Works matching IS 01973851 AND DT 2023 AND VI 43

Results: 207

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Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. i, doi. 10.1002/pd.6513

By:

Martin, Kimberly;
Norton, Mary E.;
MacPherson, Cora;
Demko, Zachary;
Egbert, Melissa;
Haeri, Sina;
Malone, Fergal;
Wapner, Ronald J.;
Roman, Ashley S.;
Khalil, Asma;
Faro, Revital;
Madankumar, Rajeevi;
Strong, Noel;
Silver, Robert;
Vohra, Nidhi;
Hyett, Jon;
Kao, Charlly;
Hakonarson, Hakon;
Jacobson, Bo;
Dar, Pe'er

Publication type:

Article

New ventures for Prenatal Diagnosis.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1573, doi. 10.1002/pd.6486

By:

Chitty, Lyn S.

Publication type:

Article

A novel SMOC1 pathogenic homozygous variant in a fetus with mesomelia of the lower limbs, micrognathia and hypertelorism and an incidental finding of CYP21A2‐related congenital adrenal hyperplasia.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1674, doi. 10.1002/pd.6485

By:

Willison, Clare;
Ramachandran, Vijaya;
Chandler, Natalie Jane;
Hillman, Sara;
Ashraf, Tazeen

Publication type:

Article

Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1574, doi. 10.1002/pd.6483

By:

Martin, Kimberly;
Norton, Mary E.;
MacPherson, Cora;
Demko, Zachary;
Egbert, Melissa;
Haeri, Sina;
Malone, Fergal;
Wapner, Ronald J.;
Roman, Ashley S.;
Khalil, Asma;
Faro, Revital;
Madankumar, Rajeevi;
Strong, Noel;
Silver, Robert;
Vohra, Nidhi;
Hyett, Jon;
Kao, Charlly;
Hakonarson, Hakon;
Jacobson, Bo;
Dar, Pe'er

Publication type:

Article

The new fetal therapy section awaits your research.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1601, doi. 10.1002/pd.6480

By:

Deprest, Jan;
Van Mieghem, Tim

Publication type:

Article

Fetal macrocephaly: Pathophysiology, prenatal diagnosis and management.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1650, doi. 10.1002/pd.6473

By:

Shinar, Shiri;
Chitayat, David;
Shannon, Patrick;
Blaser, Susan

Publication type:

Article

Prenatal diagnosis of Hartsfield syndrome with a novel genetic variant.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1671, doi. 10.1002/pd.6472

By:

Rich, Matthew;
Schroeder, Bradley;
Manning, Courtney;
Abbott, Mary‐Alice

Publication type:

Article

Biallellic variants in CACNA1S cause fetal akinesia sequence, progressive hydrops and stillbirth.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1678, doi. 10.1002/pd.6471

By:

Seed, Emma;
Noon, Fallon;
Milnes, Di;
Roscioli, Tony;
Kristensen, Karl;
Ellwood, David;
DaSilva Costa, Fabricio

Publication type:

Article

Risk factors for delayed termination of pregnancy following increased nuchal translucency.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1593, doi. 10.1002/pd.6467

By:

Bunnell, Megan E.;
Adams, Sophie;
Pelletier, Andrea;
Hoffman Sage, Yael

Publication type:

Article

Percutaneous fetal endoscopic third ventriculostomy for severe isolated cerebral ventriculomegaly.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1614, doi. 10.1002/pd.6465

By:

Peralta, Cleisson Fábio Andrioli;
Medrado, Aletea Patrícia;
Botelho, Rafael Davi;
Jorge Rodrigues da Costa, Karina;
Imada, Vanessa;
Lamis, Fabricio

Publication type:

Article

Improving the accuracy of noninvasive prenatal testing through size‐selection between fetal and maternal cfDNA.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1581, doi. 10.1002/pd.6464

By:

Kwon, Hyuk‐Jung;
Yun, Seonyoung;
Joo, Joungsu;
Park, Dabin;
Do, Woo‐Jung;
Lee, Sunghoon;
Lee, Min‐Seob

Publication type:

Article

Neu Laxova syndrome and megacystis in the first trimester: Broadening the fetal phenotype.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1666, doi. 10.1002/pd.6463

By:

