Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Deodato

Showing results (1-10 of 34) with videos related to

Pageof 4
Sort By:
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 11, 2001
Brain ischemic lesions of the newbornF Guzzetta, F Deodato, T Randò
Progress in Orthodontics|February 27, 2004
A functional approach to the TMJ disordersF Deodato, S Cristiano, R Trusendi, et al.
Journal of Inherited Metabolic Disease|July 18, 2002
Successful pregnancy in a woman with mut- methylmalonic acidaemiaF Deodato, C Rizzo, S Boenzi, et al.
Neurology|December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutationA Fogli, C Dionisi-Vici, F Deodato, et al.
Neuropediatrics|January 24, 2006
MRI and 1H-MRS findings in early-onset cobalamin C/D defectD Longo, G Fariello, C Dionisi-Vici, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|February 5, 2014
Clinical implications of different calculation algorithms in breast radiotherapy: a comparison between pencil beam and collapsed cone convolutionS Cilla, C Digesù, G Macchia, et al.
Neuropediatrics|June 10, 2005
Assessment of visual function in children with methylmalonic aciduria and homocystinuriaD Ricci, M Pane, F Deodato, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemiaF Deodato, S Boenzi, C Rizzo, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Long-Term Follow-Up of Two Siblings with a Non-Classic Infantile Variant Form of Pompe DiseaseR Taurisano, A D'Amico, G S Colafati, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiencyF Deodato, M Sabatelli, E Ricci, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 11, 2001
Brain ischemic lesions of the newbornF Guzzetta, F Deodato, T Randò
Progress in Orthodontics|February 27, 2004
A functional approach to the TMJ disordersF Deodato, S Cristiano, R Trusendi, et al.
Journal of Inherited Metabolic Disease|July 18, 2002
Successful pregnancy in a woman with mut- methylmalonic acidaemiaF Deodato, C Rizzo, S Boenzi, et al.
Neurology|December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutationA Fogli, C Dionisi-Vici, F Deodato, et al.
Neuropediatrics|January 24, 2006
MRI and 1H-MRS findings in early-onset cobalamin C/D defectD Longo, G Fariello, C Dionisi-Vici, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|February 5, 2014
Clinical implications of different calculation algorithms in breast radiotherapy: a comparison between pencil beam and collapsed cone convolutionS Cilla, C Digesù, G Macchia, et al.
Neuropediatrics|June 10, 2005
Assessment of visual function in children with methylmalonic aciduria and homocystinuriaD Ricci, M Pane, F Deodato, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemiaF Deodato, S Boenzi, C Rizzo, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Long-Term Follow-Up of Two Siblings with a Non-Classic Infantile Variant Form of Pompe DiseaseR Taurisano, A D'Amico, G S Colafati, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiencyF Deodato, M Sabatelli, E Ricci, et al.
Pageof 4