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Italian Journal of Pediatrics
|
July 8, 2020
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' project
Elisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 3, 2020
Posterior Reversible Encephalopathy Syndrome in infants and young children
Duccio Maria Cordelli, Chiara Marra, Lara Ciampoli, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
February 3, 2020
Hazard identification of pyrogenic synthetic amorphous silica (NM-203) after sub-chronic oral exposure in rat: A multitarget approach
Roberta Tassinari, Gabriella Di Felice, Cinzia Butteroni, et al.
Epilepsia
|
March 6, 2026
Efficacy and safety of continuous midazolam infusion in the treatment of acute repetitive seizures in non-intensive settings: A multicenter retrospective real-world data study
Alessandro Orsini, Lorenza Marini, Luca Bergonzini, et al.
Journal of Tissue Viability
|
March 8, 2024
Complementing Braden scale for pressure ulcer risk with clinical and demographic-related factors in a large cohort of hospitalized Italian patients
Lorenzo Giovannoni, Yari Longobucco, Paolo Iovino, et al.
Seizure
|
August 10, 2024
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study
Luca Bergonzini, Davide Leardini, Roberta Rao, et al.
Human Molecular Genetics
|
February 22, 2014
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype
Pamela Magini, Tommaso Pippucci, I-Chun Tsai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 3, 2024
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience
Alessandro Orsini, Andrea Santangelo, Giorgio Costagliola, et al.
Human Genetics
|
June 4, 2020
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East
Flavia Palombo, Claudio Graziano, Nadia Al Wardy, et al.
Cancers
|
December 11, 2022
MRI- and Histologic-Molecular-Based Radio-Genomics Nomogram for Preoperative Assessment of Risk Classes in Endometrial Cancer
Veronica Celli, Michele Guerreri, Angelina Pernazza, et al.
Page
of 52
Search research articles
Search
Showing results (191-200 of 519) with videos related to
Sort By:
Page
of 52
Italian Journal of Pediatrics
|
July 8, 2020
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' project
Elisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 3, 2020
Posterior Reversible Encephalopathy Syndrome in infants and young children
Duccio Maria Cordelli, Chiara Marra, Lara Ciampoli, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
February 3, 2020
Hazard identification of pyrogenic synthetic amorphous silica (NM-203) after sub-chronic oral exposure in rat: A multitarget approach
Roberta Tassinari, Gabriella Di Felice, Cinzia Butteroni, et al.
Epilepsia
|
March 6, 2026
Efficacy and safety of continuous midazolam infusion in the treatment of acute repetitive seizures in non-intensive settings: A multicenter retrospective real-world data study
Alessandro Orsini, Lorenza Marini, Luca Bergonzini, et al.
Journal of Tissue Viability
|
March 8, 2024
Complementing Braden scale for pressure ulcer risk with clinical and demographic-related factors in a large cohort of hospitalized Italian patients
Lorenzo Giovannoni, Yari Longobucco, Paolo Iovino, et al.
Seizure
|
August 10, 2024
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study
Luca Bergonzini, Davide Leardini, Roberta Rao, et al.
Human Molecular Genetics
|
February 22, 2014
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype
Pamela Magini, Tommaso Pippucci, I-Chun Tsai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 3, 2024
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience
Alessandro Orsini, Andrea Santangelo, Giorgio Costagliola, et al.
Human Genetics
|
June 4, 2020
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East
Flavia Palombo, Claudio Graziano, Nadia Al Wardy, et al.
Cancers
|
December 11, 2022
MRI- and Histologic-Molecular-Based Radio-Genomics Nomogram for Preoperative Assessment of Risk Classes in Endometrial Cancer
Veronica Celli, Michele Guerreri, Angelina Pernazza, et al.
Page
of 52