PAPPALARDO, XENA GIADA
PAPPALARDO, XENA GIADA
Istituto di Scienze Neurologiche - ISN - Sede Secondaria Catania (soppressa) (attivo dal 01/01/1990 al 31/12/2023)
A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement
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
2025 Rizzo, Roberta; Fusto, Gaia; Marino, Serena; Castagnola, Iside; Parano, Claudia; Pappalardo, Xena Giada; Parano, Enrico
NRXN1-related disorders, attempt to better define clinical assessment
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
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
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
2023 Pappalardo, X. G.; Testa, G.; Pellitteri, R.; Dell'Albani, P.; Rodolico, M.; Pavone, V.; Parano, E.
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
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
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
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions
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
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
2020 Pavone, Piero; Pappalardo, XENA GIADA; D Marino, Simona; Sciuto, Laura; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Piccione, Maria; Falsaperla, Raffaele
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment
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
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
2020 Pavone, Piero; Pappalardo, XENA GIADA; Incorpora, Gemma; Falsaperla, Raffaele; Domenica Marino, Simona; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino
ABUSI SUI MINORI: CORRELAZIONI CLINICHE, GENETICHE ED EPIGENETICHE
2018 Parano, Enrico; Pappalardo, XENA GIADA
Child abuse and maltratment: clinical, genetic and epigenetic correlates.
2018 Pappalardo, XENA GIADA; Parano, Enrico; Pavone, Piero; Maria Fazio, Anna; Trovato, Graziella; Rapisarda, Giovanni; Fichera, Giuseppe; Cavallaro, Sebastiano
"Maltrattamenti e Abusi sui Minori: correlazioni cliniche, genetiche ed epigenetiche"
2016 Parano, Enrico; Pappalardo, XENA GIADA
Child abuse syndrome (CAS): A newly recognized distinct entity
2016 E. Parano; X.G. Pappalardo ; P. Pavone; M. Ruggieri; S. Cavallaro
Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity
2016 Parano, Enrico; Pappalardo, XENA GIADA; Pavone, Piero; Ruggieri, Martino; Cavallaro, Sebastiano
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES
2015 Parano, E; G Pappalardo, X; Pavone, P; Ruggieri, M; Cavallaro, S
| 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 | |
| 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. | |
| 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 | |
| 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 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 | |
| ABUSI SUI MINORI: CORRELAZIONI CLINICHE, GENETICHE ED EPIGENETICHE | 1-gen-2018 | Parano, Enrico; Pappalardo, XENA GIADA | |
| Child abuse and maltratment: clinical, genetic and epigenetic correlates. | 1-gen-2018 | Pappalardo, XENA GIADA; Parano, Enrico; Pavone, Piero; Maria Fazio, Anna; Trovato, Graziella; Rapisarda, Giovanni; Fichera, Giuseppe; Cavallaro, Sebastiano | |
| "Maltrattamenti e Abusi sui Minori: correlazioni cliniche, genetiche ed epigenetiche" | 1-gen-2016 | Parano, Enrico; Pappalardo, XENA GIADA | |
| Child abuse syndrome (CAS): A newly recognized distinct entity | 1-gen-2016 | E. Parano; X.G. Pappalardo ; P. Pavone; M. Ruggieri; S. Cavallaro | |
| Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity | 1-gen-2016 | Parano, Enrico; Pappalardo, XENA GIADA; Pavone, Piero; Ruggieri, Martino; Cavallaro, Sebastiano | |
| POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES | 1-gen-2015 | Parano, E; G Pappalardo, X; Pavone, P; Ruggieri, M; Cavallaro, S |