. DOI:10.1016/j.cjca.2017.03.010; Полякова Е.Б., Щербакова Н.В. Первые результаты генетического тестирования детей с брадиаритмиями. Педиатрия им. Г.Н. Сперанского 2020; 99(3): 23–28. DOI:10.24110/0031-403X-2020-99-3-23-28; Sun B., Yao J., Ni M., Wei J., Zhong X., Guo W. et al. Cardiac ryanodine receptor calcium release deficiency syndrome. Sci Transl Med 2021; 13(579): eaba7287. DOI:10.1126/scitranslmed.aba7287; Полякова Е.Б., Школьникова М.А., Калинин Л.А. Механизмы формирования, классификация, клиническое течение и прогноз «идиопатических» нарушений функции синусового узла в детском возрасте. Вестник аритмологии 2008; 52: 5–13. DOI: estar.elpub.ru/jour/article/view/358; Giudicessi J.R., Ackerman M.J. Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes. Translat Res 2013; 161: 1–14. DOI:10.1016/j.trsl.2012.08.005; https://www.ped-perinatology.ru/jour/article/view/1662Test

الإتاحة: https://doi.org/10.21508/1027-4065-2022-67-3-117-12110.1016/j.hrthm.2011.05.02010.5339/gcsp.2015.3910.1161/CIR.000000000000062810.1155/2020/241585010.1016/j.cjca.2017.03.01010.24110/0031-403X-2020-99-3-23-2810.1126/scitranslmed.aba728710.1016/j.trsl.2012.08.005Test
https://www.ped-perinatology.ru/jour/article/view/1662Test

المؤلفون: Brunet Garcia, Laia, Hajra, Ankita, Field, Ella, Wacher, Joseph, Walsh, Helen, Norrish, Gabrielle, Manzur, Adnan, Muntoni, Francesco, Munot, Pinki, Robb, Stephanie, Quinlivan, Rosaline, Scoto, Mariacristina, Baranello, Giovanni, Sarkozy, Anna, Starling, Luke, Kaski, Juan Pablo, Cervi, Elena

المصدر: Frontiers in Pediatrics , 10 , Article 910660. (2022)

مصطلحات موضوعية: myotonic dystrophy (DM1), congenital myotonic dystrophy, pediatric population, neuromuscular disorder, cardiac conduction disease, electrocardiographic abnormalities

وصف الملف: application/pdf

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10151101/1/fped-10-910660.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10151101Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10151101/1/fped-10-910660.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10151101Test/

المؤلفون: Alberto Palladino, Andrea Antonio Papa, Roberta Petillo, Marianna Scutifero, Salvatore Morra, Luigia Passamano, Vincenzo Nigro, Luisa Politano

المصدر: Genes; Volume 13; Issue 2; Pages: 258

مصطلحات موضوعية: progressive cardiac conduction disease, atrio-ventricular block, right bundle branch block, Cardiac channelopathy

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Human Genomics and Genetic Diseases; https://dx.doi.org/10.3390/genes13020258Test

الإتاحة: https://doi.org/10.3390/genes13020258Test

المؤلفون: Aaron Isaacs, Andrei Barysenka, Rachel M.A. ter Bekke, Apollonia T.J.M. Helderman-van den Enden, Arthur van den Wijngaard, Paul G.A. Volders, Monika Stoll

المصدر: Heart Rhythm. 20(5):720-727

مصطلحات موضوعية: SELECTION, RISK, R-PACKAGE, LOCI, COMMON VARIANTS, ASSOCIATION, Family study, DISEASE, Ventricular tachyarrhythmia, Cardiac conduction disease, Modifier genes, Standing genetic variation, Physiology (medical), LINKAGE, INTERVAL, Isorhythmic atrioventricular dissociation, Com-pound variation, Cardiology and Cardiovascular Medicine

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af02934c25ef590ae5955f7c701c5adTest
https://doi.org/10.1016/j.hrthm.2023.02.004Test