Sfoglia per Autore
A New Patient with Potocki-Lupski Syndrome: A Literature Review
file da validare2018-01-01 Praticò, Andrea Domenico; Falsaperla, Raffaele; Rizzo, Renata; Ruggieri, Martino; Verrotti, Alberto; Pavone, Piero
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study
file da validare2018-01-01 Pratico, A. D.; Longo, L.; Mansueto, S.; Gozzo, L.; Barberi, I.; Tiralongo, V.; Salvo, V.; Falsaperla, R.; Vitaliti, G.; La Rosa, M.; Leonardi, S.; Rotondo, A.; Avola, N.; Sgarlata, D.; Damiano, A.; Tirantello, M.; Anzelmo, G.; Cipolla, D.; Rizzo, A.; Russo, A.; Ruggieri, M.; Salomone, S.; Drago, F.
Otorhinolaryngologic Findings in Pediatric Patients with Pandas
2018-01-01 Cocuzza, SALVATORE GIUSEPPE; Marino, Silvia; Yoon Cho, Sung; DI LUCA, Milena; Falsaperla, Raffaele Giuseppe; DI MAURO, Paola; Serra, Agostino; Jin, Dong-Kyu; Sabino, Luca; Pavone, Piero
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine
2018-01-01 Pavone, P; Praticò, Ad; Falsaperla, R; Striano, P; Ruggieri, M
Transverse cervical megapophysis as an uncommon cause of torticollis
2018-01-01 Pavone, Vito; Testa, Gianluca; Lucenti, Ludovico; Falsaperla, Raffaele; Sessa, Giuseppe
Ptosis in childhood: A clinical sign of several disorders: Case series reports and literature review
2018-01-01 Pavone, P.; Cho, Sung Yoon; Praticò, A. D.; Falsaperla, R.; Ruggieri, M.; Jin, Dong-Kyu
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
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome?
2019-01-01 Pavone, Piero; Falsaperla, Raffaele; Rizzo, Renata; Praticò, Andrea D.; Ruggieri, Martino
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi
2019-01-01 Marino, S.; Marino, S. D.; Praticò, A. D.; Marino, L.; Ruggieri, M.; Falsaperla, R.; Pavone, P.
E se non fossero solo incubi notturni?
2019-01-01 La Mendola, F. M. C.; Praticò, A. D.; Marino, S. D.; Cupitò, G.; Ruggieri, M.; Falsaperla, R.
Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome-Literature Review
file da validare2019-01-01 Pavone, P; Marino, Sd; Corsello, G; Ruggieri, M; Chiodo, Dc; Marino, S; Falsaperla, R
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis
2019-01-01 Pavone, Piero; Falsaperla, Raffaele; Marino, Silvia; Ruggieri, Martino; Praticò, Andrea D; Nardone, Beatrice
ENT involvement and orobuccal movements' disorders in Pandas patients: assessment and rehabilitations tools
2019-01-01 Cocuzza, S; Marino, S; Gulino, A; Pustorino, E; Murabito, P; Maniaci, A; Sabino, L; Taibi, R; Di Luca, M; Falsaperla, R; Campione, G; Vecchio, M; Pavone, P
Microcephaly/trigonocephaly, intellectual disability, autism spectrum disorder, and atypical dysmorphic features in a boy with Xp22.31 duplication
2019-01-01 Pavone, P.; Corsello, G.; Marino, S.; Ruggieri, M.; Falsaperla, R.
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?
2019-01-01 Pavone, P; Corsello, G; Cho, Sy; Pappalardo, Xg; Ruggieri, M; Marino, Sd; Jin, Dk; Marino, S; Falsaperla, R
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience
2019-01-01 Falsaperla, R.; Mauceri, L.; Pavone, P.; Barbagallo, M.; Vitaliti, G.; Ruggieri, M.; Pisani, F.; Corsello, G.
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review
2019-01-01 Pavone, P.; Corsello, G.; Marino, S. D.; Ruggieri, M.; Falsaperla, R.
A case of covid-19 with late-onset rash and transient loss of taste and smell in a 15-year-old boy
2020-01-01 Maniaci, A.; Iannella, G.; Vicini, C.; Pavone, P.; Nunnari, G.; Falsaperla, R.; Di Mauro, P.; Ferlito, S.; Cocuzza, S.