Bourgon, Nicolas;
Chen, Ruiqian;
Grangé, Gilles;
Grotto, Sarah;
Molac, Clémence;
Loeuillet, Laurence;
Attié‐Bitach, Tania

Publication type:

Article

Prenatal diagnosis of autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants presented with thick nuchal translucency and cardiac abnormalities.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1662, doi. 10.1002/pd.6462

By:

Yu, Qiu‐Xia;
Zhen, Li;
Lin, Xiao‐Mei;
Wen, Yun‐Jing;
Li, Dong‐Zhi

Publication type:

Article

Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1638, doi. 10.1002/pd.6460

By:

Herzeg, Akos;
Borges, Beltran;
Lianoglou, Billie R.;
Gonzalez‐Velez, Juan;
Canepa, Emma;
Munar, Dane;
Young, Sarah P.;
Bali, Deeksha;
Gelb, Michel H.;
Chakraborty, Pranesh;
Kishnani, Priya S.;
Harmatz, Paul;
Cohen, Jennifer L.;
MacKenzie, Tippi C.

Publication type:

Article

Maternal and fetal safety outcomes after in utero stem cell injection: A systematic review.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1622, doi. 10.1002/pd.6459

By:

Sagar, Rachel L.;
Walther‐Jallow, Lilian;
Götherström, Cecilia;
Westgren, Magnus;
David, Anna L.

Publication type:

Article

Simple prenatal imaging predictors for postnatal cerebrospinal fluid diversion surgery in fetuses undergoing in utero surgery for spina bifida.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1605, doi. 10.1002/pd.6453

By:

Kunpalin, Yada;
Sichitiu, Joanna;
Krishnan, Pradeep;
Blaser, Susan;
Kulkarni, Abhaya V.;
Abbasi, Nimrah;
Ryan, Greg;
Shinar, Shiri;
van Mieghem, Tim

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1571, doi. 10.1002/pd.6185
Publication type:: Article

Congenital small bowel obstruction: Prenatal detection and outcome.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1485, doi. 10.1002/pd.6461

By:

Heinrich, H.;
Pijpers, A. G. H.;
Linskens, I. H.;
van Leeuwen, E.;
Schattenkerk, L. D. Eeftinck;
Derikx, J. P. M.;
Pajkrt, E.

Publication type:

Article

Haplotype‐based noninvasive prenatal diagnosis of methylmalonic acidemia and the discovery of a recurrent pathogenic haplotype associated with c.609G>A.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1544, doi. 10.1002/pd.6458

By:

Fu, Xinyu;
Li, Shaojun;
Zhao, Zhenhua;
Kong, Lingrong;
Zhu, Jingqi;
Li, Huanyun;
Feng, Jun;
Tang, Weiqin;
Wu, Di;
Kong, Xiangdong

Publication type:

Article

Prognostic accuracy of factors associated with poor outcome in prenatally diagnosed sacrococcygeal teratoma: A systematic review and meta‐analysis.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1495, doi. 10.1002/pd.6457

By:

van Heurn, Lieke J.;
Coumans, Audrey;
Haak, Monique C.;
van der Kaaij, Annemarth;
van Heurn, L. W. Ernest;
Pajkrt, Eva;
Derikx, Joep P. M.

Publication type:

Article

The normal 14–18 gestational weeks "parasagittal complex" view of the fetal brain. A 3D transvaginal neurosonographic study.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1520, doi. 10.1002/pd.6456

By:

Birnbaum, Roee;
Kuperberg, Maya;
Brusilov, Michael;
Wolman, Igal;
Malinger, Gustavo;
Haratz, Karina Krajden

Publication type:

Article

Prenatal diagnosis of mucopolysaccharidosis type VII facilitating treatment in neonatal period.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1567, doi. 10.1002/pd.6455

By:

Chandler, Natalie Jane;
Ramachandran, Vijaya;
Beesley, Clare;
Otigbah, Chineze;
Davison, James;
Ashraf, Tazeen

Publication type:

Article

Optimal timing of delivery for growth restricted fetuses with gastroschisis: A decision analysis.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1506, doi. 10.1002/pd.6452

By:

Packer, Claire H.;
Pilliod, Rachel A.;
Caughey, Aaron B.;
Sparks, Teresa N.

