These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 29054473)

  • 21. [Clinical characteristics and research progress on the treatment of mitochondrial optic neuropathy].
    Guo ST; Jiang LB
    Zhonghua Yan Ke Za Zhi; 2021 May; 57(5):386-390. PubMed ID: 33915644
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.
    Sarzi E; Angebault C; Seveno M; Gueguen N; Chaix B; Bielicki G; Boddaert N; Mausset-Bonnefont AL; Cazevieille C; Rigau V; Renou JP; Wang J; Delettre C; Brabet P; Puel JL; Hamel CP; Reynier P; Lenaers G
    Brain; 2012 Dec; 135(Pt 12):3599-613. PubMed ID: 23250881
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetically induced impairment of retinal ganglion cells at the axonal level is linked to extrastriate cortical plasticity.
    Mateus C; d'Almeida OC; Reis A; Silva E; Castelo-Branco M
    Brain Struct Funct; 2016 Apr; 221(3):1767-80. PubMed ID: 25680704
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.
    Sarzi E; Seveno M; Angebault C; Milea D; Rönnbäck C; Quilès M; Adrian M; Grenier J; Caignard A; Lacroux A; Lavergne C; Reynier P; Larsen M; Hamel CP; Delettre C; Lenaers G; Müller A
    Hum Mol Genet; 2016 Jun; 25(12):2539-2551. PubMed ID: 27260406
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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. PubMed ID: 25690485
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Visual system involvement in patients with Friedreich's ataxia.
    Fortuna F; Barboni P; Liguori R; Valentino ML; Savini G; Gellera C; Mariotti C; Rizzo G; Tonon C; Manners D; Lodi R; Sadun AA; Carelli V
    Brain; 2009 Jan; 132(Pt 1):116-23. PubMed ID: 18931386
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
    Bosley TM; Brodsky MC; Glasier CM; Abu-Amero KK
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5250-6. PubMed ID: 18676632
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neuroglobin effectively halts vision loss in Harlequin mice at an advanced stage of optic nerve degeneration.
    Cwerman-Thibault H; Lechauve C; Malko-Baverel V; Augustin S; Le Guilloux G; Reboussin É; Degardin-Chicaud J; Simonutti M; Debeir T; Corral-Debrinski M
    Neurobiol Dis; 2021 Nov; 159():105483. PubMed ID: 34400304
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genotype-phenotype heterogeneity of ganglion cell and inner plexiform layer deficit in autosomal-dominant optic atrophy.
    Rönnbäck C; Nissen C; Almind GJ; Grønskov K; Milea D; Larsen M
    Acta Ophthalmol; 2015 Dec; 93(8):762-6. PubMed ID: 26385429
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Retinal atrophy using optical coherence tomography (OCT) in 15 patients with multiple sclerosis and comparison with healthy subjects].
    Jeanjean L; Castelnovo G; Carlander B; Villain M; Mura F; Dupeyron G; Labauge P
    Rev Neurol (Paris); 2008 Nov; 164(11):927-34. PubMed ID: 18808761
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Optic neuropathies--importance of spatial distribution of mitochondria as well as function.
    Yu Wai Man CY; Chinnery PF; Griffiths PG
    Med Hypotheses; 2005; 65(6):1038-42. PubMed ID: 16098682
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Differential diagnosis of optic nerve atrophy].
    Kommerell G
    Bull Soc Belge Ophtalmol; 1990; 236():21-33. PubMed ID: 2093405
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Leber hereditary optic neuropathy due to a new ND1 mutation.
    Soldath P; Wegener M; Sander B; Rosenberg T; Duno M; Wibrand F; Vissing J
    Ophthalmic Genet; 2017; 38(5):480-485. PubMed ID: 28139165
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Imaging of the macula indicates early completion of structural deficit in autosomal-dominant optic atrophy.
    Rönnbäck C; Milea D; Larsen M
    Ophthalmology; 2013 Dec; 120(12):2672-2677. PubMed ID: 24120325
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mitochondrial DNA abnormalities in ophthalmological disease.
    Gorman GS; Taylor RW
    Saudi J Ophthalmol; 2011 Oct; 25(4):395-404. PubMed ID: 23960954
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Movement disorders in mitochondrial diseases.
    Tranchant C; Anheim M
    Rev Neurol (Paris); 2016; 172(8-9):524-529. PubMed ID: 27476418
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Vision Recovery Despite Retinal Ganglion Cell Loss in Leber's Hereditary Optic Neuropathy.
    Webber AL
    Optom Vis Sci; 2016 Dec; 93(12):1571-1577. PubMed ID: 27741086
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy.
    Seo JH; Hwang JM; Park SS
    Eye (Lond); 2010 Jan; 24(1):107-11. PubMed ID: 19247386
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Comparison of peripapillary retinal nerve fiber layer loss and visual outcome in fellow eyes following sequential bilateral non-arteritic anterior ischemic optic neuropathy.
    Dotan G; Kesler A; Naftaliev E; Skarf B
    Curr Eye Res; 2015 May; 40(6):632-7. PubMed ID: 25153943
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [How to distinguish between autosomal dominant optic atrophy and Leber's hereditary optic neuropathy].
    Leo-Kottler B; Jägle H; Küpker T; Schimpf S
    Ophthalmologe; 2007 Dec; 104(12):1060-5. PubMed ID: 17899121
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.