P. Bardelli

4-Hydroxybutyric aciduria: Clinical findings and vigabatrin therapy

G. Uziel, C. Pantaleoni, M. Rimoldi, 1993, Journal of Inherited Metabolic Disease.

GENETIC DISORDERS: CLINICAL AND THERAPEUTICAL ASPECTS

E. Bertini, G. Uziel, M. Cappa, 1994 .

Clinical diagnosis of long-chain acyl-coenzyme A-dehydrogenase deficiency: use of stress and fat-loading tests.

S. di Donato, J. Saudubray, B. Garavaglia, 1991, The Journal of pediatrics.

Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathy.

E. Bertini, G. Uziel, M. Rimoldi, 1991, Developmental neuroscience.

Chronic GM1 Gangliosidosis Presenting as Dystonia: Clinical and Biochemical Studies in a New Case

N. Nardocci, L. Angelini, B. Bertagnolio, 1993, Neuropediatrics.