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Items: 1 to 20 of 121

1.

Inherited mitochondrial neuropathies.

Finsterer J.

J Neurol Sci. 2011 May 15;304(1-2):9-16. doi: 10.1016/j.jns.2011.02.012. Epub 2011 Mar 13. Review.

PMID:
21402391
2.

Mitochondrial ataxias.

Finsterer J.

Can J Neurol Sci. 2009 Sep;36(5):543-53. Review.

PMID:
19831121
3.

[Molecular genetics of inherited neuropathies].

Takashima H.

Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Review. Japanese.

PMID:
16541790
4.

Human mitochondrial diseases: answering questions and questioning answers.

Howell N.

Int Rev Cytol. 1999;186:49-116. Review.

PMID:
9770297
5.

Mitochondrial cytopathies.

Schmiedel J, Jackson S, Schäfer J, Reichmann H.

J Neurol. 2003 Mar;250(3):267-77. Review.

PMID:
12638015
6.

Overview on visceral manifestations of mitochondrial disorders.

Finsterer J.

Neth J Med. 2006 Mar;64(3):61-71. Review.

7.

Inherited peripheral neuropathies due to mitochondrial disorders.

Cassereau J, Codron P, Funalot B.

Rev Neurol (Paris). 2014 May;170(5):366-74. doi: 10.1016/j.neurol.2013.11.005. Epub 2014 Apr 24. Review.

PMID:
24768438
8.

Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.

Marotta R, Chin J, Quigley A, Katsabanis S, Kapsa R, Byrne E, Collins S.

Intern Med J. 2004 Jan-Feb;34(1-2):10-9.

PMID:
14748908
9.

Functional diagnostics in mitochondrial diseases.

Siciliano G, Volpi L, Piazza S, Ricci G, Mancuso M, Murri L.

Biosci Rep. 2007 Jun;27(1-3):53-67. Review.

PMID:
17492503
10.

Movement disorders in mitochondrial diseases.

Tranchant C, Anheim M.

Rev Neurol (Paris). 2016 Aug - Sep;172(8-9):524-529. doi: 10.1016/j.neurol.2016.07.003. Epub 2016 Jul 28. Review.

PMID:
27476418
11.

Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.

Isashiki Y, Nakagawa M, Ohba N, Kamimura K, Sakoda Y, Higuchi I, Izumo S, Osame M.

Acta Ophthalmol Scand. 1998 Feb;76(1):6-13.

12.

SANDO: two novel mutations in POLG1 gene.

Gago MF, Rosas MJ, Guimarães J, Ferreira M, Vilarinho L, Castro L, Carpenter S.

Neuromuscul Disord. 2006 Aug;16(8):507-9. Epub 2006 Aug 21.

PMID:
16919951
13.

[Peripheral neuropathies due to mitochondrial disorders].

Funalot B.

Rev Neurol (Paris). 2009 Dec;165(12):1118-21. doi: 10.1016/j.neurol.2009.10.001. French.

PMID:
19942242
14.

A novel mitochondrial mutation m.8989G>C associated with neuropathy, ataxia, retinitis pigmentosa - the NARP syndrome.

Duno M, Wibrand F, Baggesen K, Rosenberg T, Kjaer N, Frederiksen AL.

Gene. 2013 Feb 25;515(2):372-5. doi: 10.1016/j.gene.2012.12.066. Epub 2012 Dec 20.

PMID:
23266623
15.

Mitochondrial abnormalities in patients with LHON-like optic neuropathies.

Abu-Amero KK, Bosley TM.

Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4211-20.

PMID:
17003408
16.

Epilepsy in mitochondrial disorders.

Finsterer J, Zarrouk Mahjoub S.

Seizure. 2012 Jun;21(5):316-21. doi: 10.1016/j.seizure.2012.03.003. Epub 2012 Mar 27. Review.

17.

[Mitochondrial diseases; thinking beyond organ specialism necessary].

Smits BW, Smeitink JA, van Engelen BG.

Ned Tijdschr Geneeskd. 2008 Oct 18;152(42):2275-81. Review. Dutch.

PMID:
19009876
18.

Cognitive dysfunction in mitochondrial disorders.

Finsterer J.

Acta Neurol Scand. 2012 Jul;126(1):1-11. doi: 10.1111/j.1600-0404.2012.01649.x. Epub 2012 Feb 15.

PMID:
22335339
19.

Demyelinating polyneuropathy in Leber hereditary optic neuropathy.

Gilhuis HJ, Schelhaas HJ, Cruysberg JR, Zwarts MJ.

Neuromuscul Disord. 2006 Jun;16(6):394-5. Epub 2006 May 11.

PMID:
16690316
20.

Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.

Thorburn DR, Dahl HH.

Am J Med Genet. 2001 Spring;106(1):102-14. Review.

PMID:
11579429

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