Similar articles for PMID: 12767666

Year	Number of Results
1984	1
1987	2
1988	1
1989	2
1990	2
1991	3
1992	6
1993	4
1994	8
1995	10
1996	6
1997	4
1998	7
1999	16
2000	10
2001	11
2002	9
2003	8
2004	7
2005	9
2006	7
2007	9
2008	11
2009	14
2010	8
2011	15
2012	13
2013	13
2014	13
2015	9
2016	8
2017	6
2018	10
2019	12
2020	19
2021	11
2022	9
2023	4
2024	0

1

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM. Taylor RW, et al. J Am Coll Cardiol. 2003 May 21;41(10):1786-96. doi: 10.1016/s0735-1097(03)00300-0. J Am Coll Cardiol. 2003. PMID: 12767666 Free article.

2

Severe Antenatal Hypertrophic Cardiomyopathy Secondary to ACAD9-Related Mitochondrial Complex I Deficiency.

Dubucs C, Aziza J, Sartor A, Heitz F, Sevely A, Sternberg D, Jardel C, Cavallé-Garrido T, Albrecht S, Bernard C, De Bie I, Chassaing N. Dubucs C, et al. Mol Syndromol. 2023 Apr;14(2):101-108. doi: 10.1159/000526022. Epub 2022 Oct 21. Mol Syndromol. 2023. PMID: 37064341 Free PMC article.

3

Hypertrophic cardiomyopathy as the initial presentation of mitochondrial disease in an infant born to a diabetic mother.

Byun JC, Choi HJ. Byun JC, et al. Cardiol Young. 2023 Sep;33(9):1743-1745. doi: 10.1017/S1047951123000392. Epub 2023 Mar 23. Cardiol Young. 2023. PMID: 36950872

4

Novel ELAC2 Mutations in Individuals Presenting with Variably Severe Neurological Disease in the Presence or Absence of Cardiomyopathy.

Cafournet C, Zanin S, Guimier A, Hully M, Assouline Z, Barcia G, de Lonlay P, Steffann J, Munnich A, Bonnefont JP, Rötig A, Ruzzenente B, Metodiev MD. Cafournet C, et al. Life (Basel). 2023 Feb 4;13(2):445. doi: 10.3390/life13020445. Life (Basel). 2023. PMID: 36836802 Free PMC article.

5

A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene.

Amate-García G, Ballesta-Martínez MJ, Serrano-Lorenzo P, Garrido-Moraga R, González-Quintana A, Blázquez A, Rubio JC, García-Consuegra I, Arenas J, Ugalde C, Morán M, Guillén-Navarro E, Martín MA. Amate-García G, et al. Int J Mol Sci. 2023 Jan 16;24(2):1743. doi: 10.3390/ijms24021743. Int J Mol Sci. 2023. PMID: 36675256 Free PMC article.

6

Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA ^Lys Gene.

Maraş Genç H, Akpınar G, Kasap M, Uyur Yalçın E, Üstek D, Aslanger AD, Kara B. Maraş Genç H, et al. Mol Syndromol. 2022 Jul;13(4):305-317. doi: 10.1159/000519526. Epub 2022 Feb 9. Mol Syndromol. 2022. PMID: 36158049 Free PMC article.

7

The Mitochondrial tRNA^Phe 625G>A Mutation in Three Han Chinese Families With Cholecystolithiasis.

Hou L, Hu C, Ji L, Wang Q, Liang M. Hou L, et al. Front Genet. 2022 May 27;13:814729. doi: 10.3389/fgene.2022.814729. eCollection 2022. Front Genet. 2022. PMID: 35719381 Free PMC article.

8

Reduction of Drosophila Mitochondrial RNase P in Skeletal and Heart Muscle Causes Muscle Degeneration, Cardiomyopathy, and Heart Arrhythmia.

Saoji M, Petersen CE, Sen A, Tripoli BA, Smyth JT, Cox RT. Saoji M, et al. Front Cell Dev Biol. 2022 May 19;10:788516. doi: 10.3389/fcell.2022.788516. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35663400 Free PMC article.

9

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.

Xu C, Tong L, Rao J, Ye Q, Chen Y, Zhang Y, Xu J, Mao X, Meng F, Shen H, Lu Z, Cang X, Fu H, Wang S, Gu W, Lai EY, Guan MX, Jiang P, Mao J. Xu C, et al. JCI Insight. 2022 Jun 8;7(11):e157418. doi: 10.1172/jci.insight.157418. JCI Insight. 2022. PMID: 35472031 Free PMC article.

10

Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.

Calabrese C, Pyle A, Griffin H, Coxhead J, Hussain R, Braund PS, Li L, Burgess A, Munroe PB, Little L, Warren HR, Cabrera C, Hall A, Caulfield MJ, Rothwell PM, Samani NJ, Hudson G, Chinnery PF. Calabrese C, et al. PLoS Genet. 2022 Apr 1;18(4):e1010068. doi: 10.1371/journal.pgen.1010068. eCollection 2022 Apr. PLoS Genet. 2022. PMID: 35363781 Free PMC article.

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