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Journal Abstract Search


152 related items for PubMed ID: 11499846

  • 1. Sulfatide storage in visceral organs of arylsulfatase A-deficient mice.
    Schott I, Hartmann D, Gieselmann V, Lüllmann-Rauch R.
    Virchows Arch; 2001 Jul; 439(1):90-6. PubMed ID: 11499846
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  • 2. Lysosomal sulfatide storage in the brain of arylsulfatase A-deficient mice: cellular alterations and topographic distribution.
    Wittke D, Hartmann D, Gieselmann V, Lüllmann-Rauch R.
    Acta Neuropathol; 2004 Oct; 108(4):261-71. PubMed ID: 15322834
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  • 3. Increasing sulfatide synthesis in myelin-forming cells of arylsulfatase A-deficient mice causes demyelination and neurological symptoms reminiscent of human metachromatic leukodystrophy.
    Ramakrishnan H, Hedayati KK, Lüllmann-Rauch R, Wessig C, Fewou SN, Maier H, Goebel HH, Gieselmann V, Eckhardt M.
    J Neurosci; 2007 Aug 29; 27(35):9482-90. PubMed ID: 17728461
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  • 6. A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy.
    Saravanan K, Büssow H, Weiler N, Gieselmann V, Franken S.
    J Neurosci Methods; 2007 Apr 15; 161(2):223-33. PubMed ID: 17204333
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  • 8. Arylsulfatase A Overexpressing Human iPSC-derived Neural Cells Reduce CNS Sulfatide Storage in a Mouse Model of Metachromatic Leukodystrophy.
    Doerr J, Böckenhoff A, Ewald B, Ladewig J, Eckhardt M, Gieselmann V, Matzner U, Brüstle O, Koch P.
    Mol Ther; 2015 Sep 15; 23(9):1519-31. PubMed ID: 26061647
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  • 9. [Pathophysiology of sulfatide metabolism in metachromatic leukodystrophy].
    Wiesmann UN.
    Bull Schweiz Akad Med Wiss; 1978 Mar 15; 34(1-3):33-47. PubMed ID: 27269
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  • 10. Morphological alterations in the inner ear of the arylsulfatase A-deficient mouse.
    Coenen R, Gieselmann V, Lüllmann-Rauch R.
    Acta Neuropathol; 2001 May 15; 101(5):491-8. PubMed ID: 11484821
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  • 14. Bone marrow stem cell-based gene transfer in a mouse model for metachromatic leukodystrophy: effects on visceral and nervous system disease manifestations.
    Matzner U, Hartmann D, Lüllmann-Rauch R, Coenen R, Rothert F, Månsson JE, Fredman P, D'Hooge R, De Deyn PP, Gieselmann V.
    Gene Ther; 2002 Jan 15; 9(1):53-63. PubMed ID: 11850723
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  • 16. Ex vivo cell-mediated gene therapy for metachromatic leukodystrophy using neurospheres.
    Kawabata K, Migita M, Mochizuki H, Miyake K, Igarashi T, Fukunaga Y, Shimada T.
    Brain Res; 2006 Jun 13; 1094(1):13-23. PubMed ID: 16729983
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  • 19. Gene therapy in metachromatic leukodystrophy.
    Sevin C, Cartier-Lacave N, Aubourg P.
    Int J Clin Pharmacol Ther; 2009 Jun 13; 47 Suppl 1():S128-31. PubMed ID: 20040324
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  • 20. Non-inhibitory antibodies impede lysosomal storage reduction during enzyme replacement therapy of a lysosomal storage disease.
    Matzner U, Matthes F, Weigelt C, Andersson C, Eistrup C, Fogh J, Gieselmann V.
    J Mol Med (Berl); 2008 Apr 13; 86(4):433-42. PubMed ID: 18360747
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