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Molecular Genetics and Metabolism|January 4, 2001
Two new severe mutations causing guanidinoacetate methyltransferase deficiencyC Carducci, V Leuzzi, C Carducci, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
The spectrum of phenylalanine variations under tetrahydrobiopterin load in subjects affected by phenylalanine hydroxylase deficiencyV Leuzzi, C Carducci, C Carducci, et al.
Journal of Chromatography. A|July 27, 1999
Automated high-performance liquid chromatographic method for the determination of homocysteine in plasma samplesC Carducci, M Birarelli, M Nola, et al.
Neuropediatrics|December 7, 2007
Tyrosine hydroxylase deficiency presenting with a biphasic clinical courseT Giovanniello, V Leuzzi, C Carducci, et al.
Biotechniques|November 1, 1992
DNA elution and amplification by polymerase chain reaction from dried blood spotsC Carducci, L Ellul, I Antonozzi, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 29, 2013
Pregnancy in a methylmalonic acidemia patient with kidney transplantation: a case reportR Lubrano, E Bellelli, I Gentile, et al.
Journal of Chromatography|December 28, 1988
Rapid and sensitive method for high-performance liquid chromatographic analysis of pterins in biological fluidsI Antonozzi, C Carducci, L Vestri, et al.
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