249 related articles for article (PubMed ID: 10098545)
1. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.
Bhatti MT; Newman NJ
J Neuroophthalmol; 1999 Mar; 19(1):28-33. PubMed ID: 10098545
[TBL] [Abstract][Full Text] [Related]
2. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE
Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
[TBL] [Abstract][Full Text] [Related]
3. Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
La Russa A; Cittadella R; Andreoli V; Valentino P; Trecroci F; Caracciolo M; Gallo O; Gambardella A; Quattrone A
Mult Scler; 2011 Jun; 17(6):763-6. PubMed ID: 21685233
[TBL] [Abstract][Full Text] [Related]
4. Leber's hereditary optic neuropathy.
Letchavanakul A; Dechphongsaphilas W; Dhamcharee V
J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
[TBL] [Abstract][Full Text] [Related]
5. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
6. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
Hotta Y; Fujiki K; Hayakawa M; Nakajima A; Kanai A; Mashima Y; Hiida Y; Shinoda K; Yamada K; Oguchi Y
Jpn J Ophthalmol; 1995; 39(1):96-108. PubMed ID: 7643491
[TBL] [Abstract][Full Text] [Related]
7. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
Leo-Kottler B; Christ-Adler M; Baumann B; Zrenner E; Wissinger B
Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108
[TBL] [Abstract][Full Text] [Related]
8. [Atypical presentation of Leber's optic neuropathy].
Borruat FX; Sanders MD
Klin Monbl Augenheilkd; 1994 May; 204(5):400-2. PubMed ID: 8051882
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial DNA analysis of Leber's hereditary optic neuropathy.
Hiida Y; Mashima Y; Oguchi Y; Uemura Y; Kudoh J; Sakai K; Shimizu N
Jpn J Ophthalmol; 1991; 35(1):102-6. PubMed ID: 1895564
[TBL] [Abstract][Full Text] [Related]
10. [Leber's hereditary optic neuropathy].
Konrádová V; Zeman J; Stratilová L; Hermanská J; Vseticka I; Misovicová N; Kurca E; Gerinec A; Houstĕk J
Cas Lek Cesk; 1999 Oct; 138(18):565-8. PubMed ID: 10596473
[TBL] [Abstract][Full Text] [Related]
11. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
Wilichowski E; Ohlenbusch A; Hanefeld F
Neuropediatrics; 1998 Dec; 29(6):307-12. PubMed ID: 10029350
[TBL] [Abstract][Full Text] [Related]
12. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation.
Yamada K; Mashima Y; Kigasawa K; Miyashita K; Wakakura M; Oguchi Y
J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781
[TBL] [Abstract][Full Text] [Related]
13. Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.
Mojon DS; Fujihara K; Hirano M; Miller C; Lincoff NS; Jacobs LD; Greenberg SJ
Graefes Arch Clin Exp Ophthalmol; 1999 Apr; 237(4):348-50. PubMed ID: 10208269
[TBL] [Abstract][Full Text] [Related]
14. Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.
Stone EM; Newman NJ; Miller NR; Johns DR; Lott MT; Wallace DC
J Clin Neuroophthalmol; 1992 Mar; 12(1):10-4. PubMed ID: 1532593
[TBL] [Abstract][Full Text] [Related]
15. Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON).
Meire GM; Cochaux P; Candaele C; Broux C
Bull Soc Belge Ophtalmol; 1994; 254():137-46. PubMed ID: 7493114
[TBL] [Abstract][Full Text] [Related]
16. Peripapillary fluorescein leakage in 11778 Leber's optic neuropathy.
Yen MY; Wei YH; Liu JH
J Neuroophthalmol; 1996 Sep; 16(3):178-81. PubMed ID: 8865009
[TBL] [Abstract][Full Text] [Related]
17. [Sudden blindness: consider Leber's hereditary optic neuropathy].
Schieving JH; de Vries BB; Hol F; Stroink H
Ned Tijdschr Geneeskd; 2008 Oct; 152(43):2313-6. PubMed ID: 19024058
[TBL] [Abstract][Full Text] [Related]
18. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve.
Howell N
Vision Res; 1997 Dec; 37(24):3495-507. PubMed ID: 9425526
[TBL] [Abstract][Full Text] [Related]
19. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON.
Rödel G; Laubhan R; Scheuerle A; Skowronek P; Haferkamp O
Eur J Med Res; 1996 Jul; 1(10):491-4. PubMed ID: 9438147
[TBL] [Abstract][Full Text] [Related]
20. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
Zhang LS; Huang Y; Li FY
Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]