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AJNR. American Journal of Neuroradiology|March 14, 2007
Treatment monitoring of brain creatine deficiency syndromes: a 1H- and 31P-MR spectroscopy studyM C Bianchi, M Tosetti, R Battini, 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.
Journal of Inherited Metabolic Disease|January 1, 1987
Plasma amino acid values and pancreatic beta-cell function in phenylketonuriaI Antonozzi, C Carducci, L Vestri, et al.
Parkinsonism & Related Disorders|April 9, 2019
PNKP deficiency mimicking a benign hereditary chorea: The misleading presentation of a neurodegenerative disorderC Caputi, M Tolve, S Galosi, 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.
Acta Neurologica Scandinavica|September 23, 1997
LHON mutations in Italian patients affected by multiple sclerosisV Leuzzi, C Carducci, M Lenza, 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.
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