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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
280 related items for PubMed ID: 24167936
1. [Leber's hereditary optic neuropathy]. Hilo W, Jabaly-Habib H, Modi N, Briscoe D. Harefuah; 2013 Aug; 152(8):486-9, 498, 497. PubMed ID: 24167936 [Abstract] [Full Text] [Related]
2. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation. Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T. Eur J Paediatr Neurol; 2002 Aug; 6(2):121-3. PubMed ID: 11995959 [Abstract] [Full Text] [Related]
3. Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation. Chuenkongkaew W, Lertrit P, Suphavilai R. Southeast Asian J Trop Med Public Health; 2004 Mar; 35(1):167-8. PubMed ID: 15272763 [Abstract] [Full Text] [Related]
4. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation]. Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565 [Abstract] [Full Text] [Related]
5. The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction. Eichhorn-Mulligan K, Cestari DM. Semin Ophthalmol; 2008 Oct; 23(1):27-37. PubMed ID: 18214789 [Abstract] [Full Text] [Related]
6. Leber hereditary optic neuropathy - historical report in comparison with the current knowledge. Piotrowska A, Korwin M, Bartnik E, Tońska K. Gene; 2015 Jan 15; 555(1):41-9. PubMed ID: 25261848 [Abstract] [Full Text] [Related]
7. [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. PubMed ID: 19024058 [Abstract] [Full Text] [Related]
8. Leber's hereditary optic neuropathy: a multifactorial disease. Yen MY, Wang AG, Wei YH. Prog Retin Eye Res; 2006 Jul 25; 25(4):381-96. PubMed ID: 16829155 [Abstract] [Full Text] [Related]
9. 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 25; 30(1):171-4. PubMed ID: 16617593 [Abstract] [Full Text] [Related]
10. Three Cases of Leber's Hereditary Optic Neuropathy with Rapid Increase in Visual Acuity After Gene Therapy. Zhang Y, Yuan JJ, Liu HL, Tian Z, Liu SW, Li B. Curr Gene Ther; 2019 Mar 25; 19(2):134-138. PubMed ID: 31237206 [Abstract] [Full Text] [Related]
11. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy]. Mao YJ, Qu J, Guan MX. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 25; 25(1):45-9. PubMed ID: 18247303 [Abstract] [Full Text] [Related]
12. Leber's hereditary optic neuropathy with childhood onset. Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V. Invest Ophthalmol Vis Sci; 2006 Dec 25; 47(12):5303-9. PubMed ID: 17122117 [Abstract] [Full Text] [Related]
13. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families. Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX. Biochem Biophys Res Commun; 2006 Aug 18; 347(1):221-5. PubMed ID: 16806060 [Abstract] [Full Text] [Related]
14. The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy. Zhang Y, Tian Z, Yuan J, Liu C, Liu HL, Ma SQ, Li B. Curr Gene Ther; 2017 Aug 18; 17(4):320-326. PubMed ID: 29189152 [Abstract] [Full Text] [Related]
15. [Hyperintense optic nerve lesion on T2-weighted MRI imaging in the acute stage of Leber's hereditary optic neuropathy: a case report]. Honda H, Tsujihata M, Ochi M, Satoh A, Tomita I, Fujikawa A. Rinsho Shinkeigaku; 2006 Apr 18; 46(4):294-6. PubMed ID: 16768101 [Abstract] [Full Text] [Related]
16. Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation. Hwang JM, Chang BL, Koh HJ, Kim JY, Park SS. J Korean Med Sci; 2002 Apr 18; 17(2):283-6. PubMed ID: 11961321 [Abstract] [Full Text] [Related]
17. Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery. Niehusmann P, Surges R, von Wrede RD, Elger CE, Wellmer J, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS. Epilepsy Behav; 2011 Jan 18; 20(1):38-43. PubMed ID: 21145289 [Abstract] [Full Text] [Related]
19. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress. Chao de la Barca JM, Simard G, Amati-Bonneau P, Safiedeen Z, Prunier-Mirebeau D, Chupin S, Gadras C, Tessier L, Gueguen N, Chevrollier A, Desquiret-Dumas V, Ferré M, Bris C, Kouassi Nzoughet J, Bocca C, Leruez S, Verny C, Miléa D, Bonneau D, Lenaers G, Martinez MC, Procaccio V, Reynier P. Brain; 2016 Nov 01; 139(11):2864-2876. PubMed ID: 27633772 [Abstract] [Full Text] [Related]
20. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy. Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V. Invest Ophthalmol Vis Sci; 2007 May 01; 48(5):2362-70. PubMed ID: 17460303 [Abstract] [Full Text] [Related] Page: [Next] [New Search]