Cargando…

Management of multiple pregnancy with an affected twin

Detalles Bibliográficos
Autores principales:	Giuffrè, Mario, Vecchio, Davide, Placa, Simona La, Pinello, Giuseppa, Piro, Ettore, MandySchierz, Ingrid Anne, Corsello, Giovanni
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Meeting Abstract
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595033/ http://dx.doi.org/10.1186/1824-7288-41-S1-A17

Ejemplares similares

Clinical cardiac assessment in newborns with prenatally diagnosed intrathoracic masses
por: Schierz, Ingrid Anne Mandy, et al.
Publicado: (2018)

An unusual association of left‐sided gastroschisis and persistent right umbilical vein
por: Schierz, Ingrid Anne Mandy, et al.
Publicado: (2018)

Growth patterns and associated risk factors of congenital malformations in twins
por: Piro, Ettore, et al.
Publicado: (2020)

Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report
por: Serra, Gregorio, et al.
Publicado: (2018)

Recognizable neonatal clinical features of aplasia cutis congenita
por: Schierz, Ingrid Anne Mandy, et al.
Publicado: (2020)

Etiological heterogeneity and clinical variability in newborns with esophageal atresia
por: Piro, Ettore, et al.
Publicado: (2018)

Neonatal ten-year retrospective study on neural tube defects in a second level University Hospital
por: Piro, Ettore, et al.
Publicado: (2020)

Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective study
por: Puccio, Giuseppe, et al.
Publicado: (2014)

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 profiles
por: Serra, Gregorio, et al.
Publicado: (2022)

Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 gene
por: Serra, Gregorio, et al.
Publicado: (2022)

Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder
por: Schierz, Ingrid Anne Mandy, et al.
Publicado: (2022)

Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case report
por: Schierz, Ingrid Anne Mandy, et al.
Publicado: (2020)

Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutation
por: Piro, Ettore, et al.
Publicado: (2020)

Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patient
por: Piro, Ettore, et al.
Publicado: (2020)

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-up
por: Serra, Gregorio, et al.
Publicado: (2021)

Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene
por: Serra, Gregorio, et al.
Publicado: (2022)

Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome
por: Serra, Gregorio, et al.
Publicado: (2020)

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 report
por: Schierz, Ingrid Anne Mandy, et al.
Publicado: (2022)

New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception
por: Serra, Gregorio, et al.
Publicado: (2023)

Report and follow-up on two new patients with congenital mesoblastic nephroma
por: Serra, Gregorio, et al.
Publicado: (2023)

Intellectual disabilitiy in developmental age
por: Giuffrè, Mario, et al.
Publicado: (2015)

Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restriction
por: Serra, Gregorio, et al.
Publicado: (2022)

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome
por: Serra, Gregorio, et al.
Publicado: (2022)

Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center Study
por: Savarino, Giovanni, et al.
Publicado: (2021)

The social role of pediatrics in the past and present times
por: Serra, Gregorio, et al.
Publicado: (2021)

Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins
por: Giuffrè, Mario, et al.
Publicado: (2011)

Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
por: Serra, Gregorio, et al.
Publicado: (2022)

Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery
por: Piro, Ettore, et al.
Publicado: (2013)

Congenital cytomegalovirus related intestinal malrotation: a case report
por: Colomba, Claudia, et al.
Publicado: (2016)

Analysis of risk and prognostic factors in a population of pediatric patients hospitalized for acute malnutrition at the Chiulo hospital, Angola
por: Tripoli, Federica Maria, et al.
Publicado: (2021)

Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study
por: Puccio, Giuseppe, et al.
Publicado: (2013)

Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene
por: Serra, Gregorio, et al.
Publicado: (2022)

Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?
por: La Placa, Simona, et al.
Publicado: (2013)

Germinal matrix hemorrhage-intraventricular hemorrhage: pathogenesis and outcomes
por: Piro, Ettore
Publicado: (2015)

Epstein-Barr virus-associated acute pancreatitis: a clinical report and review of literature
por: Accomando, Salvatore, et al.
Publicado: (2022)

Epidemiology of Toxoplasma and CMV serology and of GBS colonization in pregnancy and neonatal outcome in a Sicilian population
por: Puccio, Giuseppe, et al.
Publicado: (2014)

Atypical and incomplete Kawasaki disease
por: Maggio, Maria Cristina, et al.
Publicado: (2015)

New insights in pediatrics in 2021: choices in allergy and immunology, critical care, endocrinology, gastroenterology, genetics, haematology, infectious diseases, neonatology, neurology, nutrition, palliative care, respiratory tract illnesses and telemedicine
por: Caffarelli, Carlo, et al.
Publicado: (2022)

Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonology
por: Caffarelli, Carlo, et al.
Publicado: (2023)

Immunogenetics studies on cattle twins
por: Sellei, J
Publicado: (1978)

Cannot write session to /tmp/vufind_sessions/sess_hkks49veul5ke0no3fprdd27ev