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F Van Hoof

Showing results (61-70 of 113) with videos related to

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Transplantation|November 1, 1992
Liver transplantation for hereditary tyrosinemia--early transplantation following the patient's stabilizationE M Sokal, R Bustos, F Van Hoof, et al.
The Biochemical Journal|September 1, 1988
Effects of riboflavin deficiency and clofibrate treatment on the five acyl-CoA dehydrogenases in rat liver mitochondriaK Veitch, J P Draye, F Van Hoof, et al.
Annales De Recherches Veterinaires. Annals of Veterinary Research|January 1, 1979
Hydrolytic activities of rumen ciliatesJ Delfosse-Debusscher, F Van Hoof, P Hellings, et al.
Pediatric Research|February 1, 1990
Hormonal regulation of the rat small intestine: responsiveness of villus and crypt cells to insulin during the suckling period and unresponsiveness after weaningJ P Buts, N De Keyser, J Kolanowski, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1989
Developmental patterns of peroxisomal enzymes in amphibian liver during spontaneous and triiodothyronine-induced metamorphosisE Ciolek, J Vamecq, F Van Hoof, et al.
Birth Defects Original Article Series|March 1, 1973
Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidaseT de Barsy, P Jacquemin, F Van Hoof, et al.
Acta Neuropathologica|February 19, 1973
Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscleJ J Martin, T de Barsy, F van Hoof, et al.
Journal - Forensic Science Society|April 1, 1974
Fatal diazinon poisoning in manA Heyndrickx, F Van Hoof, L De Wolf, et al.
The Biochemical Journal|April 1, 1975
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiencyB Lederer, F Van Hoof, G Van den Berghe, et al.
Biochemical Pharmacology|December 1, 1982
Mechanism of aminoglycoside-induced lysosomal phospholipidosis: in vitro and in vivo studies with gentamicin and amikacinG Laurent, M B Carlier, B Rollman, et al.
Pageof 12

Showing results (61-70 of 113) with videos related to

Sort By:
Pageof 12
Transplantation|November 1, 1992
Liver transplantation for hereditary tyrosinemia--early transplantation following the patient's stabilizationE M Sokal, R Bustos, F Van Hoof, et al.
The Biochemical Journal|September 1, 1988
Effects of riboflavin deficiency and clofibrate treatment on the five acyl-CoA dehydrogenases in rat liver mitochondriaK Veitch, J P Draye, F Van Hoof, et al.
Annales De Recherches Veterinaires. Annals of Veterinary Research|January 1, 1979
Hydrolytic activities of rumen ciliatesJ Delfosse-Debusscher, F Van Hoof, P Hellings, et al.
Pediatric Research|February 1, 1990
Hormonal regulation of the rat small intestine: responsiveness of villus and crypt cells to insulin during the suckling period and unresponsiveness after weaningJ P Buts, N De Keyser, J Kolanowski, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1989
Developmental patterns of peroxisomal enzymes in amphibian liver during spontaneous and triiodothyronine-induced metamorphosisE Ciolek, J Vamecq, F Van Hoof, et al.
Birth Defects Original Article Series|March 1, 1973
Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidaseT de Barsy, P Jacquemin, F Van Hoof, et al.
Acta Neuropathologica|February 19, 1973
Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscleJ J Martin, T de Barsy, F van Hoof, et al.
Journal - Forensic Science Society|April 1, 1974
Fatal diazinon poisoning in manA Heyndrickx, F Van Hoof, L De Wolf, et al.
The Biochemical Journal|April 1, 1975
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiencyB Lederer, F Van Hoof, G Van den Berghe, et al.
Biochemical Pharmacology|December 1, 1982
Mechanism of aminoglycoside-induced lysosomal phospholipidosis: in vitro and in vivo studies with gentamicin and amikacinG Laurent, M B Carlier, B Rollman, et al.
Pageof 12