Mario Mastrangelo

ResearcherID Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 14

Top Topics

Temporal Lobe Epilepsy

Top Venues

Children (Basel, Switzerland)

American journal of medical genetics. Part A

Neuropediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Mario Mastrangelo, Valentina Gasparri, Katerina Bernardi, Silvia Foglietta, Georgia Ramantani, Francesco Pisani
Epilepsy Phenotypes of Vitamin B6-Dependent Diseases: An Updated Systematic Review. Children (Basel, Switzerland) 10 (3) (2023)
Mario Mastrangelo, Manuela Tolve, Cristiana Artiola, Rossella Bove, Claudia Carducci, Carla Carducci, Antonio Angeloni, Francesco Pisani, Vincenzo Leuzzi
Phenotypes and Genotypes of Inherited Disorders of Biogenic Amine Neurotransmitter Metabolism. Genes 14 (2) (2023)
Mario Mastrangelo, Manuela Tolve, Cristiana Artiola, Rossella Bove, Claudia Carducci, Carla Carducci, Antonio Angeloni, Francesco Pisani, Vincenzo Leuzzi
Phenotypes and Genotypes of Inherited Disorders of Biogenic Amine Neurotransmitter Metabolism. Genes 14 (2) (2023)
Mario Mastrangelo, Valentina Gasparri, Katerina Bernardi, Silvia Foglietta, Georgia Ramantani, Francesco Pisani
Epilepsy Phenotypes of Vitamin B6-Dependent Diseases: An Updated Systematic Review. Children (Basel, Switzerland) 10 (3) (2023)
Mario Mastrangelo, Dario Esposito, Francesco Pisani
Sudden unexpected death in epilepsy: The need for age-specific evidence-based prevention. Developmental medicine and child neurology (2023)
Mario Mastrangelo, Manuela Tolve, Cristiana Artiola, Rossella Bove, Claudia Carducci, Carla Carducci, Antonio Angeloni, Francesco Pisani, Vincenzo Leuzzi
Phenotypes and Genotypes of Inherited Disorders of Biogenic Amine Neurotransmitter Metabolism. Genes 14 (2) (2023)
Silvia Leoncini, Lidia Boasiako, Diego Lopergolo, Maria Altamura, Caterina Fazzi, Roberto Canitano, Salvatore Grosso, Ilaria Meloni, Margherita Baldassarri, Susanna Croci, Alessandra Renieri, Mario Mastrangelo, Claudio De Felice
Natural Course of IQSEC2 -Related Encephalopathy: An Italian National Structured Survey. Children (Basel, Switzerland) 10 (9) (2023)
Mario Mastrangelo, Manuela Tolve, Cristiana Artiola, Rossella Bove, Claudia Carducci, Carla Carducci, Antonio Angeloni, Francesco Pisani, Vincenzo Leuzzi
Phenotypes and Genotypes of Inherited Disorders of Biogenic Amine Neurotransmitter Metabolism. Genes 14 (2) (2023)
Serena Cesario, Consuelo Basile, Matteo Trevisan, Federica Gigliotti, Filippo Manti, Rita Maria Esposito, Giuseppe Abbracciavento, Mario Mastrangelo
Loss of Continuity of Care in Pediatric Neurology Services during COVID-19 Lockdown: An Additional Stressor for Parents. Children (Basel, Switzerland) 9 (6) (2022)
Mario Mastrangelo, Valentina Baglioni
Management of Neurological Emergencies in Children: An Updated Overview. Neuropediatrics 52 (4) (2021)
Beatrice De Maria, Simona Balestrini, Davide Mei, Federico Melani, Simona Pellacani, Tiziana Pisano, Anna Rosati, Giusi M Scaturro, Lucio Giordano, Gaetano Cantalupo, Elena Fontana, Cristina Zammarchi, Edith Said, Vincenzo Leuzzi, Mario Mastrangelo, Serena Galosi, Elena Parrini, Renzo Guerrini
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy. American journal of medical genetics. Part A (2021)
Mario Mastrangelo, Chiara Commone, Carlo Greco, Vincenzo Leuzzi
TSC1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Child with a Mild Phenotype of Tuberous Sclerosis. Neuropediatrics 52 (2) (2021)
Mario Mastrangelo
Epilepsy in inherited neurotransmitter disorders: Spotlights on pathophysiology and clinical management. Metabolic brain disease 36 (1) (2020)
Mario Mastrangelo, Manuela Tolve, Martina Martinelli, Sofia P Di Noia, Elena Parrini, Vincenzo Leuzzi
PRICKLE1-related early onset epileptic encephalopathy. American journal of medical genetics. Part A 176 (12) (2018)