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Paolo Galluzzi

Showing results (21-30 of 62) with videos related to

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American Journal of Medical Genetics. Part A|June 10, 2003
Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasiaSalvatore Grosso, Maria Angela Farnetani, Rosario Berardi, et al.
Clinical Dysmorphology|October 18, 2016
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetusesAnna Maria Pinto, Valentina Imperatore, Laura Bianciardi, et al.
European Journal of Ophthalmology|February 1, 2011
Contrast-enhanced magnetic resonance imaging of fibrovascular tissue ingrowth within synthetic hydroxyapatite orbital implants in childrenPaolo Galluzzi, Sonia De Francesco, Giovanna Giacalone, et al.
Journal of Neurology|May 28, 2004
Uncommon findings in idiopathic hypertrophic cranial pachymeningitisSimone Rossi, Fabio Giannini, Alfonso Cerase, et al.
Archives of Neurology|August 8, 2002
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degenerationRaffaella Zannolli, Sid Gilman, Simone Rossi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|August 19, 2014
First report of spondylodiscitis due to vancomycin heteroresistant Staphylococcus capitis in immunocompetent hostClaudia Bianco, Fabio Arena, Barbara Rossetti, et al.
European Journal of Ophthalmology|April 17, 2012
13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twinsSonia De Francesco, Paolo Galluzzi, Alessandra Del Longo, et al.
Neuroradiology|May 1, 2016
MRI-based assessment of the pineal gland in a large population of children aged 0-5 years and comparison with pineoblastoma: part II, the cystic glandSelma Sirin, Marcus C de Jong, Paolo Galluzzi, et al.
Neurologia I Neurochirurgia Polska|September 10, 2010
Spindle cell lipoma of the orbit: a case report of an unusual orbital pathologySimone Ulivieri, Giuseppe Olivieri, Paolo Alfonso Motolese, et al.
Journal of Neurology|May 16, 2009
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variantMaria Teresa Dotti, Rosaria Buccoliero, Andrew Lee, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|June 10, 2003
Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasiaSalvatore Grosso, Maria Angela Farnetani, Rosario Berardi, et al.
Clinical Dysmorphology|October 18, 2016
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetusesAnna Maria Pinto, Valentina Imperatore, Laura Bianciardi, et al.
European Journal of Ophthalmology|February 1, 2011
Contrast-enhanced magnetic resonance imaging of fibrovascular tissue ingrowth within synthetic hydroxyapatite orbital implants in childrenPaolo Galluzzi, Sonia De Francesco, Giovanna Giacalone, et al.
Journal of Neurology|May 28, 2004
Uncommon findings in idiopathic hypertrophic cranial pachymeningitisSimone Rossi, Fabio Giannini, Alfonso Cerase, et al.
Archives of Neurology|August 8, 2002
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degenerationRaffaella Zannolli, Sid Gilman, Simone Rossi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|August 19, 2014
First report of spondylodiscitis due to vancomycin heteroresistant Staphylococcus capitis in immunocompetent hostClaudia Bianco, Fabio Arena, Barbara Rossetti, et al.
European Journal of Ophthalmology|April 17, 2012
13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twinsSonia De Francesco, Paolo Galluzzi, Alessandra Del Longo, et al.
Neuroradiology|May 1, 2016
MRI-based assessment of the pineal gland in a large population of children aged 0-5 years and comparison with pineoblastoma: part II, the cystic glandSelma Sirin, Marcus C de Jong, Paolo Galluzzi, et al.
Neurologia I Neurochirurgia Polska|September 10, 2010
Spindle cell lipoma of the orbit: a case report of an unusual orbital pathologySimone Ulivieri, Giuseppe Olivieri, Paolo Alfonso Motolese, et al.
Journal of Neurology|May 16, 2009
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variantMaria Teresa Dotti, Rosaria Buccoliero, Andrew Lee, et al.
Pageof 7