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Anne Mandy

Showing results (31-40 of 61) with videos related to

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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 18, 2017
Transitional hemodynamics in infants of diabetic mothers by targeted neonatal echocardiography, electrocardiography and peripheral flow studyIngrid Anne Mandy Schierz, Giuseppa Pinello, Ettore Piro, et al.
Italian Journal of Pediatrics|February 20, 2020
Recognizable neonatal clinical features of aplasia cutis congenitaIngrid Anne Mandy Schierz, Mario Giuffrè, Antonello Del Vecchio, et al.
Italian Journal of Pediatrics|August 24, 2018
Clinical cardiac assessment in newborns with prenatally diagnosed intrathoracic massesIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Italian Journal of Pediatrics|March 5, 2022
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profilesGregorio Serra, Vincenzo Antona, Mario Giuffrè, et al.
Italian Journal of Pediatrics|July 29, 2022
Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorderIngrid Anne Mandy Schierz, Salvatore Amoroso, Vincenzo Antona, et al.
Italian Journal of Pediatrics|July 29, 2022
Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 geneGregorio Serra, Vincenzo Antona, Chiara Cannata, et al.
Italian Journal of Pediatrics|September 19, 2020
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutationEttore Piro, Ingrid Anne Mandy Schierz, Vincenzo Antona, et al.
Italian Journal of Pediatrics|September 19, 2020
Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case reportIngrid Anne Mandy Schierz, Marcello Cimador, Mario Giuffrè, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 5, 2022
Clinical and genetic approach in the characterization of newborns with anorectal malformationIngrid Anne Mandy Schierz, Ettore Piro, Mario Giuffrè, et al.
Italian Journal of Pediatrics|November 15, 2021
Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center StudyGiovanni Savarino, Maurizio Carta, Marcello Cimador, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 18, 2017
Transitional hemodynamics in infants of diabetic mothers by targeted neonatal echocardiography, electrocardiography and peripheral flow studyIngrid Anne Mandy Schierz, Giuseppa Pinello, Ettore Piro, et al.
Italian Journal of Pediatrics|February 20, 2020
Recognizable neonatal clinical features of aplasia cutis congenitaIngrid Anne Mandy Schierz, Mario Giuffrè, Antonello Del Vecchio, et al.
Italian Journal of Pediatrics|August 24, 2018
Clinical cardiac assessment in newborns with prenatally diagnosed intrathoracic massesIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Italian Journal of Pediatrics|March 5, 2022
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profilesGregorio Serra, Vincenzo Antona, Mario Giuffrè, et al.
Italian Journal of Pediatrics|July 29, 2022
Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorderIngrid Anne Mandy Schierz, Salvatore Amoroso, Vincenzo Antona, et al.
Italian Journal of Pediatrics|July 29, 2022
Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 geneGregorio Serra, Vincenzo Antona, Chiara Cannata, et al.
Italian Journal of Pediatrics|September 19, 2020
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutationEttore Piro, Ingrid Anne Mandy Schierz, Vincenzo Antona, et al.
Italian Journal of Pediatrics|September 19, 2020
Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case reportIngrid Anne Mandy Schierz, Marcello Cimador, Mario Giuffrè, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 5, 2022
Clinical and genetic approach in the characterization of newborns with anorectal malformationIngrid Anne Mandy Schierz, Ettore Piro, Mario Giuffrè, et al.
Italian Journal of Pediatrics|November 15, 2021
Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center StudyGiovanni Savarino, Maurizio Carta, Marcello Cimador, et al.
Pageof 7