Alessandro P. Burlina

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)

M. Durán, R. Surtees, C. Greenberg, 2007, Journal of Inherited Metabolic Disease.

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

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

Oxygen derived free radicals in patients with chronic pancreatic and other digestive diseases.

M. Plebani, C. Fabris, A. Meani, 1990, Journal of clinical pathology.

Alterations in bilirubin metabolism during extra- and intrahepatic cholestasis

M. Plebani, C. Fabris, D. Basso, 2004, The clinical investigator.

Clinical, biochemical and molecular characterization of prosaposin deficiency

M. Tartaglia, M. Motta, V. Nigro, 2016, Clinical genetics.