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Johanna Kuusisto, Petri Sipola, Pertti Jääskeläinen & Anita Naukkarinen. (2016) Current perspectives in hypertrophic cardiomyopathy with the focus on patients in the Finnish population: a review. Annals of Medicine 48:7, pages 496-508.
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Mikko Jalanko, Mika Tarkiainen, Petri Sipola, Pertti Jääskeläinen, Kirsi Lauerma, Mika Laine, Markku S. Nieminen, Markku Laakso, Tiina Heliö & Johanna Kuusisto. (2016) Left ventricular mechanical dispersion is associated with nonsustained ventricular tachycardia in hypertrophic cardiomyopathy. Annals of Medicine 48:6, pages 417-427.
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Katherine Sachs, Debbie Andersen, Jennifer Sommer, Amy Winkelman & Philip S. Mehler. (2015) Avoiding Medical Complications During the Refeeding of Patients With Anorexia Nervosa. Eating Disorders 23:5, pages 411-421.
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Pertti Jääskeläinen, Tiina Heliö, Katriina Aalto-Setälä, Maija Kaartinen, Erkki Ilveskoski, Liisa Hämäläinen, John Melin, Satu Kärkkäinen, Keijo Peuhkurinen, Markku S. Nieminen, Markku Laakso & Johanna Kuusisto. (2014) A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy. Annals of Medicine 46:6, pages 424-429.
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Articles from other publishers (29)
Olga S. Chumakova, Tatiana N. Baklanova, Natalia V. Milovanova & Dmitry A. Zateyshchikov. (2023) Hypertrophic Cardiomyopathy in Underrepresented Populations: Clinical and Genetic Landscape Based on a Russian Single-Center Cohort Study. Genes 14:11, pages 2042.
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Róbert Sepp, Lidia Hategan, Beáta Csányi, János Borbás, Annamária Tringer, Eszter Dalma Pálinkás, Viktória Nagy, Hedvig Takács, Dóra Latinovics, Noémi Nyolczas, Attila Pálinkás, Réka Faludi, Miklós Rábai, Gábor Tamás Szabó, Dániel Czuriga, László Balogh, Róbert Halmosi, Attila Borbély, Tamás Habon, Zoltán Hegedűs & István Nagy. (2022) The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes. Diagnostics 12:5, pages 1132.
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Arsonval Lamounier Junior, Alba Guitián González, Alejandro Rodríguez Vilela, Alfredo Repáraz Andrade, Álvaro Rubio Alcaide, Ana Berta Sousa, Carmen Benito López, Diego Alonso García, Germán Fernández Ferro, Inês Cruz, Ivonne Johana Cárdenas Reyes, Joel Salazar-Mendiguchía García, José María Larrañaga-Moreira, Juan Pablo Ochoa, Julián Palomino-Doza, Luis de la Higuera Romero, Marcos Nicolás Cicerchia, María Alejandra Restrepo Córdoba, María Luisa Peña-Peña, Maria Noël Brögger, Marilia Loureiro, María Victoria Mogollón Jiménez, Raquel Bilbao Quesada, Raúl Franco Gutiérrez, Soledad García Hernández, Tomás Ripoll-Vera, Xusto Fernández, Olga Azevedo, Pablo García Pavía, Luis R. Lopes, Martín Ortiz, Dulce Brito, Roberto Barriales-Villa & Lorenzo Monserrat Iglesias. (2022) Correlación genotipo-fenotipo en miocardiopatía hipertrófica: un estudio multicéntrico en Portugal y España sobre la variante p.Arg21Leu de TPM1. Revista Española de Cardiología 75:3, pages 242-250.
