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J M Trijbels

Showing results (41-50 of 177) with videos related to

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Neuropadiatrie|May 1, 1976
Cardiomyopathy and short stature associated with mitochondrial and/or lipid storage myopathy of skeletal muscleR C Sengers, A M Stadhouders, H H Jaspar, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Estimation of energy metabolism in human skeletal muscle homogenate as a diagnostic aidW Ruitenbeek, R C Sengers, J M Trijbels, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
The use of chorionic villi in prenatal diagnosis of mitochondriopathiesW Ruitenbeek, R C Sengers, J M Trijbels, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1971
Automated determination of serum iron and ferrioxamine in urineH P Werkman, J M Trijbels, P J van Munster, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Benign mitochondrial encephalomyopathy in a patient with complex I deficiencyJ M Trijbels, W Ruitenbeek, R C Sengers, et al.
The International Journal of Biochemistry|January 1, 1991
Peroxisomal oxidases and catalase in liver and kidney homogenates of normal and di(ethylhexyl)phthalate-fed ratsF A Reubsaet, J H Veerkamp, M L Brückwilder, et al.
Neuropadiatrie|November 1, 1975
Infantile Gaucher's disease: glucocerebrosidase deficiency in peripheral blood leukocytes and cultured fibroblastsR C Sengers, K J Lamers, J A Bakkeren, et al.
The Netherlands Journal of Medicine|January 1, 1980
Symptoms, diagnostic pitfalls, and treatment of homocystinuria in seven adult patientsJ I Drayer, A J Cleophas, J M Trijbels, et al.
The New England Journal of Medicine|February 14, 1974
Letter: Pyruvate decarboxylase deficiency in liverJ L Willems, L A Monnens, J M Trijbels, et al.
FEBS Letters|July 16, 1990
The involvement of fatty acid binding protein in peroxisomal fatty acid oxidationF A Reubsaet, J H Veerkamp, M L Brückwilder, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
Neuropadiatrie|May 1, 1976
Cardiomyopathy and short stature associated with mitochondrial and/or lipid storage myopathy of skeletal muscleR C Sengers, A M Stadhouders, H H Jaspar, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Estimation of energy metabolism in human skeletal muscle homogenate as a diagnostic aidW Ruitenbeek, R C Sengers, J M Trijbels, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
The use of chorionic villi in prenatal diagnosis of mitochondriopathiesW Ruitenbeek, R C Sengers, J M Trijbels, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1971
Automated determination of serum iron and ferrioxamine in urineH P Werkman, J M Trijbels, P J van Munster, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Benign mitochondrial encephalomyopathy in a patient with complex I deficiencyJ M Trijbels, W Ruitenbeek, R C Sengers, et al.
The International Journal of Biochemistry|January 1, 1991
Peroxisomal oxidases and catalase in liver and kidney homogenates of normal and di(ethylhexyl)phthalate-fed ratsF A Reubsaet, J H Veerkamp, M L Brückwilder, et al.
Neuropadiatrie|November 1, 1975
Infantile Gaucher's disease: glucocerebrosidase deficiency in peripheral blood leukocytes and cultured fibroblastsR C Sengers, K J Lamers, J A Bakkeren, et al.
The Netherlands Journal of Medicine|January 1, 1980
Symptoms, diagnostic pitfalls, and treatment of homocystinuria in seven adult patientsJ I Drayer, A J Cleophas, J M Trijbels, et al.
The New England Journal of Medicine|February 14, 1974
Letter: Pyruvate decarboxylase deficiency in liverJ L Willems, L A Monnens, J M Trijbels, et al.
FEBS Letters|July 16, 1990
The involvement of fatty acid binding protein in peroxisomal fatty acid oxidationF A Reubsaet, J H Veerkamp, M L Brückwilder, et al.
Pageof 18