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Journal Abstract Search

111 related items for PubMed ID: 8773606

  • 1. Sequence of mitochondrial DNA in patients with multiple sclerosis.
    Chalmers RM, Robertson N, DAS Compston, Harding AE.
    Ann Neurol; 1996 Aug; 40(2):239-43. PubMed ID: 8773606
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  • 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
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  • 3. 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
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  • 4. [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
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  • 5. Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations.
    Ohlenbusch A, Wilichowski E, Hanefeld F.
    Neuropediatrics; 1998 Aug; 29(4):175-9. PubMed ID: 9762692
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  • 6. Characterization of the mitochondrial genome in childhood multiple sclerosis. III. Multiple sclerosis without optic neuritis and the non-LHON-associated genes.
    Ohlenbusch A, Wilichowski E, Hanefeld F.
    Neuropediatrics; 1998 Dec; 29(6):313-9. PubMed ID: 10029351
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  • 8. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111
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  • 9. 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
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  • 10. A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.
    Tanaka A, Kiyosawa M, Mashima Y, Tokoro T.
    J Neuroophthalmol; 1998 Jun; 18(2):81-3. PubMed ID: 9621260
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  • 12. [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 20; 138(18):565-8. PubMed ID: 10596473
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  • 13. 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 20; 5(4):233-40. PubMed ID: 8854108
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  • 14. Clinical spectrum of Leber's hereditary optic neuropathy.
    Kerrison JB, Newman NJ.
    Clin Neurosci; 1997 Jul 20; 4(5):295-301. PubMed ID: 9292259
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  • 15. 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 20; 115 ( Pt 4)():979-89. PubMed ID: 1393514
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  • 20. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
    Lertrit P, Ruangvaravate N, Trongpanich Y, Imsumran A, Mungkornkarn C, Neungton N.
    J Med Assoc Thai; 1999 Jan 20; 82(1):59-64. PubMed ID: 10087740
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