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P A Ockerman

Showing results (11-20 of 60) with videos related to

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Acta Paediatrica Scandinavica|May 1, 1970
Fine-needle aspiration biopsy of human liver for enzymatic diagnosis of glycogen storage disease and gargoylismA Lundquist, P A Ockerman
Acta Paediatrica Scandinavica|March 1, 1970
The bleeding disorder in hepatomegalic forms of glycogen storage diseaseI M Nilsson, P A Ockerman
Lakartidningen|July 12, 1978
[Fasting and vegetarian food--a therapeutic alternative]K O Aly, P A Ockerman
Scandinavian Journal of Clinical and Laboratory Investigation|October 1, 1972
Urinary excretion of acid hydrolases in diseaseB Hultberg, N Nordén, P A Ockerman
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 23, 1973
4-Methylumbelliferyl-beta-glucosidase in cultured human fibroblasts from controls and patients with Gaucher's diseaseB Hultberg, S Sjöblad, P A Ockerman
Acta Paediatrica Scandinavica|September 1, 1973
Properties of five acid hydrolases in human skin fibroblast cultures. Possible use in the diagnosis of inborn lysosomal diseasesB Hultberg, S Sjöblad, P A Ockerman
European Neurology|January 1, 1972
Enzymatic and biochemical diagnosis of inborn lysosomal diseases with neurological symptomsB Hultberg, P A Ockerman, S Sjöblad
Lakartidningen|June 26, 1974
[Hereditary metabolic diseases with cumulative symptoms]B Hultberg, S Sjöblad, P A Ockerman
The Journal of Clinical Investigation|February 1, 1970
Gargoylism: hydrolysis of beta-galactosides and tissure accumulation of galactose- and mannose-containing compoundsB Hultberg, P A Ockerman, A Dahlqvist
Acta Paediatrica Scandinavica|January 1, 1975
Glycosidases in human skin fibroblast cultures. Alpha-fucosidase, alpha-galactosidase, alpha-glucosidase, beta-mannosidase, and N-acetyl-alpha-glucosaminidaseB Hultberg, S Sjöblad, P A Ockerman
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
Acta Paediatrica Scandinavica|May 1, 1970
Fine-needle aspiration biopsy of human liver for enzymatic diagnosis of glycogen storage disease and gargoylismA Lundquist, P A Ockerman
Acta Paediatrica Scandinavica|March 1, 1970
The bleeding disorder in hepatomegalic forms of glycogen storage diseaseI M Nilsson, P A Ockerman
Lakartidningen|July 12, 1978
[Fasting and vegetarian food--a therapeutic alternative]K O Aly, P A Ockerman
Scandinavian Journal of Clinical and Laboratory Investigation|October 1, 1972
Urinary excretion of acid hydrolases in diseaseB Hultberg, N Nordén, P A Ockerman
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 23, 1973
4-Methylumbelliferyl-beta-glucosidase in cultured human fibroblasts from controls and patients with Gaucher's diseaseB Hultberg, S Sjöblad, P A Ockerman
Acta Paediatrica Scandinavica|September 1, 1973
Properties of five acid hydrolases in human skin fibroblast cultures. Possible use in the diagnosis of inborn lysosomal diseasesB Hultberg, S Sjöblad, P A Ockerman
European Neurology|January 1, 1972
Enzymatic and biochemical diagnosis of inborn lysosomal diseases with neurological symptomsB Hultberg, P A Ockerman, S Sjöblad
Lakartidningen|June 26, 1974
[Hereditary metabolic diseases with cumulative symptoms]B Hultberg, S Sjöblad, P A Ockerman
The Journal of Clinical Investigation|February 1, 1970
Gargoylism: hydrolysis of beta-galactosides and tissure accumulation of galactose- and mannose-containing compoundsB Hultberg, P A Ockerman, A Dahlqvist
Acta Paediatrica Scandinavica|January 1, 1975
Glycosidases in human skin fibroblast cultures. Alpha-fucosidase, alpha-galactosidase, alpha-glucosidase, beta-mannosidase, and N-acetyl-alpha-glucosaminidaseB Hultberg, S Sjöblad, P A Ockerman
Pageof 6