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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

358 related items for PubMed ID: 22266889

  • 1. The genetics of mitochondrial disease.
    Davis RL, Sue CM.
    Semin Neurol; 2011 Nov; 31(5):519-30. PubMed ID: 22266889
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial cytopathies.
    Schmiedel J, Jackson S, Schäfer J, Reichmann H.
    J Neurol; 2003 Mar; 250(3):267-77. PubMed ID: 12638015
    [Abstract] [Full Text] [Related]

  • 3. [Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome].
    Rydzanicz M, Mrugacz M, Gajecka M.
    Klin Oczna; 2008 Mar; 110(7-9):321-4. PubMed ID: 19112871
    [Abstract] [Full Text] [Related]

  • 4. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ.
    Brain Dev; 2004 Oct; 26(7):459-62. PubMed ID: 15351082
    [Abstract] [Full Text] [Related]

  • 5. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
    Shoffner JM.
    Lancet; 1996 Nov 09; 348(9037):1283-8. PubMed ID: 8909383
    [Abstract] [Full Text] [Related]

  • 6. Headache and mitochondrial disorders.
    Rosen N.
    Headache; 2008 May 09; 48(5):733-4. PubMed ID: 18471127
    [Abstract] [Full Text] [Related]

  • 7. Genotype-phenotype correlation of maternally inherited disorders due to mutations in mitochondrial DNA.
    Thajeb P, Dai D, Chiang MF, Shyu WC.
    Taiwan J Obstet Gynecol; 2006 Sep 09; 45(3):201-7. PubMed ID: 17175464
    [Abstract] [Full Text] [Related]

  • 8. Mitochondrial disorders.
    Edmond JC.
    Int Ophthalmol Clin; 2009 Sep 09; 49(3):27-33. PubMed ID: 19584620
    [No Abstract] [Full Text] [Related]

  • 9. Mitochondrial defects in neurodegenerative disease.
    Wallace DC.
    Ment Retard Dev Disabil Res Rev; 2001 Sep 09; 7(3):158-66. PubMed ID: 11553931
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial syndromes with leukoencephalopathies.
    Wong LJ.
    Semin Neurol; 2012 Feb 09; 32(1):55-61. PubMed ID: 22422207
    [Abstract] [Full Text] [Related]

  • 11. Ophthalmological findings in 74 patients with mitochondrial disease.
    Zhu CC, Traboulsi EI, Parikh S.
    Ophthalmic Genet; 2017 Feb 09; 38(1):67-69. PubMed ID: 27029465
    [Abstract] [Full Text] [Related]

  • 12. Diagnostic challenges of mitochondrial DNA disorders.
    Wong LJ.
    Mitochondrion; 2007 Feb 09; 7(1-2):45-52. PubMed ID: 17276740
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial encephalomyopathies.
    Eymard B, Hauw JJ.
    Curr Opin Neurol Neurosurg; 1992 Dec 09; 5(6):909-16. PubMed ID: 1467585
    [Abstract] [Full Text] [Related]

  • 14. Nuclear gene defects in mitochondrial disorders.
    Scaglia F.
    Methods Mol Biol; 2012 Dec 09; 837():17-34. PubMed ID: 22215538
    [Abstract] [Full Text] [Related]

  • 15. [Mitochondrial disorders: a classification for the 21st century].
    Andreu AL, Gonzalo-Sanz R.
    Neurologia; 2004 Dec 09; 19(1):15-22. PubMed ID: 14762729
    [Abstract] [Full Text] [Related]

  • 16. [Digestive system disease as manifestation of the pleiotropic action of genes in mitochondrial dysfunction].
    Hrechanina OIa, Hrechanina IuB, Husar VA, Molodan LV.
    Lik Sprava; 2014 Nov 09; (11):29-39. PubMed ID: 25528830
    [Abstract] [Full Text] [Related]

  • 17. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].
    Arpa-Gutiérrez FJ, Cruz-Martínez A, Campos-González Y, Gutiérrez-Molina M, Santiago-Pérez S, Pérez-Conde MC, López-Pajares MR, Martín-Casarrubias MA, Rubio-Muñoz JC, del Hoyo P, Arpa-Fernández A, Arenas-Barbero J.
    Rev Neurol; 2014 Nov 09; 41(8):449-54. PubMed ID: 16224730
    [Abstract] [Full Text] [Related]

  • 18. Diagnosis and treatment of childhood mitochondrial diseases.
    Gropman AL.
    Curr Neurol Neurosci Rep; 2001 Mar 09; 1(2):185-94. PubMed ID: 11898515
    [Abstract] [Full Text] [Related]

  • 19. RNA-mediated restoration of mitochondrial function in cells harboring a Kearns Sayre Syndrome mutation.
    Mahato B, Jash S, Adhya S.
    Mitochondrion; 2011 Jul 09; 11(4):564-74. PubMed ID: 21406250
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial deafness.
    Kokotas H, Petersen MB, Willems PJ.
    Clin Genet; 2007 May 09; 71(5):379-91. PubMed ID: 17489842
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.