Galvin N - Search Results

1

Neuropathology of murine mucopolysaccharidosis type VII.

Levy B, Galvin N, Vogler C, Birkenmeier EH, Sly WS. Levy B, et al. Among authors: galvin n. Acta Neuropathol. 1996 Dec;92(6):562-8. doi: 10.1007/s004010050562. Acta Neuropathol. 1996. PMID: 8960313

2

Intravitreal gene therapy reduces lysosomal storage in specific areas of the CNS in mucopolysaccharidosis VII mice.

Hennig AK, Levy B, Ogilvie JM, Vogler CA, Galvin N, Bassnett S, Sands MS. Hennig AK, et al. Among authors: galvin n. J Neurosci. 2003 Apr 15;23(8):3302-7. doi: 10.1523/JNEUROSCI.23-08-03302.2003. J Neurosci. 2003. PMID: 12716937 Free PMC article.

3

Overcoming the blood-brain barrier with high-dose enzyme replacement therapy in murine mucopolysaccharidosis VII.

Vogler C, Levy B, Grubb JH, Galvin N, Tan Y, Kakkis E, Pavloff N, Sly WS. Vogler C, et al. Among authors: galvin n. Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14777-82. doi: 10.1073/pnas.0506892102. Epub 2005 Sep 14. Proc Natl Acad Sci U S A. 2005. PMID: 16162667 Free PMC article.

4

Early onset of lysosomal storage disease in a murine model of mucopolysaccharidosis type VII: undegraded substrate accumulates in many tissues in the fetus and very young MPS VII mouse.

Vogler C, Levy B, Galvin N, Lessard M, Soper B, Barker J. Vogler C, et al. Among authors: galvin n. Pediatr Dev Pathol. 2005 Jul-Aug;8(4):453-62. doi: 10.1007/s10024-005-0025-8. Epub 2005 Oct 12. Pediatr Dev Pathol. 2005. PMID: 16222480

5

Enzyme therapy in mannose receptor-null mucopolysaccharidosis VII mice defines roles for the mannose 6-phosphate and mannose receptors.

Sly WS, Vogler C, Grubb JH, Levy B, Galvin N, Tan Y, Nishioka T, Tomatsu S. Sly WS, et al. Among authors: galvin n. Proc Natl Acad Sci U S A. 2006 Oct 10;103(41):15172-7. doi: 10.1073/pnas.0607053103. Epub 2006 Oct 2. Proc Natl Acad Sci U S A. 2006. PMID: 17015822 Free PMC article.

6

Chemically modified beta-glucuronidase crosses blood-brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII.

Grubb JH, Vogler C, Levy B, Galvin N, Tan Y, Sly WS. Grubb JH, et al. Among authors: galvin n. Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2616-21. doi: 10.1073/pnas.0712147105. Epub 2008 Feb 11. Proc Natl Acad Sci U S A. 2008. PMID: 18268347 Free PMC article.

7

Enzyme replacement with recombinant beta-glucuronidase in murine mucopolysaccharidosis type VII: impact of therapy during the first six weeks of life on subsequent lysosomal storage, growth, and survival.

Vogler C, Sands MS, Levy B, Galvin N, Birkenmeier EH, Sly WS. Vogler C, et al. Among authors: galvin n. Pediatr Res. 1996 Jun;39(6):1050-4. doi: 10.1203/00006450-199606000-00019. Pediatr Res. 1996. PMID: 8725268

8

Murine mucopolysaccharidosis type VII: the impact of therapies on the clinical course and pathology in a murine model of lysosomal storage disease.

Vogler C, Sands MS, Galvin N, Levy B, Thorpe C, Barker J, Sly WS. Vogler C, et al. Among authors: galvin n. J Inherit Metab Dis. 1998 Aug;21(5):575-86. doi: 10.1023/a:1005423222927. J Inherit Metab Dis. 1998. PMID: 9728337 Review.

9

A novel model of murine mucopolysaccharidosis type VII due to an intracisternal a particle element transposition into the beta-glucuronidase gene: clinical and pathologic findings.

Vogler C, Levy B, Galvin N, Sands MS, Birkenmeier EH, Sly WS, Barker J. Vogler C, et al. Among authors: galvin n. Pediatr Res. 2001 Mar;49(3):342-8. doi: 10.1203/00006450-200103000-00007. Pediatr Res. 2001. PMID: 11228259

10

Murine mucopolysaccharidosis VIL: impact of therapies on the phenotype, clinical course, and pathology in a model of a lysosomal storage disease.

Vogler C, Barker J, Sands MS, Levy B, Galvin N, Sly WS. Vogler C, et al. Among authors: galvin n. Pediatr Dev Pathol. 2001 Sep-Oct;4(5):421-33. doi: 10.1007/s10024001-0079-1. Pediatr Dev Pathol. 2001. PMID: 11779044 Review.

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