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Renzo Guerrini

Showing results (321-330 of 611) with videos related to

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Journal of Neural Engineering|April 29, 2026
Effective correction of extreme capacitive artifacts in TMS-EEG via windowed detrendingAlberto Arturo Vergani, Giulio Peroni, Camilla Bruscagli, et al.
Neurology|March 6, 2016
The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWSEmanuele Bartolini, Melania Falchi, Francesco Zellini, et al.
Molecular Genetics and Metabolism|February 9, 2021
Morquio B disease: From pathophysiology towards diagnosisAnna Caciotti, Lucrezia Cellai, Rodolfo Tonin, et al.
Clinical Chemistry and Laboratory Medicine|October 15, 2015
Development and validation of a 2nd tier test for identification of purine nucleoside phosphorylase deficiency patients during expanded newborn screening by liquid chromatography-tandem mass spectrometryGiancarlo la Marca, Elisa Giocaliere, Sabrina Malvagia, et al.
Epilepsia|January 24, 2004
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutationsPaolo Bonanni, Michela Malcarne, Francesca Moro, et al.
Cellular and Molecular Life Sciences : CMLS|February 25, 2022
Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylationLaura Di Patria, Giosuè Annibalini, Amelia Morrone, et al.
Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.
CNS Drugs|July 25, 2014
Off-label prescribing of antiepileptic drugs in pharmacoresistant epilepsy: a cross-sectional drug utilization study of tertiary care centers in ItalyValentina Franco, Maria Paola Canevini, Giuseppe Capovilla, et al.
Nature Genetics|December 3, 2003
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortexVolney L Sheen, Vijay S Ganesh, Meral Topcu, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 13, 2019
SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plusFrancesca Bisulli, Laura Licchetta, Sara Baldassari, et al.
Pageof 62

Showing results (321-330 of 611) with videos related to

Sort By:
Pageof 62
Journal of Neural Engineering|April 29, 2026
Effective correction of extreme capacitive artifacts in TMS-EEG via windowed detrendingAlberto Arturo Vergani, Giulio Peroni, Camilla Bruscagli, et al.
Neurology|March 6, 2016
The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWSEmanuele Bartolini, Melania Falchi, Francesco Zellini, et al.
Molecular Genetics and Metabolism|February 9, 2021
Morquio B disease: From pathophysiology towards diagnosisAnna Caciotti, Lucrezia Cellai, Rodolfo Tonin, et al.
Clinical Chemistry and Laboratory Medicine|October 15, 2015
Development and validation of a 2nd tier test for identification of purine nucleoside phosphorylase deficiency patients during expanded newborn screening by liquid chromatography-tandem mass spectrometryGiancarlo la Marca, Elisa Giocaliere, Sabrina Malvagia, et al.
Epilepsia|January 24, 2004
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutationsPaolo Bonanni, Michela Malcarne, Francesca Moro, et al.
Cellular and Molecular Life Sciences : CMLS|February 25, 2022
Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylationLaura Di Patria, Giosuè Annibalini, Amelia Morrone, et al.
Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.
CNS Drugs|July 25, 2014
Off-label prescribing of antiepileptic drugs in pharmacoresistant epilepsy: a cross-sectional drug utilization study of tertiary care centers in ItalyValentina Franco, Maria Paola Canevini, Giuseppe Capovilla, et al.
Nature Genetics|December 3, 2003
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortexVolney L Sheen, Vijay S Ganesh, Meral Topcu, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 13, 2019
SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plusFrancesca Bisulli, Laura Licchetta, Sara Baldassari, et al.
Pageof 62