Showing results (1-10 of 370) with videos related to

Sort By:
Pageof 37
Journal of Inherited Metabolic Disease|May 26, 2004
Executive function impairment in early-treated PKU subjects with normal mental developmentV Leuzzi, M Pansini, E Sechi, et al.
Neurology|October 23, 2002
Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndromeV Leuzzi, Ca Carducci, Cl 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 Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|November 1, 1994
Visual, auditory, and somatosensorial evoked potentials in early and late treated adolescents with phenylketonuriaV Leuzzi, F Cardona, I Antonozzi, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Biochemical, clinical and neuroradiological (MRI) correlations in late-detected PKU patientsV Leuzzi, G Trasimeni, G F Gualdi, et al.
Electroencephalography and Clinical Neurophysiology|January 1, 1991
The development of auditory and visual evoked potentials in early treated phenylketonuric childrenF Cardona, V Leuzzi, I Antonozzi, 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.
Molecular Genetics and Metabolism|January 4, 2001
Two new severe mutations causing guanidinoacetate methyltransferase deficiencyC Carducci, V Leuzzi, C Carducci, et al.
Neuropediatrics|December 1, 1993
Neuroradiological (MRI) abnormalities in phenylketonuric subjects: clinical and biochemical correlationsV Leuzzi, G F Gualdi, F Fabbrizi, et al.
Pageof 37