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P Rinaldo

Showing results (11-20 of 95) with videos related to

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The New England Journal of Medicine|January 30, 1997
Liver disease in pregnancyP Rinaldo, W R Treem, C A Riely
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
A fluorogenic allele-specific amplification method for DNA-based screening for inherited metabolic disordersY Matsubara, K Fujii, P Rinaldo, et al.
Biomedical & Environmental Mass Spectrometry|July 1, 1989
Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoringP Rinaldo, J J O'Shea, R D Welch, et al.
Pediatric Research|May 1, 1990
The enzymatic basis for the dehydrogenation of 3-phenylpropionic acid: in vitro reaction of 3-phenylpropionyl-CoA with various acyl-CoA dehydrogenasesP Rinaldo, J J O'Shea, R D Welch, et al.
Journal of Inherited Metabolic Disease|July 24, 2007
Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007)D Matern, S Tortorelli, D Oglesbee, et al.
Biomedical Mass Spectrometry|December 1, 1984
CAD MIKES: a new method for a rapid and unequivocal structural identification of organic acids in biological fluids. A first application to a case of methylmalonic aciduriaP Rinaldo, L Chiandetti, F Zacchello, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old womanK Raymond, A E Bale, C A Barnes, et al.
Current Opinion in Pediatrics|December 16, 1998
Clinical and biochemical features of fatty acid oxidation disordersP Rinaldo, K Raymond, A al-Odaib, et al.
Progress in Clinical and Biological Research|January 1, 1990
Diagnosis of medium chain acyl-CoA dehydrogenase deficiency by stable isotope dilution analysis of urinary acylglycines: retrospective and prospective studies, and comparison of its accuracy to acylcarnitine identification by FAB/mass spectrometryP Rinaldo, J J O'Shea, R D Welch, et al.
Clinical Chemistry|September 3, 1999
Method for the determination of total homocysteine in plasma and urine by stable isotope dilution and electrospray tandem mass spectrometryM J Magera, J M Lacey, B Casetta, et al.
Pageof 10

Showing results (11-20 of 95) with videos related to

Sort By:
Pageof 10
The New England Journal of Medicine|January 30, 1997
Liver disease in pregnancyP Rinaldo, W R Treem, C A Riely
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
A fluorogenic allele-specific amplification method for DNA-based screening for inherited metabolic disordersY Matsubara, K Fujii, P Rinaldo, et al.
Biomedical & Environmental Mass Spectrometry|July 1, 1989
Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoringP Rinaldo, J J O'Shea, R D Welch, et al.
Pediatric Research|May 1, 1990
The enzymatic basis for the dehydrogenation of 3-phenylpropionic acid: in vitro reaction of 3-phenylpropionyl-CoA with various acyl-CoA dehydrogenasesP Rinaldo, J J O'Shea, R D Welch, et al.
Journal of Inherited Metabolic Disease|July 24, 2007
Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007)D Matern, S Tortorelli, D Oglesbee, et al.
Biomedical Mass Spectrometry|December 1, 1984
CAD MIKES: a new method for a rapid and unequivocal structural identification of organic acids in biological fluids. A first application to a case of methylmalonic aciduriaP Rinaldo, L Chiandetti, F Zacchello, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old womanK Raymond, A E Bale, C A Barnes, et al.
Current Opinion in Pediatrics|December 16, 1998
Clinical and biochemical features of fatty acid oxidation disordersP Rinaldo, K Raymond, A al-Odaib, et al.
Progress in Clinical and Biological Research|January 1, 1990
Diagnosis of medium chain acyl-CoA dehydrogenase deficiency by stable isotope dilution analysis of urinary acylglycines: retrospective and prospective studies, and comparison of its accuracy to acylcarnitine identification by FAB/mass spectrometryP Rinaldo, J J O'Shea, R D Welch, et al.
Clinical Chemistry|September 3, 1999
Method for the determination of total homocysteine in plasma and urine by stable isotope dilution and electrospray tandem mass spectrometryM J Magera, J M Lacey, B Casetta, et al.
Pageof 10