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A Vellodi

Showing results (31-40 of 57) with videos related to

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British Medical Journal (Clinical Research Ed.)|November 28, 1987
Treatment of Niemann-Pick disease type B by allogeneic bone marrow transplantationA Vellodi, J R Hobbs, N M O'Donnell, et al.
Journal of Inherited Metabolic Disease|February 11, 2005
Measurement of urinary CDH and CTH by tandem mass spectrometry in patients hemizygous and heterozygous for Fabry diseaseK Mills, P Morris, P Lee, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|February 5, 1998
Otologic and laryngologic manifestations of mucopolysaccharidoses after bone marrow transplantationB C Papsin, A Vellodi, C M Bailey, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Bone marrow transplantation for Maroteaux-Lamy syndrome (MPS VI): long-term follow-upE Herskhovitz, E Young, J Rainer, et al.
Bone Marrow Transplantation|May 1, 1994
Bone marrow transplantation for thalassaemia: experience of two British centresA Vellodi, S Picton, C J Downie, et al.
Journal of Medical Genetics|March 8, 2003
Sanfilippo syndrome type D: identification of the first mutation in the N-acetylglucosamine-6-sulphatase geneC E Beesley, D Burke, M Jackson, et al.
Fetal and Pediatric Pathology|April 19, 2007
Ultrastructural features of gaucher disease treated with enzyme replacement therapy presenting as mesenteric mass lesionsD J Fowler, M A Weber, G Anderson, et al.
Journal of Inherited Metabolic Disease|November 13, 2007
Outcome of type III Gaucher disease on enzyme replacement therapy: review of 55 casesE H Davies, A Erikson, T Collin-Histed, et al.
Neuropediatrics|August 25, 2001
Audiometric abnormalities in children with Gaucher disease type 3D E Bamiou, P Campbell, A Liasis, et al.
Bone|January 17, 2002
Macrophage colony-stimulating factor and receptor activator NF-kappaB ligand fail to rescue osteoclast-poor human malignant infantile osteopetrosis in vitroA M Flanagan, H M Massey, C Wilson, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
British Medical Journal (Clinical Research Ed.)|November 28, 1987
Treatment of Niemann-Pick disease type B by allogeneic bone marrow transplantationA Vellodi, J R Hobbs, N M O'Donnell, et al.
Journal of Inherited Metabolic Disease|February 11, 2005
Measurement of urinary CDH and CTH by tandem mass spectrometry in patients hemizygous and heterozygous for Fabry diseaseK Mills, P Morris, P Lee, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|February 5, 1998
Otologic and laryngologic manifestations of mucopolysaccharidoses after bone marrow transplantationB C Papsin, A Vellodi, C M Bailey, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Bone marrow transplantation for Maroteaux-Lamy syndrome (MPS VI): long-term follow-upE Herskhovitz, E Young, J Rainer, et al.
Bone Marrow Transplantation|May 1, 1994
Bone marrow transplantation for thalassaemia: experience of two British centresA Vellodi, S Picton, C J Downie, et al.
Journal of Medical Genetics|March 8, 2003
Sanfilippo syndrome type D: identification of the first mutation in the N-acetylglucosamine-6-sulphatase geneC E Beesley, D Burke, M Jackson, et al.
Fetal and Pediatric Pathology|April 19, 2007
Ultrastructural features of gaucher disease treated with enzyme replacement therapy presenting as mesenteric mass lesionsD J Fowler, M A Weber, G Anderson, et al.
Journal of Inherited Metabolic Disease|November 13, 2007
Outcome of type III Gaucher disease on enzyme replacement therapy: review of 55 casesE H Davies, A Erikson, T Collin-Histed, et al.
Neuropediatrics|August 25, 2001
Audiometric abnormalities in children with Gaucher disease type 3D E Bamiou, P Campbell, A Liasis, et al.
Bone|January 17, 2002
Macrophage colony-stimulating factor and receptor activator NF-kappaB ligand fail to rescue osteoclast-poor human malignant infantile osteopetrosis in vitroA M Flanagan, H M Massey, C Wilson, et al.
Pageof 6