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1979 5
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1986 4
1988 2
1989 4
1990 2
1991 3
1992 3
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1995 1
1996 2
1997 1
1998 6
1999 8
2000 2
2001 4
2002 4
2003 7
2004 8
2005 7
2006 6
2007 8
2008 10
2009 3
2010 5
2011 5
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2013 9
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2024 0

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Showing results for haskins me[au]
Your search for Gaskins ME[au] retrieved no results
Treatment of brain disease in the mucopolysaccharidoses.
Scarpa M, Orchard PJ, Schulz A, Dickson PI, Haskins ME, Escolar ML, Giugliani R. Scarpa M, et al. Among authors: haskins me. Mol Genet Metab. 2017 Dec;122S:25-34. doi: 10.1016/j.ymgme.2017.10.007. Epub 2017 Oct 16. Mol Genet Metab. 2017. PMID: 29153844 Free article. Review.
Gene therapy for mucopolysaccharidosis.
Ponder KP, Haskins ME. Ponder KP, et al. Among authors: haskins me. Expert Opin Biol Ther. 2007 Sep;7(9):1333-45. doi: 10.1517/14712598.7.9.1333. Expert Opin Biol Ther. 2007. PMID: 17727324 Free PMC article. Review.
Models of human genetic disease in domestic animals.
Patterson DF, Haskins ME, Jezyk PF. Patterson DF, et al. Among authors: haskins me. Adv Hum Genet. 1982;12:263-339. doi: 10.1007/978-1-4615-8315-8_4. Adv Hum Genet. 1982. PMID: 6751045 Review. No abstract available.
CNS-directed gene therapy for lysosomal storage diseases.
Sands MS, Haskins ME. Sands MS, et al. Among authors: haskins me. Acta Paediatr. 2008 Apr;97(457):22-7. doi: 10.1111/j.1651-2227.2008.00660.x. Acta Paediatr. 2008. PMID: 18339183 Free PMC article. Review.
Animal models of lysosomal storage diseases: their development and clinical relevance.
Haskins ME, Giger U, Patterson DF. Haskins ME, et al. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry Disease: Perspectives from 5 Years of FOS. Oxford: Oxford PharmaGenesis; 2006. Chapter 6. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry Disease: Perspectives from 5 Years of FOS. Oxford: Oxford PharmaGenesis; 2006. Chapter 6. PMID: 21290677 Free Books & Documents. Review.
163 results