Is SARSCoV-2 nasopharyngeal swab still a gold standard in children?

Por Marino, Silvia, Ruggieri, Martino, Falsaperla, Raffaele
Publicado no Med Hypotheses (2020)

Neurocutaneous disorders phakomatoses and hamartoneoplastic syndromes

Por Ruggieri, Martino., Pascual-Castroviejo, Ignacio., Di Rocco, Concezio.
Publicado em 2008

Microcephaly/Trigonocephaly, Intellectual Disability, Autism Spectrum Disorder, and Atypical Dysmorphic Features in a Boy with Xp22.31 Duplication

Por Pavone, Piero, Corsello, Giovanni, Marino, Silvia, Ruggieri, Martino, Falsaperla, Raffaele
Publicado no Mol Syndromol (2019)

West Syndrome Treatment: New Roads for an Old Syndrome

Por Pavone, Piero, Falsaperla, Raffaele, Ruggieri, Martino, Praticò, Andrea Domenico, Pavone, Lorenzo
Publicado em 2013

Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity

Por Parano, Enrico, Pappalardo, Xena Giada, Pavone, Piero, Ruggieri, Martino, Cavallaro, Sebastiano
Publicado no Open Neurol J (2016)

Highlights on Genomics Applications for Lysosomal Storage Diseases

Por La Cognata, Valentina, Guarnaccia, Maria, Polizzi, Agata, Ruggieri, Martino, Cavallaro, Sebastiano
Publicado no Cells (2020)

Gluten Psychosis: Confirmation of a New Clinical Entity

Por Lionetti, Elena, Leonardi, Salvatore, Franzonello, Chiara, Mancardi, Margherita, Ruggieri, Martino, Catassi, Carlo
Publicado no Nutrients (2015)

Benign and severe early-life seizures: a round in the first year of life

Por Pavone, Piero, Corsello, Giovanni, Ruggieri, Martino, Marino, Silvia, Marino, Simona, Falsaperla, Raffaele
Publicado no Ital J Pediatr (2018)

Propranolol: Effectiveness and Failure in Infantile Cutaneous Hemangiomas

Por Praticò, Andrea Domenico, Caraci, Filippo, Pavone, Piero, Falsaperla, Raffaele, Drago, Filippo, Ruggieri, Martino
Publicado no Drug Saf Case Rep (2015)

Clinical spectrum of woolly hair: indications for cerebral involvement

Por Pavone, Piero, Falsaperla, Raffaele, Barbagallo, Massimo, Polizzi, Agata, Praticò, Andrea D., Ruggieri, Martino
Publicado no Ital J Pediatr (2017)

A New Patient with Potocki–Lupski Syndrome: A Literature Review

Por Praticò, Andrea Domenico, Falsaperla, Raffaele, Rizzo, Renata, Ruggieri, Martino, Verrotti, Alberto, Pavone, Piero
Publicado no J Pediatr Genet (2018)

Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis

Por Pavone, Piero, Falsaperla, Raffaele, Marino, Silvia, Ruggieri, Martino, Praticò, Andrea D., Nardone, Beatrice
Publicado no Pediatr Rep (2019)

Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype

Por Sapuppo, Annamaria, Pavone, Piero, Praticò, Andrea Domenico, Ruggieri, Martino, Bertino, Gaetano, Fiumara, Agata
Publicado no BMC Med Genet (2020)

Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes

Por Pavone, Piero, Praticò, Andrea D., Falsaperla, Raffaele, Ruggieri, Martino, Zollino, Marcella, Corsello, Giovanni, Neri, Giovanni
Publicado no Ital J Pediatr (2015)

Ataxia in children: early recognition and clinical evaluation

Por Pavone, Piero, Praticò, Andrea D., Pavone, Vito, Lubrano, Riccardo, Falsaperla, Raffaele, Rizzo, Renata, Ruggieri, Martino
Publicado no Ital J Pediatr (2017)

A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment

Por Pavone, Piero, Praticò, Andrea Domenico, Rizzo, Renata, Corsello, Giovanni, Ruggieri, Martino, Parano, Enrico, Falsaperla, Raffaele
Publicado no Medicine (Baltimore) (2017)

West syndrome: a comprehensive review

Por Pavone, Piero, Polizzi, Agata, Marino, Simona Domenica, Corsello, Giovanni, Falsaperla, Raffaele, Marino, Silvia, Ruggieri, Martino
Publicado no Neurol Sci (2020)

Short-Term Neurodevelopmental Outcome in Term Neonates Treated with Phenobarbital versus Levetiracetam: A Single-Center Experience

Por Falsaperla, Raffaele, Mauceri, Laura, Pavone, Piero, Barbagallo, Massimo, Vitaliti, Giovanna, Ruggieri, Martino, Pisani, Francesco, Corsello, Giovanni
Publicado no Behav Neurol (2019)

Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome—Literature Review

Por Pavone, Piero, Marino, Simona Domenica, Corsello, Giovanni, Ruggieri, Martino, Chiodo, Danilo Castellano, Marino, Silvia, Falsaperla, Raffaele
Publicado no J Pediatr Genet (2019)

Hemihydranencephaly: living with half brain dysfunction

Por Pavone, Piero, Nigro, Francesco, Falsaperla, Raffaele, Greco, Filippo, Ruggieri, Martino, Rizzo, Renata, Praticò, Andrea D, Pavone, Lorenzo
Publicado em 2013