Publication type:

Article

PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencing.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1556, doi. 10.1002/pd.6451

By:

Brewer, Casey J.;
Makhamreh, Mona M.;
Shivashankar, Kavya;
McLaren, Rodney;
Toro, Mariella;
Berger, Seth I.;
Al‐Kouatly, Huda B.

Publication type:

Article

Fetal lung volumes measured by MRI predict pulmonary morbidity among infants with giant omphaloceles.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1514, doi. 10.1002/pd.6449

By:

Gallagher, Lauren T.;
Lyttle, Bailey D.;
Meyers, Mariana L.;
Gien, Jason;
Zaretsky, Michael V.;
Galan, Henry L.;
Behrendt, Nicholas;
Liechty, Kenneth W.;
Derderian, Sarkis Christopher

Publication type:

Article

Screen‐positive rate in cell free DNA screening for trisomy 21.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1536, doi. 10.1002/pd.6448

By:

Lüthgens, Kai;
Häbig, Karina;
Sonek, Jiri;
Kagan, Karl Oliver

Publication type:

Article

Agenesis of the corpus callosum: What to tell expecting parents?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1527, doi. 10.1002/pd.6447

By:

Tsai, Pascale;
Shinar, Shiri

Publication type:

Article

Identification of two novel MYH3 variants causing different phenotypes in prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1467, doi. 10.1002/pd.6440

By:

Yang, Yang;
Zhang, Wen;
Wang, Hao

Publication type:

Article

Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1394, doi. 10.1002/pd.6444

By:

Sahin‐Hodoglugil, Nuriye N.;
Lianoglou, Billie R.;
Ackerman, Sara;
Sparks, Teresa N.;
Norton, Mary E.

Publication type:

Article

Imaging and outcomes of fetal adrenal hemorrhage: A systematic review.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1433, doi. 10.1002/pd.6442

By:

Pham, Amelie;
Biswas, Sonia;
Levy, Ariel;
Spiliopoulos, Michail;
McLaren, Rodney;
Makhamreh, Mona M.;
Al‐Kouatly, Huda B.

Publication type:

Article

Maternal serological screening for cytomegalovirus infection may play an important role nowadays.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1477, doi. 10.1002/pd.6441

By:

Aldè, Mirko;
Ambrosetti, Umberto

Publication type:

Article

Two unrelated fetuses with ITPR1 missense variants and fetal hydrops.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1463, doi. 10.1002/pd.6439

By:

Harris, Sarah;
Putra, Manesha;
Gilmore, Kelly L.;
Vora, Neeta L.

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1483, doi. 10.1002/pd.6184
Publication type:: Article

Prenatal diagnosis of PORCN‐related developmental syndrome in a fetus: A novel phenotype.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1472, doi. 10.1002/pd.6438

By:

Kilby, Mark D.;
Castleman, James;
Allen, Stephanie;
Doyle, Samantha;
Williams, Denise K.

Publication type:

Article

Outcomes of fetal reduction versus expectant management in dichorionic triamniotic triplets.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1442, doi. 10.1002/pd.6437

By:

Meng, Xinlu;
Huang, Jiaqi;
Yuan, Pengbo;
Wang, Xueju;
Shi, Xiaoming;
Zhao, Yangyu;
Wei, Yuan

Publication type:

Article

Biometric magnetic resonance imaging analysis of fetal brain development in Down syndrome.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1450, doi. 10.1002/pd.6436

By:

Kitano, Rie;
Madan, Neel;
Mikami, Takahisa;
Madankumar, Rajeevi;
Skotko, Brian G.;
Santoro, Stephanie;
Ralston, Steven J.;
Bianchi, Diana W.;
Tarui, Tomo

Publication type:

Article

Obstetrical outcomes following amniocentesis performed after 24 weeks of gestation: A systematic review and meta‐analysis.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1425, doi. 10.1002/pd.6435

By:

Nassr, Ahmed A.;
Hessami, Kamran;
D'Alberti, Elena;
Giancotti, Antonella;
Meshinchiasl, Nazlisadat;
Evans, Mark I.;
Di Mascio, Daniele;
Shamshirsaz, Alireza A.

