PubMed (OMIM) for id: 43108

Year	Number of Results
1973	2
1974	3
1975	1
1976	4
1977	5
1978	5
1979	3
1981	2
1982	3
1984	1
1985	2
1986	1
1987	1
1988	1
1989	2
1990	3
1991	6
1992	4
1993	6
1994	2
1995	4
1996	2
1997	2
1998	6
1999	3
2001	2
2002	6
2003	3
2004	1
2024	0

1

Glycosylation-independent targeting enhances enzyme delivery to lysosomes and decreases storage in mucopolysaccharidosis type VII mice.

LeBowitz JH, Grubb JH, Maga JA, Schmiel DH, Vogler C, Sly WS. LeBowitz JH, et al. Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):3083-8. doi: 10.1073/pnas.0308728100. Epub 2004 Feb 19. Proc Natl Acad Sci U S A. 2004. PMID: 14976248 Free PMC article.

2

Mucopolysaccharidosis VII: clinical, biochemical and molecular investigation of a Brazilian family.

Schwartz I, Silva LR, Leistner S, Todeschini LA, Burin MG, Pina-Neto JM, Islam RM, Shah GN, Sly WS, Giugliani R. Schwartz I, et al. Clin Genet. 2003 Aug;64(2):172-5. doi: 10.1034/j.1399-0004.2003.00119.x. Clin Genet. 2003. PMID: 12859417 No abstract available.

3

A new case of mucopolysaccharidosis VII presenting as non immune hydrops fetalis.

Walter-Nicolet E, Rakza T, Storme L, Vaillant C, Magnenant E, Cremer R, Thumerelle C, Dobbelaere D. Walter-Nicolet E, et al. Eur J Pediatr. 2003 Jul;162(7-8):520-521. doi: 10.1007/s00431-003-1198-7. Epub 2003 May 14. Eur J Pediatr. 2003. PMID: 12748853 No abstract available.

4

Mutational analysis in longest known survivor of mucopolysaccharidosis type VII.

Storch S, Wittenstein B, Islam R, Ullrich K, Sly WS, Braulke T. Storch S, et al. Hum Genet. 2003 Feb;112(2):190-4. doi: 10.1007/s00439-002-0849-5. Epub 2002 Nov 5. Hum Genet. 2003. PMID: 12522561

5

Selective neurodegeneration in murine mucopolysaccharidosis VII is progressive and reversible.

Heuer GG, Passini MA, Jiang K, Parente MK, Lee VM, Trojanowski JQ, Wolfe JH. Heuer GG, et al. Ann Neurol. 2002 Dec;52(6):762-70. doi: 10.1002/ana.10373. Ann Neurol. 2002. PMID: 12447930

6

Missense models [Gustm(E536A)Sly, Gustm(E536Q)Sly, and Gustm(L175F)Sly] of murine mucopolysaccharidosis type VII produced by targeted mutagenesis.

Tomatsu S, Orii KO, Vogler C, Grubb JH, Snella EM, Gutierrez MA, Dieter T, Sukegawa K, Orii T, Kondo N, Sly WS. Tomatsu S, et al. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14982-7. doi: 10.1073/pnas.232570999. Epub 2002 Oct 28. Proc Natl Acad Sci U S A. 2002. PMID: 12403825 Free PMC article.

7

Therapeutic neonatal hepatic gene therapy in mucopolysaccharidosis VII dogs.

Ponder KP, Melniczek JR, Xu L, Weil MA, O'Malley TM, O'Donnell PA, Knox VW, Aguirre GD, Mazrier H, Ellinwood NM, Sleeper M, Maguire AM, Volk SW, Mango RL, Zweigle J, Wolfe JH, Haskins ME. Ponder KP, et al. Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):13102-7. doi: 10.1073/pnas.192353499. Epub 2002 Sep 13. Proc Natl Acad Sci U S A. 2002. PMID: 12232044 Free PMC article.

8

Brain-directed gene therapy for lysosomal storage disease: going well beyond the blood- brain barrier.

Sly WS, Vogler C. Sly WS, et al. Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):5760-2. doi: 10.1073/pnas.102175599. Proc Natl Acad Sci U S A. 2002. PMID: 11983877 Free PMC article. Review. No abstract available.

9

Functional correction of established central nervous system deficits in an animal model of lysosomal storage disease with feline immunodeficiency virus-based vectors.

Brooks AI, Stein CS, Hughes SM, Heth J, McCray PM Jr, Sauter SL, Johnston JC, Cory-Slechta DA, Federoff HJ, Davidson BL. Brooks AI, et al. Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6216-21. doi: 10.1073/pnas.082011999. Epub 2002 Apr 16. Proc Natl Acad Sci U S A. 2002. PMID: 11959904 Free PMC article.

10

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. Pediatr Res. 2001 Mar;49(3):342-8. doi: 10.1203/00006450-200103000-00007. Pediatr Res. 2001. PMID: 11228259

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