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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.
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.
Neurology|April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletionD Pareyson, V Scaioli, F Taroni, et al.
International Journal of Legal Medicine|September 1, 2005
Forensic identification of urine samples: a comparison between nuclear and mitochondrial DNA markersV Castella, N Dimo-Simonin, C Brandt-Casadevall, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 15, 1991
cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferaseG Finocchiaro, F Taroni, M Rocchi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 20, 2013
[Effect of prematurity on fat mass distribution and blood pressure at prepubertal age: a follow-up study]P Piemontese, N Liotto, F Garbarino, et al.
Muscle & Nerve|December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathyD Pareyson, A Solari, F Taroni, et al.
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