Publication type:

Article

An overview of reproductive carrier screening panels for autosomal recessive and/or X‐linked conditions: How much do we know?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1416, doi. 10.1002/pd.6434

By:

Wang, Tianjiao;
Scuffham, Paul;
Byrnes, Joshua;
Delatycki, Martin B.;
Downes, Martin

Publication type:

Article

Fetal de novo heterozygous variant in the isocitrate dehydrogenase 1 gene associated with growth restriction, skeletal, cerebral and vascular anomalies.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1459, doi. 10.1002/pd.6433

By:

Illi, Clara;
Koenigbauer, Josefine;
Henrich, Wolfgang;
Fangmann, Laura;
Reinhardt, Charlotte;
Ossmann, Sophia;
Weichert, Alexander

Publication type:

Article

Droplet digital PCR is a cost‐effective method for analyzing long cell‐free DNA in maternal plasma: Application in preeclampsia.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1385, doi. 10.1002/pd.6432

By:

Gai, Wanxia;
Yu, Stephanie C. Y.;
Chan, W. T. Charlotte;
Peng, Wenlei;
Lau, So Ling;
Leung, Tak Y.;
Jiang, Peiyong;
Chan, K. C. Allen;
Lo, Y. M. Dennis

Publication type:

Article

Factors associated with late gestational age of diagnosis and/or delayed referral of fetuses with major structural malformations: A study in a tertiary care hospital in South India.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1406, doi. 10.1002/pd.6431

By:

Yadav, Manisha;
Gowda, Mamatha;
Chinta, Navya;
Deodhare, Kirti;
Murugesan, Sneha

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1383, doi. 10.1002/pd.6183
Publication type:: Article

Correction to Laser therapy versus expectant management for selective fetal growth restriction in monochorionic twins: A systematic review.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1378, doi. 10.1002/pd.6430
Publication type:: Article

Cx43 regulates mechanotransduction mechanisms in human preterm amniotic membrane defects.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1284, doi. 10.1002/pd.6429

By:

Costa, Eleni;
Thrasivoulou, Christopher;
Becker, David L.;
Deprest, Jan A.;
David, Anna L.;
Chowdhury, Tina T.

Publication type:

Article

A novel PIEZO2 mutation in a fetus from a Chinese family with Gordon syndrome.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1370, doi. 10.1002/pd.6422

By:

Pu, Lihong;
Dai, Xiaohui;
Liu, Dan;
Wang, Yu;
Liu, Hanmin;
He, Xiaolan;
Chen, Jiao

Publication type:

Article

Performance of single‐gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1344, doi. 10.1002/pd.6427

By:

Wynn, Julia;
Hoskovec, Jennifer;
Carter, Rebecca D.;
Ross, Meredith J.;
Perni, Sriram C.

Publication type:

Article

SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1374, doi. 10.1002/pd.6426

By:

Hourvitz, Noa;
Kurolap, Alina;
Mory, Adi;
Haratz, Karina Krajden;
Kidron, Dvora;
Malinger, Gustavo;
Baris Feldman, Hagit;
Yaron, Yuval

Publication type:

Article

What helps define outcomes in persistent uninterpretable non‐invasive prenatal testing: Maternal factors, fetal fraction or quality scores?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1333, doi. 10.1002/pd.6423

By:

Lannoo, Lore;
Van Camp, Joke;
Brison, Nathalie;
Parijs, Ilse;
Vancoillie, Leen;
Van Den Bogaert, Kris;
Vermeesch, Joris Robert;
Devriendt, Koen;
Van Calsteren, Kristel

Publication type:

Article

Prenatal diagnosis of cleft lip and/or palate: What do we tell prospective parents?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1310, doi. 10.1002/pd.6418

By:

Wilkes, Courtney;
Graetz, Melissa;
Downie, Lilian;
Bethune, Michael;
Chong, David

Publication type:

Article

Lung proliferation is dependent on the duration not the timepoint of tracheal occlusion in nitrofen rats with diaphragmatic hernia.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1274, doi. 10.1002/pd.6428

By:

Beck, Veronika;
Froyen, Guy;
Deckx, Sebastiaan;
Sandaite, Inga;
Deprest, Thomas;
Plevoets, Koen;
Deprest, Jan A.

Publication type:

Article