Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mestra CF"'
Autor:
Huertas-Quiñones VM; Division of Pediatric Cardiology, Fundación Cardioinfantil, Cardiology Institute, Bogotá, Colombia.; School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia., Mestra CF; Division of Pediatric Cardiology, Fundación Cardioinfantil, Cardiology Institute, Bogotá, Colombia., Peña-Trujillo V; Division of Pediatric Cardiology, Fundación Cardioinfantil, Cardiology Institute, Bogotá, Colombia.; School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia., Gallo-Bernal S; Division of Pediatric Cardiology, Fundación Cardioinfantil, Cardiology Institute, Bogotá, Colombia.; School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia., Villaveces M; Division of Pediatric Cardiology, Fundación Cardioinfantil, Cardiology Institute, Bogotá, Colombia.; School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia., Alarcón-Forero LC; Division of Pediatric Cardiology, Fundación Cardioinfantil, Cardiology Institute, Bogotá, Colombia.; School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Publikováno v:
Cardiology in the young [Cardiol Young] 2020 Apr; Vol. 30 (4), pp. 462-467. Date of Electronic Publication: 2020 Feb 17.
Autor:
Cano Sierra JD; 1Pediatric Cardiology Hospitalist,Fundación Cardioinfantil,Bogotá,Colombia., Mestra CF; 2Pediatric Cardiology Department,Universidad Del Rosario,Bogotá,Colombia., Ronderos Dumit MA; 3Pediatric Interventional Cardiology Department,Fundación Cardioinfantil,Bogotá,Colombia.
Publikováno v:
Cardiology in the young [Cardiol Young] 2018 Aug; Vol. 28 (8), pp. 1074-1076. Date of Electronic Publication: 2018 Jun 29.
Autor:
Cano Sierra JD; Pediatric Cardiology Hospitalist, Fundación Cardioinfantil, Bogotá, Colombia., Mestra CF; Pediatric Cardiology Department, Universidad del Rosario, Bogotá, Colombia., Nieto JCG; Pediatrics Department, Universidad del Rosario, Bogotá, Colombia., Ronderos Dumit M; Pediatric Interventional Cardiology Department, Fundación Cardioinfantil, Bogotá, Colombia., García-Torres A; Pediatric Interventional Cardiology Department, Fundación Cardioinfantil, Bogotá, Colombia.
Publikováno v:
Annals of translational medicine [Ann Transl Med] 2018 Apr; Vol. 6 (7), pp. 118.
Autor:
Güleray Lafcı, Naz, Karaosmanoglu, Beren, Taskiran, Ekim Z., Simsek-Kiper, Pelin Ozlem, Utine, Gülen Eda
Publikováno v:
Molecular Syndromology; 2023, Vol. 14 Issue 3, p258-266, 8p
Publikováno v:
Pharmacogenomics & Personalized Medicine; Nov2022, Vol. 15, p913-918, 6p
Autor:
Ziogas, Ioannis1 ivz2@cornell.edu
Publikováno v:
Mnemosyne. 2011, Vol. 64 Issue 2, p249-270. 22p.
Publikováno v:
1. De Angelis G, Bobbo M, Paldino A, D’Agata Mottolese B, Altinier A, Dal Ferro M, et al. Cardiomyopathies in children. Curr Opin Organ Transplant [Internet]. 2020Jun;25(3):218–30. Available from: http://journals.lww.com/10.1097/MOT.0000000000000755
2. Lipshultz SE, Cochran TR, Briston DA, Brown SR, Sambatakos PJ, Miller TL, et al. Pediatric cardiomyopathies: causes, epidemiology, clinical course, preventive estrategies and therapies. Future Cardiol [Internet]. 2013 Nov;9(6):817–48. Available from: https://www.futuremedicine.com/doi/abs/10.2217/fca.13.66
3. Konta L, Franklin RCG, Kaski JP. Nomenclature and systems of classification for cardiomyopathy in children. Cardiol Young [Internet]. 2015 Aug 17;25(S2):31–42.Availablefrom:https://www.cambridge.org/core/product/identifier/S1047951115001201/type/journal_article
4. Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies. Heart [Internet]. 1980 Dec 1;44(6):672–3. Available from:http://heart.bmj.com/cgi/doi/10.1136/hrt.44.6.672
5. Mathew J, Zahavich L, Lafreniere-Roula M, Wilson J, George K, Benson L, et al. Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy. Clin Genet[Internet]. 2018 Feb;93(2):310–9.Available from: http://doi.wiley.com/10.1111/cge.13157
6. Ware SM. Cardiomyopathy in Children. J Am Coll Cardiol [Internet]. 2018Nov;72(19):2339–41. Available from:https://linkinghub.elsevier.com/retrieve/pii/S073510971838402X
7. Huertas-Quiñones VM, Restrepo CM. Genética de las Cardiopatías Congénitas. Capítulo 15. Bloque 4-Genética del Corazón y sus estructuras. En López-Farré. Cardio-Genética. Primera ed. Sociedad Española de Cardiología, Universidad Complutense de Madrid. Editorial médica CTO. Madrid (España) 2015:175-202.ISBN 978-84-16153-91-6.
