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Piero Pavone

Showing results (151-160 of 255) with videos related to

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European Journal of Medical Genetics|March 17, 2016
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent featuresPiero Pavone, Andrea Domenico Praticò, Giulia Gentile, et al.
Italian Journal of Pediatrics|September 1, 2016
Congenital muscular dystrophy: from muscle to brainRaffaele Falsaperla, Andrea D Praticò, Martino Ruggieri, et al.
Acta Orthopaedica|April 12, 2012
Congenital talipes equinovarus: an epidemiological study in SicilyVito Pavone, Sebastiano Bianca, Giuseppe Grosso, et al.
Italian Journal of Pediatrics|December 16, 2022
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new casesPiero Pavone, Giovanni Corsello, Umberto Raucci, et al.
Pediatric Neurology|February 13, 2021
Ocular Motor Paroxysmal Events in Neonates and Infants: A Review of the LiteratureRaffaele Falsaperla, Marco Andrea Nicola Saporito, Francesco Pisani, et al.
European Journal of Medical Genetics|October 4, 2012
Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlationTeresa Mattina, Orazio Palumbo, Raffaella Stallone, et al.
Journal of Pediatric Genetics|July 28, 2020
Primary Microcephaly with Novel Variant of <i>MCPH1</i> Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's ThyroiditisPiero Pavone, Xena Giada Pappalardo, Andrea Domenico Praticò, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 23, 2009
Recurrent obstructive hydrocephalus in a 4-month-old infantDanilo Castellano-Chiodo, Piero Pavone, Andrea Domenico Praticò, et al.
Frontiers in Pediatrics|October 12, 2020
Intronic Variant in <i>CNTNAP2</i> Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and SeizuresRaffaele Falsaperla, Xena Giada Pappalardo, Catia Romano, et al.
World Neurosurgery|February 25, 2019
Grisel Syndrome in Pediatric Age: A Single-Center Italian Experience and Review of the LiteraturePasquale Anania, Piero Pavone, Mattia Pacetti, et al.
Pageof 26

Showing results (151-160 of 255) with videos related to

Sort By:
Pageof 26
European Journal of Medical Genetics|March 17, 2016
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent featuresPiero Pavone, Andrea Domenico Praticò, Giulia Gentile, et al.
Italian Journal of Pediatrics|September 1, 2016
Congenital muscular dystrophy: from muscle to brainRaffaele Falsaperla, Andrea D Praticò, Martino Ruggieri, et al.
Acta Orthopaedica|April 12, 2012
Congenital talipes equinovarus: an epidemiological study in SicilyVito Pavone, Sebastiano Bianca, Giuseppe Grosso, et al.
Italian Journal of Pediatrics|December 16, 2022
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new casesPiero Pavone, Giovanni Corsello, Umberto Raucci, et al.
Pediatric Neurology|February 13, 2021
Ocular Motor Paroxysmal Events in Neonates and Infants: A Review of the LiteratureRaffaele Falsaperla, Marco Andrea Nicola Saporito, Francesco Pisani, et al.
European Journal of Medical Genetics|October 4, 2012
Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlationTeresa Mattina, Orazio Palumbo, Raffaella Stallone, et al.
Journal of Pediatric Genetics|July 28, 2020
Primary Microcephaly with Novel Variant of <i>MCPH1</i> Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's ThyroiditisPiero Pavone, Xena Giada Pappalardo, Andrea Domenico Praticò, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 23, 2009
Recurrent obstructive hydrocephalus in a 4-month-old infantDanilo Castellano-Chiodo, Piero Pavone, Andrea Domenico Praticò, et al.
Frontiers in Pediatrics|October 12, 2020
Intronic Variant in <i>CNTNAP2</i> Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and SeizuresRaffaele Falsaperla, Xena Giada Pappalardo, Catia Romano, et al.
World Neurosurgery|February 25, 2019
Grisel Syndrome in Pediatric Age: A Single-Center Italian Experience and Review of the LiteraturePasquale Anania, Piero Pavone, Mattia Pacetti, et al.
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