Works matching IS 01973851 AND DT 2024 AND VI 44 AND IP 5

Results: 17

Eliminating first trimester combined testing: Consequences for early detection of significant fetal anomalies.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 544, doi. 10.1002/pd.6552

By:

Lugthart, M. A.;
Heinrich, H.;
Ertugrul, I.;
Nsiah‐Asare, E. N.;
van de Kamp, K.;
Linskens, I. H.;
van Maarle, M. C.;
van Leeuwen, E.;
Pajkrt, E.

Publication type:

Article

Prenatal diagnosis and in utero treatment of congenital adrenal hyperplasia: An up‐to‐date comprehensive review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 635, doi. 10.1002/pd.6542

By:

Okpaise, Oluwateniayo O.;
Ahn, Hyunyoung;
Tonni, Gabriele;
Ruano, Rodrigo

Publication type:

Article

Isolated fetal umbilical vein varix and the association with intrauterine fetal death and fetal growth restriction: A systematic review, meta‐analysis, and nested retrospective cohort study.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 595, doi. 10.1002/pd.6538

By:

Koorn, Ian;
Heinrich, Hanna;
Nelissen, Anne;
Denswil, Nerissa;
Linskens, Ingeborg H.;
Jansen, Charlotte H. J. R.;
Wortelboer, Esther W.;
Pajkrt, Eva

Publication type:

Article

Postmortem imaging of fetuses at early gestations: A comparison of microfocus computed tomography with postmortem magnetic resonance at 9.4 T and postmortem ultrasound.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 572, doi. 10.1002/pd.6532

By:

Ibarra Vilar, Patricia;
Jani, Jacques C.;
Cannie, Mieke M.;
Shelmerdine, Susan C.;
Lecomte, Sophie;
Verhoye, Marleen;
Hutchinson, Ciaran J.;
Arthurs, Owen J.;
Carlin, Andrew;
Kang, Xin

Publication type:

Article

Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 614, doi. 10.1002/pd.6569

By:

Lemin, Sara;
van Bosse, Harold J. P.;
Hutka, Lauren;
Soberdash, Shea;
Patibandla, Jay

Publication type:

Article

"The anxiety coming up to every scan—It destroyed me": A qualitative study of the lived experience of cytomegalovirus infection during pregnancy.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 623, doi. 10.1002/pd.6564

By:

Tripathi, Tanya;
Watson, Jotara;
Skrzypek, Hannah;
Stump, Hanako;
Lewis, Sharon;
Hui, Lisa

Publication type:

Article

Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 665, doi. 10.1002/pd.6563

By:

Burrill, Natalie;
Khalek, Nahla;
Oliver, Edward R.;
Linn, Rebecca;
Victoria, Teresa;
Yates, Carin;
Moldenhauer, Julie S.

Publication type:

Article

Deep‐learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 535, doi. 10.1002/pd.6559

By:

Kasera, Bhavya;
Shinar, Shiri;
Edke, Parinita;
Pruthi, Vagisha;
Goldenberg, Anna;
Erdman, Lauren;
Van Mieghem, Tim

Publication type:

Article

Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 661, doi. 10.1002/pd.6560

By:

Burrill, Natalie;
Khalek, Nahla;
Cristancho, Ana G.;
Coleman, Beverly;
Murrell, Jill;
Moldenhauer, Julie S.

Publication type:

Article

Use of cell‐free non‐invasive prenatal testing in pregnancies affected by placental mosaicism.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 562, doi. 10.1002/pd.6558

By:

Lund, Ida Charlotte Bay;
Becher, Naja;
Lildballe, Dorte;
Andreasen, Lotte;
Horsholt Thomsen, Simon;
Vestergaard, Else Marie;
Vogel, Ida

Publication type:

Article

Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 586, doi. 10.1002/pd.6554

By:

Johansen, Margriet;
Haskell, Gloria T.;
Arreola, Alexandra;
Riordan, Christine;
Gadi, Inder K.;
Penton, Andrea;
Papenhausen, Peter R.;
Schwartz, Stuart

Publication type:

Article

Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 580, doi. 10.1002/pd.6520

By:

Liu, Xijing;
Zhang, Zhu;
Zhang, Xuan;
Wang, Jiamin;
Jiang, Jieni;
Li, Lingping;
Wang, He;
Liu, Shanling;
Hu, Ting

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2024, v. 44, n. 5, p. 533, doi. 10.1002/pd.6373
Publication type:: Article

Performance of cell‐free DNA testing for common fetal trisomies in triplet pregnancies.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 555, doi. 10.1002/pd.6548

By:

Zakaria, Hoda;
Kleinfinger, Pascale;
Lohmann, Laurence;
Costa, Jean‐Marc;
Tsatsaris, Vassilis;
Salomon, Laurent J.;
Jouannic, Jean‐Marie;
Rosenblatt, Jonathan;
Demain, Adèle;
Benachi, Alexandra;
El Khattabi, Laïla;
Vivanti, Alexandre J.

Publication type:

Article

Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 644, doi. 10.1002/pd.6547

By:

Watananirun, Kanokwaroon;
Vargas, Anna M. L. F.;
Vergote, Simen;
Lewi, Liesbeth;
Filippo, Marcelo O. L.;
McCulloch, Peter;
Devlieger, Roland;
Peralta, Cleisson F. A.;
Deprest, Jan

Publication type:

Article

Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 657, doi. 10.1002/pd.6546

By:

Vanden Eynde, Nathalie;
Van den Mooter, Eve;
Vantroys, Elise;
De Schutter, Elke;
Leus, Astrid;
Keymolen, Kathelijn;
Dimitrov, Boyan;
van Berkel, Kim

Publication type:

Article

Prenatal diagnosis of ROR‐2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 5, p. 653, doi. 10.1002/pd.6543

By:

Yang, Liying;
Shannon, Patrick;
Silver, Rachel;
Roifman, Maian;
Yates, Carin;
Chitayat, David

Publication type:

Article