ROMANO, CATIA
ROMANO, CATIA
MEDICINA CLINICA E SPERIMENTALE
ALDH7A1 Gene and Its Related Pyridoxine-Dependent Epilepsy
file da validare2021-01-01 La Mendola, Flavia Maria Consuelo; Timpanaro, Tiziana; Caruso, Daniela; Garozzo, Maria Teresa; Presti, Santiago; Romano, Catia; Praticò, Elena R.; Lombardo, Giulia; Zanghì, Antonio; Falsaperla, Raffaele
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy
file da validare2020-01-01 Pavone, P.; Ruggieri, M.; Marino, S. D.; Corsello, G.; Pappalardo, X.; Polizzi, A.; Parano, E.; Romano, C.; Marino, S.; Pratico, A. D.; Falsaperla, R.
Congenital muscular dystrophy and epilepsy: A prospective case series of pediatric patients
2016-01-01 Vitaliti, G.; Pavone, P.; Romano, C.; Barbagallo, M.; Vecchio, M.; Ledda, C.; Lubrano, R.; Falsaperla, R.
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study
2018-01-01 Falsaperla, Raffaele; Vitaliti, Giovanna; Collotta, Ausilia Desiree; Fiorillo, Chiara; Pulvirenti, Alfredo; Alaimo, Salvatore; Romano, Catia; Ruggieri, Martino
Gamma-aminobutyric acid type a receptor genes and their related epilepsies
file da validare2021-01-01 Musicoro, V. B.; Sortino, V.; Pecora, G.; Tosto, M.; Bianco, M. L.; Soma, R.; Romano, C.; Falsaperla, R.; Pratico, A. D.
HyperCKemia as a biomarker for muscular diseases
file da validare2010-01-01 Falsaperla, R.; Parano, E.; Romano, C.; Praticò, Andrea Domenico; Pavone, P.
Plexus Neuropathy in Infants Secondary to Arthro-Osteomyelitis: Report of 2 Cases and Review of the Literature
2012-01-01 Pavone, Vito; Politi, MARIA ROSARIA; Vecchio, Michele; Romano, Catia; Falsaperla, Raffaele Giuseppe; Pavone, Piero; Carboni, Roberta; Fanos, Vassilios
PRRT2 Related Epilepsies: A Gene Review
file da validare2021-01-01 Portale, Laura; Massimino, Carmela Rita; Sapuppo, Annamaria; Pizzo, Francesco; Sciuto, Laura; Romano, Catia; Salafia, Stefania; Falsaperla, Raffaele
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
ALDH7A1 Gene and Its Related Pyridoxine-Dependent Epilepsy | 1-gen-2021 | La Mendola, Flavia Maria Consuelo; Timpanaro, Tiziana; Caruso, Daniela; Garozzo, Maria Teresa; Presti, Santiago; Romano, Catia; Praticò, Elena R.; Lombardo, Giulia; Zanghì, Antonio; Falsaperla, Raffaele | file da validare |
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy | 1-gen-2020 | Pavone, P.; Ruggieri, M.; Marino, S. D.; Corsello, G.; Pappalardo, X.; Polizzi, A.; Parano, E.; Romano, C.; Marino, S.; Pratico, A. D.; Falsaperla, R. | file da validare |
Congenital muscular dystrophy and epilepsy: A prospective case series of pediatric patients | 1-gen-2016 | Vitaliti, G.; Pavone, P.; Romano, C.; Barbagallo, M.; Vecchio, M.; Ledda, C.; Lubrano, R.; Falsaperla, R. | |
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study | 1-gen-2018 | Falsaperla, Raffaele; Vitaliti, Giovanna; Collotta, Ausilia Desiree; Fiorillo, Chiara; Pulvirenti, Alfredo; Alaimo, Salvatore; Romano, Catia; Ruggieri, Martino | |
Gamma-aminobutyric acid type a receptor genes and their related epilepsies | 1-gen-2021 | Musicoro, V. B.; Sortino, V.; Pecora, G.; Tosto, M.; Bianco, M. L.; Soma, R.; Romano, C.; Falsaperla, R.; Pratico, A. D. | file da validare |
HyperCKemia as a biomarker for muscular diseases | 1-gen-2010 | Falsaperla, R.; Parano, E.; Romano, C.; Praticò, Andrea Domenico; Pavone, P. | file da validare |
Plexus Neuropathy in Infants Secondary to Arthro-Osteomyelitis: Report of 2 Cases and Review of the Literature | 1-gen-2012 | Pavone, Vito; Politi, MARIA ROSARIA; Vecchio, Michele; Romano, Catia; Falsaperla, Raffaele Giuseppe; Pavone, Piero; Carboni, Roberta; Fanos, Vassilios | |
PRRT2 Related Epilepsies: A Gene Review | 1-gen-2021 | Portale, Laura; Massimino, Carmela Rita; Sapuppo, Annamaria; Pizzo, Francesco; Sciuto, Laura; Romano, Catia; Salafia, Stefania; Falsaperla, Raffaele | file da validare |