Works matching IS 01973851 AND DT 2018 AND VI 38

Results: 218

Cover Image, Volume 38, Issue 4.

Published in:

Prenatal Diagnosis, 2018, v. 38, n. 4, p. i, doi. 10.1002/pd.5244

By:

Philipp, Tom;
Terry, Jefferson;
Feichtinger, Michael;
Grillenberger, Sandra;
Hartmann, Beda;
Jirecek, Stefan

Publication type:

Article

Corrigendum for Peng, Zhou, Xie, et al. (2017) DOI: 10.1002/pd.5015.

Published in:

2018

By:

Peng, Ruan;
Xie, Hong‐Ning;
Zheng, Ju;
Zhou, Yi;
Lin, Mei‐Fang;
Xie, Hong-Ning;
Lin, Mei-Fang

Publication type:

journal article

When ultrasound anomalies are present: An estimation of the frequency of chromosome abnormalities not detected by cell-free DNA aneuploidy screens.

Published in:

2018

By:

Reimers, Rebecca M.;
Mason‐Suares, Heather;
Little, Sarah E.;
Bromley, Bryann;
Reiff, Emily S.;
Dobson, Lori J.;
Wilkins‐Haug, Louise;
Mason-Suares, Heather;
Wilkins-Haug, Louise

Publication type:

journal article

Early hemodynamic changes after fetal aortic stenosis valvuloplasty predict biventricular circulation at birth.

Published in:

2018

By:

Prosnitz, Aaron R.;
Drogosz, Monika;
Marshall, Audrey C.;
Wilkins‐Haug, Louise E.;
Benson, Carol B.;
Sleeper, Lynn A.;
Tworetzky, Wayne;
Friedman, Kevin G.;
Wilkins-Haug, Louise E

Publication type:

journal article

Morphology of early intrauterine deaths with full trisomy 15.

Published in:

2018

By:

Philipp, Tom;
Terry, Jefferson;
Feichtinger, Michael;
Grillenberger, Sandra;
Hartmann, Beda;
Jirecek, Stefan

Publication type:

journal article

Cerebellar herniation demonstrated by the occipitum-dens line: Ultrasonography assessment of normal fetuses, fetuses with myelomeningocele, and fetuses that underwent antenatal myelomeningocele surgery.

Published in:

2018

By:

Barreto, Enoch Quinderé de Sá;
Cavalheiro, Sérgio;
Milani, Herbene José Figuinha;
Barbosa, Maurício Mendes;
Araujo Júnior, Edward;
Nardozza, Luciano Marcondes Machado;
Moron, Antonio Fernandes

Publication type:

journal article

What is the real "price" of more prenatal screening and fewer diagnostic procedures? Costs and trade-offs in the genomic era.

Published in:

2018

By:

Hui, Lisa;
Norton, Mary

Publication type:

journal article

Impact of laser therapy for twin-to-twin transfusion syndrome on subsequent pregnancy.

Published in:

2018

By:

Le Lous, Maela;
Mediouni, Imen;
Chalouhi, Gihad;
Salomon, Laurent J.;
Bussières, Laurence;
Carrier, Aude;
Bernard, Jean‐Pierre;
Ville, Yves;
Bernard, Jean-Pierre

Publication type:

journal article

The price of abandoning diagnostic testing for cell-free fetal DNA screening.

Published in:

2018

By:

Evans, Mark I.;
Evans, Shara M.;
Bennett, Terry Ann;
Wapner, Ronald J.

Publication type:

Editorial

Fetal pulmonary valve stenosis or atresia with intact ventricular septum: Predictors of need for neonatal intervention.

Published in:

2018

By:

Wang, Qing;
Wu, Yu Rong;
Jiao, Xian Ting;
Wu, Peng Fei;
Zhao, Li Qing;
Chen, Sun;
Sun, Kun

Publication type:

journal article

Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.

Published in:

2018

By:

Brison, Nathalie;
Neofytou, Maria;
Dehaspe, Luc;
Bayindir, Baran;
Van Den Bogaert, Kris;
Dardour, Leila;
Peeters, Hilde;
Van Esch, Hilde;
Van Buggenhout, Griet;
Vogels, Annick;
de Ravel, Thomy;
Legius, Eric;
Devriendt, Koen;
Vermeesch, Joris R.

