about
Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid.Abnormal skull findings in neural tube defects.Two-dimensional fetal echocardiography: where we are.Newborns with congenital heart diseases: epidemiological data from a single reference center in Brazil.Comparison of maternal and neonatal outcomes in women with HELLP syndrome and women with severe preeclampsia without HELLP syndrome.US-color Doppler early diagnosis of uterine rupture with protrusion of umbilical cordManagement, prognosis and reproductive outcomes of borderline ovarian tumor relapse during pregnancy: from diagnosis to potential treatment options.Fetal-MRI prenatal diagnosis of severe bilateral lung hypoplasia: alveolar capillary dysplasia case reportA case of polimalformed fetus with a microdeletion of CTNNA3 gene.Predictive value of procalcitonin or c-reactive protein for subclinical intrauterine infection in patients with premature rupture of membranes (PROM).Shoulder dystocia: an Evidence-Based approach.Fetal weight estimation for prediction of fetal macrosomia: does additional clinical and demographic data using pattern recognition algorithm improve detection?Obstetric management in Rh alloimmunizated pregnancy.Postpartum period: three distinct but continuous phases.Level of C - reactive protein as an indicator for prognosis of premature uterine contractionsSix consecutive false positive cases from cell-free fetal DNA testing in a single referring centreIntroducing the next generation sequencing in genomic amnio and villuos sampling. The so called "Next Generation Prenatal Diagnosis" (NGPD).Thyroid physiology and common diseases in pregnancy: review of literatureAntepartum haemorrhage.Putative protective effects of cesarean section on pelvic floor disorders.Uterine rupture after prostaglandin analogues to induce midtrimester abortion.Obesity and fetal-maternal outcomes.Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening.Preterm delivery at low gestational age: risk factors for short latency. A multivariated analysis.Severe, early onset hypertrophic cardiomyopathy in a family with LEOPARD syndromeHistory of colposcopy: a brief biography of Hinselmann.Analysis of fetal biometric measurements in the last 30 yearsPrenatal screening of Cystic Fibrosis: a single centre experience.Exploring SOD1 Gene for the Detection of Fetal Down Syndrome.Indication of prenatal diagnosis in pregnancies complicated by undetectable second-trimester maternal serum estriol levels.Prenatal third trimester sonographic behavior of a thanatophoric dwarfsAn isolated fetal cor triatriatum dexter during a targeted anatomic survey at 22 weeks' gestation.Prevention of Neural Tube Defects and proper folate periconceptional supplementationManagement of molar pregnancy.Case report: successful of a spontaneous quadruplet pregnancyObstetric management of IUGRNow you can! Reality & Future Applications of array CGH in prenatal diagnosis.The amniotic fluid-derived cells: the biomedical challenge for the third millennium.Proteomic analysis for the study of amniotic fluid protein compositionAddison's disease and pregnancy: case report.
P1433
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P1433
description
czasopismo naukowe
@pl
journal
@en
revista científica
@es
rivista scientifica
@it
wetenschappelijk tijdschrift
@nl
wissenschaftliche Fachzeitschrift
@de
name
Journal of prenatal medicine
@ast
Journal of prenatal medicine
@en
Journal of prenatal medicine
@es
Journal of prenatal medicine
@nl
type
label
Journal of prenatal medicine
@ast
Journal of prenatal medicine
@en
Journal of prenatal medicine
@es
Journal of prenatal medicine
@nl
altLabel
J Prenat Med
@en
prefLabel
Journal of prenatal medicine
@ast
Journal of prenatal medicine
@en
Journal of prenatal medicine
@es
Journal of prenatal medicine
@nl
P3181
P1055
P1476
Journal of prenatal medicine
@en