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Epilepsy & Behavior : E&B
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September 10, 2013
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosome
Maria 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 artery
Ettore 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 protocol
Maria 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 study
Giuseppe 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 microduplication
Maria 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 protocol
Maria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
Italian Journal of Pediatrics
|
April 13, 2013
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study
Giuseppe 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 findings
Maria Piccione, Emiliano Maresi, Marcella Zollino, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2008
10qter deletion: a new case
Maria 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 report
Sergio Salerno, Maria Chiara Terranova, Mario Rossello, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 74) with videos related to
Sort By:
Page
of 8
Epilepsy & Behavior : E&B
|
September 10, 2013
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosome
Maria 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 artery
Ettore 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 protocol
Maria 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 study
Giuseppe 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 microduplication
Maria 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 protocol
Maria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
Italian Journal of Pediatrics
|
April 13, 2013
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study
Giuseppe 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 findings
Maria Piccione, Emiliano Maresi, Marcella Zollino, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2008
10qter deletion: a new case
Maria 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 report
Sergio Salerno, Maria Chiara Terranova, Mario Rossello, et al.
Page
of 8