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Journal Abstract Search

453 related items for PubMed ID: 24014506

  • 1. Regional brain atrophy in mouse models of neuronal ceroid lipofuscinosis: a new rostrocaudal perspective.
    Kühl TG, Dihanich S, Wong AM, Cooper JD.
    J Child Neurol; 2013 Sep; 28(9):1117-22. PubMed ID: 24014506
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  • 2. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E, Dyken PR, Phillips P, Brodsky M, Bates S, Glasier C, Mrak RE.
    J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383
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  • 3. A novel c.1135_1138delCTGT mutation in CLN3 leads to juvenile neuronal ceroid lipofuscinosis.
    Drack AV, Miller JN, Pearce DA.
    J Child Neurol; 2013 Sep; 28(9):1112-6. PubMed ID: 23877479
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  • 5. Hippocampal volumes in juvenile neuronal ceroid lipofuscinosis: a longitudinal magnetic resonance imaging study.
    Tokola AM, Salli EK, Åberg LE, Autti TH.
    Pediatr Neurol; 2014 Feb; 50(2):158-63. PubMed ID: 24411222
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  • 6. Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease).
    Seigel GM, Lotery A, Kummer A, Bernard DJ, Greene ND, Turmaine M, Derksen T, Nussbaum RL, Davidson B, Wagner J, Mitchison HM.
    Mol Cell Neurosci; 2002 Apr; 19(4):515-27. PubMed ID: 11988019
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  • 7. Gene symbol: CLN3. Disease: juvenile neuronal ceroid lipofuscinosis (Batten disease).
    Leman AR, Pearce DA, Rothberg PG.
    Hum Genet; 2005 Feb; 116(3):236. PubMed ID: 15818814
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  • 8. Gene symbol: CLN3. Disease: Juvenile neuronal ceroid lipofuscinosis (Batten disease).
    Leman AR, Pearce DA, Rothberg PG.
    Hum Genet; 2005 May; 116(6):544. PubMed ID: 15991331
    [No Abstract] [Full Text] [Related]

  • 9. Developmental impairments of select neurotransmitter systems in brains of Cln3(Deltaex7/8) knock-in mice, an animal model of juvenile neuronal ceroid lipofuscinosis.
    Herrmann P, Druckrey-Fiskaaen C, Kouznetsova E, Heinitz K, Bigl M, Cotman SL, Schliebs R.
    J Neurosci Res; 2008 Jun; 86(8):1857-70. PubMed ID: 18265413
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  • 14. Altered gene expression in the eye of a mouse model for batten disease.
    Chattopadhyay S, Kingsley E, Serour A, Curran TM, Brooks AI, Pearce DA.
    Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):2893-905. PubMed ID: 15326100
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  • 15. Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten disease.
    Pontikis CC, Cotman SL, MacDonald ME, Cooper JD.
    Neurobiol Dis; 2005 Dec; 20(3):823-36. PubMed ID: 16006136
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  • 17. Microglia in juvenile neuronal ceroid lipofuscinosis are primed toward a pro-inflammatory phenotype.
    Xiong J, Kielian T.
    J Neurochem; 2013 Oct; 127(2):245-58. PubMed ID: 23919525
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  • 18. Altered arginine metabolism in the central nervous system (CNS) of the Cln3-/- mouse model of juvenile Batten disease.
    Chan CH, Ramirez-Montealegre D, Pearce DA.
    Neuropathol Appl Neurobiol; 2009 Apr; 35(2):189-207. PubMed ID: 19284480
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  • 19. Molecular genetic analysis of neuronal ceroid lipofuscinosis.
    Mole SE, Gardiner M.
    Int J Neurol; 2009 Apr; 25-26():52-9. PubMed ID: 11980063
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