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Alfonso Romano

Showing results (21-30 of 39) with videos related to

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Journal of Child Neurology|December 7, 2016
Clinical Value of Perfusion Abnormalities of Brain on Technetium-99m HMPAO Single-Photon Emission Computed Tomography in Children With Sydenham ChoreaSara Maria Delle Acque Giorgio, Maria Grazia Caprio, Flavia Galante, et al.
Italian Journal of Pediatrics|May 15, 2013
Improvement of dysphagia in a child affected by Pompe disease treated with enzyme replacement therapySimona Fecarotta, Serena Ascione, Giuseppe Montefusco, et al.
Pediatric Research|January 24, 2007
Neonatal urinary cotinine correlates with behavioral alterations in newborns prenatally exposed to tobacco smokeGiuseppina Mansi, Francesco Raimondi, Simona Pichini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 26, 2022
COVID-19-associated severe mono-hemispheric encephalitis in a young infantFrancesco Nunziata, Edoardo Vassallo, Maria Alessio, et al.
Neurology|January 1, 2014
Child neurology: Recurrent rhabdomyolysis due to a fatty acid oxidation disorderGaetano Terrone, Margherita Ruoppolo, Nicola Brunetti-Pierri, et al.
JIMD Reports|March 11, 2020
Cavitating and tigroid-like leukoencephalopathy in a case of <i>NDUFA2</i>-related disorderMarianna Alagia, Gerarda Cappuccio, Annalaura Torella, et al.
Journal of Child Neurology|August 11, 2007
Long-term enzyme replacement therapy for pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cellsMassimiliano Rossi, Giancarlo Parenti, Roberto Della Casa, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Cerebellar vermis aplasia: patient report and exclusion of the candidate genes EN2 and ZIC1Luigi Titomanlio, Nicola Brunetti Pierri, Alfonso Romano, et al.
Seizure|May 17, 2020
A further contribution to the delineation of epileptic phenotype in PACS2-related syndromeGaetano Terrone, Francesca Marchese, Maria Stella Vari, et al.
European Journal of Medical Genetics|June 5, 2012
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: central nervous involvement in two Italian patientsGaetano Terrone, Alessandra D'Amico, Floriana Imperati, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

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Pageof 4
Journal of Child Neurology|December 7, 2016
Clinical Value of Perfusion Abnormalities of Brain on Technetium-99m HMPAO Single-Photon Emission Computed Tomography in Children With Sydenham ChoreaSara Maria Delle Acque Giorgio, Maria Grazia Caprio, Flavia Galante, et al.
Italian Journal of Pediatrics|May 15, 2013
Improvement of dysphagia in a child affected by Pompe disease treated with enzyme replacement therapySimona Fecarotta, Serena Ascione, Giuseppe Montefusco, et al.
Pediatric Research|January 24, 2007
Neonatal urinary cotinine correlates with behavioral alterations in newborns prenatally exposed to tobacco smokeGiuseppina Mansi, Francesco Raimondi, Simona Pichini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 26, 2022
COVID-19-associated severe mono-hemispheric encephalitis in a young infantFrancesco Nunziata, Edoardo Vassallo, Maria Alessio, et al.
Neurology|January 1, 2014
Child neurology: Recurrent rhabdomyolysis due to a fatty acid oxidation disorderGaetano Terrone, Margherita Ruoppolo, Nicola Brunetti-Pierri, et al.
JIMD Reports|March 11, 2020
Cavitating and tigroid-like leukoencephalopathy in a case of <i>NDUFA2</i>-related disorderMarianna Alagia, Gerarda Cappuccio, Annalaura Torella, et al.
Journal of Child Neurology|August 11, 2007
Long-term enzyme replacement therapy for pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cellsMassimiliano Rossi, Giancarlo Parenti, Roberto Della Casa, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Cerebellar vermis aplasia: patient report and exclusion of the candidate genes EN2 and ZIC1Luigi Titomanlio, Nicola Brunetti Pierri, Alfonso Romano, et al.
Seizure|May 17, 2020
A further contribution to the delineation of epileptic phenotype in PACS2-related syndromeGaetano Terrone, Francesca Marchese, Maria Stella Vari, et al.
European Journal of Medical Genetics|June 5, 2012
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: central nervous involvement in two Italian patientsGaetano Terrone, Alessandra D'Amico, Floriana Imperati, et al.
Pageof 4