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PUBMED FOR HANDHELDS

Journal Abstract Search


335 related items for PubMed ID: 22403016

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  • 6. Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcome.
    de Laat P, Fleuren LH, Bekker MN, Smeitink JA, Janssen MC.
    Mitochondrion; 2015 Nov; 25():98-103. PubMed ID: 26455484
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  • 8. [Mitochondrial DNA heteroplasmy of the m.3243A>G mutation in maternally inherited diabetes and deafness].
    Cataldo LR, Olmos P, Valerie Smalley S, Díez A, Parada A, Gejman R, Fadic R, Santos JL.
    Rev Med Chil; 2013 Mar; 141(3):305-12. PubMed ID: 23900320
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  • 9. Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
    Niedermayr K, Pölzl G, Scholl-Bürgi S, Fauth C, Schweigmann U, Haberlandt E, Albrecht U, Zlamy M, Sperl W, Mayr JA, Karall D.
    Congenit Heart Dis; 2018 Sep; 13(5):671-677. PubMed ID: 30133155
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  • 13. The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management.
    Nesbitt V, Pitceathly RD, Turnbull DM, Taylor RW, Sweeney MG, Mudanohwo EE, Rahman S, Hanna MG, McFarland R.
    J Neurol Neurosurg Psychiatry; 2013 Aug; 84(8):936-8. PubMed ID: 23355809
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  • 15. Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.
    Procaccio V, Neckelmann N, Paquis-Flucklinger V, Bannwarth S, Jimenez R, Davila A, Poole JC, Wallace DC.
    Mol Diagn Ther; 2006 Aug; 10(6):381-9. PubMed ID: 17154655
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  • 18. Dysphagia, malnutrition and gastrointestinal problems in patients with mitochondrial disease caused by the m3243A>G mutation.
    de Laat P, Zweers HE, Knuijt S, Smeitink JA, Wanten GJ, Janssen MC.
    Neth J Med; 2015 Jan; 73(1):30-6. PubMed ID: 26219939
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  • 19. Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study.
    Haast RAM, Ivanov D, IJsselstein RJT, Sallevelt SCEH, Jansen JFA, Smeets HJM, de Coo IFM, Formisano E, Uludağ K.
    Neuroimage Clin; 2018 Jan; 18():231-244. PubMed ID: 29868447
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