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A Vellodi

Showing results (51-60 of 57) with videos related to

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The Journal of Pediatrics|December 1, 1994
Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation GroupE J Gerritsen, J M Vossen, A Fasth, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotypeJ J Hopwood, A Vellodi, H S Scott, et al.
Molecular Genetics and Metabolism Reports|March 1, 2017
Evaluation of impact of anti-idursulfase antibodies during long-term idursulfase enzyme replacement therapy in mucopolysaccharidosis II patientsR Giugliani, P Harmatz, S A Jones, et al.
Health Technology Assessment (Winchester, England)|October 24, 2012
The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disordersK Wyatt, W Henley, L Anderson, et al.
Pediatrics|September 1, 1996
Bone marrow transplantation from genetically HLA-nonidentical donors in children with fatal inherited disorders excluding severe combined immunodeficiencies: use of two monoclonal antibodies to prevent graft rejectionN Jabado, F Le Deist, A Cant, et al.
JIMD Reports|January 31, 2016
Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell TransplantationA S Kunin-Batson, E G Shapiro, K D Rudser, et al.
Journal of Inherited Metabolic Disease|October 27, 2015
Response of 33 UK patients with infantile-onset Pompe disease to enzyme replacement therapyA Broomfield, J Fletcher, J Davison, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
The Journal of Pediatrics|December 1, 1994
Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation GroupE J Gerritsen, J M Vossen, A Fasth, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotypeJ J Hopwood, A Vellodi, H S Scott, et al.
Molecular Genetics and Metabolism Reports|March 1, 2017
Evaluation of impact of anti-idursulfase antibodies during long-term idursulfase enzyme replacement therapy in mucopolysaccharidosis II patientsR Giugliani, P Harmatz, S A Jones, et al.
Health Technology Assessment (Winchester, England)|October 24, 2012
The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disordersK Wyatt, W Henley, L Anderson, et al.
Pediatrics|September 1, 1996
Bone marrow transplantation from genetically HLA-nonidentical donors in children with fatal inherited disorders excluding severe combined immunodeficiencies: use of two monoclonal antibodies to prevent graft rejectionN Jabado, F Le Deist, A Cant, et al.
JIMD Reports|January 31, 2016
Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell TransplantationA S Kunin-Batson, E G Shapiro, K D Rudser, et al.
Journal of Inherited Metabolic Disease|October 27, 2015
Response of 33 UK patients with infantile-onset Pompe disease to enzyme replacement therapyA Broomfield, J Fletcher, J Davison, et al.
Pageof 6