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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 11, 2010
Ehlers-Danlos syndrome and neurological features: a reviewSalvatore Savasta, Pietro Merli, Martino Ruggieri, et al.
Therapeutic Hypothermia and Temperature Management|October 21, 2022
Prolonged Background Suppression Induced by Anticonvulsants Misleading Amplitude-Integrated Electroencephalography's Interpretation: A Single Case ReportRaffaele Falsaperla, Bruna Scalia, Emanuele A Liotta, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 28, 2017
Resuming the obsolete term "small head": when microcephaly occurs without cognitive impairmentPiero Pavone, Andrea D Praticò, Martino Ruggieri, et al.
European Journal of Medical Genetics|June 5, 2018
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome?Piero Pavone, Raffaele Falsaperla, Renata Rizzo, et al.
Cells|August 23, 2020
Highlights on Genomics Applications for Lysosomal Storage DiseasesValentina La Cognata, Maria Guarnaccia, Agata Polizzi, et al.
Frontiers in Chemistry|April 27, 2023
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanineMaria Anna Messina, Ludovica Maugeri, Giuseppe Forte, et al.
Epilepsy Research|November 11, 2019
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature reviewPiero Pavone, Giovanni Corsello, Simona Domenica Marino, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Scimitar vein anomaly with multiple cardiac malformations, craniofacial, and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome?Martino Ruggieri, Mauro Abbate, Enrico Parano, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 29, 2005
Callosal anomalies with interhemispheric cyst: expanding the phenotypePiero Pavone, Rita Barone, Sabrina Baieli, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2010
Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)Martino Ruggieri, Mario Roggini, Ingo Kennerknecht, et al.
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