MS and Mito

[Guest guest]

These peer reviewed articles indicate the potential relationship between MS and

Mito (for those who are interested).

Iniguez C, Arenas J, Montoya J, Mostacero E, del Val J,

[Mitochondrial respiratory chain deficiency may present as multiple sclerosis]

Neurologia. 1998 Apr;13(4):199-203. Spanish.

PMID: 9608760 [PubMed - indexed for MEDLINE]

RW, Chinnery PF, Bates MJ, MJ, MA, s RM, Turnbull

DM.

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a

patient presenting with chronic progressive external ophthalmoplegia and

multiple sclerosis.

Biochem Biophys Res Commun. 1998 Feb 4;243(1):47-51.

PMID: 9473477 [PubMed - indexed for MEDLINE]

Bet L, Moggio M, Comi GP, ni C, Prelle A, Checcarelli N, Bordoni A,

Bresolin N, Scarpini E, Scarlato G

Multiple sclerosis and mitochondrial myopathy: an unusual combination of

diseases.

J Neurol. 1994 Jul;241(8):511-6.

PMID: 7964921 [PubMed - indexed for MEDLINE]

Quan D, Kleinschmidt-DeMasters BK. A 71-year-old male with 4 decades of

symptoms referable to both central and peripheral nervous system.

Brain Pathol. 2005 Oct;15(4):369-70, 373.

PMID: 16389949 [PubMed - indexed for MEDLINE]

Aboul-Enein F, Lassmann H.

Mitochondrial damage and histotoxic hypoxia: a pathway of tissue injury in

inflammatory brain disease?

Acta Neuropathol (Berl). 2005 Jan;109(1):49-55. Epub 2005 Jan 11. Review.

PMID: 15645261 [PubMed - indexed for MEDLINE]

Kovacs GG, Hoftberger R, Majtenyi K, Horvath R, Barsi P, Komoly S, Lassmann H,

Budka H, Jakab G

Neuropathology of white matter disease in Leber's hereditary optic neuropathy.

Brain. 2005 Jan;128(Pt 1):35-41. Epub 2004 Oct 13.

PMID: 15483043 [PubMed - indexed for MEDLINE]

Kalman B, Leist TP.

Familial multiple sclerosis and other inherited disorders of the white matter.

Neurologist. 2004 Jul;10(4):201-15. Review.

PMID: 15245586 [PubMed - indexed for MEDLINE]

Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J

Lack of association between Leber's hereditary optic neuropathy primary point

mutations and multiple sclerosis in Iran.

Eur Neurol. 2004;51(2):68-71. Epub 2003 Dec 10.

PMID: 14671420 [PubMed - indexed for MEDLINE]

Jamrozik Z, Tutaj A, Piechowski-Jozwiak B, Mroczek-Tonska K, Bartnik E,

[Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like

phenotype]

Neurol Neurochir Pol. 2003 May-Jun;37(3):713-20. Review. Polish.

PMID: 14593764 [PubMed - indexed for MEDLINE]

El'chaninov AP, Malashenko AV, Volkov VK, Simonova LIa

[Clinical and anatomical observation of mitochondrial encephalopathy]

Zh Nevrol Psikhiatr Im S S Korsakova. 2001;101(2):44-5. Russian. No abstract

available.

PMID: 11243035 [PubMed - indexed for MEDLINE]

Joanne Kocourek (mom to , lies, and )

visit us at: http://www.caringbridge.org/il/annakris