BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 8139599)

  • 1. Platelet mitochondrial DNA in Parkinson's disease.
    Schapira AH; Marsden CD
    Mov Disord; 1994 Jan; 9(1):119-21. PubMed ID: 8139599
    [No Abstract]   [Full Text] [Related]  

  • 2. Mitochondrial DNA in Parkinson's disease.
    Schapira AH
    Adv Neurol; 1999; 80():233-7. PubMed ID: 10410727
    [No Abstract]   [Full Text] [Related]  

  • 3. PCR analysis of platelet mtDNA: lack of specific changes in Parkinson's disease.
    Sandy MS; Langston JW; Smith MT; Di Monte DA
    Mov Disord; 1993; 8(1):74-82. PubMed ID: 8419811
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Respiratory chain and mitochondrial deoxyribonucleic acid in blood cells from patients with focal and generalized dystonia.
    Reichmann H; Naumann M; Hauck S; Janetzky B
    Mov Disord; 1994 Nov; 9(6):597-600. PubMed ID: 7845398
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA analysis in Parkinson's disease.
    Schapira AH; Holt IJ; Sweeney M; Harding AE; Jenner P; Marsden CD
    Mov Disord; 1990; 5(4):294-7. PubMed ID: 1979656
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene of the month.
    Nat Biotechnol; 1996 Dec; 14(13):1638. PubMed ID: 9634834
    [No Abstract]   [Full Text] [Related]  

  • 7. [Parkinson disease--a mitochondrial myopathy?].
    Reichmann H; Janetzky B; Klinge M; Riederer P
    Nervenarzt; 1993 Apr; 64(4):215-20. PubMed ID: 8506008
    [No Abstract]   [Full Text] [Related]  

  • 8. The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction.
    Kösel S; Egensperger R; Schnopp NM; Graeber MB
    Mov Disord; 1997 Sep; 12(5):639-45. PubMed ID: 9380043
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Absence of 4,977-bp deletion of blood cell mitochondrial DNA in patients with young-onset Parkinson's disease.
    Shan DE; Yeh SI; Wan YC; Wei YH
    Acta Neurol Scand; 1995 Feb; 91(2):149-52. PubMed ID: 7785427
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The mitochondrial genome and its relation to human pathology].
    López de Munain A; Martí-Massó JF
    Neurologia; 1991; 6(7):251-5. PubMed ID: 1768444
    [No Abstract]   [Full Text] [Related]  

  • 11. Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease.
    Gu M; Cooper JM; Taanman JW; Schapira AH
    Ann Neurol; 1998 Aug; 44(2):177-86. PubMed ID: 9708539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial complex I deficiency in Parkinson's disease.
    Schapira AH
    Adv Neurol; 1993; 60():288-91. PubMed ID: 8420145
    [No Abstract]   [Full Text] [Related]  

  • 13. Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family.
    Swerdlow RH; Parks JK; Davis JN; Cassarino DS; Trimmer PA; Currie LJ; Dougherty J; Bridges WS; Bennett JP; Wooten GF; Parker WD
    Ann Neurol; 1998 Dec; 44(6):873-81. PubMed ID: 9851431
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisal.
    Schapira AH
    Mov Disord; 1994 Mar; 9(2):125-38. PubMed ID: 8196673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human mitochondrial complex I dysfunction.
    Cooper JM; Mann VM; Krige D; Schapira AH
    Biochim Biophys Acta; 1992 Jul; 1101(2):198-203. PubMed ID: 1633185
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial energy crisis in Parkinson's disease.
    Mizuno Y; Ikebe S; Hattori N; Kondo T; Tanaka M; Ozawa T
    Adv Neurol; 1993; 60():282-7. PubMed ID: 8420144
    [No Abstract]   [Full Text] [Related]  

  • 17. Mitochondrial DNA in focal dystonia: a cybrid analysis.
    Tabrizi SJ; Cooper JM; Schapira AH
    Ann Neurol; 1998 Aug; 44(2):258-61. PubMed ID: 9708550
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sequence analysis of the entire mitochondrial genome in Parkinson's disease.
    Vives-Bauza C; Andreu AL; Manfredi G; Beal MF; Janetzky B; Gruenewald TH; Lin MT
    Biochem Biophys Res Commun; 2002 Feb; 290(5):1593-601. PubMed ID: 11820805
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.
    Pyle A; Foltynie T; Tiangyou W; Lambert C; Keers SM; Allcock LM; Davison J; Lewis SJ; Perry RH; Barker R; Burn DJ; Chinnery PF
    Ann Neurol; 2005 Apr; 57(4):564-7. PubMed ID: 15786469
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Origin and functional consequences of the complex I defect in Parkinson's disease.
    Swerdlow RH; Parks JK; Miller SW; Tuttle JB; Trimmer PA; Sheehan JP; Bennett JP; Davis RE; Parker WD
    Ann Neurol; 1996 Oct; 40(4):663-71. PubMed ID: 8871587
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.