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Piero Pavone

Showing results (31-40 of 255) with videos related to

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Molecular Syndromology|February 9, 2019
Microcephaly/Trigonocephaly, Intellectual Disability, Autism Spectrum Disorder, and Atypical Dysmorphic Features in a Boy with Xp22.31 DuplicationPiero Pavone, Giovanni Corsello, Silvia Marino, et al.
Journal of Orthopaedic Case Reports|October 21, 2017
Early Motor Delay: An Outstanding, Initial Sign of Osteogenesis Imperfecta Type 1Vito Pavone, Teresa Mattina, Piero Pavone, et al.
Journal of Pediatric Hematology/Oncology|September 19, 2008
Pseudohypoparathyroidism Ia with Evans syndromePiero Pavone, Andrea Domenico Praticò, Danilo Castellano-Chiodo, et al.
Expert Review of Respiratory Medicine|October 22, 2013
Noninvasive ventilation in pediatric emergency care: a literature review and description of our experienceGiovanna Vitaliti, Anette Wenzel, Francesco Bellia, et al.
Brain & Development|November 26, 2013
Infantile spasms syndrome, West syndrome and related phenotypes: what we know in 2013Piero Pavone, Pasquale Striano, Raffaele Falsaperla, et al.
Human Vaccines & Immunotherapeutics|March 11, 2014
Targeting inflammation as a therapeutic strategy for drug-resistant epilepsies: an update of new immune-modulating approachesGiovanna Vitaliti, Piero Pavone, Fahad Mahmood, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 14, 2012
Apneic crises: a clue for MECP2 testing in severe neonatal hypotonia-respiratory failureRaffaele Falsaperla, Lorenzo Pavone, Marco Fichera, 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.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 27, 2010
First case of dizygous twins with X-linked alpha-thalassemia/mental retardation syndrome showing wide clinical variabilityPiero Pavone, Rosaria Taibi, Elena Lionetti, 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.
Pageof 26

Showing results (31-40 of 255) with videos related to

Sort By:
Pageof 26
Molecular Syndromology|February 9, 2019
Microcephaly/Trigonocephaly, Intellectual Disability, Autism Spectrum Disorder, and Atypical Dysmorphic Features in a Boy with Xp22.31 DuplicationPiero Pavone, Giovanni Corsello, Silvia Marino, et al.
Journal of Orthopaedic Case Reports|October 21, 2017
Early Motor Delay: An Outstanding, Initial Sign of Osteogenesis Imperfecta Type 1Vito Pavone, Teresa Mattina, Piero Pavone, et al.
Journal of Pediatric Hematology/Oncology|September 19, 2008
Pseudohypoparathyroidism Ia with Evans syndromePiero Pavone, Andrea Domenico Praticò, Danilo Castellano-Chiodo, et al.
Expert Review of Respiratory Medicine|October 22, 2013
Noninvasive ventilation in pediatric emergency care: a literature review and description of our experienceGiovanna Vitaliti, Anette Wenzel, Francesco Bellia, et al.
Brain & Development|November 26, 2013
Infantile spasms syndrome, West syndrome and related phenotypes: what we know in 2013Piero Pavone, Pasquale Striano, Raffaele Falsaperla, et al.
Human Vaccines & Immunotherapeutics|March 11, 2014
Targeting inflammation as a therapeutic strategy for drug-resistant epilepsies: an update of new immune-modulating approachesGiovanna Vitaliti, Piero Pavone, Fahad Mahmood, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 14, 2012
Apneic crises: a clue for MECP2 testing in severe neonatal hypotonia-respiratory failureRaffaele Falsaperla, Lorenzo Pavone, Marco Fichera, 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.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 27, 2010
First case of dizygous twins with X-linked alpha-thalassemia/mental retardation syndrome showing wide clinical variabilityPiero Pavone, Rosaria Taibi, Elena Lionetti, 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.
Pageof 26