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Items: 1 to 20 of 136

1.

Clinical and electrophysiological recovery in Leber hereditary optic neuropathy with G3460A mutation.

Sharkawi E, Oleszczuk JD, Holder GE, Raina J.

Doc Ophthalmol. 2012 Aug;125(1):71-4. doi: 10.1007/s10633-012-9328-z.

PMID:
22684678
2.

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.

PMID:
25690485
3.

Visual electrophysiologic findings in patients from an extensive Brazilian family with Leber's hereditary optic neuropathy.

Salomão SR, Berezovsky A, Andrade RE, Belfort R Jr, Carelli V, Sadun AA.

Doc Ophthalmol. 2004 Mar;108(2):147-55.

PMID:
15455797
4.
5.

Retinal function and neural conduction along the visual pathways in affected and unaffected carriers with Leber's hereditary optic neuropathy.

Ziccardi L, Sadun F, De Negri AM, Barboni P, Savini G, Borrelli E, La Morgia C, Carelli V, Parisi V.

Invest Ophthalmol Vis Sci. 2013 Oct 21;54(10):6893-901. doi: 10.1167/iovs.13-12894.

PMID:
24071953
6.

Visual recovery in a patient with Leber hereditary optic neuropathy and the 14484 mutation.

Hrynchak PK, Spafford MM.

Optom Vis Sci. 1994 Oct;71(10):604-12.

PMID:
7877803
7.

Visual recovery patterns in children with Leber's hereditary optic neuropathy.

Acaroğlu G, Kansu T, Doğulu CF.

Int Ophthalmol. 2001;24(6):349-55.

PMID:
14750573
8.

[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
10.

Leber's hereditary optic neuropathy with the 3434, 9011 mitochondrial DNA point mutation.

Shidara K, Wakakura M.

Jpn J Ophthalmol. 2012 Mar;56(2):175-80. doi: 10.1007/s10384-011-0106-3.

PMID:
22183138
11.

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.

12.

Leber hereditary optic neuropathy gene therapy clinical trial recruitment: year 1.

Lam BL, Feuer WJ, Abukhalil F, Porciatti V, Hauswirth WW, Guy J.

Arch Ophthalmol. 2010 Sep;128(9):1129-35. doi: 10.1001/archophthalmol.2010.201.

13.

Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.

Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.

Coll Antropol. 2006 Mar;30(1):171-4.

PMID:
16617593
14.

[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
15.
16.

Visual improvement in Leber congenital amaurosis and the CRX genotype.

Koenekoop RK, Loyer M, Dembinska O, Beneish R.

Ophthalmic Genet. 2002 Mar;23(1):49-59.

PMID:
11910559
17.

Retinal ganglion cell dysfunction in asymptomatic G11778A: Leber hereditary optic neuropathy.

Guy J, Feuer WJ, Porciatti V, Schiffman J, Abukhalil F, Vandenbroucke R, Rosa PR, Lam BL.

Invest Ophthalmol Vis Sci. 2014 Feb 10;55(2):841-8. doi: 10.1167/iovs.13-13365.

18.
19.

Multifocal VEP provide electrophysiological evidence of predominant dysfunction of the optic nerve fibers derived from the central retina in Leber's hereditary optic neuropathy.

Ziccardi L, Parisi V, Giannini D, Sadun F, De Negri AM, Barboni P, La Morgia C, Sadun AA, Carelli V.

Graefes Arch Clin Exp Ophthalmol. 2015 Sep;253(9):1591-600. doi: 10.1007/s00417-015-2979-1.

PMID:
25773998
20.

Visual evoked potentials findings in non-affected subjects from a large Brazilian pedigree of 11778 Leber's hereditary optic neuropathy.

Sacai PY, Salomão SR, Carelli V, Pereira JM, Belfort R Jr, Sadun AA, Berezovsky A.

Doc Ophthalmol. 2010 Oct;121(2):147-54. doi: 10.1007/s10633-010-9241-2.

PMID:
20676915

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