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 *

152 related articles for article (PubMed ID: 9925234)

  • 1. Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians.
    Kalman B; Li S; Chatterjee D; O'Connor J; Voehl MR; Brown MD; Alder H
    Acta Neurol Scand; 1999 Jan; 99(1):16-25. PubMed ID: 9925234
    [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. Is the mitochondrial DNA involved in determining susceptibility to multiple sclerosis?
    Kalman B; Alder H
    Acta Neurol Scand; 1998 Oct; 98(4):232-7. PubMed ID: 9808271
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
    Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M
    Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
    Brown MD; Torroni A; Reckord CL; Wallace DC
    Hum Mutat; 1995; 6(4):311-25. PubMed ID: 8680405
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.
    Houshmand M; Sanati MH; Babrzadeh F; Ardalan A; Teimori M; Vakilian M; Akuchekian M; Farhud D; Lotfi J
    Mult Scler; 2005 Dec; 11(6):728-30. PubMed ID: 16320736
    [TBL] [Abstract][Full Text] [Related]  

  • 9. mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.
    Lamminen T; Huoponen K; Sistonen P; Juvonen V; Lahermo P; Aula P; Nikoskelainen E; Savontaus ML
    Eur J Hum Genet; 1997; 5(5):271-9. PubMed ID: 9412783
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis.
    Mihailova SM; Ivanova MI; Quin LM; Naumova EJ
    Eur J Neurol; 2007 Jan; 14(1):44-7. PubMed ID: 17222112
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
    Brown MD; Sun F; Wallace DC
    Am J Hum Genet; 1997 Feb; 60(2):381-7. PubMed ID: 9012411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis.
    Kalman B; Rodriguez-Valdez JL; Bosch U; Lublin FD
    Mult Scler; 1997 Jan; 2(6):279-82. PubMed ID: 9065918
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
    Khan NA; Govindaraj P; Soumittra N; Sharma S; Srilekha S; Ambika S; Vanniarajan A; Meena AK; Uppin MS; Sundaram C; Bindu PS; Gayathri N; Taly AB; Thangaraj K
    Invest Ophthalmol Vis Sci; 2017 Aug; 58(10):3923-3930. PubMed ID: 28768321
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.
    Torroni A; Petrozzi M; D'Urbano L; Sellitto D; Zeviani M; Carrara F; Carducci C; Leuzzi V; Carelli V; Barboni P; De Negri A; Scozzari R
    Am J Hum Genet; 1997 May; 60(5):1107-21. PubMed ID: 9150158
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in italian patients presenting with sporadic bilateral optic neuritis.
    Sartore M; Grasso M; Piccolo G; Fasani R; Bergamaschi R; Malaspina A; Ceroni M; Kobayashi M; Semeraro A; Arbustini E
    Biochem Mol Med; 1995 Oct; 56(1):45-51. PubMed ID: 8593537
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
    Brown MD; Voljavec AS; Lott MT; Torroni A; Yang CC; Wallace DC
    Genetics; 1992 Jan; 130(1):163-73. PubMed ID: 1732158
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
    Houshmand M; Sanati MH; Rashedi I; Sharifpanah F; Asghari E; Lotfi J
    Eur Neurol; 2004; 51(2):68-71. PubMed ID: 14671420
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
    Brown MD; Starikovskaya E; Derbeneva O; Hosseini S; Allen JC; Mikhailovskaya IE; Sukernik RI; Wallace DC
    Hum Genet; 2002 Feb; 110(2):130-8. PubMed ID: 11935318
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.