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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 25724872)

  • 1. Parkinsonism, cognitive deficit and behavioural disturbance caused by a novel mutation in the polymerase gamma gene.
    Delgado-Alvarado M; de la Riva P; Jiménez-Urbieta H; Gago B; Gabilondo A; Bornstein B; Rodríguez-Oroz MC
    J Neurol Sci; 2015 Mar; 350(1-2):93-7. PubMed ID: 25724872
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
    Luoma P; Melberg A; Rinne JO; Kaukonen JA; Nupponen NN; Chalmers RM; Oldfors A; Rautakorpi I; Peltonen L; Majamaa K; Somer H; Suomalainen A
    Lancet; 2004 Sep 4-10; 364(9437):875-82. PubMed ID: 15351195
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neuromelanin MRI in a family with mitochondrial parkinsonism harboring a Y955C mutation in POLG1.
    Mukai M; Sugaya K; Yabe I; Goto Y; Yokochi F; Miyamoto K; Cai H; Sasaki H; Matsubara S
    Parkinsonism Relat Disord; 2013 Sep; 19(9):821-4. PubMed ID: 23673011
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
    Mancuso M; Filosto M; Oh SJ; DiMauro S
    Arch Neurol; 2004 Nov; 61(11):1777-9. PubMed ID: 15534189
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Familial progressive external opthalmoplegia, parkinsonism and polyneuropathy associated with POLG1 mutation].
    Mukai M; Sugaya K; Matsubara S; Cai H; Yabe I; Sasaki H; Nakano I
    Rinsho Shinkeigaku; 2014; 54(5):417-22. PubMed ID: 24943079
    [TBL] [Abstract][Full Text] [Related]  

  • 6. POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
    Di Fonzo A; Bordoni A; Crimi M; Sara G; Del Bo R; Bresolin N; Comi GP
    Hum Mutat; 2003 Dec; 22(6):498-9. PubMed ID: 14635118
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism.
    Hudson G; Schaefer AM; Taylor RW; Tiangyou W; Gibson A; Venables G; Griffiths P; Burn DJ; Turnbull DM; Chinnery PF
    Arch Neurol; 2007 Apr; 64(4):553-7. PubMed ID: 17420318
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonism.
    Invernizzi F; Varanese S; Thomas A; Carrara F; Onofrj M; Zeviani M
    Neuromuscul Disord; 2008 Jun; 18(6):460-4. PubMed ID: 18502641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial DNA depletion in progressive external ophthalmoplegia caused by POLG1 mutations.
    Tzoulis C; Papingji M; Fiskestrand T; Røste LS; Bindoff LA
    Acta Neurol Scand Suppl; 2009; (189):38-41. PubMed ID: 19566497
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders.
    Palin EJ; Paetau A; Suomalainen A
    Brain; 2013 Aug; 136(Pt 8):2379-92. PubMed ID: 23811324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progressive external ophthalmoplegia and multiple mitochondrial DNA deletions.
    Van Goethem G; Martin JJ; Van Broeckhoven C
    Acta Neurol Belg; 2002 Mar; 102(1):39-42. PubMed ID: 12094562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
    Komulainen T; Hinttala R; Kärppä M; Pajunen L; Finnilä S; Tuominen H; Rantala H; Hassinen I; Majamaa K; Uusimaa J
    BMC Neurol; 2010 May; 10():29. PubMed ID: 20438629
    [TBL] [Abstract][Full Text] [Related]  

  • 13. POLG1-related levodopa-responsive parkinsonism.
    Miguel R; Gago MF; Martins J; Barros P; Vale J; Rosas MJ
    Clin Neurol Neurosurg; 2014 Nov; 126():47-54. PubMed ID: 25203713
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.
    Van Goethem G; Dermaut B; Löfgren A; Martin JJ; Van Broeckhoven C
    Nat Genet; 2001 Jul; 28(3):211-2. PubMed ID: 11431686
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia].
    Posada IJ; Gallardo ME; Domínguez C; Rivera H; Cabello A; Arenas J; Martín MA; Garesse R; Bornstein B
    Med Clin (Barc); 2010 Oct; 135(10):452-5. PubMed ID: 20576279
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The in cis T251I and P587L POLG1 base changes: description of a new family and literature review.
    Scuderi C; Borgione E; Castello F; Lo Giudice M; Santa Paola S; Giambirtone M; Di Blasi FD; Elia M; Amato C; Città S; Gagliano C; Barbarino G; Vitello GA; Musumeci SA
    Neuromuscul Disord; 2015 Apr; 25(4):333-9. PubMed ID: 25660390
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sensory ataxic neuropathy with ophthalmoparesis caused by POLG mutations.
    Milone M; Brunetti-Pierri N; Tang LY; Kumar N; Mezei MM; Josephs K; Powell S; Simpson E; Wong LJ
    Neuromuscul Disord; 2008 Aug; 18(8):626-32. PubMed ID: 18585914
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene.
    Remes AM; Hinttala R; Kärppä M; Soini H; Takalo R; Uusimaa J; Majamaa K
    Parkinsonism Relat Disord; 2008 Dec; 14(8):652-4. PubMed ID: 18321754
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic analysis of two Japanese families with progressive external ophthalmoplegia and parkinsonism.
    Sato K; Yabe I; Yaguchi H; Nakano F; Kunieda Y; Saitoh S; Sasaki H
    J Neurol; 2011 Jul; 258(7):1327-32. PubMed ID: 21301859
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymerase gamma 1 mutations: clinical correlations.
    Milone M; Massie R
    Neurologist; 2010 Mar; 16(2):84-91. PubMed ID: 20220442
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.