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Results by year

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

Year Number of Results
1988 3
1990 2
1991 1
1993 2
1994 2
1995 1
1996 3
1997 2
1998 3
1999 1
2000 2
2001 2
2003 3
2004 3
2005 3
2006 3
2007 3
2010 1
2011 3
2012 5
2013 2
2014 3
2017 2
2018 2
2019 1
2024 0

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Similar articles for PMID: 1978914

53 results

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Page 1
Mitochondrial mutation in fatal infantile cardiomyopathy.
Tanaka M, Ino H, Ohno K, Hattori K, Sato W, Ozawa T, Tanaka T, Itoyama S. Tanaka M, et al. Lancet. 1990 Dec 8;336(8728):1452. doi: 10.1016/0140-6736(90)93162-i. Lancet. 1990. PMID: 1978914 No abstract available.
Functional analysis of DES-p.L398P and RBM20-p.R636C.
Brodehl A, Ebbinghaus H, Gaertner-Rommel A, Stanasiuk C, Klauke B, Milting H. Brodehl A, et al. Genet Med. 2019 May;21(5):1246-1247. doi: 10.1038/s41436-018-0291-2. Epub 2018 Sep 28. Genet Med. 2019. PMID: 30262925 Free article. No abstract available.
First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy.
Alila-Fersi O, Tabebi M, Maalej M, Belguith N, Keskes L, Mkaouar-Rebai E, Fakhfakh F. Alila-Fersi O, et al. Biochem Biophys Res Commun. 2018 Mar 18;497(4):1049-1054. doi: 10.1016/j.bbrc.2018.02.173. Epub 2018 Feb 23. Biochem Biophys Res Commun. 2018. PMID: 29481798
Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening.
Alila-Fersi O, Chamkha I, Majdoub I, Gargouri L, Mkaouar-Rebai E, Tabebi M, Tlili A, Keskes L, Mahfoudh A, Fakhfakh F. Alila-Fersi O, et al. Biochem Biophys Res Commun. 2017 Feb 26;484(1):71-78. doi: 10.1016/j.bbrc.2017.01.070. Epub 2017 Jan 16. Biochem Biophys Res Commun. 2017. PMID: 28104394
53 results