8. Miocardiopatia dilatada [Internet]. 2018. Available from: https://healthincode.com/en/panels/cardiology/cardiomyopathy/dilated-cardiomyopathy/
9. Huertas-Quiñones VM. Cardiomiopatías en edad pediátrica. En “Cardiología Pediátrica”. Díaz GF, Sandoval N, Vélez JF, ed. Segunda ed. Sociedad Colombiana de Cardiología. Editorial Distribuna. Bogotá (Colombia)2018:941-974. ISBN 978-958-8813-70-7.
11. Monserrat L, Ochoa J, Garcia D, Ortiz M. Genética de la miocardiopatia hipertrofica. In: CTO E médica, editor. Cardio-genética. Primera ed. Madrid, España; 2015. p. 41–53.
12. Levine GN. Restrictive Cardiomyopathy. In: Cardiology Secrets [Internet]. Elsevier;2010. p. 203–6. Available from: https://www.elsevier.com/books/cardiology-secrets/levine/978-0-323-47870-0
13. Barredo M, Gonzalez J. Genética de la miocardiopatía restrictiva cardiaca. In: Cardiogenética. Primera edición. Madrid, España: Editorial médica CTO; 2015. p. 57–66.
14. Sabaté Rotés A, Huertas-Quiñones VM, Betrián P, Carretero J, Jiménez L, Girona J, et al. Miocardiopatía no compactada: características clínicas, evolutivas y pronósticas en edad pediátrica. Resultados de un estudio multicéntrico. An Pediatr. 2012 Dec;77(6):360–5
15. Miocardiopatia no compacta [Internet]. 2018. Available from:https://cardio.healthincode.com/genetica-cardiovascular/miocardiopatias/no-compactada
16. Monserrat Iglesias L. Miocardiopatía no compactada: una enfermedad en busca de criterios. Rev Española Cardiol [Internet]. 2008 Feb;61(2):112–5. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0300893208733566
17. Lee TM, Hsu DT, Kantor P, Towbin JA, Ware SM, Colan SD, et al. Pediatric Cardiomyopathies. Circ Res [Internet]. 2017 Sep 15;121(7):855–73. Available from: https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.116.309386
18. Yuan S-M. Cardiomyopathy in the pediatric patients. Pediatr Neonatol [Internet]. 2018Apr;59(2):120–8. Available from: https://www.sciencedirect.com/science/article/pii/S1875957218300342
19. Huertas-Quiñones VM, Mestra CF, Peña-Trujillo V, Gallo-Bernal S, Villaveces M, Alarcón-Forero LC. Paediatric cardiomyopathies: echocardiographic diagnosis, clinical profile, and demographic characteristics: the experience of a tertiary referral centre for Latin American paediatric cardiology. Cardiol Young [Internet]. 2020 Apr 17;30(4):462– Available from:https://www.cambridge.org/core/product/identifier/S1047951120000281/type/journal_article
20. Lipshultz SE, Law YM, Asante-Korang A, Austin ED, Dipchand AI, Everitt MD, et al. Cardiomyopathy in Children: Classification and Diagnosis: A Scientific Statement From the American Heart Association. Circulation [Internet]. 2019 Jul 2;140(1). Available from: https://www.ahajournals.org/doi/10.1161/CIR.0000000000000682
21. Yotti R, Seidman CE, Seidman JG. Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies. Annu Rev Genomics Hum Genet [Internet]. 2019 Aug 31;20(1):129–53. Available from: https://www.annualreviews.org/doi/10.1146/annurev-genom-083118-015306
22. Jordan E, Peterson L, Ai T, Asatryan B, Bronicki L, Brown E, et al. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Circulation [Internet]. 2021 Jul 6;144(1):7–19. Available from: https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.120.053033
23. Lakdawala NK, Dellefave L, Redwood CS, Sparks E, Cirino AL, Depalma S, et al. Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation. J Am Coll Cardiol [Internet]. 2010 Jan;55(4):320–9. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0735109709037784
