Works matching IS 01973851 AND DT 2024 AND VI 44

Results: 223

Response to Correspondence: "Do We Really Want to Go Fishing for Fetal CC Dysgenesis (Whatever This Means...)? Extreme Caution is Needed".

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1677, doi. 10.1002/pd.6703

By:

Rodríguez, M. Angeles

Publication type:

Article

Do We Really Want to Go Fishing for Foetal CC Dysgenesis (Whatever This Means...)? Extreme Caution is Needed.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1675, doi. 10.1002/pd.6704

By:

Paladini, Dario

Publication type:

Article

Post‐Abortem Detection of a Pathogenic Somatic PIK3CA‐Variant in an Abdominal Lymphangioma That Is Not Present in Cultured Amniotic Fluid Cells.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1671, doi. 10.1002/pd.6702

By:

Roggia, Cristiana;
Ballin, Nadja;
Faust, Ulrike;
Kagan, Karl Oliver;
Dufke, Andreas

Publication type:

Article

Fetal Presentation of MYRF‐Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1647, doi. 10.1002/pd.6700

By:

Favier, Maud;
Brischoux‐Boucher, Elise;
Pyle, Louise C.;
Mottet, Nicolas;
Auber‐Lenoir, Marion;
Cattin, Julie;
Dahlen, Eric;
Cabrol, Christelle;
Arbez‐Gindre, Francine;
Attié‐Bitach, Tania;
Boute, Odile;
Devisme, Louise;
Trost, Detlef;
Boughalem, Aicha;
Chitayat, David;
Prasov, Lev;
Chorin, Odelia;
Rein‐Rothschild, Annick;
Kassif, Eran;
Weissbach, Tal

Publication type:

Article

Hypospadias Associated With Fetal Growth Restriction: A Multicentric Descriptive and Prognostic Cohort Study.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1567, doi. 10.1002/pd.6699

By:

Marquet, Manon;
Anselem, Olivia;
Bouvattier, Claire;
Vivanti, Alexandre J.;
Benachi, Alexandra;
Jouannic, Jean‐Marie;
Picone, Olivier;
Rosenblatt, Jonathan;
Salomon, Laurent J.;
Tsatsaris, Vassilis;
Athiel, Yoann

Publication type:

Article

Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1659, doi. 10.1002/pd.6698

By:

Birnbaum, Roee;
Malinger, Gustavo;
Ben Sira, Liat;
Goldenberg‐Furmanov, Mirela;
Miremberg, Hadas;
Shohat, Mordechai;
Haratz, Karina Krajden

Publication type:

Article

The Association of Prenatal Alcohol Exposure With Brain Development During the First 1000 Days of Life: A Systematic Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1603, doi. 10.1002/pd.6694

By:

Pielage, Marin;
Rousian, Melek;
van Heteren, Sem;
Groenenberg, Irene A. L.;
Hillegers, Manon H. J.;
Steegers, Eric A. P.;
Marroun, Hanan El

Publication type:

Article

Short‐ and Long‐Term Outcomes of Prenatally Identified Congenital Aqueductal Stenosis by Fetal MRI.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1574, doi. 10.1002/pd.6690

By:

Smith, Noah J.;
Nagaraj, Usha D.;
Kline‐Fath, Beth M.;
Bierbrauer, Karin S.;
Habli, Mounira;
Venkatesan, Charu

Publication type:

Article

Contemporary Outcomes of a National Fetal Spina Bifida Surgery Service.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1635, doi. 10.1002/pd.6689

By:

Kik, Charlotte C.;
Kunpalin, Yada;
Kulkarni, Abhaya V.;
Varghese, Abby;
Abbasi, Nimrah;
Ryan, Greg;
Dekoninck, Philip L. J.;
Church, Paige T.;
Malhotra, Armaan;
Raghuram, Kamini;
Kelly, Edmond;
Van Mieghem, Tim

Publication type:

Article

Aberrant Fetal Brain Sulcus Formation: A Clue to the Diagnosis of Sotos Syndrome.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1641, doi. 10.1002/pd.6686

By:

Luo, Caiqun;
Liu, Yang;
Wang, Hui;
Chen, LiYuan;
Wu, XiaoXia;
Geng, Qian;
Wen, Huaxuan;
Li, Shengli;
Wu, Weiqing;
Zhong, Mei

