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J-E Månsson

Showing results (1-10 of 112) with videos related to

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The Journal of Nutrition|October 1, 1985
Incorporation of 14C into tissue lipids after oral administration of [1-14C]linoleic acid in rats fed different levels of essential fatty acidsW Becker, J E Månsson
European Child & Adolescent Psychiatry|November 24, 1998
Is monoamine oxidase activity elevated in Prader-Willi syndrome?A Akefeldt, J E Månsson
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 9, 1982
The use of galactosylceramides with uniform fatty acids as substrates in the diagnosis and carrier detection of Krabbe diseaseJ E Månsson, L Svennerholm
Journal of Inherited Metabolic Disease|September 5, 1998
Animal models of lysosomal disease: an overviewK Suzuki, J E Månsson
Acta Paediatrica (Oslo, Norway : 1992)|March 27, 2010
Mucopolysaccharidosis type III (Sanfilippo disease) in Sweden: clinical presentation of 22 children diagnosed during a 30-year periodG Malm, J-E Månsson
Clinical Genetics|August 1, 1986
Cerebroside-beta-glucosidase activity in Gaucher brainL Svennerholm, J E Månsson, B Rosengren
Biochimica Et Biophysica Acta|July 22, 1991
Characterization of glucosylceramide from plasma membranes of plant root cellsP Norberg, J E Månsson, C Liljenberg
Neuropediatrics|August 1, 1995
Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher diseaseA Erikson, M Aström, J E Månsson
Journal of Chromatography|April 10, 1985
Separation of gangliosides by anion-exchange chromatography on Mono QJ E Månsson, B Rosengren, L Svennerholm
Journal of Neurochemistry|September 1, 1987
Composition of gangliosides and neutral glycosphingolipids of brain in classical Tay-Sachs and Sandhoff disease: more lyso-GM2 in Sandhoff disease?B Rosengren, J E Månsson, L Svennerholm
Pageof 12

Showing results (1-10 of 112) with videos related to

Sort By:
Pageof 12
The Journal of Nutrition|October 1, 1985
Incorporation of 14C into tissue lipids after oral administration of [1-14C]linoleic acid in rats fed different levels of essential fatty acidsW Becker, J E Månsson
European Child & Adolescent Psychiatry|November 24, 1998
Is monoamine oxidase activity elevated in Prader-Willi syndrome?A Akefeldt, J E Månsson
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 9, 1982
The use of galactosylceramides with uniform fatty acids as substrates in the diagnosis and carrier detection of Krabbe diseaseJ E Månsson, L Svennerholm
Journal of Inherited Metabolic Disease|September 5, 1998
Animal models of lysosomal disease: an overviewK Suzuki, J E Månsson
Acta Paediatrica (Oslo, Norway : 1992)|March 27, 2010
Mucopolysaccharidosis type III (Sanfilippo disease) in Sweden: clinical presentation of 22 children diagnosed during a 30-year periodG Malm, J-E Månsson
Clinical Genetics|August 1, 1986
Cerebroside-beta-glucosidase activity in Gaucher brainL Svennerholm, J E Månsson, B Rosengren
Biochimica Et Biophysica Acta|July 22, 1991
Characterization of glucosylceramide from plasma membranes of plant root cellsP Norberg, J E Månsson, C Liljenberg
Neuropediatrics|August 1, 1995
Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher diseaseA Erikson, M Aström, J E Månsson
Journal of Chromatography|April 10, 1985
Separation of gangliosides by anion-exchange chromatography on Mono QJ E Månsson, B Rosengren, L Svennerholm
Journal of Neurochemistry|September 1, 1987
Composition of gangliosides and neutral glycosphingolipids of brain in classical Tay-Sachs and Sandhoff disease: more lyso-GM2 in Sandhoff disease?B Rosengren, J E Månsson, L Svennerholm
Pageof 12