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Ferdinando Aliberti

Showing results (31-40 of 39) with videos related to

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European Journal of Medical Genetics|March 16, 2021
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndromeClaudia Santoro, Simona Riccio, Federica Palladino, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 25, 2021
Dural venous sinus anatomy in children with external hydrocephalus: analysis of a series of 97 patientsGiuseppe Cinalli, Giuliana di Martino, Carmela Russo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2021
Temporal lobe malformations, focal epilepsy, and FGFR3 mutations: a non-causal association?Pia Bernardo, Mauro Budetta, Ferdinando Aliberti, et al.
Journal of Neurosurgery. Pediatrics|December 23, 2017
Surgical treatment of thalamic tumors in childrenGiuseppe Cinalli, Daniel T Aguirre, Giuseppe Mirone, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 23, 2024
Correction: Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocolLucia De Martino, Peppino Mirabelli, Lucia Quaglietta, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 5, 2004
Imbalance of osteoclastogenesis-regulating factors in patients with celiac diseaseAnna Taranta, Dario Fortunati, Maurizio Longo, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 12, 2024
Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocolLucia De Martino, Peppino Mirabelli, Lucia Quaglietta, et al.
Diagnostics (Basel, Switzerland)|September 14, 2024
Neuroimaging in Nonsyndromic Craniosynostosis: Key Concepts to Unlock InnovationCamilla Russo, Ferdinando Aliberti, Ursula Pia Ferrara, et al.
Orphanet Journal of Rare Diseases|February 3, 2025
XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomesLothar Seefried, Ferdinando Aliberti, Cathrine Alsaker Heier, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
European Journal of Medical Genetics|March 16, 2021
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndromeClaudia Santoro, Simona Riccio, Federica Palladino, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 25, 2021
Dural venous sinus anatomy in children with external hydrocephalus: analysis of a series of 97 patientsGiuseppe Cinalli, Giuliana di Martino, Carmela Russo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2021
Temporal lobe malformations, focal epilepsy, and FGFR3 mutations: a non-causal association?Pia Bernardo, Mauro Budetta, Ferdinando Aliberti, et al.
Journal of Neurosurgery. Pediatrics|December 23, 2017
Surgical treatment of thalamic tumors in childrenGiuseppe Cinalli, Daniel T Aguirre, Giuseppe Mirone, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 23, 2024
Correction: Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocolLucia De Martino, Peppino Mirabelli, Lucia Quaglietta, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 5, 2004
Imbalance of osteoclastogenesis-regulating factors in patients with celiac diseaseAnna Taranta, Dario Fortunati, Maurizio Longo, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 12, 2024
Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocolLucia De Martino, Peppino Mirabelli, Lucia Quaglietta, et al.
Diagnostics (Basel, Switzerland)|September 14, 2024
Neuroimaging in Nonsyndromic Craniosynostosis: Key Concepts to Unlock InnovationCamilla Russo, Ferdinando Aliberti, Ursula Pia Ferrara, et al.
Orphanet Journal of Rare Diseases|February 3, 2025
XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomesLothar Seefried, Ferdinando Aliberti, Cathrine Alsaker Heier, et al.
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