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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1987 1
1989 2
1990 4
1991 1
1992 8
1993 3
1994 2
1995 3
1996 1
1997 5
1998 2
1999 2
2000 6
2001 2
2002 2
2003 4
2004 5
2005 3
2006 4
2007 2
2008 7
2009 5
2010 13
2011 6
2012 3
2013 3
2014 5
2015 8
2016 5
2017 4
2018 6
2019 6
2020 8
2021 7
2022 8
2023 2

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PubMed for id: 382807

142 results

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Page 1
Genetic Basis of Childhood Cardiomyopathy.
Bagnall RD, Singer ES, Wacker J, Nowak N, Ingles J, King I, Macciocca I, Crowe J, Ronan A, Weintraub RG, Semsarian C. Bagnall RD, et al. Circ Genom Precis Med. 2022 Dec;15(6):e003686. doi: 10.1161/CIRCGEN.121.003686. Epub 2022 Oct 11. Circ Genom Precis Med. 2022. PMID: 36252119
ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium.
Bermúdez-Jiménez FJ, Carriel V, Santos-Mateo JJ, Fernández A, García-Hernández S, Ramos KA, Piqueras-Flores J, Cabrera-Romero E, Barriales-Villa R, de la Higuera Romero L, Alcalá López JE, Gimeno Blanes JR, Sánchez-Porras D, Campos F, Alaminos M, Oyonarte-Ramírez JM, Álvarez M, Tercedor L, Brodehl A, Jiménez-Jáimez J. Bermúdez-Jiménez FJ, et al. Rev Esp Cardiol (Engl Ed). 2023 May;76(5):301-311. doi: 10.1016/j.rec.2022.08.002. Epub 2022 Aug 8. Rev Esp Cardiol (Engl Ed). 2023. PMID: 35952944 English, Spanish.
142 results