24. Xiao L, Li C, Sun Y, Chen Y, Wei H, Hu D, et al. Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy. Front Cardiovasc Med [Internet]. 2021 Apr 30;8. Available from: https://www.frontiersin.org/articles/10.3389/fcvm.2021.657689/full
25. Liew C-C, Sole MJ, Yamauchi-Takihara K, Kellam B, Anderson DH, Lin L, et al. Complete sequence and organization of the human cardiac β-myosin heavy chain gene. Nucleic Acids Res [Internet]. 1990;18(12):3647–51. Available from: https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/18.12.3647
26. Bang M-L, Centner T, Fornoff F, Geach AJ, Gotthardt M, McNabb M, et al. The Complete Gene Sequence of Titin, Expression of an Unusual ≈700-kDa Titin Isoform, and Its Interaction With Obscurin Identify a Novel Z-Line to I-Band Linking System. Circ Res [Internet]. 2001 Nov 23;89(11):1065–72. Available from: https://www.ahajournals.org/doi/10.1161/hh2301.100981
27. Fananapazir L, Dalakas MC, Cyran F, Cohn G, Epstein ND. Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy. Proc Natl Acad Sci [Internet]. 1993 May;90(9):3993–7. Available from: https://pnas.org/doi/full/10.1073/pnas.90.9.3993
28. Myosin, heavy chain 7, cardiac muscle, beta; MYH7 [Internet]. 2018. Available from: https://www.omim.org/entry/160760
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
2. Lipshultz SE, Cochran TR, Briston DA, Brown SR, Sambatakos PJ, Miller TL, et al. Pediatric cardiomyopathies: causes, epidemiology, clinical course, preventive estrategies and therapies. Future Cardiol [Internet]. 2013 Nov;9(6):817–48. Available from: https://www.futuremedicine.com/doi/abs/10.2217/fca.13.66
3. Konta L, Franklin RCG, Kaski JP. Nomenclature and systems of classification for cardiomyopathy in children. Cardiol Young [Internet]. 2015 Aug 17;25(S2):31–42.Availablefrom:https://www.cambridge.org/core/product/identifier/S1047951115001201/type/journal_article
4. Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies. Heart [Internet]. 1980 Dec 1;44(6):672–3. Available from:http://heart.bmj.com/cgi/doi/10.1136/hrt.44.6.672
5. Mathew J, Zahavich L, Lafreniere-Roula M, Wilson J, George K, Benson L, et al. Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy. Clin Genet[Internet]. 2018 Feb;93(2):310–9.Available from: http://doi.wiley.com/10.1111/cge.13157
6. Ware SM. Cardiomyopathy in Children. J Am Coll Cardiol [Internet]. 2018Nov;72(19):2339–41. Available from:https://linkinghub.elsevier.com/retrieve/pii/S073510971838402X
7. Huertas-Quiñones VM, Restrepo CM. Genética de las Cardiopatías Congénitas. Capítulo 15. Bloque 4-Genética del Corazón y sus estructuras. En López-Farré. Cardio-Genética. Primera ed. Sociedad Española de Cardiología, Universidad Complutense de Madrid. Editorial médica CTO. Madrid (España) 2015:175-202.ISBN 978-84-16153-91-6.
8. Miocardiopatia dilatada [Internet]. 2018. Available from: https://healthincode.com/en/panels/cardiology/cardiomyopathy/dilated-cardiomyopathy/
9. Huertas-Quiñones VM. Cardiomiopatías en edad pediátrica. En “Cardiología Pediátrica”. Díaz GF, Sandoval N, Vélez JF, ed. Segunda ed. Sociedad Colombiana de Cardiología. Editorial Distribuna. Bogotá (Colombia)2018:941-974. ISBN 978-958-8813-70-7.
11. Monserrat L, Ochoa J, Garcia D, Ortiz M. Genética de la miocardiopatia hipertrofica. In: CTO E médica, editor. Cardio-genética. Primera ed. Madrid, España; 2015. p. 41–53.
12. Levine GN. Restrictive Cardiomyopathy. In: Cardiology Secrets [Internet]. Elsevier;2010. p. 203–6. Available from: https://www.elsevier.com/books/cardiology-secrets/levine/978-0-323-47870-0
13. Barredo M, Gonzalez J. Genética de la miocardiopatía restrictiva cardiaca. In: Cardiogenética. Primera edición. Madrid, España: Editorial médica CTO; 2015. p. 57–66.
