Lüllmann-Rauch R - Search Results

1

Lysosomal sulfoglycolipid storage in the kidneys of mice deficient for arylsulfatase A (ASA) and of double-knockout mice deficient for ASA and galactosylceramide synthase.

Lüllmann-Rauch R, Matzner U, Franken S, Hartmann D, Gieselmann V. Lüllmann-Rauch R, et al. Histochem Cell Biol. 2001 Aug;116(2):161-9. doi: 10.1007/s004180100286. Histochem Cell Biol. 2001. PMID: 11685544

2

Sulfatide storage in visceral organs of arylsulfatase A-deficient mice.

Schott I, Hartmann D, Gieselmann V, Lüllmann-Rauch R. Schott I, et al. Virchows Arch. 2001 Jul;439(1):90-6. doi: 10.1007/s004280000360. Virchows Arch. 2001. PMID: 11499846

3

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. Wittke D, et al. Acta Neuropathol. 2004 Oct;108(4):261-71. doi: 10.1007/s00401-004-0883-6. Epub 2004 Aug 20. Acta Neuropathol. 2004. PMID: 15322834

4

Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene.

Franken S, Wittke D, Mansson JE, D'Hooge R, De Deyn PP, Lüllmann-Rauch R, Matzner U, Gieselmann V. Franken S, et al. Lipids Health Dis. 2006 Aug 7;5:21. doi: 10.1186/1476-511X-5-21. Lipids Health Dis. 2006. PMID: 16893448 Free PMC article.

5

Morphological alterations in the inner ear of the arylsulfatase A-deficient mouse.

Coenen R, Gieselmann V, Lüllmann-Rauch R. Coenen R, et al. Acta Neuropathol. 2001 May;101(5):491-8. doi: 10.1007/s004010000318. Acta Neuropathol. 2001. PMID: 11484821

6

Induction of tolerance to human arylsulfatase A in a mouse model of metachromatic leukodystrophy.

Matzner U, Matthes F, Herbst E, Lüllmann-Rauch R, Callaerts-Vegh Z, D'Hooge R, Weigelt C, Eistrup C, Fogh J, Gieselmann V. Matzner U, et al. Mol Med. 2007 Sep-Oct;13(9-10):471-9. doi: 10.2119/2007-00063.Matzner. Mol Med. 2007. PMID: 17660863 Free PMC article.

7

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. Matzner U, et al. Gene Ther. 2002 Jan;9(1):53-63. doi: 10.1038/sj.gt.3301593. Gene Ther. 2002. PMID: 11850723

8

Metachromatic leukodystrophy: consequences of sulphatide accumulation.

Gieselmann V, Franken S, Klein D, Mansson JE, Sandhoff R, Lüllmann Rauch R, Hartmann D, Saravanan VP, De Deyn PP, D'Hooge R, Van Der Linden AM, Schaeren-Wiemers N. Gieselmann V, et al. Acta Paediatr Suppl. 2003 Dec;92(443):74-9; discussion 45. doi: 10.1111/j.1651-2227.2003.tb00225.x. Acta Paediatr Suppl. 2003. PMID: 14989469

9

Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy.

Hess B, Saftig P, Hartmann D, Coenen R, Lüllmann-Rauch R, Goebel HH, Evers M, von Figura K, D'Hooge R, Nagels G, De Deyn P, Peters C, Gieselmann V. Hess B, et al. Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14821-6. doi: 10.1073/pnas.93.25.14821. Proc Natl Acad Sci U S A. 1996. PMID: 8962139 Free PMC article.

10

Metachromatic leukodystrophy: molecular genetics and an animal model.

Gieselmann V, Matzner U, Hess B, Lüllmann-Rauch R, Coenen R, Hartmann D, D'Hooge R, DeDeyn P, Nagels G. Gieselmann V, et al. J Inherit Metab Dis. 1998 Aug;21(5):564-74. doi: 10.1023/a:1005471106088. J Inherit Metab Dis. 1998. PMID: 9728336 Review.

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