Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R C Sengers

Showing results (61-70 of 144) with videos related to

Pageof 15
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1977
L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retinaJ M Trijbels, R C Sengers, J A Bakkeren, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Predictors of mean phenylalanine levels during the first five years of life in patients with phenylketonuria who were treated early. Dutch National PKU Steering CommitteeP H Verkerk, F J van Spronsen, M van Houten, et al.
European Journal of Pediatrics|August 1, 1986
Maternal phenylketonuria: comparison of two treated full term pregnanciesR P Soeters, R C Sengers, P W van Dongen, et al.
Biochemical Medicine|December 1, 1978
Pyruvate oxidation in rat and human skeletal muscle mitochondriaH Bookelman, J M Trijbels, R C Sengers, et al.
The International Journal of Biochemistry|January 1, 1979
Reconstitution of malate-aspartate and alpha-glycerophosphate shuttle activity in rat skeletal muscle mitochondriaH Bookelman, J M Trijbels, R C Sengers, et al.
Archives of Neurology|March 1, 1991
Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitineP L Bernsen, F J Gabreëls, W Ruitenbeek, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Mitochondrial myopathies: multiple enzyme defects in the respiratory chainW Ruitenbeek, J M Trijbels, J C Fischer, et al.
Acta Neuropathologica|February 7, 1998
Infantile motor neuron disease with autonomic dysfunction and bunina bodiesB A Semmekrot, P Wesseling, J F Bruinenberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 1997
Multicore myopathy with restrictive cardiomyopathyM A Willemsen, A M van Oort, H J ter Laak, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1977
L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retinaJ M Trijbels, R C Sengers, J A Bakkeren, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Predictors of mean phenylalanine levels during the first five years of life in patients with phenylketonuria who were treated early. Dutch National PKU Steering CommitteeP H Verkerk, F J van Spronsen, M van Houten, et al.
European Journal of Pediatrics|August 1, 1986
Maternal phenylketonuria: comparison of two treated full term pregnanciesR P Soeters, R C Sengers, P W van Dongen, et al.
Biochemical Medicine|December 1, 1978
Pyruvate oxidation in rat and human skeletal muscle mitochondriaH Bookelman, J M Trijbels, R C Sengers, et al.
The International Journal of Biochemistry|January 1, 1979
Reconstitution of malate-aspartate and alpha-glycerophosphate shuttle activity in rat skeletal muscle mitochondriaH Bookelman, J M Trijbels, R C Sengers, et al.
Archives of Neurology|March 1, 1991
Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitineP L Bernsen, F J Gabreëls, W Ruitenbeek, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Mitochondrial myopathies: multiple enzyme defects in the respiratory chainW Ruitenbeek, J M Trijbels, J C Fischer, et al.
Acta Neuropathologica|February 7, 1998
Infantile motor neuron disease with autonomic dysfunction and bunina bodiesB A Semmekrot, P Wesseling, J F Bruinenberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 1997
Multicore myopathy with restrictive cardiomyopathyM A Willemsen, A M van Oort, H J ter Laak, et al.
Pageof 15