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Showing results (331-340 of 347) with videos related to

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Epilepsy & Behavior : E&B|November 5, 2019
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up studyGiulia Iapadre, Luca Zagaroli, Nicola Cimini, et al.
Orphanet Journal of Rare Diseases|February 10, 2018
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapyRossella Parini, Paola De Lorenzo, Andrea Dardis, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 4, 2017
Parapelvic cysts, a distinguishing feature of renal Fabry diseaseAntonio Pisani, Luigi Petruzzelli Annicchiarico, Angela Pellegrino, et al.
Acta Neurologica Scandinavica|January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)S Matricardi, F Darra, A Spalice, et al.
Annals of Neurology|October 31, 2012
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsyRita Barone, Chiara Aiello, Valérie Race, et al.
Neuroradiology|April 8, 2017
Corpus callosum involvement: a useful clue for differentiating Fabry Disease from Multiple SclerosisSirio Cocozza, Gaia Olivo, Eleonora Riccio, et al.
Journal of Inherited Metabolic Disease|April 6, 2011
Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapyRenzo Manara, Elena Priante, Marco Grimaldi, et al.
Internal and Emergency Medicine|March 7, 2023
Acid sphingomyelinase deficiency (ASMD): addressing knowledge gaps in unmet needs and patient journey in Italy-a Delphi consensusMaurizio Scarpa, Antonio Barbato, Annalisa Bisconti, et al.
Molecular Genetics and Metabolism Reports|July 14, 2017
Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative groupD Concolino, L Amico, M D Cappellini, et al.
Cancers|October 14, 2022
BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-MakingFrancesco Pavese, Ettore Domenico Capoluongo, Margherita Muratore, et al.
Pageof 35

Showing results (331-340 of 347) with videos related to

Sort By:
Pageof 35
Epilepsy & Behavior : E&B|November 5, 2019
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up studyGiulia Iapadre, Luca Zagaroli, Nicola Cimini, et al.
Orphanet Journal of Rare Diseases|February 10, 2018
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapyRossella Parini, Paola De Lorenzo, Andrea Dardis, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 4, 2017
Parapelvic cysts, a distinguishing feature of renal Fabry diseaseAntonio Pisani, Luigi Petruzzelli Annicchiarico, Angela Pellegrino, et al.
Acta Neurologica Scandinavica|January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)S Matricardi, F Darra, A Spalice, et al.
Annals of Neurology|October 31, 2012
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsyRita Barone, Chiara Aiello, Valérie Race, et al.
Neuroradiology|April 8, 2017
Corpus callosum involvement: a useful clue for differentiating Fabry Disease from Multiple SclerosisSirio Cocozza, Gaia Olivo, Eleonora Riccio, et al.
Journal of Inherited Metabolic Disease|April 6, 2011
Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapyRenzo Manara, Elena Priante, Marco Grimaldi, et al.
Internal and Emergency Medicine|March 7, 2023
Acid sphingomyelinase deficiency (ASMD): addressing knowledge gaps in unmet needs and patient journey in Italy-a Delphi consensusMaurizio Scarpa, Antonio Barbato, Annalisa Bisconti, et al.
Molecular Genetics and Metabolism Reports|July 14, 2017
Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative groupD Concolino, L Amico, M D Cappellini, et al.
Cancers|October 14, 2022
BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-MakingFrancesco Pavese, Ettore Domenico Capoluongo, Margherita Muratore, et al.
Pageof 35