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A. Praticò · SciRah

Researcher profile · Semantic Scholar

A. Praticò

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A. Praticò — researcher profile on SciRah

h-index: 37
Works: 180
Citations: 2,846

Most-cited papers

Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD
M. Nosadini, M. Eyre, Thea Giacomini, Massimiliano Valeriani +43 more
2022Neurology: Neuroimmunology & Neuroinflammation67 citations Open access
Semantic Scholar
Early history of the different forms of neurofibromatosis from ancient Egypt to the British Empire and beyond: First descriptions, medical curiosities, misconceptions, landmarks, and the persons behind the syndromes
M. Ruggieri, A. Praticò, R. Caltabiano, A. Polizzi
2018American Journal of Medical Genetics. Part A66 citations
Semantic Scholar
Introduction to phacomatoses (neurocutaneous disorders) in childhood
M. Ruggieri, A. Polizzi, G. P. Marceca, S. Catanzaro +2 more
2020Child's Nervous System58 citations
Semantic Scholar
Ketogenic diet for infants with epilepsy: A literature review.
R. Falsaperla, G. D'Angelo, A. Praticò, L. Mauceri +6 more
2020Epilepsy & Behavior56 citations
Semantic Scholar
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases
A. Fiumara, Giuseppina Lanzafame, A. Arena, A. Sapuppo +4 more
2020Journal of Clinical Medicine44 citations Open access
Semantic Scholar
A Probable Topiramate-Induced Limbs Paraesthesia and Rigid Fingers Flexion.
A. Praticò, M. Ruggieri, R. Falsaperla, P. Pavone
2018Current Drug Safety41 citations
Semantic Scholar
Neurocutaneous melanocytosis (melanosis)
M. Ruggieri, A. Polizzi, S. Catanzaro, M. L. Bianco +2 more
2020Child's Nervous System40 citations
Semantic Scholar
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype
A. Sapuppo, P. Pavone, A. Praticò, M. Ruggieri +2 more
2020BMC Medical Genetics35 citations Open access
Semantic Scholar
Graph theory in paediatric epilepsy: A systematic review
R. Falsaperla, G. Vitaliti, S. Marino, A. Praticò +5 more
2021Dialogues in Clinical Neuroscience32 citations Open access
Semantic Scholar
Ptosis in childhood: A clinical sign of several disorders
P. Pavone, S. Cho, A. Praticò, R. Falsaperla +2 more
2018Medicine31 citations Open access
Semantic Scholar
COVID-19 vaccination for children: may be necessary for the full eradication of the disease
A. Praticò, M. Ruggieri
2021Pediatric Research27 citations Open access
Semantic Scholar
COVID-19 pandemic for Pediatric Health Care: disadvantages and opportunities
A. Praticò
2020Pediatric Research27 citations Open access
Semantic Scholar
Case report: A gain-of-function of hamartin may lead to a distinct “inverse TSC1-hamartin” phenotype characterized by reduced cell growth
A. Praticò, R. Falsaperla, M. Comella, G. Belfiore +2 more
2023Frontiers in Pediatrics19 citations Open access
Semantic Scholar
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review
R. Falsaperla, L. Sciuto, L. La Spina, Sarah Sciuto +2 more
2021Metabolic brain disease18 citations Open access
Semantic Scholar
Megalencephaly Capillary Malformation Syndrome
A. Praticò, A. Polizzi, Stefania Salafia, E. Praticò +9 more
2018Journal of Pediatric Neurology online18 citations
Semantic Scholar
SCN2A and Its Related Epileptic Phenotypes
A. Praticò, Alessandro Giallongo, M. Arrabito, Silvia D'amico +5 more
2021Journal of Pediatric Neurology online16 citations
Semantic Scholar
Pediatric Lemierre’s Syndrome: A Comprehensive Literature Review
S. Lavalle, Edoardo Masiello, S. Cocuzza, P. Pavone +11 more
2024Pediatric Reports14 citations Open access
Semantic Scholar
Neurocutaneous syndromes in art and antiquities
M. Ruggieri, A. Gentile, Vincenza Ferrara, M. Papi +5 more
2021American Journal of Medical Genetics. Part C, Seminars in Medical Genetics9 citations Open access
Semantic Scholar
Magnetic Resonance Imaging of Central Nervous System Manifestations of Type 1 Neurofibromatosis: Pictorial Review and Retrospective Study of Their Frequency in a Cohort of Patients
Stefano Di Pietro, Linda Reali, Emanuela Tona, Giuseppe Belfiore +7 more
2024Journal of Clinical Medicine7 citations Open access
Semantic Scholar
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature
G. Leone, Concetta Meli, R. Falsaperla, Federica Gullo +12 more
2025Nutrients6 citations Open access
Semantic Scholar
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis
P. Pavone, X. Pappalardo, A. Praticò, A. Polizzi +4 more
2020Journal of Pediatric Genetics6 citations Open access
Semantic Scholar
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
P. Pavone, M. Ruggieri, S. Marino, G. Corsello +7 more
2020Molecular Genetics & Genomic Medicine6 citations Open access
Semantic Scholar
From abnormal fetal movements to neonatal seizures: A literature review.
R. Falsaperla, Martino Ruggieri, A. Polizzi, A. Praticò
2025Epilepsy Research5 citations Open access
Semantic Scholar
Investigating the Role of the Zinc Finger Protein ZC2HC1C on Autism Spectrum Disorder Susceptibility
Simone Treccarichi, M. Vinci, A. Musumeci, R. G. Rando +8 more
2025Medicina5 citations Open access
Semantic Scholar
The Impact of Vitamin D Supplementation Duration on Early Childhood Developmental Milestones: A Retrospective Study
