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

Alberto Spalice

Showing results (81-90 of 182) with videos related to

Pageof 19
Sort By:
European Journal of Pediatrics|December 12, 2025
Beyond endocrine features in non-classical congenital adrenal hyperplasia: a narrative review of psychoneuro-social perspectives in pediatric and adolescent patientsRoberto Paparella, Fabiola Panvino, Ida Pucarelli, et al.
Journal of Clinical Medicine|March 17, 2025
Polymerized Molecular Allergoid Alt a1: Effective SCIT in Pediatric Asthma PatientsGiulia Brindisi, Alessandra Gori, Caterina Anania, et al.
Brain & Development|January 1, 2013
Metabolic epilepsy: an updateLaura Papetti, Pasquale Parisi, Vincenzo Leuzzi, et al.
Pediatric Neurology|August 1, 2014
Novel mutations in the glycine receptor alpha subunit gene in two sisters with hyperekplexiaFabiana Ursitti, Fiorenza Ulgiati, Laura Papetti, et al.
Current Pediatric Reviews|November 30, 2021
Pediatrics for Disability: A Comprehensive Approach to Children with Syndromic Psychomotor DelayLuigi Tarani, Debora Rasio, Francesca Tarani, et al.
Allergy and Asthma Proceedings|September 2, 2020
Nasal reactivity evaluation in children with allergic rhinitis receiving grass pollen sublingual immunotherapyLaura Schiavi, Giulia Brindisi, Giovanna De Castro, et al.
Frontiers in Neurology|April 18, 2022
Case Report: Cerebral Venous Sinus Thrombosis in a Young Child With SARS-CoV-2 Infection: The Italian ExperiencePaola Silvestri, Anna Clemente, Alberto Spalice, et al.
Journal of Genetics|June 17, 2011
Novel missense mutation (L1917P) involving sac-domain of NSD1 gene in a patient with Sotos syndromeFrancesco Nicita, Luigi Tarani, Alberto Spalice, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1Martino Ruggieri, Mario Mastrangelo, Alberto Spalice, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 21, 2025
A novel NKX2-1 frameshift variant expanding the genetic landscape of benign hereditary choreaSimone Aloisio, Martina De Riggi, Adriana Martini, et al.
Pageof 19

Showing results (81-90 of 182) with videos related to

Sort By:
Pageof 19
European Journal of Pediatrics|December 12, 2025
Beyond endocrine features in non-classical congenital adrenal hyperplasia: a narrative review of psychoneuro-social perspectives in pediatric and adolescent patientsRoberto Paparella, Fabiola Panvino, Ida Pucarelli, et al.
Journal of Clinical Medicine|March 17, 2025
Polymerized Molecular Allergoid Alt a1: Effective SCIT in Pediatric Asthma PatientsGiulia Brindisi, Alessandra Gori, Caterina Anania, et al.
Brain & Development|January 1, 2013
Metabolic epilepsy: an updateLaura Papetti, Pasquale Parisi, Vincenzo Leuzzi, et al.
Pediatric Neurology|August 1, 2014
Novel mutations in the glycine receptor alpha subunit gene in two sisters with hyperekplexiaFabiana Ursitti, Fiorenza Ulgiati, Laura Papetti, et al.
Current Pediatric Reviews|November 30, 2021
Pediatrics for Disability: A Comprehensive Approach to Children with Syndromic Psychomotor DelayLuigi Tarani, Debora Rasio, Francesca Tarani, et al.
Allergy and Asthma Proceedings|September 2, 2020
Nasal reactivity evaluation in children with allergic rhinitis receiving grass pollen sublingual immunotherapyLaura Schiavi, Giulia Brindisi, Giovanna De Castro, et al.
Frontiers in Neurology|April 18, 2022
Case Report: Cerebral Venous Sinus Thrombosis in a Young Child With SARS-CoV-2 Infection: The Italian ExperiencePaola Silvestri, Anna Clemente, Alberto Spalice, et al.
Journal of Genetics|June 17, 2011
Novel missense mutation (L1917P) involving sac-domain of NSD1 gene in a patient with Sotos syndromeFrancesco Nicita, Luigi Tarani, Alberto Spalice, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1Martino Ruggieri, Mario Mastrangelo, Alberto Spalice, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 21, 2025
A novel NKX2-1 frameshift variant expanding the genetic landscape of benign hereditary choreaSimone Aloisio, Martina De Riggi, Adriana Martini, et al.
Pageof 19