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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

197 related items for PubMed ID: 17175464

  • 1.
    ; . PubMed ID:
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  • 2. Prevalence and progression of mitochondrial diseases: a study of 50 patients.
    Arpa J, Cruz-Martínez A, Campos Y, Gutiérrez-Molina M, García-Rio F, Pérez-Conde C, Martín MA, Rubio JC, Del Hoyo P, Arpa-Fernández A, Arenas J.
    Muscle Nerve; 2003 Dec; 28(6):690-5. PubMed ID: 14639582
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial cytopathies.
    Schmiedel J, Jackson S, Schäfer J, Reichmann H.
    J Neurol; 2003 Mar; 250(3):267-77. PubMed ID: 12638015
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  • 6. Mitochondrial disorders.
    Edmond JC.
    Int Ophthalmol Clin; 2009 Mar; 49(3):27-33. PubMed ID: 19584620
    [No Abstract] [Full Text] [Related]

  • 7. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation.
    Finsterer J.
    Acta Neurol Scand; 2007 Jul; 116(1):1-14. PubMed ID: 17587249
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  • 9. Value of brain magnetic resonance imaging in mitochondrial respiratory chain disorders.
    Diogo L, Cordeiro M, Garcia P, Fineza I, Moura C, Oliveira CR, Veiga M, Garcia T, Grazina M.
    Pediatr Neurol; 2010 Mar; 42(3):196-200. PubMed ID: 20159429
    [Abstract] [Full Text] [Related]

  • 10. [Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF].
    Goto Y.
    Nihon Rinsho; 1997 Dec; 55(12):3259-64. PubMed ID: 9436447
    [Abstract] [Full Text] [Related]

  • 11. The genetics of mitochondrial disease.
    Davis RL, Sue CM.
    Semin Neurol; 2011 Nov; 31(5):519-30. PubMed ID: 22266889
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  • 12. Diagnostic challenges of mitochondrial DNA disorders.
    Wong LJ.
    Mitochondrion; 2007 Nov; 7(1-2):45-52. PubMed ID: 17276740
    [Abstract] [Full Text] [Related]

  • 13. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
    Spruijt L, Smeets HJ, Hendrickx A, Bettink-Remeijer MW, Maat-Kievit A, Schoonderwoerd KC, Sluiter W, de Coo IF, Hintzen RQ.
    Arch Neurol; 2007 Jun; 64(6):890-3. PubMed ID: 17562939
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  • 14. [Leigh syndrome caused by the mitochondrial DNA G14459A mutation in a Mexican family].
    Gutiérrez A, Saldaña-Martínez A, García-Ramírez R, Rayo-Mares D, Carreras M, López-Pérez MJ, Ruiz-Pesini E, Montoya J, Montiel-Sosa JF.
    Rev Neurol; 2007 Jun; 49(5):248-50. PubMed ID: 19714555
    [Abstract] [Full Text] [Related]

  • 15. PGD to reduce reproductive risk: the case of mitochondrial DNA disorders.
    Bredenoord AL, Dondorp W, Pennings G, De Die-Smulders CE, De Wert G.
    Hum Reprod; 2008 Nov; 23(11):2392-401. PubMed ID: 18664474
    [Abstract] [Full Text] [Related]

  • 16. Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation.
    McFarland R, Clark KM, Morris AA, Taylor RW, Macphail S, Lightowlers RN, Turnbull DM.
    Nat Genet; 2002 Feb; 30(2):145-6. PubMed ID: 11799391
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  • 17. [Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome].
    Rydzanicz M, Mrugacz M, Gajecka M.
    Klin Oczna; 2008 Feb; 110(7-9):321-4. PubMed ID: 19112871
    [Abstract] [Full Text] [Related]

  • 18. The molecular genetics of mitochondrial cytopathies: the Melbourne experience.
    Thyagarajan D, Byrne E, Dennet X, Marzuki S.
    Clin Exp Neurol; 1992 Feb; 29():172-81. PubMed ID: 1343860
    [Abstract] [Full Text] [Related]

  • 19. Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
    Blok MJ, Spruijt L, de Coo IF, Schoonderwoerd K, Hendrickx A, Smeets HJ.
    J Med Genet; 2007 Apr; 44(4):e74. PubMed ID: 17400793
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  • 20. Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.
    Grönlund MA, Honarvar AK, Andersson S, Moslemi AR, Oldfors A, Holme E, Tulinius M, Darin N.
    Br J Ophthalmol; 2010 Jan; 94(1):121-7. PubMed ID: 20385529
    [Abstract] [Full Text] [Related]

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