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F Taroni

Showing results (111-120 of 172) with videos related to

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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.
Neurology|April 2, 1999
Charcot-Marie-Tooth disease type 2 and P0 gene mutationsD Pareyson, A Sghirlanzoni, S Bolti, 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.
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.
Science & Justice : Journal of the Forensic Science Society|December 15, 2015
The importance of distinguishing information from evidence/observations when formulating propositionsT Hicks, A Biedermann, J A de Koeijer, et al.
Science & Justice : Journal of the Forensic Science Society|September 12, 2017
Reply to Morrison et al. (2016) Refining the relevant population in forensic voice comparison - A response to Hicks et alii (2015) The importance of distinguishing information from evidence/observations when formulating propositionsT Hicks, A Biedermann, J A de Koeijer, et al.
Pageof 18

Showing results (111-120 of 172) with videos related to

Sort By:
Pageof 18
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.
Neurology|April 2, 1999
Charcot-Marie-Tooth disease type 2 and P0 gene mutationsD Pareyson, A Sghirlanzoni, S Bolti, 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.
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.
Science & Justice : Journal of the Forensic Science Society|December 15, 2015
The importance of distinguishing information from evidence/observations when formulating propositionsT Hicks, A Biedermann, J A de Koeijer, et al.
Science & Justice : Journal of the Forensic Science Society|September 12, 2017
Reply to Morrison et al. (2016) Refining the relevant population in forensic voice comparison - A response to Hicks et alii (2015) The importance of distinguishing information from evidence/observations when formulating propositionsT Hicks, A Biedermann, J A de Koeijer, et al.
Pageof 18