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F Van Hoof

Showing results (91-100 of 113) with videos related to

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Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1977
[Mannosidosis: diagnosis by conjunctival biopsy and enzymatic analysis of the tears]J Libert, F Van Hoof, J P Farriaux, et al.
American Journal of Medical Genetics|October 23, 1997
Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal formA Verloes, M Massin, J Lombet, et al.
Biochimica Et Biophysica Acta|December 18, 1989
Altered acyl-CoA metabolism in riboflavin deficiencyK Veitch, J P Draye, J Vamecq, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 18, 2000
Identification of undescribed medium-chain acylcarnitines present in urine of patients with propionic and methylmalonic acidemiasR Libert, F Van Hoof, M Thillaye, et al.
Prenatal Diagnosis|January 1, 1988
Prenatal diagnosis of Hunter syndrome using fetal plasmaW Lissens, M Van Lierde, J Decaluwe, et al.
The American Journal of Cardiology|December 1, 1984
Effects of nicardipine and nisoldipine on myocardial metabolism, coronary blood flow and oxygen supply in angina pectorisM F Rousseau, M F Vincent, F Van Hoof, et al.
Acta Paediatrica Belgica|January 1, 1980
Niemann-Pick type C disease and early cholestasis in three brothersJ Jaeken, W Proesmans, E Eggermont, et al.
European Journal of Pediatrics|March 1, 1992
Progressive cardiac failure following orthotopic liver transplantation for type IV glycogenosisE M Sokal, F Van Hoof, D Alberti, et al.
Archives Francaises De Pediatrie|June 1, 1973
[Type II mucolipidosis (I-cell disease)]R Walbaum, P Dehaene, W Scharfman, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Identification of new medium-chain acylcarnitines present in urine of a patient with medium-chain acyl-CoA dehydrogenase deficiencyR Libert, F Van Hoof, M Thillaye, et al.
Pageof 12

Showing results (91-100 of 113) with videos related to

Sort By:
Pageof 12
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1977
[Mannosidosis: diagnosis by conjunctival biopsy and enzymatic analysis of the tears]J Libert, F Van Hoof, J P Farriaux, et al.
American Journal of Medical Genetics|October 23, 1997
Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal formA Verloes, M Massin, J Lombet, et al.
Biochimica Et Biophysica Acta|December 18, 1989
Altered acyl-CoA metabolism in riboflavin deficiencyK Veitch, J P Draye, J Vamecq, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 18, 2000
Identification of undescribed medium-chain acylcarnitines present in urine of patients with propionic and methylmalonic acidemiasR Libert, F Van Hoof, M Thillaye, et al.
Prenatal Diagnosis|January 1, 1988
Prenatal diagnosis of Hunter syndrome using fetal plasmaW Lissens, M Van Lierde, J Decaluwe, et al.
The American Journal of Cardiology|December 1, 1984
Effects of nicardipine and nisoldipine on myocardial metabolism, coronary blood flow and oxygen supply in angina pectorisM F Rousseau, M F Vincent, F Van Hoof, et al.
Acta Paediatrica Belgica|January 1, 1980
Niemann-Pick type C disease and early cholestasis in three brothersJ Jaeken, W Proesmans, E Eggermont, et al.
European Journal of Pediatrics|March 1, 1992
Progressive cardiac failure following orthotopic liver transplantation for type IV glycogenosisE M Sokal, F Van Hoof, D Alberti, et al.
Archives Francaises De Pediatrie|June 1, 1973
[Type II mucolipidosis (I-cell disease)]R Walbaum, P Dehaene, W Scharfman, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Identification of new medium-chain acylcarnitines present in urine of a patient with medium-chain acyl-CoA dehydrogenase deficiencyR Libert, F Van Hoof, M Thillaye, et al.
Pageof 12