Publication type:

Article

Agenesis of the Ductus Venosus and Its Association With Genetic Abnormalities.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1585, doi. 10.1002/pd.6678

By:

Mash, Yarin;
Bardin, Ron;
Gilboa, Yinon;
Geron, Yossi;
Romano, Asaf;
Hadar, Eran;
Goldstein, Dana Brabbing;
Davidov, Bella;
Houri, Ohad

Publication type:

Article

Parental Management Choices and Discordant Ultrasound Findings in Referrals for Fetal Spina Bifida.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1628, doi. 10.1002/pd.6677

By:

Van den Eede, Emma;
Vergote, Simen;
Van der Veeken, Lennart;
Russo, Francesca;
Van der Merwe, Johannes;
Mastrodima‐Polychroniou, Sofia;
De Catte, Luc;
Deprest, Jan

Publication type:

Article

Clinical Characteristics and Outcomes of Intrauterine Blood Transfusion (IUT) for Infectious Etiologies.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1622, doi. 10.1002/pd.6671

By:

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

Publication type:

Article

Safety of Intrauterine Transfusion Performed Beyond 34 weeks of Gestation.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1614, doi. 10.1002/pd.6670

By:

Youssefzadeh, Ariane C.;
Masri, Jinnen;
Korst, Lisa M.;
Llanes, Arlyn;
Hamzeh, Catherine;
Chmait, Ramen H.

Publication type:

Article

Predicting the Difficult Neonatal Airway in Fetuses With Micrognathia, Oropharyngeal or Neck Mass Lesions: Two‐Center Experience With Fetal MRI.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1593, doi. 10.1002/pd.6651

By:

Goergen, Stacy;
Christie, James;
Jackson, Tracy;
Smet, Maria‐Elisabeth;
Robertson, Simon;
Malhotra, Atul;
Kroushev, Annie;
Lovell, Mark

Publication type:

Article

Prenatal Ultrasonographic Features Associated With ARSL and X‐Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1663, doi. 10.1002/pd.6649

By:

Broeren, Eleanor;
Stover, Samantha;
Bennett, Katya;
Giordano, Jessica;
Galloway, Stephanie;
Lauzon, Julie;
Rust, Laura;
Suerink, Manon;
van Haeringen, Arie;
Reimers, Rebecca

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2024, v. 44, n. 13, p. 1565, doi. 10.1002/pd.6381
Publication type:: Article

Predictive Indicators and Outcomes of Pregnancies Affected by Stage I Twin–Twin Transfusion Syndrome Treated With Fetoscopic Laser Photocoagulation.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1548, doi. 10.1002/pd.6691

By:

Wagata, Maiko;
Wada, Seiji;
Sago, Haruhiko;
Shimabukuro, Makiko;
Nakata, Masahiko;
Iwagaki, Shigenori;
Takahashi, Yuichiro;
Konno, Hiroko;
Murakoshi, Takeshi;
Ishii, Keisuke

Publication type:

Article

Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra‐Cerebral Malformations.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1526, doi. 10.1002/pd.6684

By:

Kratochwila, C.;
Pomar, L.;
Lebon, S.;
Gengler, C.;
Pavlidou, D. C.;
Good, J.‐M.;
Kumps, C.;
Sichitiu, J.

Publication type:

Article

Novel Missense Variant in the SMARCD1 Gene as the Cause of Coffin–Siris Syndrome 11 in a Fetus With Ambiguous Genitalia and Multiple Dysmorphic Features.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1522, doi. 10.1002/pd.6683

By:

Veazey, Rachel A.;
Fisher, Allan J.;
Talati, Asha N.;
Hardisty, Emily;
Gilmore, Kelly L.;
Vora, Neeta L.

