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Items: 16

1.

POLG-Related Disorders.

Cohen BH, Chinnery PF, Copeland WC.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2010 Mar 16 [updated 2018 Mar 1].

3.

What Can Mitochondrial DNA Analysis Tell Us About Mood Disorders?

Kasahara T, Kato T.

Biol Psychiatry. 2018 May 1;83(9):731-738. doi: 10.1016/j.biopsych.2017.09.010. Epub 2017 Sep 21. Review.

4.

Depression-like episodes in mice harboring mtDNA deletions in paraventricular thalamus.

Kasahara T, Takata A, Kato TM, Kubota-Sakashita M, Sawada T, Kakita A, Mizukami H, Kaneda D, Ozawa K, Kato T.

Mol Psychiatry. 2016 Jan;21(1):39-48. doi: 10.1038/mp.2015.156. Epub 2015 Oct 20.

5.

A composite peripheral blood gene expression measure as a potential diagnostic biomarker in bipolar disorder.

Munkholm K, Peijs L, Vinberg M, Kessing LV.

Transl Psychiatry. 2015 Aug 4;5:e614. doi: 10.1038/tp.2015.110.

6.

Mitochondrial dysfunction in migraine.

Yorns WR Jr, Hardison HH.

Semin Pediatr Neurol. 2013 Sep;20(3):188-93. doi: 10.1016/j.spen.2013.09.002.

PMID:
24331360
7.

Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: a case report and an update on the state of art.

Kiferle L, Orsucci D, Mancuso M, Lo Gerfo A, Petrozzi L, Siciliano G, Ceravolo R, Bonuccelli U.

Neurosci Lett. 2013 Nov 27;556:1-4. doi: 10.1016/j.neulet.2013.09.034. Epub 2013 Sep 26. Review.

PMID:
24076137
8.

POLG1 Arg953Cys mutation: expanded phenotype and recessive inheritance in a Brazilian family.

Gurgel-Giannetti J, Camargos ST, Cardoso F, Hirano M, DiMauro S.

Muscle Nerve. 2012 Mar;45(3):453-4. doi: 10.1002/mus.22330. No abstract available.

9.

Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation?

Verhoeven WM, Egger JI, Kremer BP, de Pont BJ, Marcelis CL.

Neuropsychiatr Dis Treat. 2011;7:293-6. doi: 10.2147/NDT.S20153. Epub 2011 May 15.

10.

Disease impact in chronic progressive external ophthalmoplegia: more than meets the eye.

Smits BW, Fermont J, Delnooz CC, Kalkman JS, Bleijenberg G, van Engelen BG.

Neuromuscul Disord. 2011 Apr;21(4):272-8. doi: 10.1016/j.nmd.2010.12.008. Epub 2011 Jan 13.

11.

Translational research in bipolar disorder: emerging insights from genetically based models.

Chen G, Henter ID, Manji HK.

Mol Psychiatry. 2010 Sep;15(9):883-95. doi: 10.1038/mp.2010.3. Epub 2010 Feb 9. Review.

12.

Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism.

Synofzik M, Asmus F, Reimold M, Schöls L, Berg D.

Mov Disord. 2010 Jan 30;25(2):243-5. doi: 10.1002/mds.22865. No abstract available.

PMID:
19998270
13.

Reverse translational strategies for developing animal models of bipolar disorder.

Malkesman O, Austin DR, Chen G, Manji HK.

Dis Model Mech. 2009 May-Jun;2(5-6):238-45. doi: 10.1242/dmm.001628. Review.

14.

Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy.

Galassi G, Lamantea E, Invernizzi F, Tavani F, Pisano I, Ferrero I, Palmieri L, Zeviani M.

Neuromuscul Disord. 2008 Jun;18(6):465-70. doi: 10.1016/j.nmd.2008.03.013. Epub 2008 May 27.

PMID:
18504126
15.

Molecular genetics of bipolar disorder and depression.

Kato T.

Psychiatry Clin Neurosci. 2007 Feb;61(1):3-19. Review.

16.

Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes.

Kasahara T, Kubota M, Miyauchi T, Noda Y, Mouri A, Nabeshima T, Kato T.

Mol Psychiatry. 2006 Jun;11(6):577-93, 523.

PMID:
16619054

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