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Sabina Barresi

Showing results (41-50 of 90) with videos related to

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Oncotarget|July 7, 2023
Intrathoracic synovial sarcoma with BRAF V600E mutationIda Russo, Sabina Barresi, Pier Luigi Di Paolo, et al.
Frontiers in Genetics|November 16, 2020
A Recurrent Pathogenic Variant of <i>INPP5K</i> Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern ItalyAdele D'Amico, Fabiana Fattori, Francesco Nicita, et al.
Virchows Archiv : an International Journal of Pathology|November 28, 2025
Novel HSPA8-NR4A2 rearrangement in extraskeletal myxoid chondrosarcoma: a sarcoma mimicker of neuroendocrine neoplasiaSabina Barresi, Roberto Passa, Silvia Vallese, et al.
Virchows Archiv : an International Journal of Pathology|December 5, 2024
Reappraisal of soft tissue myoepithelial tumors by DNA methylation profiling reveals an epigenetically distinct group of mostly fusion-driven neoplasmsFaizan Malik, Selene C Koo, Nasir Ud Din, et al.
Acta Neuropathologica Communications|June 13, 2023
Intracranial mesenchymal tumor with (novel) COX14::PTEN rearrangementAntonio d'Amati, Francesca Gianno, Luciana Scuccimarri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 30, 2011
The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in childrenAlessandra Terracciano, Florence Renaldo, Ginevra Zanni, et al.
Neurogenetics|April 26, 2018
The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genesLorena Travaglini, Chiara Aiello, Fabrizia Stregapede, et al.
Pediatric Neurology|December 15, 2019
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G MutationsSabina Barresi, Maria Lisa Dentici, Francesca Manzoni, et al.
Frontiers in Surgery|July 5, 2022
Rethinking the Management of Optic Pathway Gliomas: A Single Center ExperienceGiada Del Baldo, Antonella Cacchione, Vito Andrea Dell'Anna, et al.
Neurogenetics|January 1, 2013
Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotypeCarlo C Quattrocchi, Ginevra Zanni, Antonio Napolitano, et al.
Pageof 9

Showing results (41-50 of 90) with videos related to

Sort By:
Pageof 9
Oncotarget|July 7, 2023
Intrathoracic synovial sarcoma with BRAF V600E mutationIda Russo, Sabina Barresi, Pier Luigi Di Paolo, et al.
Frontiers in Genetics|November 16, 2020
A Recurrent Pathogenic Variant of <i>INPP5K</i> Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern ItalyAdele D'Amico, Fabiana Fattori, Francesco Nicita, et al.
Virchows Archiv : an International Journal of Pathology|November 28, 2025
Novel HSPA8-NR4A2 rearrangement in extraskeletal myxoid chondrosarcoma: a sarcoma mimicker of neuroendocrine neoplasiaSabina Barresi, Roberto Passa, Silvia Vallese, et al.
Virchows Archiv : an International Journal of Pathology|December 5, 2024
Reappraisal of soft tissue myoepithelial tumors by DNA methylation profiling reveals an epigenetically distinct group of mostly fusion-driven neoplasmsFaizan Malik, Selene C Koo, Nasir Ud Din, et al.
Acta Neuropathologica Communications|June 13, 2023
Intracranial mesenchymal tumor with (novel) COX14::PTEN rearrangementAntonio d'Amati, Francesca Gianno, Luciana Scuccimarri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 30, 2011
The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in childrenAlessandra Terracciano, Florence Renaldo, Ginevra Zanni, et al.
Neurogenetics|April 26, 2018
The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genesLorena Travaglini, Chiara Aiello, Fabrizia Stregapede, et al.
Pediatric Neurology|December 15, 2019
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G MutationsSabina Barresi, Maria Lisa Dentici, Francesca Manzoni, et al.
Frontiers in Surgery|July 5, 2022
Rethinking the Management of Optic Pathway Gliomas: A Single Center ExperienceGiada Del Baldo, Antonella Cacchione, Vito Andrea Dell'Anna, et al.
Neurogenetics|January 1, 2013
Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotypeCarlo C Quattrocchi, Ginevra Zanni, Antonio Napolitano, et al.
Pageof 9