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Ettore Piro

Showing results (11-20 of 70) with videos related to

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Clinical Case Reports|February 16, 2018
Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first reportGregorio Serra, Vincenzo Antona, Mandy Schierz, et al.
American Journal of Perinatology|February 2, 2019
Methemoglobinemia Associated with Late-Onset Neonatal Sepsis: A Single-Center ExperienceIngrid Anne Mandy Schierz, Giuseppa Pinello, Ettore Piro, et al.
Italian Journal of Pediatrics|May 26, 2020
Neonatal ten-year retrospective study on neural tube defects in a second level University HospitalEttore Piro, Gregorio Serra, Ingrid Anne Mandy Schierz, et al.
Metabolites|November 26, 2024
Antioxidant Therapy in Neonatal Hypoxic Ischemic Encephalopathy: Adjuvant or Future Alternative to Therapeutic Hypothermia?Veronica Notarbartolo, Bintu Ayla Badiane, Vita Maria Angileri, 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.
Pediatrics|January 19, 2018
A Case of Cardiomyopathy Due to Premature Ductus Arteriosus Closure: The Flip Side of ParacetamolIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 18, 2020
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?Rosaria Nardello, Giuseppe Donato Mangano, Francesco Miceli, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
10qter deletion: a new caseMaria Piccione, Vincenzo Antona, Ettore Piro, et al.
Clinical Dysmorphology|May 21, 2020
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletionIngrid Anne Mandy Schierz, Gregorio Serra, Vincenzo Antona, et al.
Early Human Development|January 6, 2020
Congenital pelvic skeletal anomalies: Clinical and radiographic evaluation of newborns with gastrointestinal malformationIngrid Anne Mandy Schierz, Giuseppa Pinello, Ettore Piro, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
Clinical Case Reports|February 16, 2018
Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first reportGregorio Serra, Vincenzo Antona, Mandy Schierz, et al.
American Journal of Perinatology|February 2, 2019
Methemoglobinemia Associated with Late-Onset Neonatal Sepsis: A Single-Center ExperienceIngrid Anne Mandy Schierz, Giuseppa Pinello, Ettore Piro, et al.
Italian Journal of Pediatrics|May 26, 2020
Neonatal ten-year retrospective study on neural tube defects in a second level University HospitalEttore Piro, Gregorio Serra, Ingrid Anne Mandy Schierz, et al.
Metabolites|November 26, 2024
Antioxidant Therapy in Neonatal Hypoxic Ischemic Encephalopathy: Adjuvant or Future Alternative to Therapeutic Hypothermia?Veronica Notarbartolo, Bintu Ayla Badiane, Vita Maria Angileri, 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.
Pediatrics|January 19, 2018
A Case of Cardiomyopathy Due to Premature Ductus Arteriosus Closure: The Flip Side of ParacetamolIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 18, 2020
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?Rosaria Nardello, Giuseppe Donato Mangano, Francesco Miceli, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
10qter deletion: a new caseMaria Piccione, Vincenzo Antona, Ettore Piro, et al.
Clinical Dysmorphology|May 21, 2020
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletionIngrid Anne Mandy Schierz, Gregorio Serra, Vincenzo Antona, et al.
Early Human Development|January 6, 2020
Congenital pelvic skeletal anomalies: Clinical and radiographic evaluation of newborns with gastrointestinal malformationIngrid Anne Mandy Schierz, Giuseppa Pinello, Ettore Piro, et al.
Pageof 7