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John J Hopwood

Showing results (1-10 of 141) with videos related to

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Prenatal Diagnosis|February 16, 2005
Prenatal diagnosis of Sanfilippo syndromeJohn J Hopwood
Biochimica Et Biophysica Acta|April 18, 2002
alpha-Mannosidosis in the guinea pig: cloning of the lysosomal alpha-mannosidase cDNA and identification of a missense mutation causing alpha-mannosidosisThomas Berg, John J Hopwood
Journal of Inherited Metabolic Disease|May 8, 2010
Lessons learnt from animal models: pathophysiology of neuropathic lysosomal storage disordersKim M Hemsley, John J Hopwood
European Journal of Pediatrics|November 12, 2003
Lysosomal storage disorders: emerging therapeutic options require early diagnosisPeter J Meikle, John J Hopwood
Pediatric Research|May 7, 2004
Enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA miceBriony L Gliddon, John J Hopwood
Behavioural Brain Research|February 9, 2005
Development of motor deficits in a murine model of mucopolysaccharidosis type IIIA (MPS-IIIA)Kim M Hemsley, John J Hopwood
Human Mutation|June 29, 2010
Functional analysis of the HGSNAT gene in patients with mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)Anthony O Fedele, John J Hopwood
Journal of Inherited Metabolic Disease|May 18, 2011
Emerging therapies for neurodegenerative lysosomal storage disorders - from concept to realityKim M Hemsley, John J Hopwood
Biochimica Et Biophysica Acta. Proteins and Proteomics|December 24, 2016
Analysis of sheep α-synuclein provides a molecular strategy for the reduction of fibrillationLungisa Bickle, John J Hopwood, Litsa Karageorgos
Nature Reviews. Drug Discovery|March 9, 2006
GalsulfaseJohn J Hopwood, Guy Bate, Peter Kirkpatrick
Pageof 15

Showing results (1-10 of 141) with videos related to

Sort By:
Pageof 15
Prenatal Diagnosis|February 16, 2005
Prenatal diagnosis of Sanfilippo syndromeJohn J Hopwood
Biochimica Et Biophysica Acta|April 18, 2002
alpha-Mannosidosis in the guinea pig: cloning of the lysosomal alpha-mannosidase cDNA and identification of a missense mutation causing alpha-mannosidosisThomas Berg, John J Hopwood
Journal of Inherited Metabolic Disease|May 8, 2010
Lessons learnt from animal models: pathophysiology of neuropathic lysosomal storage disordersKim M Hemsley, John J Hopwood
European Journal of Pediatrics|November 12, 2003
Lysosomal storage disorders: emerging therapeutic options require early diagnosisPeter J Meikle, John J Hopwood
Pediatric Research|May 7, 2004
Enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA miceBriony L Gliddon, John J Hopwood
Behavioural Brain Research|February 9, 2005
Development of motor deficits in a murine model of mucopolysaccharidosis type IIIA (MPS-IIIA)Kim M Hemsley, John J Hopwood
Human Mutation|June 29, 2010
Functional analysis of the HGSNAT gene in patients with mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)Anthony O Fedele, John J Hopwood
Journal of Inherited Metabolic Disease|May 18, 2011
Emerging therapies for neurodegenerative lysosomal storage disorders - from concept to realityKim M Hemsley, John J Hopwood
Biochimica Et Biophysica Acta. Proteins and Proteomics|December 24, 2016
Analysis of sheep α-synuclein provides a molecular strategy for the reduction of fibrillationLungisa Bickle, John J Hopwood, Litsa Karageorgos
Nature Reviews. Drug Discovery|March 9, 2006
GalsulfaseJohn J Hopwood, Guy Bate, Peter Kirkpatrick
Pageof 15