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Journal Abstract Search

127 related items for PubMed ID: 8884581

  • 1. Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism.
    Ruitenbeek W, Wendel U, Hamel BC, Trijbels JM.
    J Inherit Metab Dis; 1996; 19(4):581-7. PubMed ID: 8884581
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  • 2. [Genetic counseling and prenatal diagnosis in mitochondrial diseases].
    Klopstock T, Gasser T.
    Nervenarzt; 1999 Jun; 70(6):504-8. PubMed ID: 10412694
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  • 7. Prerequisites and strategies for prenatal diagnosis of respiratory chain deficiency in chorionic villi.
    Niers L, van den Heuvel L, Trijbels F, Sengers R, Smeitink J, Nijmegen Centre for Mitochondrial Disorders, The Netherlands.
    J Inherit Metab Dis; 2003 Jun; 26(7):647-58. PubMed ID: 14707513
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  • 8. [Mutations of mitochondrial DNA and their relation to neuromuscular diseases].
    Wunderlich V.
    Zentralbl Allg Pathol; 1990 Jun; 136(4):305-16. PubMed ID: 2205992
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  • 9. Mitochondrial encephalomyopathies.
    DiMauro S, Moraes CT.
    Arch Neurol; 1993 Nov; 50(11):1197-208. PubMed ID: 8215979
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  • 11. [Diagnosis and therapy of mitochondriopathies].
    Sperl W.
    Wien Klin Wochenschr; 1997 Feb 14; 109(3):93-9. PubMed ID: 9139466
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  • 12. LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation.
    Blakely EL, de Silva R, King A, Schwarzer V, Harrower T, Dawidek G, Turnbull DM, Taylor RW.
    Eur J Hum Genet; 2005 May 14; 13(5):623-7. PubMed ID: 15657614
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  • 13. Mitochondrial DNA in migraine with aura.
    Klopstock T, May A, Seibel P, Papagiannuli E, Diener HC, Reichmann H.
    Neurology; 1996 Jun 14; 46(6):1735-8. PubMed ID: 8649580
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  • 15. [Prenatal diagnosis and genetic counseling of X-linked Alport syndrome in China].
    Zhang HW, Ding J, Wang F, Yang HX.
    Zhonghua Er Ke Za Zhi; 2007 Jul 14; 45(7):484-9. PubMed ID: 17953801
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  • 18. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
    Shoffner JM.
    Lancet; 1996 Nov 09; 348(9037):1283-8. PubMed ID: 8909383
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  • 19. Mitochondrial DNA and genetic disease.
    Poulton J.
    Bioessays; 1992 Nov 09; 14(11):763-8. PubMed ID: 1365889
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