Italo Antonozzi

DNA elution and amplification by polymerase chain reaction from dried blood spots.

A. Pontecorvi, I. Antonozzi, C. Carducci, 1992, BioTechniques.

Phenotypic variability, neurological outcome and genetics background of 6‐pyruvoyl‐tetrahydropterin synthase deficiency

N. Blau, A. Burlina, P. Strisciuglio, 2010, Clinical genetics.

The spectrum of phenylalanine variations under tetrahydrobiopterin load in subjects affected by phenylalanine hydroxylase deficiency

F. Chiarotti, V. Leuzzi, C. Carducci, 2006, Journal of Inherited Metabolic Disease.

Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome.

F. Cardona, V. Leuzzi, C. Carducci, 2002, Neurology.