Works matching IS 01973851 AND DT 2024 AND VI 44 AND IP 8

Results: 15

Structured reporting in fetal magnetic resonance imaging with congenital diaphragmatic hernia.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 988, doi. 10.1002/pd.6593

By:

Thater, G.;
Weidner, A.;
Rafat, N.;
Nowak, O.;
Otto, C.;
Zahn, K.;
Boettcher, M.;
Schönberg, S. O.;
Schaible, T.;
Weis, M.

Publication type:

Article

Delivery room and early postnatal management of neonates with congenital heart disease.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 915, doi. 10.1002/pd.6617

By:

Ali, Noorjahan;
Donofrio, Mary T.

Publication type:

Article

Novel variant in ACTA1 identified in a fetus with akinesia deformation sequence and cortical development delay.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 996, doi. 10.1002/pd.6568

By:

Martínez‐Diago, Clara;
Mademont‐Soler, Irene;
Bonmatí, Alexandra;
Rodo, Carlota;
Alberch, Ariadna;
Obon, María;
Fuertes, Begoña;
Maroto, Anna

Publication type:

Article

Cell‐free DNA screening for common autosomal trisomies using rolling‐circle replication in twin pregnancies.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 953, doi. 10.1002/pd.6615

By:

Vivanti, Alexandre J.;
Maestroni, Camille;
Benachi, Alexandra;
Conotte, Stéphanie;
Geipel, Annegret;
Kagan, Karl Oliver;
Borrell, Antoni;
El Kenz, Hanane;
Costa, Jean‐Marc;
Jani, Jacques C.

Publication type:

Article

National registry of thoracoamniotic shunting using a double‐basket catheter: A post‐marketing surveillance registry of 295 patients with fetal hydrothorax.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 971, doi. 10.1002/pd.6587

By:

Takahashi, Yuichiro;
Ishii, Keisuke;
Ishikawa, Hiroshi;
Imai, Kenji;
Baba, Kazunori;
Sago, Haruhiko

Publication type:

Article

Numbers of prenatal cell‐free DNA screens performed: Results of a 2022 CAP exercise.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 946, doi. 10.1002/pd.6574

By:

Palomaki, Glenn E.;
Wyatt, Philip;
Rowsey, Ross;
Cacheris, Phillip Michael;
Lepage, Nathalie;
Natowicz, Marvin R.;
Long, Thomas;
Moyer, Ann M.

Publication type:

Article

Truncating variants in PAPSS2 gene: A cause of early prenatal onset brachyolmia?

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 1003, doi. 10.1002/pd.6596

By:

Biancotto, Giulia;
Rosti, Giulia;
Madia, Francesca;
Capra, Valeria;
Scala, Marcello;
Aleo, Elena;
Paladini, Dario

Publication type:

Article

Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy–Walker malformation and single ventricle heart.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 1008, doi. 10.1002/pd.6614

By:

Stanković, Anđela;
Toljić, Mina;
Orlić, Nataša Karadžov;
Miković, Željko;
Joksić, Ivana

Publication type:

Article

Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 959, doi. 10.1002/pd.6588

By:

Dreux, Sophie;
Rosenblatt, Jonathan;
Massardier, Jérôme;
Benachi, Alexandra;
Voirin‐Mathieu, Etienne;
Muller, Françoise;
Boitte, F.;
Moal, V.;
Denis, M. C.;
Lorenter, P.;
Jouval, M.;
Sitruk, B.;
Suybeng, V.;
Verchain, S.;
Herbreteau, S.;
Treyssac, F.;
Gras, V.;
Guiot, J.;
Savarit, D.;
Blouin, P.

Publication type:

Article

A novel MED12 pathogenic variant in a female fetus with facial cleft and cardiac defects identified in the first trimester.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 999, doi. 10.1002/pd.6594

By:

Dai, Wei‐Si;
Yang, Yan‐Dong;
Li, Dong‐Zhi

Publication type:

Article

High positive predictive value 22q11.2 microdeletion screening by prenatal cell‐free DNA testing that incorporates fetal fraction amplification.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 925, doi. 10.1002/pd.6562

By:

Hammer, Carly;
Pierson, Summer;
Acevedo, Ashley;
Goldberg, James;
Westover, Thomas;
Chawla, Devika;
Mabey, Brent;
Muzzey, Dale;
Johansen Taber, Katherine

Publication type:

Article

Maternal "mirror" syndrome: Evaluating the benefits of fetal therapy.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 979, doi. 10.1002/pd.6589

By:

Sichitiu, Joanna;
Alkazaleh, Fawaz;
de Heus, Roel;
Abbasi, Nimrah;
van Mieghem, Tim;
Keunen, Johannes;
Windrim, Rory;
Seaward, Gareth;
Kelly, Edmond N.;
Lewi, Liesbeth;
Deprest, Jan;
Ryan, Greg;
Shinar, Shiri

Publication type:

Article

Test performance and clinical utility of expanded non‐invasive prenatal test: Experience on 71,883 unselected routine cases from one single center.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 936, doi. 10.1002/pd.6580

By:

Faieta, Monica;
Falcone, Rossella;
Duca, Sara;
Corsetti, Elena;
Giannico, Riccardo;
Gigante, Laura;
Diano, Laura;
Calugi, Graziella;
Spinella, Francesca;
Pizzuti, Francesca

Publication type:

Article

Perinatal outcomes of fetoscopic selective laser photocoagulation for spontaneous twin‐anemia polycythemia sequence.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 8, p. 965, doi. 10.1002/pd.6576

By:

Munoz, Jessian L.;
Buskmiller, Cara;
Sanz Cortes, Magdalena;
Donepudi, Roopali V.;
Belfort, Michael A.;
Nassr, Ahmed A.

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2024, v. 44, n. 8, p. 913, doi. 10.1002/pd.6376
Publication type:: Article