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Journal Abstract Search

64 related items for PubMed ID: 25816977

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  • 4. Congenital ataxia and mental retardation in three brothers.
    Margari L, Ventura P, Presicci A, Buttiglione M, Perniola T.
    Pediatr Neurol; 2004 Jul; 31(1):59-63. PubMed ID: 15246495
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  • 9. Diagnostic imaging and clinical findings in rhombencephalosynapsis: case report and literature review.
    Oei AS, Vanzieleghem BD, Kunnen MF.
    JBR-BTR; 2001 Jul; 84(5):197-200. PubMed ID: 11757675
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  • 10. GLUT1 deficiency with delayed myelination responding to ketogenic diet.
    Klepper J, Engelbrecht V, Scheffer H, van der Knaap MS, Fiedler A.
    Pediatr Neurol; 2007 Aug; 37(2):130-3. PubMed ID: 17675029
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  • 12. [Rhombencephalosynapsis as a rare anomaly of the posterior skull base].
    Caffier S, Kittner T, Laniado M.
    Rofo; 2001 Sep; 173(9):850-1. PubMed ID: 11582567
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  • 13. Preservation of language in the ataxic infant in a case of cerebellar agenesis.
    Jacob FD, Goez HR.
    Can J Neurol Sci; 2011 Jan; 38(1):143-4. PubMed ID: 21156446
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  • 15. Cognitive outcome in children with rhombencephalosynapsis.
    Poretti A, Alber FD, Bürki S, Toelle SP, Boltshauser E.
    Eur J Paediatr Neurol; 2009 Jan; 13(1):28-33. PubMed ID: 18407532
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  • 16. Isolated rhombencephalosynapsis diagnosed by magnetic resonance imaging.
    Savolaine ER, Fadell RJ, Patel YP.
    Clin Imaging; 1991 Jan; 15(2):125-9. PubMed ID: 1913312
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  • 17. Disorders of cognitive and affective development in cerebellar malformations.
    Tavano A, Grasso R, Gagliardi C, Triulzi F, Bresolin N, Fabbro F, Borgatti R.
    Brain; 2007 Oct; 130(Pt 10):2646-60. PubMed ID: 17872929
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  • 18. Rhombencephalosynapsis: a rare congenital anomaly presenting with seizure and developmental delay.
    Shahrzad M, Gold M.
    Acta Neurol Belg; 2015 Dec; 115(4):685-6. PubMed ID: 26013386
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  • 19. Macrocephaly in association with pontocerebellar hypoplasia type 1: a paradox.
    Tamhankar PM, Suvarna JC, Deshmukh CT.
    Indian J Med Sci; 2009 Mar; 63(3):120-3. PubMed ID: 19359782
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  • 20. Teaching NeuroImages: Molar tooth sign with hypotonia, ataxia, and nystagmus (Joubert syndrome) and hypothyroidism.
    Graber JJ, Lau H, Sathe S.
    Neurology; 2009 Dec 15; 73(24):e106. PubMed ID: 20018634
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