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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 Chromatography. B, Biomedical Sciences and Applications|June 8, 2001
Automated high-performance liquid chromatographic method for the determination of guanidinoacetic acid in dried blood spots: a tool for early diagnosis of guanidinoacetate methyltransferase deficiencyC Carducci, M Birarelli, P Santagata, 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|April 5, 1996
Automated method for the measurement of amino acids in urine by high-performance liquid chromatographyC Carducci, M Birarelli, V Leuzzi, et al.Neuropediatrics|December 7, 2007
Tyrosine hydroxylase deficiency presenting with a biphasic clinical courseT Giovanniello, V Leuzzi, C Carducci, et al.Neurology|November 23, 2000
Brain creatine depletion: guanidinoacetate methyltransferase deficiency (improving with creatine supplementation)V Leuzzi, M C Bianchi, M Tosetti, 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.Biotechniques|November 1, 1992
DNA elution and amplification by polymerase chain reaction from dried blood spotsC Carducci, L Ellul, I Antonozzi, et al.Journal of Chromatography|August 16, 1991
Rapid and sensitive high-performance liquid chromatographic method for the analysis of tryptophan, tyrosine and phenylalanine in biological samplesC Carducci, F Moretti, M Birarelli, et al.Human Genetics|October 1, 1991
Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathyC Carducci, V Leuzzi, M Scuderi, et al.Pageof 14