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Maria Piccione

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Epilepsy & Behavior : E&B|September 10, 2013
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosomeMaria Piccione, Davide Vecchio, Emanuela Salzano, et al.
Italian Journal of Pediatrics|May 16, 2013
Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral arteryEttore Piro, Maria Piccione, Gianluca Marrone, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
Italian Journal of Pediatrics|June 3, 2014
Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective studyGiuseppe Puccio, Mario Giuffré, Maria Piccione, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplicationMaria Piccione, Davide Vecchio, Simona Cavani, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
Italian Journal of Pediatrics|April 13, 2013
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological studyGiuseppe Puccio, Mario Giuffré, Maria Piccione, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Sex reversal from functional disomy of Xp: prenatal and post-mortem findingsMaria Piccione, Emiliano Maresi, Marcella Zollino, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
10qter deletion: a new caseMaria Piccione, Vincenzo Antona, Ettore Piro, et al.
Molecular and Clinical Oncology|April 18, 2017
Whole-body magnetic resonance imaging in the diagnosis and follow-up of multicentric infantile myofibromatosis: A case reportSergio Salerno, Maria Chiara Terranova, Mario Rossello, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Epilepsy & Behavior : E&B|September 10, 2013
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosomeMaria Piccione, Davide Vecchio, Emanuela Salzano, et al.
Italian Journal of Pediatrics|May 16, 2013
Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral arteryEttore Piro, Maria Piccione, Gianluca Marrone, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
Italian Journal of Pediatrics|June 3, 2014
Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective studyGiuseppe Puccio, Mario Giuffré, Maria Piccione, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplicationMaria Piccione, Davide Vecchio, Simona Cavani, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
Italian Journal of Pediatrics|April 13, 2013
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological studyGiuseppe Puccio, Mario Giuffré, Maria Piccione, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Sex reversal from functional disomy of Xp: prenatal and post-mortem findingsMaria Piccione, Emiliano Maresi, Marcella Zollino, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
10qter deletion: a new caseMaria Piccione, Vincenzo Antona, Ettore Piro, et al.
Molecular and Clinical Oncology|April 18, 2017
Whole-body magnetic resonance imaging in the diagnosis and follow-up of multicentric infantile myofibromatosis: A case reportSergio Salerno, Maria Chiara Terranova, Mario Rossello, et al.
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