Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 949

1.

Hormone replacement therapy in Leber's hereditary optic neuropathy: Accelerated visual recovery in vivo.

Fantini M, Asanad S, Karanjia R, Sadun A.

J Curr Ophthalmol. 2018 Nov 3;31(1):102-105. doi: 10.1016/j.joco.2018.10.003. eCollection 2019 Mar.

2.

Late-onset Leber's hereditary optic neuropathy: the role of environmental factors in hereditary diseases.

Moura-Coelho N, Pinto Proença R, Tavares Ferreira J, Cunha JP.

BMJ Case Rep. 2019 Mar 20;12(3). pii: e227977. doi: 10.1136/bcr-2018-227977.

PMID:
30898963
3.

[LHON-Treatment option despite poor initial visual acuity?]

Rickmann A, Wocker L, Damm LJ, Ivanescu C, Szurman P, Pérez Guerra N.

Ophthalmologe. 2019 Mar 18. doi: 10.1007/s00347-019-0864-8. [Epub ahead of print] German.

PMID:
30887114
4.

Leber's hereditary optic neuropathy: Severe vascular pathology in a severe primary mutation.

Asanad S, Meer E, Tian JJ, Fantini M, Nassisi M, Sadun AA.

Intractable Rare Dis Res. 2019 Feb;8(1):52-55. doi: 10.5582/irdr.2018.01126.

5.

Analysis of Inherited Optic Neuropathies.

Lazdinyte S, Schorderet DF, Schaller A, Valmaggia C, Todorova MG.

Klin Monbl Augenheilkd. 2019 Mar 4. doi: 10.1055/a-0829-6828. [Epub ahead of print]

PMID:
30831606
6.

Functional changes of retinal ganglion cells and visual pathways in patients with Leber's hereditary optic neuropathy during one year of follow-up in chronic phase.

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

Ophthalmology. 2019 Feb 26. pii: S0161-6420(18)33301-3. doi: 10.1016/j.ophtha.2019.02.018. [Epub ahead of print]

7.
8.

Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene: A Secondary Analysis of a Phase 1/2 Clinical Trial.

Bouquet C, Vignal Clermont C, Galy A, Fitoussi S, Blouin L, Munk MR, Valero S, Meunier S, Katz B, Sahel JA, Thomasson N.

JAMA Ophthalmol. 2019 Feb 7. doi: 10.1001/jamaophthalmol.2018.6902. [Epub ahead of print]

PMID:
30730541
9.

[Raxone in the Leber optical neuropathy: Parisian experience].

Orssaud C, Bidot S, Lamirel C, Brémond Gignac D, Touitou V, Vignal C.

J Fr Ophtalmol. 2019 Jan 31. pii: S0181-5512(18)30539-4. doi: 10.1016/j.jfo.2018.06.010. [Epub ahead of print] French.

PMID:
30712826
10.

Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy.

Miyaue N, Yamanishi Y, Tada S, Ando R, Yabe H, Nagai M, Nomoto M.

eNeurologicalSci. 2019 Jan 11;14:74-76. doi: 10.1016/j.ensci.2019.01.002. eCollection 2019 Mar.

11.

Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy.

Asanad S, Tian JJ, Frousiakis S, Jiang JP, Kogachi K, Felix CM, Fatemeh D, Irvine AG, Ter-Zakarian A, Falavarjani KG, Barboni P, Karanjia R, Sadun AA.

Curr Eye Res. 2019 Jan 16:1-7. doi: 10.1080/02713683.2019.1567792. [Epub ahead of print]

PMID:
30649972
12.

[Mitochondrial diseases].

Radelfahr F, Klopstock T.

Nervenarzt. 2019 Feb;90(2):121-130. doi: 10.1007/s00115-018-0666-2. Review. German.

PMID:
30643957
13.

Bilateral striatal necrosis due to homoplasmic mitochondrial 3697G>A mutation presents with incomplete penetrance and sex bias.

Zhong S, Wen S, Qiu Y, Yu Y, Xin L, He Y, Gao X, Fang H, Hong D, Zhang J.

Mol Genet Genomic Med. 2019 Mar;7(3):e541. doi: 10.1002/mgg3.541. Epub 2019 Jan 8.

14.

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.

Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, Li Q, Jin X, Wei Y, Meng F, Gao Y, Cang X, Tong Y, Liu X, Zhang M, Jiang P, Zhu T, Mo JQ, Huang T, Jiang P, Guan MX.

Hum Mol Genet. 2018 Dec 31. doi: 10.1093/hmg/ddy450. [Epub ahead of print]

PMID:
30597069
15.

Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye.

Mauri E, Dilena R, Boccazzi A, Ronchi D, Piga D, Triulzi F, Gagliardi D, Brusa R, Faravelli I, Bresolin N, Magri F, Corti S, Comi GP.

BMC Neurol. 2018 Dec 27;18(1):220. doi: 10.1186/s12883-018-1227-9.

16.

Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers.

Bianco A, Valletti A, Longo G, Bisceglia L, Montoya J, Emperador S, Guerriero S, Petruzzella V.

BMC Res Notes. 2018 Dec 20;11(1):911. doi: 10.1186/s13104-018-4025-y.

17.

Leber's hereditary optic neuropathy misdiagnosed as optic neuritis and Lyme disease in a patient with multiple sclerosis.

Chang M.

BMJ Case Rep. 2018 Dec 7;11(1). pii: e227109. doi: 10.1136/bcr-2018-227109.

PMID:
30567205
18.

Juvenile open-angle Glaucoma associated with Leber's hereditary optic neuropathy: a case report and literature review.

Lin YH, Wang NK, Yeung L, Lai CC, Chuang LH.

BMC Ophthalmol. 2018 Dec 17;18(1):323. doi: 10.1186/s12886-018-0980-2. Review.

19.

Leber's hereditary optic neuropathy: Shifting our attention to the macula.

Asanad S, Meer E, Fantini M, Borrelli E, Sadun AA.

Am J Ophthalmol Case Rep. 2018 Nov 13;13:13-15. doi: 10.1016/j.ajoc.2018.11.010. eCollection 2019 Mar.

20.

Treatment strategies for Leber hereditary optic neuropathy.

Jurkute N, Harvey J, Yu-Wai-Man P.

Curr Opin Neurol. 2019 Feb;32(1):99-104. doi: 10.1097/WCO.0000000000000646.

PMID:
30516647

Supplemental Content

Loading ...
Support Center