PANS/PANDAS: Clinical Experience in IVIG Treatment and State of the Art in Rehabilitation Approaches
2020-01-01 Pavone, Piero; Falsaperla, Raffaele Giuseppe; Cacciaguerra, Giovanni; Sapuppo, Annamaria; Chiaramonte, Rita; Lubrano, Riccardo; Messina, Giulia; Sciuto, Sarah; Sabino, Luca; Cocuzza, SALVATORE GIUSEPPE; Maniaci, Antonino; Fontana, Alessandra; Marino, Lidia; Oliva, CLAUDIA FRANCESCA; Grazia Pappalardo, Maria; Vecchio, Michele
Clinicoradiographic data and management of children with Chiari malformation type 1 and 1.5: an Italian case series
2020-01-01 Giallongo, A.; Pavone, P.; Tomarchio, S. P.; Filosco, F.; Falsaperla, R.; Testa, G.; Pavone, V.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A New Patient with Potocki-Lupski Syndrome: A Literature Review | 1-gen-2018 | Praticò, Andrea Domenico; Falsaperla, Raffaele; Rizzo, Renata; Ruggieri, Martino; Verrotti, Alberto; Pavone, Piero | file da validare |
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study | 1-gen-2018 | Pratico, A. D.; Longo, L.; Mansueto, S.; Gozzo, L.; Barberi, I.; Tiralongo, V.; Salvo, V.; Falsaperla, R.; Vitaliti, G.; La Rosa, M.; Leonardi, S.; Rotondo, A.; Avola, N.; Sgarlata, D.; Damiano, A.; Tirantello, M.; Anzelmo, G.; Cipolla, D.; Rizzo, A.; Russo, A.; Ruggieri, M.; Salomone, S.; Drago, F. | file da validare |
Otorhinolaryngologic Findings in Pediatric Patients with Pandas | 1-gen-2018 | Cocuzza, SALVATORE GIUSEPPE; Marino, Silvia; Yoon Cho, Sung; DI LUCA, Milena; Falsaperla, Raffaele Giuseppe; DI MAURO, Paola; Serra, Agostino; Jin, Dong-Kyu; Sabino, Luca; Pavone, Piero | |
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine | 1-gen-2018 | Pavone, P; Praticò, Ad; Falsaperla, R; Striano, P; Ruggieri, M | |
Transverse cervical megapophysis as an uncommon cause of torticollis | 1-gen-2018 | Pavone, Vito; Testa, Gianluca; Lucenti, Ludovico; Falsaperla, Raffaele; Sessa, Giuseppe | |
Ptosis in childhood: A clinical sign of several disorders: Case series reports and literature review | 1-gen-2018 | Pavone, P.; Cho, Sung Yoon; Praticò, A. D.; Falsaperla, R.; Ruggieri, M.; Jin, Dong-Kyu | |
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 | |
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? | 1-gen-2019 | Pavone, Piero; Falsaperla, Raffaele; Rizzo, Renata; Praticò, Andrea D.; Ruggieri, Martino | |
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi | 1-gen-2019 | Marino, S.; Marino, S. D.; Praticò, A. D.; Marino, L.; Ruggieri, M.; Falsaperla, R.; Pavone, P. | |
E se non fossero solo incubi notturni? | 1-gen-2019 | La Mendola, F. M. C.; Praticò, A. D.; Marino, S. D.; Cupitò, G.; Ruggieri, M.; Falsaperla, R. | |
Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome-Literature Review | 1-gen-2019 | Pavone, P; Marino, Sd; Corsello, G; Ruggieri, M; Chiodo, Dc; Marino, S; Falsaperla, R | file da validare |
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis | 1-gen-2019 | Pavone, Piero; Falsaperla, Raffaele; Marino, Silvia; Ruggieri, Martino; Praticò, Andrea D; Nardone, Beatrice | |
ENT involvement and orobuccal movements' disorders in Pandas patients: assessment and rehabilitations tools | 1-gen-2019 | Cocuzza, S; Marino, S; Gulino, A; Pustorino, E; Murabito, P; Maniaci, A; Sabino, L; Taibi, R; Di Luca, M; Falsaperla, R; Campione, G; Vecchio, M; Pavone, P | |
Microcephaly/trigonocephaly, intellectual disability, autism spectrum disorder, and atypical dysmorphic features in a boy with Xp22.31 duplication | 1-gen-2019 | Pavone, P.; Corsello, G.; Marino, S.; Ruggieri, M.; Falsaperla, R. | |
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? | 1-gen-2019 | Pavone, P; Corsello, G; Cho, Sy; Pappalardo, Xg; Ruggieri, M; Marino, Sd; Jin, Dk; Marino, S; Falsaperla, R | |
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience | 1-gen-2019 | Falsaperla, R.; Mauceri, L.; Pavone, P.; Barbagallo, M.; Vitaliti, G.; Ruggieri, M.; Pisani, F.; Corsello, G. | |
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review | 1-gen-2019 | Pavone, P.; Corsello, G.; Marino, S. D.; Ruggieri, M.; Falsaperla, R. | |
A case of covid-19 with late-onset rash and transient loss of taste and smell in a 15-year-old boy | 1-gen-2020 | Maniaci, A.; Iannella, G.; Vicini, C.; Pavone, P.; Nunnari, G.; Falsaperla, R.; Di Mauro, P.; Ferlito, S.; Cocuzza, S. | |
PANS/PANDAS: Clinical Experience in IVIG Treatment and State of the Art in Rehabilitation Approaches | 1-gen-2020 | Pavone, Piero; Falsaperla, Raffaele Giuseppe; Cacciaguerra, Giovanni; Sapuppo, Annamaria; Chiaramonte, Rita; Lubrano, Riccardo; Messina, Giulia; Sciuto, Sarah; Sabino, Luca; Cocuzza, SALVATORE GIUSEPPE; Maniaci, Antonino; Fontana, Alessandra; Marino, Lidia; Oliva, CLAUDIA FRANCESCA; Grazia Pappalardo, Maria; Vecchio, Michele | |
Clinicoradiographic data and management of children with Chiari malformation type 1 and 1.5: an Italian case series | 1-gen-2020 | Giallongo, A.; Pavone, P.; Tomarchio, S. P.; Filosco, F.; Falsaperla, R.; Testa, G.; Pavone, V. |
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