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Journal of Inherited Metabolic Disease|January 5, 2002
Lethal neonatal presentation of carnitine palmitoyltransferase I deficiencyF Invernizzi, A B Burlina, A Donadio, et al.Forensic Science International|February 19, 2003
Evaluation of links in heroin seizuresL Dujourdy, G Barbati, F Taroni, et al.Journal of Epidemiology and Community Health|January 20, 2004
Impact of regionalisation of cardiac surgery in Emilia-Romagna, ItalyL Nobilio, D Fortuna, M Vizioli, et al.Neurology|December 31, 1997
Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsiesJ M Gabriel, B Erne, D Pareyson, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 12, 2016
Early white matter involvement in an infant carrying a novel mutation in ACOX1R Masson, S Guerra, R Cerini, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 27, 2009
[Quality of growth in preterm infants assessed at term equivalent age: a pilot study]F Taroni, N Liotto, O Amato, et al.Minerva Pediatrica|May 24, 2007
[Proposal for a protocol for the staging of incontinentia pigmenti in pediatric age]D Portaleone, F Taroni, S Micheli, et al.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.Pageof 16