Works matching IS 01973851 AND DT 2023 AND VI 43 AND IP 3

Results: 19

Clinical application of long‐read nanopore sequencing in a preimplantation genetic testing pre‐clinical workup to identify the junction for complex Xq chromosome rearrangement‐related disease.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 304, doi. 10.1002/pd.6334

By:

Mariya, Tasuku;
Shichiri, Yui;
Sugimoto, Takeshi;
Kawamura, Rie;
Miyai, Syunsuke;
Inagaki, Hidehito;
Sugihara, Eiji;
Ikeda, Keiko;
Baba, Tsuyoshi;
Ishikawa, Aki;
Ammae, Michiko;
Nakaoka, Yoshiharu;
Saito, Tsuyoshi;
Sakurai, Akihiro;
Kurahashi, Hiroki

Publication type:

Article

nanoNIPT: Short‐fragment nanopore sequencing of cell‐free DNA for non‐invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 314, doi. 10.1002/pd.6331

By:

Jørgensen, Maria Winther;
Miceikaitė, Ieva;
Larsen, Martin J.

Publication type:

Article

A cross‐country comparison of pregnant women's decision‐making and perspectives when opting for non‐invasive prenatal testing in the Netherlands and Belgium.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 294, doi. 10.1002/pd.6329

By:

Lannoo, Lore;
van der Meij, Karuna R. M.;
Bekker, Mireille N.;
De Catte, Luc;
Deckers, Sarah;
Devriendt, Koenraad;
Roggen, Nele;
Galjaard, Robert‐Jan H.;
Gitsels‐van der Wal, Janneke;
Macville, Merryn V. E.;
Martin, Linda;
Sistermans, Erik A.;
Van Calsteren, Kristel;
Van Keirsbilck, Joachim;
Crombag, Neeltje;
Henneman, Lidewij

Publication type:

Article

Screen‐positive rate in cell‐free DNA screening for microdeletion 22q11.2.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 288, doi. 10.1002/pd.6328

By:

Lüthgens, Kai;
Sinzel, Monika;
Kolar, Miriam;
Kagan, Karl Oliver

Publication type:

Article

Perioperative risk factors of preterm delivery after fetoscopic laser photocoagulation for twin–twin transfusion syndrome.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 393, doi. 10.1002/pd.6325

By:

Yamamoto, Rumiko;
Yamada, Takuma;
Yamamoto, Ryo;
Wagata, Maiko;
Hayashi, Shusaku;
Ishii, Keisuke

Publication type:

Article

Prenatal diagnosis of SMPD4 loss ‐ A neurodevelopmental disorder with microcephaly, arthrogryposis and structural brain anomalies.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 284, doi. 10.1002/pd.6324

By:

Theresia, Koenigbauer Josefine;
Wolfgang, Henrich;
Gundula, Girschick;
Michael, Entezami;
Alexander, Weichert;
Caroline, Gabrysch;
Laura, Fangmann;
Rabih, Chaoui;
Heinz‐Peter, Gabriel

Publication type:

Article

Prenatal diagnosis of vascular anomalies.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 318, doi. 10.1002/pd.6321

By:

Agarwal, Shreya;
Mehollin‐Ray, Amy;
Sutton, Vernon R.;
Iacobas, Ionela

Publication type:

Article

Fetal surgery is not associated with increased inflammatory placental pathology.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 382, doi. 10.1002/pd.6319

By:

Cardenas, Maria C.;
Cheek‐Norgan, E. Heidi;
Branda, Megan E.;
Norgan, Andrew P.;
Schenone, Mauro H.;
Lemens, Maureen A.;
Chakraborty, Rana;
Ruano, Rodrigo;
Enninga, Elizabeth Ann L.

Publication type:

Article

Local host response of commercially available dural patches for fetal repair of spina bifida aperta in rabbit model.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 370, doi. 10.1002/pd.6315

By:

Kunpalin, Yada;
Vergote, Simen;
Joyeux, Luc;
Telli, Onur;
David, Anna L.;
Belfort, Michael;
De Coppi, Paolo;
Deprest, Jan

Publication type:

Article

Prenatal and postnatal echocardiographic imaging of a rare congenital cardiac diverticulum.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 402, doi. 10.1002/pd.6313

By:

Zhang, Yichan;
Wu, Wenqian;
Yang, Yali;
Xie, Mingxing;
Wang, Jing

Publication type:

Article

Brain development is altered in rabbit fetuses with congenital diaphragmatic hernia.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 359, doi. 10.1002/pd.6309

By:

Van der Veeken, Lennart;
Russo, Francesca Maria;
Bleeser, Tom;
Basurto, David;
Emam, Doaa;
Regin, Yannick;
Gsell, Willy;
Himmelreich, Uwe;
De Catte, Luc;
Rex, Steffen;
Deprest, Jan

Publication type:

Article

Development of a simulator for training of fetoscopic myelomeningocele surgery.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 355, doi. 10.1002/pd.6308

By:

Spoor, Jochem K. H.;
van Gastel, Lis;
Tahib, Fatima;
van Grieken, Amanda;
van Weteringen, Willem;
Sterke, Frank;
Baschat, Ahmet A.;
Miller, Jena L.;
de Jong, Tjeerd H. R.;
Wijnen, René M. H.;
Eggink, Alex E.;
DeKoninck, Philip L. J.

Publication type:

Article

Addressing expectations of therapeutic options for children with hydrocephalus—A comment on "Fetal Cerebral Ventriculomegaly. What do we tell the prospective parents?".

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 404, doi. 10.1002/pd.6304

By:

Poliseli, Gianfelipe Belini;
Hamamoto, Juliana Fattori;
Rugolo, Ligia Maria Suppo de Souza;
Zanini, Marco Antonio;
Hamamoto Filho, Pedro Tadao

Publication type:

Article

Patient‐reported outcomes for congenital diaphragmatic hernia: A qualitative study.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 339, doi. 10.1002/pd.6303

By:

Taillieu, Aymara;
Deprest, Jan;
Vergote, Simen;
Debeer, Anne;
Russo, Francesca Maria;
Power, Beverley;
Meijer, Frank;
Crombag, Neeltje

Publication type:

Article

Fetal intestinal loop dilatation: Follow‐up and outcome of a series of 133 consecutive cases (the DILDIG study).

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 328, doi. 10.1002/pd.6300

By:

Mangione, Raphaële;
Voirin‐Mathieu, Etienne;
Yvert, Marianne;
Fries, Nicolas;
Mousty, Eve;
Castaigne, Vanina;
Muller, Françoise;
Dreux, Sophie

Publication type:

Article

A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 275, doi. 10.1002/pd.6294

By:

Wang, Yu;
Dai, Xiaohui;
Liu, Hanmin;
Peng, Jin;
Chen, Jiao

Publication type:

Article

A novel NOTCH1 missense variant in two fetuses with a non‐syndromic conotruncal heart defect from a single family.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 280, doi. 10.1002/pd.6290

By:

Zhou, Jie;
Dai, Xiaohui;
Liu, Hanmin;
Zhou, Shu;
Wu, Ting;
Guo, Nan;
Chen, Jiao

Publication type:

Article

RE: Wang et al. Diagnosis of fetal total anomalous pulmonary venous connection based on the post‐left atrium space ratio using artificial intelligence.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 3, p. 400, doi. 10.1002/pd.6287

By:

Day, Thomas George;
Kainz, Bernhard;
Razavi, Reza;
Simpson, John

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 3, p. 273, doi. 10.1002/pd.6175
Publication type:: Article