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Renzo Guerrini

Showing results (331-340 of 611) with videos related to

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Archives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.
Thescientificworldjournal|December 3, 2013
Medium-chain acyl-CoA deficiency: outlines from newborn screening, in silico predictions, and molecular studiesSerena Catarzi, Anna Caciotti, Janita Thusberg, et al.
European Radiology|September 5, 2020
Changes in appearance of cortical formation abnormalities in the foetus detected on sequential in utero MR imagingPaul D Griffiths, Mariasavina Severino, Deborah Jarvis, et al.
Biomedical Optics Express|July 5, 2021
Large-scale, cell-resolution volumetric mapping allows layer-specific investigation of human brain cytoarchitectureIrene Costantini, Giacomo Mazzamuto, Matteo Roffilli, et al.
Brain : a Journal of Neurology|September 15, 2012
Atypical face shape and genomic structural variants in epilepsyKrishna Chinthapalli, Emanuele Bartolini, Jan Novy, et al.
Endocrine Connections|August 30, 2024
Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literatureAlessandro Barbato, Giulia Gori, Michele Sacchini, et al.
Orphanet Journal of Rare Diseases|July 17, 2014
Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatmentCatia Cavicchi, Maria Donati, Rossella Parini, et al.
Epilepsia|April 17, 2015
Early and effective treatment of KCNQ2 encephalopathyTiziana Pisano, Adam L Numis, Sinéad B Heavin, et al.
Epilepsia|August 5, 2025
Is there really evidence for neurodegeneration in Dravet syndrome? Commentary on the publication by Selvarajah et alSanjay M Sisodiya, Simona Balestrini, Samuel F Berkovic, et al.
Neurology. Genetics|December 26, 2025
DNAJC12 Disease: Clinical Spectrum and Long-Term OutcomesFilippo Manti, Giacomina Ricciardi, Francesca Nardecchia, et al.
Pageof 62

Showing results (331-340 of 611) with videos related to

Sort By:
Pageof 62
Archives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.
Thescientificworldjournal|December 3, 2013
Medium-chain acyl-CoA deficiency: outlines from newborn screening, in silico predictions, and molecular studiesSerena Catarzi, Anna Caciotti, Janita Thusberg, et al.
European Radiology|September 5, 2020
Changes in appearance of cortical formation abnormalities in the foetus detected on sequential in utero MR imagingPaul D Griffiths, Mariasavina Severino, Deborah Jarvis, et al.
Biomedical Optics Express|July 5, 2021
Large-scale, cell-resolution volumetric mapping allows layer-specific investigation of human brain cytoarchitectureIrene Costantini, Giacomo Mazzamuto, Matteo Roffilli, et al.
Brain : a Journal of Neurology|September 15, 2012
Atypical face shape and genomic structural variants in epilepsyKrishna Chinthapalli, Emanuele Bartolini, Jan Novy, et al.
Endocrine Connections|August 30, 2024
Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literatureAlessandro Barbato, Giulia Gori, Michele Sacchini, et al.
Orphanet Journal of Rare Diseases|July 17, 2014
Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatmentCatia Cavicchi, Maria Donati, Rossella Parini, et al.
Epilepsia|April 17, 2015
Early and effective treatment of KCNQ2 encephalopathyTiziana Pisano, Adam L Numis, Sinéad B Heavin, et al.
Epilepsia|August 5, 2025
Is there really evidence for neurodegeneration in Dravet syndrome? Commentary on the publication by Selvarajah et alSanjay M Sisodiya, Simona Balestrini, Samuel F Berkovic, et al.
Neurology. Genetics|December 26, 2025
DNAJC12 Disease: Clinical Spectrum and Long-Term OutcomesFilippo Manti, Giacomina Ricciardi, Francesca Nardecchia, et al.
Pageof 62