Publication type:

journal article

Safety and efficacy of fetal surgery techniques to close a spina bifida defect in the fetal lamb model: A systematic review.

Published in:

2018

By:

Joyeux, Luc;
De Bie, Felix;
Danzer, Enrico;
Van Mieghem, Tim;
Flake, Alan W.;
Deprest, Jan

Publication type:

journal article

Issue Information.

Published in:: Prenatal Diagnosis, 2018, v. 38, n. 4, p. 229, doi. 10.1002/pd.5124
Publication type:: Article

Cover Image, Volume 38, Issue 3.

Published in:

Prenatal Diagnosis, 2018, v. 38, n. 3, p. i, doi. 10.1002/pd.5237

By:

Sun, Kun;
Lun, Fiona M. F.;
Leung, Tak Y.;
Chiu, Rossa W. K.;
Lo, Y. M. Dennis;
Sun, Hao

Publication type:

Article

Current controversies in prenatal diagnosis 3: Fetal MRI should be performed in all prenatally detected fetuses with a major structural abnormality.

Published in:

2018

By:

Platt, Lawrence D.;
Barth, Richard A.;
Pugash, Denise

Publication type:

Editorial

Erratum for Peng, Zhou, Xie, et al. (2017) DOI: 10.1002/pd.5169.

Published in:

2018

By:

Peng, Ruan;
Yang, Jian‐Bo;
Xie, Hong‐Ning;
Lin, Mei‐Fang;
Zheng, Ju;
Yang, Jian-Bo;
Xie, Hong-Ning;
Lin, Mei-Fang

Publication type:

journal article

Clinical experience of laboratory follow-up with noninvasive prenatal testing using cell-free DNA and positive microdeletion results in 349 cases.

Published in:

2018

By:

Schwartz, S.;
Kohan, M.;
Pasion, R.;
Papenhausen, P. R.;
Platt, L. D.

Publication type:

journal article

Current controversies in prenatal diagnosis 2: Cell-free DNA prenatal screening should be used to identify all chromosome abnormalities.

Published in:

2018

By:

Chitty, Lyn S.;
Hudgins, Louanne;
Norton, Mary E.

Publication type:

Editorial

Patient-controlled tissue collection for genetic testing after early pregnancy loss: A pilot study.

Published in:

2018

By:

Kucherov, Alexander;
Atrio, Jessica;
Williams, Zev

Publication type:

journal article

Noninvasive reconstruction of placental methylome from maternal plasma DNA: Potential for prenatal testing and monitoring.

Published in:

2018

By:

Sun, Kun;
Lun, Fiona M. F.;
Leung, Tak Y.;
Chiu, Rossa W. K.;
Lo, Y. M. Dennis;
Sun, Hao

Publication type:

journal article

Myocardial injury in fetal aortic stenosis: Insights from amniotic fluid analysis.

Published in:

2018

By:

Friedman, Kevin G.;
Sleeper, Lynn A.;
Fichorova, Raina N.;
Weilnau, Taylor;
Tworetzky, Wayne;
Wilkins‐Haug, Louise E.;
Wilkins-Haug, Louise E

Publication type:

journal article

ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?

Published in:

2018

By:

Hay, Sara B.;
Sahoo, Trilochan;
Travis, Mary K.;
Hovanes, Karine;
Dzidic, Natasa;
Doherty, Charles;
Strecker, Michelle N.

Publication type:

journal article

Current controversies in prenatal diagnosis 1: All prenatally detected lower urinary tract obstructions should be shunted.

Published in:

2018

By:

Devlieger, Roland;
Douglas Wilson, R.;
Ruano, Rodrigo

Publication type:

Editorial

Conflict of interest related to clinical practice is underreported: The case of noninvasive prenatal testing.

Published in:

2018

By:

Wolfberg, Adam J.

Publication type:

journal article

Severe fetal hydronephrosis: the added value of associated congenital anomalies of the kidneys and urinary tract (CAKUT) in the prediction of postnatal outcome.