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Arsonval Lamounier Junior, Alba Guitián González, Alejandro Rodríguez Vilela, Alfredo Repáraz Andrade, Álvaro Rubio Alcaide, Ana Berta Sousa, Carmen Benito López, Diego Alonso García, Germán Fernández Ferro, Inês Cruz, Ivonne Johana Cárdenas Reyes, Joel Salazar-Mendiguchía García, José María Larrañaga-Moreira, Juan Pablo Ochoa, Julián Palomino-Doza, Luis de la Higuera Romero, Marcos Nicolás Cicerchia, María Alejandra Restrepo Córdoba, María Luisa Peña-Peña, Maria Noël Brögger, Marilia Loureiro, María Victoria Mogollón Jiménez, Raquel Bilbao Quesada, Raúl Franco Gutiérrez, Soledad García Hernández, Tomás Ripoll-Vera, Xusto Fernández, Olga Azevedo, Pablo García Pavía, Luis R. Lopes, Martín Ortiz, Dulce Brito, Roberto Barriales-Villa & Lorenzo Monserrat Iglesias. (2022) Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant. Revista Española de Cardiología (English Edition) 75:3, pages 242-250.
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Chee Jian Pua, Nevin ThamCalvin W.L. Chin, Roddy Walsh, Chiea Chuen KhorChristopher N. Toepfer, Giuliana G. Repetti, Amanda C. GarfinkelJourdan F. EwoldtPaige CloonanChristopher S. ChenShi Qi LimJiashen Cai, Li Yang LooSiew Ching KongCharleston W.K. ChiangNicola WhiffinAntonio de Marvao, Pei Min LioAn An HiiCheng Xi YangThu Thao LeYasmin BylstraWeng Khong LimJing Xian TeoKallyandra PadilhaGabriela V. SilvaBangfen PanRisha Govind, Rachel J. Buchan, Paul J.R. Barton, Patrick TanRoger Foo, James W.L. YipRaymond C.C. WongWan Xian ChanAlexandre C. PereiraHak Chiaw TangSaumya Shekhar JamuarJames S. Ware, Jonathan G. Seidman, Christine E. Seidman & Stuart A. Cook. (2020)
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Mohammed Arif, Pooneh Nabavizadeh, Taejeong Song, Darshini Desai, Rohit Singh, Sholeh Bazrafshan, Mohit Kumar, Yigang Wang, Richard J. Gilbert, Perundurai S. Dhandapany, Richard C. Becker, Evangelia G. Kranias & Sakthivel Sadayappan. (2020) Genetic, clinical, molecular, and pathogenic aspects of the South Asian–specific polymorphic MYBPC3Δ25bp variant. Biophysical Reviews 12:4, pages 1065-1084.
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Berglind Adalsteinsdottir, Michael Burke, Barry J Maron, Ragnar Danielsen, Begoña Lopez, Javier Diez, Petr Jarolim, Jonathan Seidman, Christine E. Seidman, Carolyn Y Ho & Gunnar Th Gunnarsson. (2020)
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Minh Thu Tran Vu, Thuy Vy Nguyen, Nha Van Huynh, Hoang Tam Nguyen Thai, Vinh Pham Nguyen & Thuy Duong Ho Huynh. (2019) Presence of Hypertrophic Cardiomyopathy Related Gene Mutations and Clinical Manifestations in Vietnamese Patients With Hypertrophic Cardiomyopathy. Circulation Journal 83:9, pages 1908-1916.
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Mika Tarkiainen, Petri Sipola, Mikko Jalanko, Tiina Heliö, Pertti Jääskeläinen, Kati Kivelä, Mika Laine, Kirsi Lauerma & Johanna Kuusisto. (2019) CMR derived left ventricular septal convexity in carriers of the hypertrophic cardiomyopathy-causing MYBPC3-Q1061X mutation. Scientific Reports 9:1.
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Pertti Jääskeläinen, Jagadish Vangipurapu, Joose Raivo, Teemu Kuulasmaa, Tiina Heliö, Katriina Aalto‐Setälä, Maija Kaartinen, Erkki Ilveskoski, Sari Vanninen, Liisa Hämäläinen, John Melin, Jorma Kokkonen, Markku S. Nieminen, Markku Laakso & Johanna Kuusisto. (2019) Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy. ESC Heart Failure 6:2, pages 436-445.
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