323 related articles for article (PubMed ID: 9027481)
1. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease.
Hofmann S; Jaksch M; Bezold R; Mertens S; Aholt S; Paprotta A; Gerbitz KD
Hum Mol Genet; 1997 Oct; 6(11):1835-46. PubMed ID: 9302261
[TBL] [Abstract][Full Text] [Related]
4. Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndrome.
Hofmann S; Bezold R; Jaksch M; Kaufhold P; Obermaier-Kusser B; Gerbitz KD
Mol Cell Biochem; 1997 Sep; 174(1-2):209-13. PubMed ID: 9309689
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
Tharaphan P; Chuenkongkaew WL; Luangtrakool K; Sanpachudayan T; Suktitipat B; Suphavilai R; Srisawat C; Sura T; Lertrit P
J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR
Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
Nakamura M; Ara F; Yamada M; Hotta Y; Hayakawa M; Fujiki K; Kanai A; Sakai J; Inoue M; Yamamoto M
Jpn J Ophthalmol; 1992; 36(1):56-61. PubMed ID: 1635296
[TBL] [Abstract][Full Text] [Related]
10. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
Sudoyo H; Suryadi H; Lertrit P; Pramoonjago P; Lyrawati D; Marzuki S
J Hum Genet; 2002; 47(11):594-604. PubMed ID: 12436196
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA mutations in Cuban optic and peripheral neuropathy.
Johns DR; Neufeld MJ; Hedges TR
J Neuroophthalmol; 1994 Sep; 14(3):135-40. PubMed ID: 7804416
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.
Gómez-Zaera M; Strom TM; Rodríguez B; Estivill X; Meitinger T; Nunes V
Mol Genet Metab; 2001 Jan; 72(1):72-81. PubMed ID: 11161832
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [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]
16. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
Brown MD; Allen JC; Van Stavern GP; Newman NJ; Wallace DC
Am J Med Genet; 2001 Dec; 104(4):331-8. PubMed ID: 11754070
[TBL] [Abstract][Full Text] [Related]
17. Cuban epidemic optic neuropathy. Mitochondrial DNA analysis.
Johns DR; Sadun AA
J Neuroophthalmol; 1994 Sep; 14(3):130-4. PubMed ID: 7804415
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease.
Sawano T; Tanaka M; Ohno K; Yoneda M; Ota Y; Terasaki H; Awaya S; Ozawa T
Biochem Mol Biol Int; 1996 Apr; 38(4):693-700. PubMed ID: 8728098
[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. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
Nakamura M
Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]