A. Praticò, Manuela Lo Bianco, R. Leonardi, A. Polizzi +1 more
2024Nutrients5 citations
Semantic Scholar
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome?
P. Pavone, R. Falsaperla, R. Rizzo, A. Praticò +1 more
2019European Journal of Medical Genetics5 citations
Semantic Scholar
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome)
Federica Sullo, A. Praticò, A. Polizzi, S. Catanzaro +11 more
2018Journal of Pediatric Neurology online5 citations
Semantic Scholar
Congenital toxoplasmosis: an observational retrospective study in the Eastern Sicily
M. Garozzo, R. Garozzo, P. Betta, Salvatore Cilauro +14 more
2025Frontiers in Pediatrics4 citations Open access
Semantic Scholar
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up
M. Consentino, L. La Spina, Concetta Meli, Marianna Messina +9 more
2025Nutrients4 citations Open access
Semantic Scholar
The Spectrum of KCNQ2- and KCNQ3-Related Epilepsy
A. Portale, M. Comella, Giulia Salomone, A. Di Nora +4 more
2021Journal of Pediatric Neurology online4 citations
Semantic Scholar
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa
V. Venti, B. Scalia, A. Sauna, M. Nasca +5 more
2019Molecular Syndromology4 citations Open access
Semantic Scholar
Determinants of Rotavirus Vaccine Acceptance in an Area of Southern Italy with Low Vaccination Coverage: A Case-Control Study by the Health Belief Model Questionnaire
D. Anzà, Massimiliano Esposito, Giorgio Bertolazzi, A. Fallucca +6 more
2025Vaccines3 citations
Semantic Scholar
Genetic screening of tuberous sclerosis complex in Sicily with a focus on neurological manifestations
A. Praticò, C. Di Napoli, Stefania Salafia, Edoardo Dammino +10 more
2025Scientific Reports3 citations Open access
Semantic Scholar
Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
Vincenzo Sortino, A. Praticò, S. Marino, Roberta Criscione +3 more
2022Acta bio-medica : Atenei Parmensis3 citations
Semantic Scholar
GRIN2A and GRIN2B and Their Related Phenotypes
A. Sapuppo, Laura Portale, C. R. Massimino, S. Presti +5 more
2021Journal of Pediatric Neurology online3 citations
Semantic Scholar
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause–Effect Hypothesis
A. Fontana, F. Greco, P. Smilari, A. Praticò +3 more
2020Journal of Pediatric Neurology online3 citations
Semantic Scholar
Wyburn-Mason syndrome
Stefania Tomarchio, A. Portale, A. Praticò, S. Catanzaro +9 more
2018British medical journal3 citations
Semantic Scholar
Becker's Nevus Syndrome
M. Cucuzza, S. Paternò, D. Attardo, A. Praticò +13 more
2018Journal of Pediatric Neurology online3 citations
Semantic Scholar
Did Cro-Magnon 1 have neurofibromatosis type 2?
M. Ruggieri, A. Praticò, S. Catanzaro, S. Palmucci +1 more
2018The Lancet3 citations Open access
Semantic Scholar
Sleep Disorders in Pediatric Patients Affected by Neurofibromatosis Type 1: Reports of a Questionnaire and an Apple Watch Sleep Assessment
Alessia Migliore, Manuela Lo Bianco, R. Leonardi, Stefania Salafia +4 more
2025Biomedicines2 citations Open access
Semantic Scholar
Cardiac rhabdomyomas in tuberous sclerosis complex: clinical manifestations and genotype correlations
A. Praticò, Manuela Lo Bianco, A. Laganà, C. Di Napoli +4 more
2025BMC Pediatrics2 citations Open access
Semantic Scholar
Clinical, Genetic, EEG, Neuroimaging Insights and Conservative Treatment in Pediatric Focal Epilepsy: A Retrospective Observational Study
M. Gauci, Rosaria Gauci, Martino Ruggieri, A. Polizzi +1 more
2025Journal of Clinical Medicine2 citations Open access
Semantic Scholar
TSC1 and TSC2 : Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype
C. Di Napoli, Alessia Gennaro, C. Lupica, R. Falsaperla +6 more
2021Journal of Pediatric Neurology online2 citations
Semantic Scholar
SCN1A and Its Related Epileptic Phenotypes
Federica Sullo, Elisa Pasquetti, F. Patanè, Manuela Lo Bianco +6 more
2021Journal of Pediatric Neurology online2 citations
Semantic Scholar
SCN1B Gene: A Close Relative to SCN1A
Elisa Pasquetti, Manuela Lo Bianco, Federica Sullo, F. Patanè +5 more
2021Journal of Pediatric Neurology online2 citations
Semantic Scholar
Neurocutaneous Disorders
M. Ruggieri, A. Praticò, A. Polizzi
2020Textbook of Pediatric Neurosurgery2 citations
Semantic Scholar
Aicardi–Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations
A. Portale, Marina Mazzurco, Laura Portale, P. Pavone +4 more
2019Journal of Pediatric Neurology online2 citations
Semantic Scholar
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis
P. Pavone, R. Falsaperla, S. Marino, M. Ruggieri +2 more
2019Pediatric Reports2 citations Open access
Semantic Scholar
Eczema herpeticum in a patient with atopic dermatitis, coxsackie B virus, and staphylococcal infection: A double skin damage
A. Praticò, Valentina Fatuzzo, M. Cucuzza, Flavia C. La Mendola
20182 citations Open access
Semantic Scholar
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome)
M. Garozzo, D. Attardo, P. Smilari, F. Greco +10 more
2018Journal of Pediatric Neurology online2 citations
Semantic Scholar

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R. Falsaperla×19
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