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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.JAMA|April 12, 1985
Comparison of the acute cardiopulmonary effects of oral albuterol, metaproterenol, and terbutaline in asthmaticsJ D Wolfe, M Yamate, A A Biedermann, et al.Physical Review Letters|January 22, 2002
Real-space study of the pathway for dissociative adsorption of H2 on Si(001)M Dürr, Z Hu, A Biedermann, 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.Journal of Health Services Research & Policy|September 4, 1997
Variation in hospital use and avoidable patient morbidityF Taroni, F Repetto, D Z Louis, et al.The Journal of Pediatrics|July 1, 1996
Hypoparathyroidism in mitochondrial trifunctional protein deficiencyC Dionisi-Vici, B Garavaglia, A B Burlina, et al.European Journal of Epidemiology|September 1, 1990
The nature content and interpractice variation of general practice: a regional study in ItalyF Taroni, R Stiassi, G Traversa, et al.Pageof 18