Works matching IS 01973851 AND DT 2023 AND VI 43 AND IP 13

Results: 17

Cover Image.

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

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

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

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

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

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

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

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

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

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

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