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Items: 1 to 20 of 118

1.
2.

[Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].

Chelstowska J, Mroczek K, Niebudek D, Małecka-Idzikowska A, Bartnik E, Hanna Nizankowska M, Sasiadek M.

Przegl Lek. 2002;59(10):777-9. Polish.

PMID:
12632910
3.

[A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis].

Lubos L, Wajgt A, Maciejowski M, Mroczek-Tońska K, Bartnik E, Dziekanowska D.

Neurol Neurochir Pol. 2003 Jan-Feb;37(1):229-34. Polish.

PMID:
12910843
4.

Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.

Korkiamäki P, Kervinen M, Karjalainen K, Majamaa K, Uusimaa J, Remes AM.

Acta Ophthalmol. 2013 Nov;91(7):630-4. doi: 10.1111/j.1755-3768.2012.02506.x. Epub 2012 Sep 12.

5.
6.

[A clinical study of Leber hereditary optic neuropathy].

Wei QP, Sun YH, Zhou XT, Zhou J, Gong XH, Jia XY.

Zhonghua Yan Ke Za Zhi. 2012 Dec;48(12):1065-8. Chinese.

PMID:
23336408
7.

[Research progress of Leber hereditary optic neuropathy].

Zhang AM, Yao YG.

Yi Chuan. 2013 Feb;35(2):123-35. Review. Chinese.

PMID:
23448924
8.

Clinical and electrophysiology findings in Slovene patients with Leber hereditary optic neuropathy.

Jarc-Vidmar M, Tajnik M, Brecelj J, Fakin A, Sustar M, Naji M, Stirn-Kranjc B, Glavač D, Hawlina M.

Doc Ophthalmol. 2015 Jun;130(3):179-87. doi: 10.1007/s10633-015-9489-7. Epub 2015 Feb 19.

PMID:
25690485
9.

Meta-analysis of the prevalence of Leber hereditary optic neuropathy mtDNA mutations in Europe.

Mascialino B, Leinonen M, Meier T.

Eur J Ophthalmol. 2012 May-Jun;22(3):461-5. doi: 10.5301/ejo.5000055.

PMID:
21928272
10.

m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.

Kodroń A, Krawczyński MR, Tońska K, Bartnik E.

J Clin Pathol. 2014 Jul;67(7):639-41. doi: 10.1136/jclinpath-2014-202192. Epub 2014 Apr 19.

PMID:
24747208
11.

[Rapid onset of visual recovery following acute visual loss due to leber's hereditary optic neuropathy].

Kawasaki A, Borruat FX.

Rev Neurol (Paris). 2005 May;161(5):599-601. French.

PMID:
16106816
12.

A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON).

Du WD, Chen G, Cao HM, Jin QH, Liao RF, He XC, Chen DB, Huang SR, Zhao H, Lv YM, Tang HY, Tang XF, Wang YQ, Sun S, Zhao JL, Zhang XJ.

Dis Markers. 2011;30(4):181-90. doi: 10.3233/DMA-2011-0767.

13.

Leber's hereditary optic neuropathy--case report and literature review.

Teive HA, Troiano AR, Raskin S, Werneck LC.

Sao Paulo Med J. 2004 Nov 4;122(6):276-9. Epub 2005 Feb 2. Review.

14.

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.

Arch Neurol. 2004 May;61(5):727-33.

PMID:
15148151
15.

mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.

Jia X, Li S, Wang P, Guo X, Zhang Q.

Biochem Biophys Res Commun. 2010 Dec 10;403(2):237-41. doi: 10.1016/j.bbrc.2010.11.017. Epub 2010 Nov 11.

PMID:
21074518
16.
17.

[Sudden blindness: consider Leber's hereditary optic neuropathy].

Schieving JH, de Vries BB, Hol F, Stroink H.

Ned Tijdschr Geneeskd. 2008 Oct 25;152(43):2313-6. Dutch.

PMID:
19024058
18.

Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.

Grazina MM, Diogo LM, Garcia PC, Silva ED, Garcia TD, Robalo CB, Oliveira CR.

Eur J Paediatr Neurol. 2007 Mar;11(2):115-8. Epub 2007 Jan 24.

PMID:
17254817
19.

Leber's hereditary optic neuropathy masquerading as optic neuritis with spontaneous visual recovery.

Hsu TK, Wang AG, Yen MY, Liu JH.

Clin Exp Optom. 2014 Jan;97(1):84-6. doi: 10.1111/cxo.12100. Epub 2013 Aug 1.

20.

[Clinical and molecular genetic analysis of hereditary optic neuropathies].

Avetisov SÉ, Sheremet NL, Vorob'eva OK, Eliseeva ÉG, Chukhrova AL, Loginova AN, Khanakova NA, Poliakov AV.

Vestn Oftalmol. 2013 Mar-Apr;129(2):8-13. Russian.

PMID:
23808173

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