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Journal Abstract Search

149 related items for PubMed ID: 23644319

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  • 2. Pantothenate-kinase associated neurodegeneration (PKAN) "eye of the tiger" sign.
    Renaud DL, Kotagal S.
    Pediatr Neurol; 2007 Jan; 36(1):70-1. PubMed ID: 17162204
    [No Abstract] [Full Text] [Related]

  • 3. A novel PANK2 gene mutation in a Persian boy: the first report from Iran.
    Aryani O, Houshmand M, Fatehi F.
    Clin Neurol Neurosurg; 2013 Jul; 115(7):1170-2. PubMed ID: 23116688
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  • 6. Chorea-acanthocytosis with upper motor neuron degeneration and 3419_3420 delCA and 3970_3973 delAGTC VPS13A mutations.
    Miki Y, Nishie M, Ichiba M, Nakamura M, Mori F, Ogawa M, Kaimori M, Sano A, Wakabayashi K.
    Acta Neuropathol; 2010 Feb; 119(2):271-3. PubMed ID: 19949804
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  • 8. Magnetic resonance imaging and Hallervorden-Spatz syndrome.
    Trimble M.
    CNS Spectr; 2003 Jun; 8(6):420. PubMed ID: 12868452
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  • 10. First cases in the Czech Republic of the Hallervorden-Spatz disease resulting from mutation in the pantothenate kinase 2 gene.
    Zumrová A, Krepelová A, Kyncl M, Maríková T, Prosková M, Cíbochová R, Sebronová V, Komárek V.
    Neuro Endocrinol Lett; 2005 Jun; 26(3):213-8. PubMed ID: 15990724
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  • 12. Missense PANK2 mutation without "eye of the tiger" sign: MR findings in a large group of patients with pantothenate kinase-associated neurodegeneration (PKAN).
    Delgado RF, Sanchez PR, Speckter H, Then EP, Jimenez R, Oviedo J, Dellani PR, Foerster B, Stoeter P.
    J Magn Reson Imaging; 2012 Apr; 35(4):788-94. PubMed ID: 22127788
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  • 13. Acanthocytosis and the c.680 A>G Mutation in the PANK2 Gene: A Study Enrolling a Cohort of PKAN Patients from the Dominican Republic.
    Schiessl-Weyer J, Roa P, Laccone F, Kluge B, Tichy A, De Almeida Ribeiro E, Prohaska R, Stoeter P, Siegl C, Salzer U.
    PLoS One; 2015 Apr; 10(4):e0125861. PubMed ID: 25915509
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  • 14. Hallervorden Spatz syndrome (pantothenate kinase associated neurodegeneration) in two Sardinian brother with homozygous mutation in PANK 2 gene.
    Cossu G, Melis M, Floris G, Hayflick SJ, Spissu A.
    J Neurol; 2002 Nov; 249(11):1599-600. PubMed ID: 12532925
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  • 15. Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
    Valentino P, Annesi G, Cirò Candiano IC, Annesi F, Civitelli D, Tarantino P, Naso F, Spadafora P, Carrideo S, De Marco EV, Consoli D, Zappia M, Gambardella A, Quattrone A.
    Mov Disord; 2006 Feb; 21(2):252-4. PubMed ID: 16149094
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  • 16. Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene.
    Cangül H, Ozdemir O, Yakut T, Okan M, Morgan NV, Baytan B, Kurian MA, Spiegel R, Maher ER.
    Turk J Pediatr; 2009 Feb; 51(2):161-5. PubMed ID: 19480328
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  • 17. Pure akinesia: an unusual phenotype of Hallervorden-Spatz syndrome.
    Molinuevo JL, Martí MJ, Blesa R, Tolosa E.
    Mov Disord; 2003 Nov; 18(11):1351-3. PubMed ID: 14639680
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  • 18. Chorein-sensitive polymerization of cortical actin and suicidal cell death in chorea-acanthocytosis.
    Föller M, Hermann A, Gu S, Alesutan I, Qadri SM, Borst O, Schmidt EM, Schiele F, vom Hagen JM, Saft C, Schöls L, Lerche H, Stournaras C, Storch A, Lang F.
    FASEB J; 2012 Apr; 26(4):1526-34. PubMed ID: 22227296
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  • 19. Pantothenate kinase-associated neurodegeneration: novel mutations in the PANK2 gene in an Argentinean young woman.
    Gatto E, Etcheverry JL, Converso DP, Bidinost C, Rosa A.
    Mov Disord; 2010 Oct 15; 25(13):2262-4. PubMed ID: 20721927
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  • 20. Novel gene mutations and clinical features in patients with pantothenate kinase-associated neurodegeneration.
    Ma LY, Wang L, Yang YM, Lu Y, Cheng FB, Wan XH.
    Clin Genet; 2015 Oct 15; 87(1):93-5. PubMed ID: 24689511
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