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Emanuele Panza

Showing results (1-10 of 33) with videos related to

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International Journal of Molecular Sciences|March 13, 2025
Biomarkers in Hereditary Spastic ParaplegiasEmanuele Panza, Antonio Orlacchio
Experimental Neurology|August 15, 2022
Hereditary spastic paraplegia: Genetic heterogeneity and common pathwaysEmanuele Panza, Arun Meyyazhagan, Antonio Orlacchio
Expert Review of Proteomics|October 3, 2023
Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanismsChiara Martinello, Emanuele Panza, Antonio Orlacchio
International Journal of Molecular Sciences|September 14, 2024
Experimental Cell Models for Investigating Neurodegenerative DiseasesCecilia Evangelisti, Sherin Ramadan, Antonio Orlacchio, et al.
Nature Reviews. Gastroenterology & Hepatology|February 13, 2013
New perspectives in the diagnosis and management of enteric neuropathiesCharles H Knowles, Greger Lindberg, Emanuele Panza, et al.
Frontiers in Neurology|March 12, 2019
Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle MetabolismEmanuele Panza, Diego Martinelli, Pamela Magini, et al.
Molecular Syndromology|September 9, 2020
Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p MosaicismReha M Toydemir, Emanuele Panza, Maria C Longhurst, et al.
Thrombosis and Haemostasis|August 12, 2011
Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cellsAlessandro Pecci, Valeria Bozzi, Emanuele Panza, et al.
Acta Diabetologica|October 17, 2024
Effects of APOE isoforms in diabetic nephropathy patients of South IndiaPreethi Basavaraju, Puthamohan Vinayaga Moorthi, Arun Meyyazhagan, et al.
Frontiers in Genetics|February 27, 2023
Case report: Functional characterization of a novel <i>CHD7</i> intronic variant in patients with CHARGE syndromeCesare Rossi, Sherin Ramadan, Cecilia Evangelisti, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
International Journal of Molecular Sciences|March 13, 2025
Biomarkers in Hereditary Spastic ParaplegiasEmanuele Panza, Antonio Orlacchio
Experimental Neurology|August 15, 2022
Hereditary spastic paraplegia: Genetic heterogeneity and common pathwaysEmanuele Panza, Arun Meyyazhagan, Antonio Orlacchio
Expert Review of Proteomics|October 3, 2023
Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanismsChiara Martinello, Emanuele Panza, Antonio Orlacchio
International Journal of Molecular Sciences|September 14, 2024
Experimental Cell Models for Investigating Neurodegenerative DiseasesCecilia Evangelisti, Sherin Ramadan, Antonio Orlacchio, et al.
Nature Reviews. Gastroenterology & Hepatology|February 13, 2013
New perspectives in the diagnosis and management of enteric neuropathiesCharles H Knowles, Greger Lindberg, Emanuele Panza, et al.
Frontiers in Neurology|March 12, 2019
Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle MetabolismEmanuele Panza, Diego Martinelli, Pamela Magini, et al.
Molecular Syndromology|September 9, 2020
Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p MosaicismReha M Toydemir, Emanuele Panza, Maria C Longhurst, et al.
Thrombosis and Haemostasis|August 12, 2011
Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cellsAlessandro Pecci, Valeria Bozzi, Emanuele Panza, et al.
Acta Diabetologica|October 17, 2024
Effects of APOE isoforms in diabetic nephropathy patients of South IndiaPreethi Basavaraju, Puthamohan Vinayaga Moorthi, Arun Meyyazhagan, et al.
Frontiers in Genetics|February 27, 2023
Case report: Functional characterization of a novel <i>CHD7</i> intronic variant in patients with CHARGE syndromeCesare Rossi, Sherin Ramadan, Cecilia Evangelisti, et al.
Pageof 4