454 related articles for article (PubMed ID: 18214789)
1. The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction.
Eichhorn-Mulligan K; Cestari DM
Semin Ophthalmol; 2008; 23(1):27-37. PubMed ID: 18214789
[TBL] [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; 6(2):121-3. PubMed ID: 11995959
[TBL] [Abstract][Full Text] [Related]
3. [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. PubMed ID: 12632910
[TBL] [Abstract][Full Text] [Related]
4. Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
Rasool N; Lessell S; Cestari DM
Semin Ophthalmol; 2016; 31(1-2):107-16. PubMed ID: 26959136
[TBL] [Abstract][Full Text] [Related]
5. [A method for estimating penetrance of pathogenic mutations in a mitochondrial genome].
Kirichenko AV; Zhadanov SI; Aksenovich TI
Genetika; 2002 Jul; 38(7):992-4. PubMed ID: 12174593
[TBL] [Abstract][Full Text] [Related]
6. [Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome].
Rydzanicz M; Mrugacz M; Gajecka M
Klin Oczna; 2008; 110(7-9):321-4. PubMed ID: 19112871
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
Shafa Shariat Panahi M; Houshmand M; Tabassi AR
Arch Med Res; 2006 Nov; 37(8):1028-33. PubMed ID: 17045122
[TBL] [Abstract][Full Text] [Related]
8. Leber hereditary optic neuropathy - historical report in comparison with the current knowledge.
Piotrowska A; Korwin M; Bartnik E; Tońska K
Gene; 2015 Jan; 555(1):41-9. PubMed ID: 25261848
[TBL] [Abstract][Full Text] [Related]
9. Reduced frequency of known mutations in a cohort of LHON patients from India.
Sundaresan P; Kumar SM; Thompson S; Fingert JH
Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
[TBL] [Abstract][Full Text] [Related]
10. [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(1):45-9. PubMed ID: 18247303
[TBL] [Abstract][Full Text] [Related]
11. [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
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
Abu-Amero KK; Bosley TM
Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408
[TBL] [Abstract][Full Text] [Related]
13. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
Zheng ML; Zhang GL; Hua AL; Zhang YL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):166-7. PubMed ID: 15079802
[TBL] [Abstract][Full Text] [Related]
14. Leber's hereditary optic neuropathy: a multifactorial disease.
Yen MY; Wang AG; Wei YH
Prog Retin Eye Res; 2006 Jul; 25(4):381-96. PubMed ID: 16829155
[TBL] [Abstract][Full Text] [Related]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 16617593
[TBL] [Abstract][Full Text] [Related]
17. Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology.
Mroczek-Tońska K; Kisiel B; Piechota J; Bartnik E
J Appl Genet; 2003; 44(4):529-38. PubMed ID: 14617834
[TBL] [Abstract][Full Text] [Related]
18. Assessing mitochondrial DNA nucleotide changes in spontaneous optic neuropathies.
Bosley TM; Abu-Amero KK
Ophthalmic Genet; 2010 Dec; 31(4):163-72. PubMed ID: 21067478
[TBL] [Abstract][Full Text] [Related]
19. Hereditary optic neuropathies share a common mitochondrial coupling defect.
Chevrollier A; Guillet V; Loiseau D; Gueguen N; de Crescenzo MA; Verny C; Ferre M; Dollfus H; Odent S; Milea D; Goizet C; Amati-Bonneau P; Procaccio V; Bonneau D; Reynier P
Ann Neurol; 2008 Jun; 63(6):794-8. PubMed ID: 18496845
[TBL] [Abstract][Full Text] [Related]
20. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
Spruijt L; Smeets HJ; Hendrickx A; Bettink-Remeijer MW; Maat-Kievit A; Schoonderwoerd KC; Sluiter W; de Coo IF; Hintzen RQ
Arch Neurol; 2007 Jun; 64(6):890-3. PubMed ID: 17562939
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