Published in:

2018

By:

Perlman, Sharon;
Roitman, Lucia;
Lotan, Danny;
Kivilevitch, Zvi;
Pode‐Shakked, Naomi;
Pode‐Shakked, Ben;
Achiron, Reuven;
Dekel, Benjamin;
Gilboa, Yinon;
Pode-Shakked, Naomi;
Pode-Shakked, Ben

Publication type:

journal article

The relationship between preoperative fetal head circumference and 2-year cognitive performance after laser surgery for twin-twin transfusion syndrome.

Published in:

2018

By:

Chon, Andrew H.;
Mamey, Mary Rose;
Schrager, Sheree M.;
Vanderbilt, Douglas L.;
Chmait, Ramen H.

Publication type:

journal article

Intra uterine sludge does not rule out anal ATRESIA.

Published in:

2018

By:

Burke, Yechiel;
Gilboa, Yinon;
Bronshtein, Moshe

Publication type:

Case Study

Issue Information.

Published in:: Prenatal Diagnosis, 2018, v. 38, n. 3, p. 153, doi. 10.1002/pd.5123
Publication type:: Article

Cover Image, Volume 38, Issue 2.

Published in:

Prenatal Diagnosis, 2018, v. 38, n. 2, p. i, doi. 10.1002/pd.5221

By:

Zou, Zhiyong;
Huang, Linhuan;
Lin, Shaobin;
He, Zhiming;
Zhu, Hui;
Zhang, Yi;
Fang, Qun;
Luo, Yanmin

Publication type:

Article

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2017.

Published in:

2018

By:

Levy, Brynn;
Bianchi, Diana W.;
Van Mieghem, Tim;
Deprest, Jan;
Ghidini, Alessandro;
Chitty, Lyn S.

Publication type:

journal article

Utility of chromosomal microarray in anomalous fetuses.

Published in:

2018

By:

Parchem, Jacqueline G.;
Sparks, Teresa N.;
Gosnell, Kristen;
Norton, Mary E.

Publication type:

journal article

Ultrasound findings provide clues to investigate founder mutations expressed as runs of homozygosity in chromosomal microarray studies.

Published in:

2018

By:

Daum, Hagit;
Lerer, Israela;
Frumkin, Ayala;
Rosenak, Daniel;
Yanai, Nili;
Porat, Shay;
Yagel, Simcha;
Meiner, Vardiella

Publication type:

journal article

Prenatal diagnosis of urinary tract anomalies, a cohort study in the Northern Netherlands.

Published in:

2018

By:

Bakker, Marian K.;
Bergman, Jorieke E. H.;
Fleurke‐Rozema, Hanneke;
Streefland, Esther;
Gracchi, Valentina;
Bilardo, Caterina M.;
De Walle, Hermien E. K.;
Fleurke-Rozema, Hanneke

Publication type:

journal article

Prospective study feasibility: Screening of antenatal total abnormal pulmonary venous return.

Published in:

2018

By:

Levêque, Christine;
Paret, Louise;
Cochet, Tiffany;
Joinau‐Zoulovits, Félicia;
Chantalat, E.;
Vidal, F.;
Vayssière, Christophe;
David, Nadine;
Joinau-Zoulovits, Félicia

Publication type:

journal article

Nonisolated diaphragmatic hernia in Simpson-Golabi-Behmel syndrome.

Published in:

2018

By:

Chong, Karen;
Saleh, Maha;
Injeyan, Marie;
Miron, Ioana;
Fong, Katherine;
Shannon, Patrick

Publication type:

journal article

Comparison of umbilical cord occlusion methods: Radiofrequency ablation versus laser photocoagulation.

Published in:

2018

By:

Abdel‐Sattar, Mira;
Chon, Andrew H.;
Llanes, Arlyn;
Korst, Lisa M.;
Ouzounian, Joseph G.;
Chmait, Ramen H.;
Abdel-Sattar, Mira

Publication type:

journal article

Maternal liver transplant: Another cause of discordant fetal sex determination using cell-free DNA.

