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A Vellodi

Showing results (1-10 of 57) with videos related to

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Biochemical Society Transactions|May 18, 2000
The molecular basis of lysosomal storage diseases and their treatmentB Winchester, A Vellodi, E Young
Journal of Inherited Metabolic Disease|May 20, 2005
Evaluation of three biochemical markers in the monitoring of Gaucher diseaseA Vellodi, Y Foo, T J Cole
Journal of Clinical Pharmacology|November 1, 1987
Hemiplegia and focal convulsions as a manifestation of cyclosporine A toxicityA Vellodi, R Jayatunga, K Hugh-Jones
Clinical Radiology|January 30, 2004
Gaucher disease in children: radiology of non-central nervous system manifestationsK McHugh, Ø E Olsen E, A Vellodi
Spine|November 29, 2001
Anterior instrumented fusion for thoracolumbar kyphosis in mucopolysaccharidosisS S Dalvie, M H Noordeen, A Vellodi
Journal of Pediatric Orthopedics. Part B|January 27, 2000
Orthopaedic manifestations of mucolipidosis III: an illustrative caseF S Haddad, R A Hill, A Vellodi
Journal of Inherited Metabolic Disease|August 1, 1997
Plasma chitotriosidase activity in Gaucher disease patients who have been treated either by bone marrow transplantation or by enzyme replacement therapy with algluceraseE Young, C Chatterton, A Vellodi, et al.
Neuropediatrics|March 8, 2000
Ocular motor abnormalities in Gaucher diseaseC M Harris, D S Taylor, A Vellodi
Archives of Disease in Childhood|September 1, 1995
Cardiac involvement in mucopolysaccharidoses: effects of allogeneic bone marrow transplantationM A Gatzoulis, A Vellodi, A N Redington
Journal of Inherited Metabolic Disease|March 26, 2009
Changes in gait pattern as assessed by the GAITRite™ walkway system in MPS II patients undergoing enzyme replacement therapyM Wood, M A Cleary, L Alderson, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Biochemical Society Transactions|May 18, 2000
The molecular basis of lysosomal storage diseases and their treatmentB Winchester, A Vellodi, E Young
Journal of Inherited Metabolic Disease|May 20, 2005
Evaluation of three biochemical markers in the monitoring of Gaucher diseaseA Vellodi, Y Foo, T J Cole
Journal of Clinical Pharmacology|November 1, 1987
Hemiplegia and focal convulsions as a manifestation of cyclosporine A toxicityA Vellodi, R Jayatunga, K Hugh-Jones
Clinical Radiology|January 30, 2004
Gaucher disease in children: radiology of non-central nervous system manifestationsK McHugh, Ø E Olsen E, A Vellodi
Spine|November 29, 2001
Anterior instrumented fusion for thoracolumbar kyphosis in mucopolysaccharidosisS S Dalvie, M H Noordeen, A Vellodi
Journal of Pediatric Orthopedics. Part B|January 27, 2000
Orthopaedic manifestations of mucolipidosis III: an illustrative caseF S Haddad, R A Hill, A Vellodi
Journal of Inherited Metabolic Disease|August 1, 1997
Plasma chitotriosidase activity in Gaucher disease patients who have been treated either by bone marrow transplantation or by enzyme replacement therapy with algluceraseE Young, C Chatterton, A Vellodi, et al.
Neuropediatrics|March 8, 2000
Ocular motor abnormalities in Gaucher diseaseC M Harris, D S Taylor, A Vellodi
Archives of Disease in Childhood|September 1, 1995
Cardiac involvement in mucopolysaccharidoses: effects of allogeneic bone marrow transplantationM A Gatzoulis, A Vellodi, A N Redington
Journal of Inherited Metabolic Disease|March 26, 2009
Changes in gait pattern as assessed by the GAITRite™ walkway system in MPS II patients undergoing enzyme replacement therapyM Wood, M A Cleary, L Alderson, et al.
Pageof 6