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

Year Number of Results
1969 1
1972 1
1973 1
1983 1
1991 1
1993 2
1994 2
1995 3
1996 2
1997 4
1998 2
1999 1
2001 1
2002 1
2003 1
2004 2
2005 4
2006 3
2007 2
2008 2
2009 1
2010 2
2011 1
2012 1
2013 2
2014 3
2015 5
2016 6
2017 5
2018 6
2019 10
2020 11
2021 5
2022 5
2023 1

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88 results

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Page 1
Moclobemide overdose.
Myrenfors PG, Eriksson T, Sandsted CS, Sjöberg G. Myrenfors PG, et al. Among authors: sjoberg g. J Intern Med. 1993 Feb;233(2):113-5. doi: 10.1111/j.1365-2796.1993.tb00662.x. J Intern Med. 1993. PMID: 8433071
Transcatheter Intervention for Coarctation of the Aorta: A Nordic Population-Based Registry With Long-Term Follow-Up.
Eriksson P, Pihkala J, Jensen AS, Dohlen G, Liuba P, Wahlander H, Sjoberg G, Hlebowicz J, Furenas E, Leirgul E, Settergren M, Vithessonthi K, Nielsen NE, Christersson C, Sondergaard L, Sinisalo J, Nielsen-Kudsk JE, Dellborg M, Larsen SH. Eriksson P, et al. Among authors: sjoberg g. JACC Cardiovasc Interv. 2023 Feb 27;16(4):444-453. doi: 10.1016/j.jcin.2022.11.007. JACC Cardiovasc Interv. 2023. PMID: 36858664
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Muravyev A, Vershinina T, Tesner P, Sjoberg G, Fomicheva Y, Čajbiková NN, Kozyreva A, Zhuk S, Mamaeva E, Tarnovskaya S, Jornholt J, Sokolnikova P, Pervunina T, Vasichkina E, Sejersen T, Kostareva A. Muravyev A, et al. Among authors: sjoberg g. Orphanet J Rare Dis. 2022 Sep 14;17(1):358. doi: 10.1186/s13023-022-02477-5. Orphanet J Rare Dis. 2022. PMID: 36104822 Free PMC article.
Progressive cardiac conduction disease associated with a DSP gene mutation.
Kiselev A, Mikhaylov E, Parmon E, Sjoberg G, Sejersen T, Tarnovskaya S, Nugnyi P, Mitrofanova L, Lebedev D, Kostareva A. Kiselev A, et al. Among authors: sjoberg g. Int J Cardiol. 2016 Aug 1;216:188-9. doi: 10.1016/j.ijcard.2016.04.164. Epub 2016 Apr 30. Int J Cardiol. 2016. PMID: 27166992 No abstract available.
88 results