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Journal Abstract Search

146 related items for PubMed ID: 9382468

  • 1. In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by 31P magnetic resonance spectroscopy.
    Lodi R, Taylor DJ, Tabrizi SJ, Kumar S, Sweeney M, Wood NW, Styles P, Radda GK, Schapira AH.
    Ann Neurol; 1997 Oct; 42(4):573-9. PubMed ID: 9382468
    [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
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  • 4. 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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  • 5. [Leber's hereditary optic atrophy. A hereditary disease caused by mitochondrial DNA mutation].
    Nørby S, Rosenberg T.
    Ugeskr Laeger; 1990 Oct 22; 152(43):3149-52. PubMed ID: 2238193
    [Abstract] [Full Text] [Related]

  • 6. Leber's hereditary optic neuropathy and complex I deficiency in muscle.
    Larsson NG, Andersen O, Holme E, Oldfors A, Wahlström J.
    Ann Neurol; 1991 Nov 22; 30(5):701-8. PubMed ID: 1763894
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  • 8. [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 22; 157(5):537-41. PubMed ID: 11438773
    [Abstract] [Full Text] [Related]

  • 9. Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo.
    Chinnery PF, Taylor DJ, Brown DT, Manners D, Styles P, Lodi R.
    Ann Neurol; 2000 Mar 22; 47(3):381-4. PubMed ID: 10716261
    [Abstract] [Full Text] [Related]

  • 10. A prospective study to evaluate the impact of 31P-MRS to determinate mitochondrial dysfunction in skeletal muscle of ALS patients.
    Grehl T, Fischer S, Müller K, Malin JP, Zange J.
    Amyotroph Lateral Scler; 2007 Feb 22; 8(1):4-8. PubMed ID: 17364428
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  • 12. [Atypical presentation of Leber's optic neuropathy].
    Borruat FX, Sanders MD.
    Klin Monbl Augenheilkd; 1994 May 22; 204(5):400-2. PubMed ID: 8051882
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  • 14. Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy.
    Lodi R, Schapira AH, Manners D, Styles P, Wood NW, Taylor DJ, Warner TT.
    Ann Neurol; 2000 Jul 22; 48(1):72-6. PubMed ID: 10894218
    [Abstract] [Full Text] [Related]

  • 15. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Jun 22; 16(2):120-3. PubMed ID: 8797169
    [Abstract] [Full Text] [Related]

  • 16. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Jun 22; 6(2):121-3. PubMed ID: 11995959
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  • 17. 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 22; 82(1):59-64. PubMed ID: 10087740
    [Abstract] [Full Text] [Related]

  • 18. [Positive diagnosis of Leber's hereditary optic neuropathy using molecular genetics].
    Souied E, Pisella PJ, Ossareh B, Brézin A, Junes P, Wild-Decrette C, Munnich A, Bonnefont JP, Mondon H.
    J Fr Ophtalmol; 1997 Jan 22; 20(1):65-70. PubMed ID: 9099286
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  • 19. Coenzyme Q10 improves mitochondrial respiration in patients with mitochondrial cytopathies. An in vivo study on brain and skeletal muscle by phosphorous magnetic resonance spectroscopy.
    Barbiroli B, Frassineti C, Martinelli P, Iotti S, Lodi R, Cortelli P, Montagna P.
    Cell Mol Biol (Noisy-le-grand); 1997 Jul 22; 43(5):741-9. PubMed ID: 9298596
    [Abstract] [Full Text] [Related]

  • 20. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.
    Bhatti MT, Newman NJ.
    J Neuroophthalmol; 1999 Mar 22; 19(1):28-33. PubMed ID: 10098545
    [Abstract] [Full Text] [Related]

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