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Anne Mandy

Showing results (41-50 of 61) with videos related to

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American Journal of Perinatology|March 5, 2013
Predictive factors of abdominal compartment syndrome in neonatal ageIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Italian Journal of Pediatrics|September 25, 2020
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patientEttore Piro, Gregorio Serra, Vincenzo Antona, et al.
Italian Journal of Pediatrics|August 13, 2022
Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosisGregorio Serra, Luigi Memo, Paola Cavicchioli, et al.
Italian Journal of Pediatrics|September 29, 2021
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-upGregorio Serra, Vincenzo Antona, Mario Giuffré, et al.
Italian Journal of Pediatrics|June 20, 2025
Congenital cytomegalovirus infection and brain injury in a newborn following maternal non-primary infection: case report of an unexpected diagnosisGregorio Serra, Ettore Piro, Deborah Bacile, et al.
Italian Journal of Pediatrics|October 16, 2020
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcomeGregorio Serra, Giovanni Corsello, Vincenzo Antona, et al.
BMC Complementary and Alternative Medicine|June 1, 2013
Patients' expectations of private osteopathic care in the UK: a national survey of patientsC M Janine Leach, Anne Mandy, Matthew Hankins, et al.
Italian Journal of Pediatrics|February 4, 2022
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case reportIngrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, et al.
Advances in Experimental Medicine and Biology|February 19, 2017
Genotyping and Antifungal Susceptibility of Dipodascus capitatus Isolated in a Neonatal Intensive Care Unit of a Sicilian HospitalTeresa Fasciana, Mario Giuffrè, Cinzia Calà, et al.
Italian Journal of Pediatrics|February 10, 2023
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conceptionGregorio Serra, Vincenzo Antona, Marcello Cimador, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

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Pageof 7
American Journal of Perinatology|March 5, 2013
Predictive factors of abdominal compartment syndrome in neonatal ageIngrid Anne Mandy Schierz, Mario Giuffrè, Ettore Piro, et al.
Italian Journal of Pediatrics|September 25, 2020
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patientEttore Piro, Gregorio Serra, Vincenzo Antona, et al.
Italian Journal of Pediatrics|August 13, 2022
Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosisGregorio Serra, Luigi Memo, Paola Cavicchioli, et al.
Italian Journal of Pediatrics|September 29, 2021
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-upGregorio Serra, Vincenzo Antona, Mario Giuffré, et al.
Italian Journal of Pediatrics|June 20, 2025
Congenital cytomegalovirus infection and brain injury in a newborn following maternal non-primary infection: case report of an unexpected diagnosisGregorio Serra, Ettore Piro, Deborah Bacile, et al.
Italian Journal of Pediatrics|October 16, 2020
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcomeGregorio Serra, Giovanni Corsello, Vincenzo Antona, et al.
BMC Complementary and Alternative Medicine|June 1, 2013
Patients' expectations of private osteopathic care in the UK: a national survey of patientsC M Janine Leach, Anne Mandy, Matthew Hankins, et al.
Italian Journal of Pediatrics|February 4, 2022
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case reportIngrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, et al.
Advances in Experimental Medicine and Biology|February 19, 2017
Genotyping and Antifungal Susceptibility of Dipodascus capitatus Isolated in a Neonatal Intensive Care Unit of a Sicilian HospitalTeresa Fasciana, Mario Giuffrè, Cinzia Calà, et al.
Italian Journal of Pediatrics|February 10, 2023
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conceptionGregorio Serra, Vincenzo Antona, Marcello Cimador, et al.
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