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Roberta Biancheri

Showing results (11-20 of 65) with videos related to

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Journal of Inherited Metabolic Disease|August 10, 2011
Cerebellar hypoplasia and brainstem thinning associated with severe white matter and basal ganglia abnormalities in a child with an mtDNA deletionRoberta Biancheri, Claudio Bruno, Denise Cassandrini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 11, 2011
Anti-N-methyl-D-aspartate-receptor encephalitis: cognitive profile in two childrenEnzo Iadisernia, Francesca Maria Battaglia, Elena Vanadia, et al.
European Journal of Radiology|April 15, 2004
Imaging in spine and spinal cord malformationsAndrea Rossi, Roberta Biancheri, Armando Cama, et al.
Neuropediatrics|December 21, 2012
Magnetic resonance imaging "tigroid pattern" in Alexander diseaseRoberta Biancheri, Andrea Rossi, Isabella Ceccherini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 27, 2007
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutationRoberta Biancheri, Andrea Rossi, Giannina Alpigiani, et al.
Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findingsAndrea Rossi, Roberta Biancheri, Claudio Bruno, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
Expanded spectrum of Pelizaeus-Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe formRoberta Biancheri, Camillo Rosano, Laura Denegri, et al.
European Journal of Medical Genetics|December 3, 2014
Heterozygous deletion of CHL1 gene: detailed array-CGH and clinical characterization of a new case and review of the literatureElisa Tassano, Roberta Biancheri, Laura Denegri, et al.
Journal of Child Neurology|August 18, 2012
Lack of SLC2A1 (glucose transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhoodElisa De Grandis, Michela Stagnaro, Roberta Biancheri, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|August 10, 2011
Cerebellar hypoplasia and brainstem thinning associated with severe white matter and basal ganglia abnormalities in a child with an mtDNA deletionRoberta Biancheri, Claudio Bruno, Denise Cassandrini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 11, 2011
Anti-N-methyl-D-aspartate-receptor encephalitis: cognitive profile in two childrenEnzo Iadisernia, Francesca Maria Battaglia, Elena Vanadia, et al.
European Journal of Radiology|April 15, 2004
Imaging in spine and spinal cord malformationsAndrea Rossi, Roberta Biancheri, Armando Cama, et al.
Neuropediatrics|December 21, 2012
Magnetic resonance imaging "tigroid pattern" in Alexander diseaseRoberta Biancheri, Andrea Rossi, Isabella Ceccherini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 27, 2007
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutationRoberta Biancheri, Andrea Rossi, Giannina Alpigiani, et al.
Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findingsAndrea Rossi, Roberta Biancheri, Claudio Bruno, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
Expanded spectrum of Pelizaeus-Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe formRoberta Biancheri, Camillo Rosano, Laura Denegri, et al.
European Journal of Medical Genetics|December 3, 2014
Heterozygous deletion of CHL1 gene: detailed array-CGH and clinical characterization of a new case and review of the literatureElisa Tassano, Roberta Biancheri, Laura Denegri, et al.
Journal of Child Neurology|August 18, 2012
Lack of SLC2A1 (glucose transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhoodElisa De Grandis, Michela Stagnaro, Roberta Biancheri, et al.
Pageof 7