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

Year Number of Results
1978 1
1979 1
1980 1
1985 5
1986 3
1987 4
1988 10
1989 3
1990 5
1991 2
1992 2
1993 3
1994 4
1995 2
1996 3
1997 4
1998 1
1999 2
2000 1
2001 3
2002 4
2003 5
2004 1
2005 4
2006 4
2007 2
2009 1
2010 3
2011 4
2012 2
2013 1
2015 1
2016 2
2017 1
2018 1
2020 2
2021 2
2022 3
2024 0

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Similar articles for PMID: 3605207

99 results

Results by year

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Page 1
Dominantly inherited dilated cardiomyopathy.
Gardner RJ, Hanson JW, Ionasescu VV, Ardinger HH, Skorton DJ, Mahoney LT, Hart MN, Rose EF, Smith WL, Florentine MS, et al. Gardner RJ, et al. Am J Med Genet. 1987 May;27(1):61-73. doi: 10.1002/ajmg.1320270108. Am J Med Genet. 1987. PMID: 3605207
Familial dilated cardiomyopathy.
Schmidt MA, Michels VV, Edwards WD, Miller FA. Schmidt MA, et al. Am J Med Genet. 1988 Sep;31(1):135-43. doi: 10.1002/ajmg.1320310116. Am J Med Genet. 1988. PMID: 3223495
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F. Bonne G, et al. Ann Neurol. 2000 Aug;48(2):170-80. Ann Neurol. 2000. PMID: 10939567
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
Perrot A, Sigusch HH, Nägele H, Genschel J, Lehmkuhl H, Hetzer R, Geier C, Leon Perez V, Reinhard D, Dietz R, Josef Osterziel K, Schmidt HH. Perrot A, et al. Eur J Heart Fail. 2006 Aug;8(5):484-93. doi: 10.1016/j.ejheart.2005.11.004. Epub 2006 Jan 4. Eur J Heart Fail. 2006. PMID: 16386954 Free article.
99 results