Author:
Vairo Filippo,Netto Cristina,Dorneles Alicia,Mittelstadt Suzana,Wilke Matheus,Doneda Divair,Michelin Kristiane,Ribeiro Camila Blos,Quevedo Amanda,Vieira Tatiane,Nalin Tatiele,Lueska Sônia,Schwartz Ida Vanessa D.
Publisher
Springer Berlin Heidelberg
Reference27 articles.
1. Brazilian Ministry of Health Guidelines for Gaucher disease In Editor ed.^eds. Book Brazilian Ministry of Health Guidelines for Gaucher disease.
http://portal.saude.gov.br/portal/arquivos/pdf/pcdt_doenca_de_gaucher_pdf
2. Brumshtein B, Salinas P, Peterson B et al (2010) Characterization of gene-activated human acid-beta-glucosidase: crystal structure, glycan composition, and internalization into macrophages. Glycobiology 20(1):24–32
3. Cox T, Lachmann R, Hollak C et al (2000) Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis. Lancet 355(9214):1481–1485
4. Dahl N, Lagerstrom M, Erikson A, Pettersson U (1990) Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase gene. Am J Hum Genet 47(2):275–278
5. Davies EH, Erikson A, Collin-Histed T, Mengel E, Tylki-Szymanska A, Vellodi A (2007) Outcome of type III Gaucher disease on enzyme replacement therapy: review of 55 cases. J Inherit Metab Dis 30(6):935–942
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