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E M Kaye

Showing results (31-40 of 39) with videos related to

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Human Gene Therapy|April 11, 2000
Correction of acid beta-galactosidase deficiency in GM1 gangliosidosis human fibroblasts by retrovirus vector-mediated gene transfer: higher efficiency of release and cross-correction by the murine enzymeM Sena-Esteves, S M Camp, J Alroy, et al.
Journal of Child Neurology|January 1, 1991
Modified encephaloduroarteriosynangiosis as a surgical treatment of childhood moyamoya disease: report of five casesC M Rooney, E M Kaye, R M Scott, et al.
Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.
Pediatric Neurology|August 30, 2000
Mitochondrial activity in Pompe's diseaseM A Selak, J P de Chadarevian, J J Melvin, et al.
Pediatric Research|May 1, 1983
Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storageD A Wenger, S Roth, T Kudoh, et al.
The New England Journal of Medicine|July 8, 1993
A controlled trial of diazepam administered during febrile illnesses to prevent recurrence of febrile seizuresN P Rosman, T Colton, J Labazzo, et al.
Pediatric Neurology|July 1, 1992
Dysmyelinogenesis in animal model of GM1 gangliosidosisE M Kaye, J Alroy, S S Raghavan, et al.
Clinical and Diagnostic Laboratory Immunology|January 5, 1999
Angiocentric CD3(+) T-cell infiltrates in human immunodeficiency virus type 1-associated central nervous system disease in childrenC D Katsetos, J E Fincke, A Legido, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiencyC P Venditti, M C Harris, D Huff, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Human Gene Therapy|April 11, 2000
Correction of acid beta-galactosidase deficiency in GM1 gangliosidosis human fibroblasts by retrovirus vector-mediated gene transfer: higher efficiency of release and cross-correction by the murine enzymeM Sena-Esteves, S M Camp, J Alroy, et al.
Journal of Child Neurology|January 1, 1991
Modified encephaloduroarteriosynangiosis as a surgical treatment of childhood moyamoya disease: report of five casesC M Rooney, E M Kaye, R M Scott, et al.
Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.
Pediatric Neurology|August 30, 2000
Mitochondrial activity in Pompe's diseaseM A Selak, J P de Chadarevian, J J Melvin, et al.
Pediatric Research|May 1, 1983
Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storageD A Wenger, S Roth, T Kudoh, et al.
The New England Journal of Medicine|July 8, 1993
A controlled trial of diazepam administered during febrile illnesses to prevent recurrence of febrile seizuresN P Rosman, T Colton, J Labazzo, et al.
Pediatric Neurology|July 1, 1992
Dysmyelinogenesis in animal model of GM1 gangliosidosisE M Kaye, J Alroy, S S Raghavan, et al.
Clinical and Diagnostic Laboratory Immunology|January 5, 1999
Angiocentric CD3(+) T-cell infiltrates in human immunodeficiency virus type 1-associated central nervous system disease in childrenC D Katsetos, J E Fincke, A Legido, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiencyC P Venditti, M C Harris, D Huff, et al.
Pageof 4