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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 13, 2009
[Body composition in small for gestational age newborns]F Taroni, N Liotto, L Morlacchi, et al.
Pediatric Neurology|March 30, 2000
Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiencyR Pons, P Cavadini, S Baratta, et al.
Human Molecular Genetics|February 9, 1999
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosisA Wong, J Yang, P Cavadini, et al.
Experimental Brain Research|February 3, 1999
Estimation of PC12 cell numbers with acid phosphatase assay and mitochondrial dehydrogenase assay: dopamine interferes with assay based on tetrazoliumF Si, S H Shin, A Biedermann, et al.
Human Genetics|March 1, 1996
Inheritance of the S113L mutation within an inbred family with carnitine palmitoyltransferase enzyme deficiencyI Handig, E Dams, F Taroni, et al.
Italian Journal of Neurological Sciences|October 1, 1995
Kennedy's disease: clinical and molecular study of two Italian familiesD Pareyson, B Castellotti, S Botti, et al.
Cancer Research|March 15, 1993
Characterization of the DNA double strand break repair defect in scid miceC Chang, K A Biedermann, M Mezzina, et al.
Neurology|July 1, 1986
Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductaseS Di Donato, F E Frerman, M Rimoldi, et al.
Gastroenterology|September 1, 1989
Gallstone recurrence after successful oral bile acid treatment. A 12-year follow-up study and evaluation of long-term postdissolution treatmentN Villanova, F Bazzoli, F Taroni, et al.
Neurology|April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutationD Pareyson, F Taroni, S Botti, et al.
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