PARANO, ENRICO
PARANO, ENRICO
CHIRURGIA GENERALE E SPECIALITA' MEDICO-CHIRURGICHE
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment
2017-01-01 Pavone, Piero; Praticò, Andrea Domenico; Rizzo, Renata; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Falsaperla, Raffaele
A novel GABRB3 variant in Dravet syndrome: Case report and literature review
2020-01-01 Pavone, P.; Pappalardo, X. G.; Marino, S. D.; Sciuto, L.; Corsello, G.; Ruggieri, M.; Parano, E.; Piccione, M.; Falsaperla, R.
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report
2023-01-01 Pavone, Piero; Falsaperla, Raffaele; Ruggieri, Martino; Marino, Simona Domenica; Parano, Enrico; Pappalardo, Xena Giada
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis
file da validare2010-01-01 Pavone, P; Pettoello-Mantovano, M; Le Pira, A; Giardino, I; Pulvirenti, A; Giugno, R; Parano, E; Polizzi, A; Distefano, A; Ferro, A; Pavone, L; Ruggieri, M.
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review
2022-01-01 Pavone, Piero; Pappalardo, Xena Giada; Ruggieri, Martino; Falsaperla, Raffaele; Parano, Enrico
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability
2022-01-01 Pavone, Piero; Pappalardo, XENA GIADA; Mustafa, Naira; Yoon Cho, Sung; Kyu Jin, Dong; Incorpora, Gemma; Falsaperla, Raffaele; Marino, SIMONA DOMENICA; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse
2016-01-01 Pavone, Vito; Lucenti, Ludovico; Testa, Gianluca; Pappalardo, Xena; Parano, Enrico
Blepharoptosis in children: Our experience at the light of literature
file da validare2010-01-01 Pavone, P.; Mackey, D. A.; Parano, E.; Barbagallo, M.; Praticò, Andrea Domenico; Trifiletti, R. R.
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
2020-01-01 Pavone, P.; Ruggieri, M.; Marino, S. D.; Corsello, G.; Pappalardo, X.; Polizzi, A.; Parano, E.; Romano, C.; Marino, S.; Pratico, A. D.; Falsaperla, R.
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review
2022-01-01 Pavone, V.; Vescio, A.; Lucenti, L.; Amico, M.; Caldaci, A.; Pappalardo, X. G.; Parano, E.; Testa, G.
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development
2023-01-01 Pappalardo, X. G.; Testa, G.; Pellitteri, R.; Dell'Albani, P.; Rodolico, M.; Pavone, V.; Parano, E.
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases
2022-01-01 Pavone, P.; Corsello, G.; Raucci, U.; Lubrano, R.; Parano, E.; Ruggieri, M.; Greco, F.; Marino, S.; Falsaperla, R.
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions
2022-01-01 Pavone, P; Pappalardo, Xg; Parano, E; Falsaperla, R; Marino, Sd; Fink, Jk; Ruggieri, M
HOLOPROSENCEPHALY (LOBAR FORM) ASSOCIATED WITH BILATERAL VOCAL CORD PALSY
2001-01-01 Smilari, P.; Serra, Agostino; LA MANTIA, Ignazio; Parano, Enrico; Pavone, Piero
HyperCKemia as a biomarker for muscular diseases
file da validare2010-01-01 Falsaperla, R.; Parano, E.; Romano, C.; Praticò, Andrea Domenico; Pavone, P.
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures
2020-01-01 Falsaperla, R.; Pappalardo, X. G.; Romano, C.; Marino, S. D.; Corsello, G.; Ruggieri, M.; Parano, E.; Pavone, P.
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review
2023-01-01 Pavone, Piero; Marino, Lidia; Cacciaguerra, Giovanni; Di Nora, Alessandra; Parano, Enrico; Musumeci, Giuseppe; Ruggieri, Martino; Polizzi, Agata; Falsaperla, Raffaele
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2
2020-01-01 Pavone, P.; Pappalardo, X. G.; Incorpora, G.; Falsaperla, R.; Marino, S. D.; Corsello, G.; Parano, E.; Ruggieri, M.
Mental retardation in muscular dystrophy: A study from Catania, Italy, with a review of the literature
file da validare1994-01-01 Trifiletti, R. R.; Falsaperla, R.; Fiumara, A.; Parano, E.; Pavone, L.
