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Items: 1 to 20 of 98

1.

The brain is hypothermic in patients with mitochondrial diseases.

Rango M, Arighi A, Bonifati C, Del Bo R, Comi G, Bresolin N.

J Cereb Blood Flow Metab. 2014 May;34(5):915-20. doi: 10.1038/jcbfm.2014.38. Epub 2014 Mar 12.

2.

Increased brain temperature in Parkinson's disease.

Rango M, Arighi A, Bonifati C, Bresolin N.

Neuroreport. 2012 Feb 15;23(3):129-33. doi: 10.1097/WNR.0b013e32834e8fac.

PMID:
22186803
3.

Phosphorus and proton magnetic resonance spectroscopy demonstrates mitochondrial dysfunction in early and advanced Parkinson's disease.

Hattingen E, Magerkurth J, Pilatus U, Mozer A, Seifried C, Steinmetz H, Zanella F, Hilker R.

Brain. 2009 Dec;132(Pt 12):3285-97. doi: 10.1093/brain/awp293. Epub .

4.

Role of mitochondrial dysfunction in Alzheimer's disease.

Castellani R, Hirai K, Aliev G, Drew KL, Nunomura A, Takeda A, Cash AD, Obrenovich ME, Perry G, Smith MA.

J Neurosci Res. 2002 Nov 1;70(3):357-60. Review.

PMID:
12391597
6.

Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.

Del Bo R, Moggio M, Rango M, Bonato S, D'Angelo MG, Ghezzi S, Airoldi G, Bassi MT, Guglieri M, Napoli L, Lamperti C, Corti S, Federico A, Bresolin N, Comi GP.

Neurology. 2008 Dec 9;71(24):1959-66. doi: 10.1212/01.wnl.0000327095.32005.a4. Epub 2008 Oct 22.

PMID:
18946002
7.

Multimodal evoked potentials in three siblings with mitochondrial disease.

Lai KL, Liu CY, Liu YC, Lin CY, Chen JT, Liao KK, Wu ZA.

Acta Neurol Taiwan. 2006 Jun;15(2):92-7.

PMID:
16871895
8.

The role of mitochondrial dysfunction in bipolar disorder.

Kato T.

Drug News Perspect. 2006 Dec;19(10):597-602. Review.

PMID:
17299601
9.

Multisystem manifestations of mitochondrial disorders.

Di Donato S.

J Neurol. 2009 May;256(5):693-710. doi: 10.1007/s00415-009-5028-3. Epub 2009 Mar 1. Review.

PMID:
19252802
10.

Diagnosis of mitochondrial myopathies.

Milone M, Wong LJ.

Mol Genet Metab. 2013 Sep-Oct;110(1-2):35-41. doi: 10.1016/j.ymgme.2013.07.007. Epub 2013 Jul 17. Review.

PMID:
23911206
11.

Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutation.

Betts J, Barron MJ, Needham SJ, Schaefer AM, Taylor RW, Turnbull DM.

Neurology. 2008 Apr 8;70(15):1290-2. doi: 10.1212/01.wnl.0000308940.38092.74. No abstract available.

PMID:
18391161
13.

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency.

Kemp JP, Smith PM, Pyle A, Neeve VC, Tuppen HA, Schara U, Talim B, Topaloglu H, Holinski-Feder E, Abicht A, Czermin B, Lochmüller H, McFarland R, Chinnery PF, Chrzanowska-Lightowlers ZM, Lightowlers RN, Taylor RW, Horvath R.

Brain. 2011 Jan;134(Pt 1):183-95. doi: 10.1093/brain/awq320. Epub 2010 Dec 17.

14.

Autistic disorder in 2 children with mitochondrial disorders.

Tsao CY, Mendell JR.

J Child Neurol. 2007 Sep;22(9):1121-3.

PMID:
17890412
16.
17.

Cerebral oxygen and glucose metabolism in patients with mitochondrial m.3243A>G mutation.

Lindroos MM, Borra RJ, Parkkola R, Virtanen SM, Lepomäki V, Bucci M, Virta JR, Rinne JO, Nuutila P, Majamaa K.

Brain. 2009 Dec;132(Pt 12):3274-84. doi: 10.1093/brain/awp259. Epub .

19.

POLG1 mutations associated with progressive encephalopathy in childhood.

Kollberg G, Moslemi AR, Darin N, Nennesmo I, Bjarnadottir I, Uvebrant P, Holme E, Melberg A, Tulinius M, Oldfors A.

J Neuropathol Exp Neurol. 2006 Aug;65(8):758-68.

20.

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect.

Nochez Y, Arsene S, Gueguen N, Chevrollier A, Ferré M, Guillet V, Desquiret V, Toutain A, Bonneau D, Procaccio V, Amati-Bonneau P, Pisella PJ, Reynier P.

Mol Vis. 2009;15:598-608. Epub 2009 Mar 27.

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