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V Leuzzi

Showing results (11-20 of 64) with videos related to

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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. 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|August 13, 1998
Subclinical visual impairment in phenylketonuria. A neurophysiological study (VEP-P) with clinical, biochemical, and neuroradiological (MRI) correlationsV Leuzzi, S Rinalduzzi, F Chiarotti, 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|July 15, 2000
Derangement of the dopaminergic system in phenylketonuria: study of the event-related potential (P300)V Leuzzi, S Seri, A Cerquiglini, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1992
Bilateral striatal necrosis, dystonia and optic atrophy in two siblingsV Leuzzi, E Bertini, A M De Negri, et al.
Neurology|November 24, 2004
Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutationV Leuzzi, M L Di Sabato, M Zollino, et al.
Pediatric Neurology|November 27, 1998
Childhood Leber's hereditary optic neuropathy (ND1/3460) with visual recoveryP P Pezzi, A M De Negri, F Sadun, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
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. 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|August 13, 1998
Subclinical visual impairment in phenylketonuria. A neurophysiological study (VEP-P) with clinical, biochemical, and neuroradiological (MRI) correlationsV Leuzzi, S Rinalduzzi, F Chiarotti, 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|July 15, 2000
Derangement of the dopaminergic system in phenylketonuria: study of the event-related potential (P300)V Leuzzi, S Seri, A Cerquiglini, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1992
Bilateral striatal necrosis, dystonia and optic atrophy in two siblingsV Leuzzi, E Bertini, A M De Negri, et al.
Neurology|November 24, 2004
Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutationV Leuzzi, M L Di Sabato, M Zollino, et al.
Pediatric Neurology|November 27, 1998
Childhood Leber's hereditary optic neuropathy (ND1/3460) with visual recoveryP P Pezzi, A M De Negri, F Sadun, et al.
Pageof 7