BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 25586537)

  • 1. Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed.
    Mignarri A; Cenciarelli S; Da Pozzo P; Cardaioli E; Malandrini A; Federico A; Dotti MT
    J Neurol Sci; 2015 Feb; 349(1-2):254-5. PubMed ID: 25586537
    [No Abstract]   [Full Text] [Related]  

  • 2. Mitochondrial recessive ataxia syndrome mimicking dominant spinocerebellar ataxia.
    Palin EJ; Hakonen AH; Korpela M; Paetau A; Suomalainen A
    J Neurol Sci; 2012 Apr; 315(1-2):160-3. PubMed ID: 22166854
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Movement disorders in mitochondrial diseases.
    Tranchant C; Anheim M
    Rev Neurol (Paris); 2016; 172(8-9):524-529. PubMed ID: 27476418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. POLG1 manifestations in childhood.
    Isohanni P; Hakonen AH; Euro L; Paetau I; Linnankivi T; Liukkonen E; Wallden T; Luostarinen L; Valanne L; Paetau A; Uusimaa J; Lönnqvist T; Suomalainen A; Pihko H
    Neurology; 2011 Mar; 76(9):811-5. PubMed ID: 21357833
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Do carriers of POLG mutation W748S have disease manifestations?
    Rantamäki M; Luoma P; Virta JJ; Rinne JO; Paetau A; Suomalainen A; Udd B
    Clin Genet; 2007 Dec; 72(6):532-7. PubMed ID: 17894835
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Friedreich ataxia--diagnosis after a decade. Differential diagnosis of inherited spinocerebellar ataxias].
    Vitaszil E; Jelencsik I; Szirmai I
    Ideggyogy Sz; 2002 Nov; 55(11-12):382-93. PubMed ID: 12632799
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Melas associated with mutations in the polg1 gene.
    Tzoulis C; Bindoff LA
    Neurology; 2008 Mar; 70(13):1054; author reply 1054-5. PubMed ID: 18362288
    [No Abstract]   [Full Text] [Related]  

  • 8. Inherited ataxia with slow saccades.
    Chakor RT; Bharote H
    J Postgrad Med; 2012; 58(4):318-25. PubMed ID: 23298936
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neuropsychological performance in patients with POLG1 mutations and the syndrome of mitochondrial spinocerebellar ataxia and epilepsy.
    Gramstad A; Bindoff LA; Lillebø A; Tzoulis C; Engelsen BA
    Epilepsy Behav; 2009 Sep; 16(1):172-4. PubMed ID: 19435586
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dystonia in mitochondrial spinocerebellar ataxia and epilepsy syndrome associated with novel recessive POLG mutations.
    Hinnell C; Haider S; Delamont S; Clough C; Hadzic N; Samuel M
    Mov Disord; 2012 Jan; 27(1):162-3. PubMed ID: 21956653
    [No Abstract]   [Full Text] [Related]  

  • 11. Keys to overcoming the challenge of diagnosing autosomal recessive spinocerebellar ataxia.
    Arias M
    Neurologia (Engl Ed); 2019 May; 34(4):248-258. PubMed ID: 27460185
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI; Koenig M
    Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical features and diagnosis of spinocerebellar ataxia].
    Klivényi P; Horváth Z; Vécsei L
    Ideggyogy Sz; 2004 Jan; 57(1-2):11-22. PubMed ID: 15042864
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Chronic ataxia in childhood].
    Erazo Torricelli R
    Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?
    Wictorin K; Brådvik B; Nilsson K; Soller M; van Westen D; Bynke G; Bauer P; Schöls L; Puschmann A
    Parkinsonism Relat Disord; 2014 Jul; 20(7):748-54. PubMed ID: 24787759
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirable.
    Gupta SN; Marks HG
    J Neurol Sci; 2008 Jan; 264(1-2):173-6. PubMed ID: 17720198
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FGF21 in ataxia patients with spinocerebellar atrophy and mitochondrial disease.
    Su SL; Wang WF; Wu SL; Wu HM; Chang JC; Huang CS; Cheng WL; Soong BW; Lee YC; Li JY; Kuo SJ; Chen M; Huang CN; Liu CS
    Clin Chim Acta; 2012 Dec; 414():225-7. PubMed ID: 23031666
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.
    Gücüyener K; Ozgül K; Paternotte C; Erdem H; Prud'homme JF; Ozgüç M; Topaloğlu H
    Neuropediatrics; 2001 Jun; 32(3):142-6. PubMed ID: 11521210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ocular apraxia in recessive ataxia.
    Koeppen AH
    Arch Neurol; 2002 May; 59(5):874; author reply 874. PubMed ID: 12020276
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.