Published in:

2018

By:

Neofytou, Maria;
Brison, Nathalie;
Van den Bogaert, Kris;
Dehaspe, Luc;
Devriendt, Koen;
Geerts, Anja;
Vermeesch, Joris R.

Publication type:

Letter

Impact of a shift in nuchal translucency measurements on the detection rate of first-trimester Down syndrome screening: A population-based study.

Published in:

2018

By:

Fries, Nicolas;
Salomon, Laurent J.;
Muller, Françoise;
Dreux, Sophie;
Houfflin‐Debarge, Véronique;
Coquel, Philippe;
Kleinfinger, Pascale;
Dommergues, Marc;
for the BioNuQual User Club, Paris;
Houfflin-Debarge, Véronique;
BioNuQual User Club, Paris

Publication type:

journal article

Tissuepatch is biocompatible and seals iatrogenic membrane defects in a rabbit model.

Published in:

2018

By:

Engels, Alexander C.;
Joyeux, Luc;
Van der Merwe, Johannes;
Jimenez, Julio;
Prapanus, Savitree;
Barrett, David W.;
Connon, Che;
Chowdhury, Tina T.;
David, Anna L.;
Deprest, Jan;
Pranpanus, Savitree

Publication type:

journal article

Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia.

Published in:

2018

By:

Zou, Zhiyong;
Huang, Linhuan;
Lin, Shaobin;
He, Zhiming;
Zhu, Hui;
Zhang, Yi;
Fang, Qun;
Luo, Yanmin

Publication type:

journal article

Issue Information.

Published in:: Prenatal Diagnosis, 2018, v. 38, n. 2, p. 81, doi. 10.1002/pd.5122
Publication type:: Article

Cover Image, Volume 38, Issue 1.

Published in:

Prenatal Diagnosis, 2018, v. 38, n. 1, p. i, doi. 10.1002/pd.5220

By:

Jenkins, Lucy A.;
Deans, Zandra C.;
Lewis, Celine;
Allen, Stephanie

Publication type:

Article

Advances in the prenatal diagnosis of monogenic disorders.

Published in:

2018

By:

Chitty, Lyn S.

Publication type:

Editorial

cfDNA screening and diagnosis of monogenic disorders - where are we heading?

Published in:

2018

By:

Chiu, Eunice Ka Long;
Hui, Winnie Wai In;
Chiu, Rossa Wai Kwun

Publication type:

journal article

Delivering an accredited non-invasive prenatal diagnosis service for monogenic disorders and recommendations for best practice.

Published in:

2018

By:

Jenkins, Lucy A.;
Deans, Zandra C.;
Lewis, Celine;
Allen, Stephanie

Publication type:

journal article

Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis.

Published in:

2018

By:

The International Society for Prenatal Diagnosis;
The Society for Maternal and Fetal Medicine;
The Perinatal Quality Foundation;
Henson, Melissa;
International Society for Prenatal Diagnosis;
Society for Maternal and Fetal Medicine;
Perinatal Quality Foundation

Publication type:

journal article

Diagnosis of lethal or prenatal-onset autosomal recessive disorders by parental exome sequencing.

Published in:

2018

By:

Stals, Karen L.;
Wakeling, Matthew;
Baptista, Júlia;
Caswell, Richard;
Parrish, Andrew;
Rankin, Julia;
Tysoe, Carolyn;
Jones, Garan;
Gunning, Adam C.;
Lango Allen, Hana;
Bradley, Lisa;
Brady, Angela F.;
Carley, Helena;
Carmichael, Jenny;
Castle, Bruce;
Cilliers, Deirdre;
Cox, Helen;
Deshpande, Charu;
Dixit, Abhijit;
Eason, Jacqueline

Publication type:

journal article

Issue Information.

Published in:: Prenatal Diagnosis, 2018, v. 38, n. 1, p. 1, doi. 10.1002/pd.5121
Publication type:: Article

Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.

Published in:

2018

By:

Horn, Ruth;
Parker, Michael

Publication type:

journal article

Expanded carrier screening for monogenic disorders: where are we now?

Published in:

2018

By:

Chokoshvili, Davit;
Vears, Danya;
Borry, Pascal

Publication type:

journal article