Search research articles
Contact Us
Filters
Showing results (1-10 of 112) with videos related to
Page
of 12
Sort By:
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 acids
W 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 disease
J E Månsson, L Svennerholm
Journal of Inherited Metabolic Disease
|
September 5, 1998
Animal models of lysosomal disease: an overview
K 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 period
G Malm, J-E Månsson
Clinical Genetics
|
August 1, 1986
Cerebroside-beta-glucosidase activity in Gaucher brain
L Svennerholm, J E Månsson, B Rosengren
Biochimica Et Biophysica Acta
|
July 22, 1991
Characterization of glucosylceramide from plasma membranes of plant root cells
P Norberg, J E Månsson, C Liljenberg
Neuropediatrics
|
August 1, 1995
Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher disease
A Erikson, M Aström, J E Månsson
Journal of Chromatography
|
April 10, 1985
Separation of gangliosides by anion-exchange chromatography on Mono Q
J 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
Page
of 12
Search research articles
Search
Showing results (1-10 of 112) with videos related to
Sort By:
Page
of 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 acids
W 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 disease
J E Månsson, L Svennerholm
Journal of Inherited Metabolic Disease
|
September 5, 1998
Animal models of lysosomal disease: an overview
K 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 period
G Malm, J-E Månsson
Clinical Genetics
|
August 1, 1986
Cerebroside-beta-glucosidase activity in Gaucher brain
L Svennerholm, J E Månsson, B Rosengren
Biochimica Et Biophysica Acta
|
July 22, 1991
Characterization of glucosylceramide from plasma membranes of plant root cells
P Norberg, J E Månsson, C Liljenberg
Neuropediatrics
|
August 1, 1995
Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher disease
A Erikson, M Aström, J E Månsson
Journal of Chromatography
|
April 10, 1985
Separation of gangliosides by anion-exchange chromatography on Mono Q
J 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
Page
of 12