CNR Institutional Research Information System

PARANO, ENRICO

PARANO, ENRICO  

Istituto per la Ricerca e l'Innovazione Biomedica - IRIB - Sede Secondaria Catania  

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Risultati 1 - 20 di 98 (tempo di esecuzione: 0.044 secondi).
Titolo Data di pubblicazione Autore(i) File
A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement 1-gen-2025 Pavone, Piero; Pappalardo, Xena Giada; Scrofani, Francesca; Falsaperla, Raffaele; Pizzo, Francesco; Polizzi, Agata; Corsello, Antonio; Chiara Consentino, Maria; Parano, Enrico; Ruggieri, Martino
Molecular and Neurobiological Imbalance from the Use of Technological Devices During Early Child Development Stages 1-gen-2025 Rizzo, Roberta; Fusto, Gaia; Marino, Serena; Castagnola, Iside; Parano, Claudia; Pappalardo, Xena Giada; Parano, Enrico
The Many Faces of Child Abuse: How Clinical, Genetic and Epigenetic Correlates Help Us See the Full Picture 1-gen-2025 Parano, Enrico; Pavone, Vito; Ruggieri, Martino; Castagnola, Iside; Ettore, Giuseppe; Fusto, Gaia; Rizzo, Roberta; Pavone, Piero
NRXN1-related disorders, attempt to better define clinical assessment 1-gen-2024 Pavone, Piero; Pappalardo, Xena Giada; Parano, Claudia; Falsaperla, Raffaele; Corsello, Antonio; Parano, Enrico; Polizzi, Agata; Ruggieri, Martino
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
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 1-gen-2023 Pavone, Piero; Striano, Pasquale; Cacciaguerra, Giovanni; Domenica Marino, Simona; Parano, Enrico; Pappalardo, XENA GIADA; Falsaperla, Raffaele; Ruggieri, Martino
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.
of 1 Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 1-gen-2023 Piero Pavone; Lidia Marino; Giovanni Cacciaguerra; Alessandra Di Nora; Enrico Parano; Giuseppe Musumeci; Martino Ruggieri; Agata Polizzi; Raffaele Falsaperla
Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype-Phenotype Correlation 1-gen-2023 Pavone, Piero; Pappalardo, Xena Giada; Parano, Claudia; Parano, Enrico; Corsello, Antonio; Ruggieri, Martino; Cacciaguerra, Giovanni; Falsaperla, Raffaele
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; Domenica Marino, Simona; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 1-gen-2022 Vito Pavone; Andrea Vescio; Ludovico Lucenti; Mirko Amico; Alessia Caldaci; Xena Giada Pappalardo; Enrico Parano; Gianluca Testa
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases 1-gen-2022 Pavone Piero; Corsello Giovanni; Raucci Umberto; Lubrano Riccardo; Parano Enrico; Ruggieri Martino; Greco Filippo; Marino Silvia; Falsaperla Raffaele
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 1-gen-2022 Piero Pavone; Xena Giada Pappalardo; Enrico Parano; Raffaele Falsaperla; Simona Domenica Marino; John Kane Fink; Martino Ruggieri
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; Domenica Marino, Simona; Corsello, Giovanni; Bianca, Sebastiano; Parano, Enrico; Ruggieri, Martino
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 1-gen-2020 Pavone, Piero; Pappalardo, XENA GIADA; D Marino, Simona; Sciuto, Laura; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Piccione, Maria; 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 1-gen-2020 Pavone, Piero; Ruggieri, Martino; D Marino, Simona; Corsello, Giovanni; Pappalardo, Xena; Polizzi, Agata; Parano, Enrico; Romano, Catia; Marino, Silvia; Domenico Pratico, Andrea; Falsaperla, Raffaele
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment 1-gen-2020 Pavone, Piero; Pappalardo, XENA GIADA; Ngaobiri Nelly Ohazuruike, Ugochi; Striano, Pasquale; Parisi, Pasquale; Corsello, Giovanni; Domenica Marino, Simona; Ruggieri, Martino; Parano, Enrico; Falsaperla, Raffaele
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 1-gen-2020 Falsaperla, Raffaele; Pappalardo, XENA GIADA; Romano, Catia; Marino Simona, Domenica; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Parano, Piero
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, Piero; Pappalardo, XENA GIADA; Incorpora, Gemma; Falsaperla, Raffaele; Domenica Marino, Simona; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino
Severe psychotic symptoms in youth with PANS/PANDAS: case-series 1-gen-2020 Pavone, Piero; Parano, Enrico; Battaglia, Chiara; Marino, Silvia; Rich Trifiletti, Rosario; D Marino, Simona; Falsaperla, Raffaele