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R Santer

Showing results (61-70 of 110) with videos related to

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Journal of Inherited Metabolic Disease|February 6, 2009
Phenylalanine tolerance in three phenylketonuric women pregnant with fetuses of different genetic PKU statusB Kohlschütter, M Ellerbrok, M Merkel, et al.
The Prostate|September 23, 2010
Transcriptional coactivators p300 and CBP stimulate estrogen receptor-beta signaling and regulate cellular events in prostate cancerJan Bouchal, Frédéric R Santer, Philipp P S Höschele, et al.
Applied Optics|October 1, 1986
Stratospheric aerosol observations from a balloon-borne polarimetric experimentM Herman, J Y Balois, L Gonzalez, et al.
The Journal of Pediatrics|May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic methodE Schmidt-Sommerfeld, D Penn, M Duran, et al.
European Journal of Pediatrics|April 1, 1993
Isolated defect of peroxisomal beta-oxidation in a 16-year-old patientR Santer, A Claviez, H D Oldigs, et al.
Nuklearmedizin. Nuclear Medicine|February 13, 2009
Computer simulations suggest that acute correction of hyperglycaemia with an insulin bolus protocol might be useful in brain FDG PETR Buchert, R Santer, W Brenner, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 9, 2007
High bone mineral density in pycnodysostotic patients with a novel mutation in the propeptide of cathepsin KA F Schilling, C Mülhausen, W Lehmann, et al.
Progress in Clinical and Biological Research|January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidationE Schmidt-Sommerfeld, D Penn, M Duran, et al.
Human Mutation|September 5, 2003
MLYCD mutation analysis: evidence for protein mistargeting as a cause of MLYCD deficiencyP J Wightman, R Santer, A Ribes, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
A secondary respiratory chain defect in a patient with Fanconi-Bickel syndromeM H Odièvre, A Lombès, P Dessemme, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Journal of Inherited Metabolic Disease|February 6, 2009
Phenylalanine tolerance in three phenylketonuric women pregnant with fetuses of different genetic PKU statusB Kohlschütter, M Ellerbrok, M Merkel, et al.
The Prostate|September 23, 2010
Transcriptional coactivators p300 and CBP stimulate estrogen receptor-beta signaling and regulate cellular events in prostate cancerJan Bouchal, Frédéric R Santer, Philipp P S Höschele, et al.
Applied Optics|October 1, 1986
Stratospheric aerosol observations from a balloon-borne polarimetric experimentM Herman, J Y Balois, L Gonzalez, et al.
The Journal of Pediatrics|May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic methodE Schmidt-Sommerfeld, D Penn, M Duran, et al.
European Journal of Pediatrics|April 1, 1993
Isolated defect of peroxisomal beta-oxidation in a 16-year-old patientR Santer, A Claviez, H D Oldigs, et al.
Nuklearmedizin. Nuclear Medicine|February 13, 2009
Computer simulations suggest that acute correction of hyperglycaemia with an insulin bolus protocol might be useful in brain FDG PETR Buchert, R Santer, W Brenner, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 9, 2007
High bone mineral density in pycnodysostotic patients with a novel mutation in the propeptide of cathepsin KA F Schilling, C Mülhausen, W Lehmann, et al.
Progress in Clinical and Biological Research|January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidationE Schmidt-Sommerfeld, D Penn, M Duran, et al.
Human Mutation|September 5, 2003
MLYCD mutation analysis: evidence for protein mistargeting as a cause of MLYCD deficiencyP J Wightman, R Santer, A Ribes, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
A secondary respiratory chain defect in a patient with Fanconi-Bickel syndromeM H Odièvre, A Lombès, P Dessemme, et al.
Pageof 11