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Results: 1 to 20 of 97

1.

Chewing-induced segmental myoclonus in a patient with Leigh syndrome.

Navarro-Otano J, Valls-Solé J, Guaita M, Santamaria J, Cardellach F, Muñoz E.

Mov Disord. 2013 Oct;28(12):1756-7. doi: 10.1002/mds.25516. Epub 2013 Jun 18. No abstract available.

PMID:
23780927
[PubMed - indexed for MEDLINE]
2.

Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.

Monden Y, Mori M, Kuwajima M, Goto T, Yamagata T, Momoi MY.

Brain Dev. 2013 Jun;35(6):582-5. doi: 10.1016/j.braindev.2012.08.006. Epub 2012 Sep 13.

PMID:
22981260
[PubMed - indexed for MEDLINE]
3.

Leigh syndrome, cytochrome C oxidase deficiency and hypsarrhythmia with infantile spasms.

Tsao CY, Luquette M, Rusin JA, Herr GM, Kien CL, Morrow G 3rd.

Clin Electroencephalogr. 1997 Oct;28(4):214-7.

PMID:
9343714
[PubMed - indexed for MEDLINE]
4.

[Leigh syndrome with facial abnormalities: a neurocristopathy].

Berio A, Piazzi A.

Pediatr Med Chir. 2007 Jan-Feb;29(1):50-4. Italian.

PMID:
17557512
[PubMed - indexed for MEDLINE]
5.

Efficacy of idebenone for respiratory failure in a patient with Leigh syndrome: a long-term follow-up study.

Haginoya K, Miyabayashi S, Kikuchi M, Kojima A, Yamamoto K, Omura K, Uematsu M, Hino-Fukuyo N, Tanaka S, Tsuchiya S.

J Neurol Sci. 2009 Mar 15;278(1-2):112-4. doi: 10.1016/j.jns.2008.11.008. Epub 2008 Dec 20.

PMID:
19101701
[PubMed - indexed for MEDLINE]
6.

Childhood moyamoya disease accompanying Leigh syndrome.

Cullu N, Karakas E, Karakas O, Deveer M, Calik M, Boyaci FN.

J Pak Med Assoc. 2013 Dec;63(12):1538-40.

PMID:
24397103
[PubMed - indexed for MEDLINE]
7.

Subacute necrotizing encephalomyelopathy (Leigh disease): report of a case with Lennox-Gastaut syndrome.

Matsuishi T, Yoshino M, Tokunaga O, Katafuchi Y, Yamashita F.

Brain Dev. 1985;7(5):500-4.

PMID:
4083386
[PubMed - indexed for MEDLINE]
8.

3-methylglutaconic aciduria type 4 manifesting as Leigh syndrome in 2 siblings.

Jareño NM, Fernández-Mayoralas DM, Silvestre CP, Cortés BM, Pérez MU, Campos-Castelló J.

J Child Neurol. 2007 Feb;22(2):218-21.

PMID:
17621487
[PubMed - indexed for MEDLINE]
9.

Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.

Funalot B, Reynier P, Vighetto A, Ranoux D, Bonnefont JP, Godinot C, Malthièry Y, Mas JL.

Ann Neurol. 2002 Sep;52(3):374-7.

PMID:
12205655
[PubMed - indexed for MEDLINE]
10.

Cardiac mitochondrial dysfunction in Leigh syndrome.

Marin-Garcia J, Ananthakrishnan R, Korson M, Goldenthal MJ, Perez-Atayde A.

Pediatr Cardiol. 1996 Nov-Dec;17(6):387-9.

PMID:
8781089
[PubMed - indexed for MEDLINE]
11.

Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.

Zhang Y, Yang YL, Sun F, Cai X, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Zhang YH, Jiang YW, Qin J, Wu XR.

J Inherit Metab Dis. 2007 Apr;30(2):265. Epub 2007 Feb 24.

PMID:
17323145
[PubMed - indexed for MEDLINE]
12.

G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.

Shtilbans A, Shanske S, Goodman S, Sue CM, Bruno C, Johnson TL, Lava NS, Waheed N, DiMauro S.

J Child Neurol. 2000 Nov;15(11):759-61.

PMID:
11108511
[PubMed - indexed for MEDLINE]
13.

[Dystonia as a principal manifestation of Leigh syndrome in an infant].

Muñoz Hiraldo ME, Martínez Bermejo A, Gutiérrez Molina M, García Melián RM, Arcas Martínez J, Pascual-Castroviejo I.

An Esp Pediatr. 1993 Apr;38(4):348-50. Spanish. No abstract available.

PMID:
8480948
[PubMed - indexed for MEDLINE]
14.

Hypertension in Leigh syndrome--a case report.

Narita T, Yamano T, Ohno M, Takano T, Ito R, Shimada M.

Neuropediatrics. 1998 Oct;29(5):265-7.

PMID:
9810562
[PubMed - indexed for MEDLINE]
15.

de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency.

Ogier H, Lombes A, Scholte HR, Poll-The BT, Fardeau M, Alcardi J, Vignes B, Niaudet P, Saudubray JM.

J Pediatr. 1988 May;112(5):734-9.

PMID:
2834526
[PubMed - indexed for MEDLINE]
16.

Vocal cord paralysis and hypoventilation in a patient with suspected Leigh disease.

Lin YC, Lee WT, Wang PJ, Shen YZ.

Pediatr Neurol. 1999 Mar;20(3):223-5.

PMID:
10207933
[PubMed - indexed for MEDLINE]
17.

Bicarbonate-lactate peritoneal dialysis in a patient with a mitochondriopathy.

Doorenbos CJ.

Perit Dial Int. 2001 Sep-Oct;21(5):518-9. No abstract available.

PMID:
11757838
[PubMed - indexed for MEDLINE]
Free Article
18.

Creatine monohydrate therapy in a Leigh syndrome patient with A8344G mutation.

Komura K, Nakano K, Ishigaki K, Tarashima M, Nakayama T, Sasaki K, Saito K, Osawa M.

Pediatr Int. 2006 Aug;48(4):409-12. No abstract available.

PMID:
16911089
[PubMed - indexed for MEDLINE]
19.

Adult Leigh syndrome with mitochondrial DNA mutation at 8993.

Nagashima T, Mori M, Katayama K, Nunomura M, Nishihara H, Hiraga H, Tanaka S, Goto Y, Nagashima K.

Acta Neuropathol. 1999 Apr;97(4):416-22. Review.

PMID:
10208283
[PubMed - indexed for MEDLINE]
20.

Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua.

Elia M, Musumeci SA, Ferri R, Colamaria V, Azan G, Greco D, Stefanini MC.

Brain Dev. 1996 May-Jun;18(3):207-11.

PMID:
8836502
[PubMed - indexed for MEDLINE]

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