14. Sabaté Rotés A, Huertas-Quiñones VM, Betrián P, Carretero J, Jiménez L, Girona J, et al. Miocardiopatía no compactada: características clínicas, evolutivas y pronósticas en edad pediátrica. Resultados de un estudio multicéntrico. An Pediatr. 2012 Dec;77(6):360–5
15. Miocardiopatia no compacta [Internet]. 2018. Available from:https://cardio.healthincode.com/genetica-cardiovascular/miocardiopatias/no-compactada
16. Monserrat Iglesias L. Miocardiopatía no compactada: una enfermedad en busca de criterios. Rev Española Cardiol [Internet]. 2008 Feb;61(2):112–5. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0300893208733566
17. Lee TM, Hsu DT, Kantor P, Towbin JA, Ware SM, Colan SD, et al. Pediatric Cardiomyopathies. Circ Res [Internet]. 2017 Sep 15;121(7):855–73. Available from: https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.116.309386
18. Yuan S-M. Cardiomyopathy in the pediatric patients. Pediatr Neonatol [Internet]. 2018Apr;59(2):120–8. Available from: https://www.sciencedirect.com/science/article/pii/S1875957218300342
19. Huertas-Quiñones VM, Mestra CF, Peña-Trujillo V, Gallo-Bernal S, Villaveces M, Alarcón-Forero LC. Paediatric cardiomyopathies: echocardiographic diagnosis, clinical profile, and demographic characteristics: the experience of a tertiary referral centre for Latin American paediatric cardiology. Cardiol Young [Internet]. 2020 Apr 17;30(4):462– Available from:https://www.cambridge.org/core/product/identifier/S1047951120000281/type/journal_article
20. Lipshultz SE, Law YM, Asante-Korang A, Austin ED, Dipchand AI, Everitt MD, et al. Cardiomyopathy in Children: Classification and Diagnosis: A Scientific Statement From the American Heart Association. Circulation [Internet]. 2019 Jul 2;140(1). Available from: https://www.ahajournals.org/doi/10.1161/CIR.0000000000000682
21. Yotti R, Seidman CE, Seidman JG. Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies. Annu Rev Genomics Hum Genet [Internet]. 2019 Aug 31;20(1):129–53. Available from: https://www.annualreviews.org/doi/10.1146/annurev-genom-083118-015306
22. Jordan E, Peterson L, Ai T, Asatryan B, Bronicki L, Brown E, et al. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Circulation [Internet]. 2021 Jul 6;144(1):7–19. Available from: https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.120.053033
23. Lakdawala NK, Dellefave L, Redwood CS, Sparks E, Cirino AL, Depalma S, et al. Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation. J Am Coll Cardiol [Internet]. 2010 Jan;55(4):320–9. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0735109709037784
24. Xiao L, Li C, Sun Y, Chen Y, Wei H, Hu D, et al. Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy. Front Cardiovasc Med [Internet]. 2021 Apr 30;8. Available from: https://www.frontiersin.org/articles/10.3389/fcvm.2021.657689/full
25. Liew C-C, Sole MJ, Yamauchi-Takihara K, Kellam B, Anderson DH, Lin L, et al. Complete sequence and organization of the human cardiac β-myosin heavy chain gene. Nucleic Acids Res [Internet]. 1990;18(12):3647–51. Available from: https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/18.12.3647
26. Bang M-L, Centner T, Fornoff F, Geach AJ, Gotthardt M, McNabb M, et al. The Complete Gene Sequence of Titin, Expression of an Unusual ≈700-kDa Titin Isoform, and Its Interaction With Obscurin Identify a Novel Z-Line to I-Band Linking System. Circ Res [Internet]. 2001 Nov 23;89(11):1065–72. Available from: https://www.ahajournals.org/doi/10.1161/hh2301.100981
27. Fananapazir L, Dalakas MC, Cyran F, Cohn G, Epstein ND. Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy. Proc Natl Acad Sci [Internet]. 1993 May;90(9):3993–7. Available from: https://pnas.org/doi/full/10.1073/pnas.90.9.3993
28. Myosin, heavy chain 7, cardiac muscle, beta; MYH7 [Internet]. 2018. Available from: https://www.omim.org/entry/160760
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Introducción: Las miocardiopatías son un grupo heterogéneo de entidades que comprometen la función y estructura del músculo cardíaco, generando disfunción miocárdica, falla cardíaca e inclusive muerte súbita. La literatura Latinoamérica es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07e86139abd08216d585f6ef3ed2c13a
https://repository.urosario.edu.co/handle/10336/34538
https://repository.urosario.edu.co/handle/10336/34538
Publikováno v:
Cardiology in the Young; Apr2019, Vol. 29 Issue 4, p538-540, 3p
Autor:
KONSTANTAKOS, IOANNIS M.
Publikováno v:
Logeion: Periodiko gia to Archaio Theatro; 2017, Issue 7, p108-144, 37p