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Renzo Guerrini

Showing results (231-240 of 611) with videos related to

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JIMD Reports|February 23, 2013
Newborn Screening for Tyrosinemia Type I: Further Evidence that Succinylacetone Determination on Blood Spot Is EssentialGiancarlo la Marca, Sabrina Malvagia, Elisabetta Pasquini, et al.
Developmental Medicine and Child Neurology|May 14, 2016
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancyCarmen Barba, Francesca Darra, Raffaella Cusmai, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1Stefanie Brock, Katrien Stouffs, Emmanuel Scalais, et al.
Brain : a Journal of Neurology|November 29, 2005
Periventricular nodular heterotopia with overlying polymicrogyriaGretchen Wieck, Richard J Leventer, Waney M Squier, et al.
Journal of Neuropsychology|August 30, 2018
Left inferior frontal cortex can compensate the inhibitory functions of right inferior frontal cortex and pre-supplementary motor areaGioele Gavazzi, Matteo Lenge, Emanuele Bartolini, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Computer-based automatic identification of neurons in gigavoxel-sized 3D human brain imagesPaolo Soda, Ludovica Acciai, Ermanno Cordelli, et al.
Epilepsia Open|October 8, 2023
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variantsNorman Panza, Claudia Bianchini, Valentina Cetica, et al.
Neuropediatrics|December 6, 2021
SLC7A3: In Silico Prediction of a Potential New Cause of Childhood EpilepsyJo Sourbron, Katrien Jansen, Davide Mei, et al.
Cerebellum (London, England)|January 17, 2017
Fast Progression of Cerebellar Atrophy in PLA2G6-Associated Infantile Neuronal Axonal DystrophyMario Mascalchi, Francesco Mari, Beatrice Berti, et al.
Orphanet Journal of Rare Diseases|March 3, 2026
Advancing clinical insight into creatine transporter deficiency: long term outcome and new observations from the Italian cohortMaria Grazia Alessandrì, Chiara Bosetti, Elena Scaffei, et al.
Pageof 62

Showing results (231-240 of 611) with videos related to

Sort By:
Pageof 62
JIMD Reports|February 23, 2013
Newborn Screening for Tyrosinemia Type I: Further Evidence that Succinylacetone Determination on Blood Spot Is EssentialGiancarlo la Marca, Sabrina Malvagia, Elisabetta Pasquini, et al.
Developmental Medicine and Child Neurology|May 14, 2016
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancyCarmen Barba, Francesca Darra, Raffaella Cusmai, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1Stefanie Brock, Katrien Stouffs, Emmanuel Scalais, et al.
Brain : a Journal of Neurology|November 29, 2005
Periventricular nodular heterotopia with overlying polymicrogyriaGretchen Wieck, Richard J Leventer, Waney M Squier, et al.
Journal of Neuropsychology|August 30, 2018
Left inferior frontal cortex can compensate the inhibitory functions of right inferior frontal cortex and pre-supplementary motor areaGioele Gavazzi, Matteo Lenge, Emanuele Bartolini, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Computer-based automatic identification of neurons in gigavoxel-sized 3D human brain imagesPaolo Soda, Ludovica Acciai, Ermanno Cordelli, et al.
Epilepsia Open|October 8, 2023
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variantsNorman Panza, Claudia Bianchini, Valentina Cetica, et al.
Neuropediatrics|December 6, 2021
SLC7A3: In Silico Prediction of a Potential New Cause of Childhood EpilepsyJo Sourbron, Katrien Jansen, Davide Mei, et al.
Cerebellum (London, England)|January 17, 2017
Fast Progression of Cerebellar Atrophy in PLA2G6-Associated Infantile Neuronal Axonal DystrophyMario Mascalchi, Francesco Mari, Beatrice Berti, et al.
Orphanet Journal of Rare Diseases|March 3, 2026
Advancing clinical insight into creatine transporter deficiency: long term outcome and new observations from the Italian cohortMaria Grazia Alessandrì, Chiara Bosetti, Elena Scaffei, et al.
Pageof 62