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome
2022-01-01 Pavone, Piero; Pappalardo, Xena Giada; Mustafa, Naira; Falsaperla, Raffaele; Marino, Simona Domenica; Corsello, Giovanni; Bianca, Sebastiano; Parano, Enrico; Ruggieri, Martino
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment | 1-gen-2017 | Pavone, Piero; Praticò, Andrea Domenico; Rizzo, Renata; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Falsaperla, Raffaele | |
| A novel GABRB3 variant in Dravet syndrome: Case report and literature review | 1-gen-2020 | Pavone, P.; Pappalardo, X. G.; Marino, S. D.; Sciuto, L.; Corsello, G.; Ruggieri, M.; Parano, E.; Piccione, M.; Falsaperla, R. | |
| A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report | 1-gen-2023 | Pavone, Piero; Falsaperla, Raffaele; Ruggieri, Martino; Marino, Simona Domenica; Parano, Enrico; Pappalardo, Xena Giada | |
| Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis | 1-gen-2010 | Pavone, P; Pettoello-Mantovano, M; Le Pira, A; Giardino, I; Pulvirenti, A; Giugno, R; Parano, E; Polizzi, A; Distefano, A; Ferro, A; Pavone, L; Ruggieri, M. | file da validare |
| Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review | 1-gen-2022 | Pavone, Piero; Pappalardo, Xena Giada; Ruggieri, Martino; Falsaperla, Raffaele; Parano, Enrico | |
| Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability | 1-gen-2022 | Pavone, Piero; Pappalardo, XENA GIADA; Mustafa, Naira; Yoon Cho, Sung; Kyu Jin, Dong; Incorpora, Gemma; Falsaperla, Raffaele; Marino, SIMONA DOMENICA; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino | |
| Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse | 1-gen-2016 | Pavone, Vito; Lucenti, Ludovico; Testa, Gianluca; Pappalardo, Xena; Parano, Enrico | |
| Blepharoptosis in children: Our experience at the light of literature | 1-gen-2010 | Pavone, P.; Mackey, D. A.; Parano, E.; Barbagallo, M.; Praticò, Andrea Domenico; Trifiletti, R. R. | 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. | |
| Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review | 1-gen-2022 | Pavone, V.; Vescio, A.; Lucenti, L.; Amico, M.; Caldaci, A.; Pappalardo, X. G.; Parano, E.; Testa, G. | |
| Early Life Stress (ELS) Effects on Fetal and Adult Bone Development | 1-gen-2023 | Pappalardo, X. G.; Testa, G.; Pellitteri, R.; Dell'Albani, P.; Rodolico, M.; Pavone, V.; Parano, E. | |
| Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases | 1-gen-2022 | Pavone, P.; Corsello, G.; Raucci, U.; Lubrano, R.; Parano, E.; Ruggieri, M.; Greco, F.; Marino, S.; Falsaperla, R. | |
| Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions | 1-gen-2022 | Pavone, P; Pappalardo, Xg; Parano, E; Falsaperla, R; Marino, Sd; Fink, Jk; Ruggieri, M | |
| HOLOPROSENCEPHALY (LOBAR FORM) ASSOCIATED WITH BILATERAL VOCAL CORD PALSY | 1-gen-2001 | Smilari, P.; Serra, Agostino; LA MANTIA, Ignazio; Parano, Enrico; Pavone, Piero | |
| HyperCKemia as a biomarker for muscular diseases | 1-gen-2010 | Falsaperla, R.; Parano, E.; Romano, C.; Praticò, Andrea Domenico; Pavone, P. | file da validare |
| Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures | 1-gen-2020 | Falsaperla, R.; Pappalardo, X. G.; Romano, C.; Marino, S. D.; Corsello, G.; Ruggieri, M.; Parano, E.; Pavone, P. | |
| Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review | 1-gen-2023 | Pavone, Piero; Marino, Lidia; Cacciaguerra, Giovanni; Di Nora, Alessandra; Parano, Enrico; Musumeci, Giuseppe; Ruggieri, Martino; Polizzi, Agata; Falsaperla, Raffaele | |
| Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 | 1-gen-2020 | Pavone, P.; Pappalardo, X. G.; Incorpora, G.; Falsaperla, R.; Marino, S. D.; Corsello, G.; Parano, E.; Ruggieri, M. | |
| Mental retardation in muscular dystrophy: A study from Catania, Italy, with a review of the literature | 1-gen-1994 | Trifiletti, R. R.; Falsaperla, R.; Fiumara, A.; Parano, E.; Pavone, L. | file da validare |
| Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome | 1-gen-2022 | Pavone, Piero; Pappalardo, Xena Giada; Mustafa, Naira; Falsaperla, Raffaele; Marino, Simona Domenica; Corsello, Giovanni; Bianca, Sebastiano; Parano, Enrico; Ruggieri, Martino |