Similar articles for PMID: 16738010

Year	Number of Results
1994	2
1995	1
1998	1
1999	1
2000	1
2001	4
2002	4
2003	2
2004	4
2005	3
2006	6
2007	5
2008	2
2009	2
2010	6
2011	7
2012	4
2014	3
2015	2
2016	2
2017	2
2018	5
2019	2
2020	1
2021	2
2022	1
2024	0

1

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

Hinttala R, Smeets R, Moilanen JS, Ugalde C, Uusimaa J, Smeitink JA, Majamaa K. Hinttala R, et al. J Med Genet. 2006 Nov;43(11):881-6. doi: 10.1136/jmg.2006.042168. Epub 2006 May 31. J Med Genet. 2006. PMID: 16738010 Free PMC article.

2

Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variants.

Wani AA, Ahanger SH, Bapat SA, Rangrez AY, Hingankar N, Suresh CG, Barnabas S, Patole MS, Shouche YS. Wani AA, et al. PLoS One. 2007 Sep 26;2(9):e942. doi: 10.1371/journal.pone.0000942. PLoS One. 2007. PMID: 17895983 Free PMC article.

3

Animal models for mitochondrial disease.

Wallace DC. Wallace DC. Methods Mol Biol. 2002;197:3-54. doi: 10.1385/1-59259-284-8:003. Methods Mol Biol. 2002. PMID: 12013805 Review.

4

Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations.

Rubio-Gozalbo ME, Dijkman KP, van den Heuvel LP, Sengers RC, Wendel U, Smeitink JA. Rubio-Gozalbo ME, et al. Hum Mutat. 2000;15(6):522-32. doi: 10.1002/1098-1004(200006)15:6<522::AID-HUMU4>3.0.CO;2-Y. Hum Mutat. 2000. PMID: 10862082

5

Molecular genetic and clinical aspects of mitochondrial disorders in childhood.

Moslemi AR, Darin N. Moslemi AR, et al. Mitochondrion. 2007 Jul;7(4):241-52. doi: 10.1016/j.mito.2007.02.002. Epub 2007 Feb 14. Mitochondrion. 2007. PMID: 17376748 Review.

6

Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.

Bosley TM, Brodsky MC, Glasier CM, Abu-Amero KK. Bosley TM, et al. Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5250-6. doi: 10.1167/iovs.08-2193. Epub 2008 Aug 1. Invest Ophthalmol Vis Sci. 2008. PMID: 18676632

7

The molecular basis of human complex I deficiency.

Tucker EJ, Compton AG, Calvo SE, Thorburn DR. Tucker EJ, et al. IUBMB Life. 2011 Sep;63(9):669-77. doi: 10.1002/iub.495. Epub 2011 Jul 15. IUBMB Life. 2011. PMID: 21766414 Free article. Review.

8

Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease.

Kirby DM, Boneh A, Chow CW, Ohtake A, Ryan MT, Thyagarajan D, Thorburn DR. Kirby DM, et al. Ann Neurol. 2003 Oct;54(4):473-8. doi: 10.1002/ana.10687. Ann Neurol. 2003. PMID: 14520659

9

Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency.

Meulemans A, Lissens W, Van Coster R, De Meirleir L, Smet J, Nassogne MC, Liebaers I, Seneca S. Meulemans A, et al. Eur J Paediatr Neurol. 2004;8(6):299-306. doi: 10.1016/j.ejpn.2004.07.006. Eur J Paediatr Neurol. 2004. PMID: 15542384

10

Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.

Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K, Tanaka M. Kato T, et al. J Hum Genet. 2010 Mar;55(3):147-54. doi: 10.1038/jhg.2009.143. Epub 2010 Jan 29. J Hum Genet. 2010. PMID: 20111055

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

64 results

Results by year