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 *

121 related articles for article (PubMed ID: 8867075)

  • 1. HLA class I genotypes in Leber's hereditary optic neuropathy.
    Chalmers RM; Govan GG; Schapira AH; Harding AE
    J Neurol Sci; 1996 Feb; 135(2):173-5. PubMed ID: 8867075
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HLA class II genotypes in Leber's hereditary optic neuropathy.
    Govan GG; Smith PR; Kellar-Wood H; Schapira AH; Harding AE
    J Neurol Sci; 1994 Nov; 126(2):193-6. PubMed ID: 7853025
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
    Brown MD; Voljavec AS; Lott MT; MacDonald I; Wallace DC
    FASEB J; 1992 Jul; 6(10):2791-9. PubMed ID: 1634041
    [TBL] [Abstract][Full Text] [Related]  

  • 5. mtDNA mutations in Leber's hereditary optic neuropathy.
    Savontaus ML
    Biochim Biophys Acta; 1995 May; 1271(1):261-3. PubMed ID: 7599218
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N
    Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.
    Harding AE; Sweeney MG; Miller DH; Mumford CJ; Kellar-Wood H; Menard D; McDonald WI; Compston DA
    Brain; 1992 Aug; 115 ( Pt 4)():979-89. PubMed ID: 1393514
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotypes of aldehyde dehydrogenase and alcohol dehydrogenase polymorphisms in patients with Leber's hereditary optic neuropathy.
    Isashiki Y; Tabata Y; Kamimura K; Ohba N
    Jpn J Hum Genet; 1997 Mar; 42(1):187-91. PubMed ID: 9183998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
    Poulton J; Deadman ME; Bronte-Stewart J; Foulds WS; Gardiner RM
    J Med Genet; 1991 Nov; 28(11):765-70. PubMed ID: 1770533
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nonfamilial and unusual cases of Leber's hereditary optic neuropathy identified by mitochondrial DNA analysis.
    Isashiki Y; Ohba N; Uto M; Nakagawa M; Nakano T; Kitahara K; Hotta A; Okamura R; Ozaki M; Futami Y
    Jpn J Ophthalmol; 1992; 36(2):197-204. PubMed ID: 1513067
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
    Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M
    J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation.
    Black GC; Morten K; Laborde A; Poulton J
    Br J Ophthalmol; 1996 Oct; 80(10):915-7. PubMed ID: 8976705
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pre-excitation syndrome in Leber's hereditary optic neuropathy.
    Nikoskelainen EK; Savontaus ML; Huoponen K; Antila K; Hartiala J
    Lancet; 1994 Sep; 344(8926):857-8. PubMed ID: 7916404
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leber's hereditary optic neuropathy: clinical and molecular genetic aspects. Preliminary results in our families.
    Van Caelenberghe E; Meire F; Broux C; Vassart G; Cochaux P
    Bull Soc Belge Ophtalmol; 1992; 243():139-46. PubMed ID: 1302143
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathy.
    Harding AE; Riordan-Eva P; Govan GG
    Muscle Nerve Suppl; 1995; 3():S82-4. PubMed ID: 7603533
    [TBL] [Abstract][Full Text] [Related]  

  • 20. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
    Gerbitz KD; Paprotta A; Obermaier-Kusser B; Rietschel M; Zerres K
    FEBS Lett; 1992 Dec; 314(3):251-5. PubMed ID: 1361456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.