Publication type:

Article

Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1518, doi. 10.1002/pd.6682

By:

Miremberg, Hadas;
Birnbaum, Roee;
Trigubov, Dorin;
Botvinik, Adi;
Yaron, Yuval;
Mory, Adi;
Malinger, Gustavo;
Haratz, Karina Krajden

Publication type:

Article

Role of Amniotic Fluid Toxicity in the Pathophysiology of Myelomeningocele: A Narrative Literature Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1530, doi. 10.1002/pd.6681

By:

Athiel, Yoann;
Jouannic, Jean‐Marie;
Lépine, Matthieu;
Maillet, Corentin;
de Saint Denis, Timothée;
Larghero, Jérôme;
Guilbaud, Lucie

Publication type:

Article

Confined Placental Mosaicism Detected With Non‐Invasive Prenatal Testing: Is There an Association Between Mosaic Ratio and Pregnancy Outcome?

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1462, doi. 10.1002/pd.6680

By:

Eggenhuizen, Geerke M.;
Go, Attie T. J. I.;
Hoffer, Mariëtte J. V.;
Goedegebuur‐Zwalua, Eveline;
Srebniak, Malgorzata I.;
Van Opstal, Diane

Publication type:

Article

The High Diagnostic Yield of Prenatal Exome Sequencing Followed by 3400 Gene Panel Analysis in 629 Ongoing Pregnancies With Ultrasound Anomalies.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1444, doi. 10.1002/pd.6676

By:

Diderich, Karin E. M.;
Bruggenwirth, Hennie T.;
Joosten, Marieke;
Thurik, Florentine;
Mijalkovic, Jona;
Polak, Marike;
Kromosoeto, Joan;
Somers‐Bolman, Galhana M.;
van den Born, Myrthe;
Drost, Mark;
Galjaard, Robert Jan H.;
Galjaard, Sander;
Hoefsloot, Lies H.;
Knapen, Maarten F. C. M.;
van Minkelen, Rick;
van der Schoot, Vyne;
van Slegtenhorst, Marjon A.;
Sleutels, Frank;
Stuurman, Kyra E.;
Weerts, Marjolein J. A.

Publication type:

Article

Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi‐Center Cohort Study.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1451, doi. 10.1002/pd.6674

By:

Li, Keying;
Wang, Huilin;
Chau, Matthew Hoi Kin;
Dong, Zirui;
Cao, Ye;
Zheng, Yu;
Leung, Tak Yeung;
Choy, Kwong Wai;
Zhu, Yuanfang

Publication type:

Article

Prenatal Phenotypic Analysis of Branchio‐Oto‐Renal Spectrum Disorder Attributable to EYA1 Gene Pathogenic Variants and Systematic Literature Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1509, doi. 10.1002/pd.6673

By:

Tian, Yuan;
Lv, Yuexia;
Wang, Handuo;
Che, Jia;
Cui, Fangying;
Guo, Jing;
Tian, Weifang;
Peng, Jia;
Yang, Bo;
Li, Haiyu;
Zhou, Baixue;
Zhu, Xiaolu;
Cui, Xueyin;
Liu, Ling

Publication type:

Article

Fetal Speckle Tracking Echocardiography Measured Global Longitudinal Strain and Strain Rate in Congenital Heart Disease: A Systematic Review and Meta‐Analysis.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1479, doi. 10.1002/pd.6672

By:

van den Wildenberg, Sarah;
van Beynum, Ingrid M.;
Havermans, Malou E. C.;
Boersma, Eric;
DeVore, Greggory R.;
Simpson, John M.;
Steegers, Eric A. P.;
Go, Attie T. J. I.;
Cornette, Jérôme M. J.

Publication type:

Article

Prenatal Sonographic Features of Rubinstein–Taybi Syndrome—A Small Case Series of a Rare Syndrome.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1502, doi. 10.1002/pd.6668

By:

Zloto, K.;
Weissbach, T.;
Messing, B.;
Birnbaum, R.;
Gindes, L.;
Levy, M.;
Lerman‐Sagie, T.;
Hadi, E.;
Eliyahu, A.;
Feinstein‐Goren, N.;
Kassif, E.

Publication type:

Article

Maternal Complications After Laser Surgery for Twin‐to‐Twin Transfusion Syndrome, a Cohort Study.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1556, doi. 10.1002/pd.6663

By:

Gijtenbeek, M.;
Prein, F. M. M.;
Verweij, E. J. T.;
Middeldorp, J. M.;
Slaghekke, F.;
Haak, M. C.

Publication type:

Article

Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1423, doi. 10.1002/pd.6659

By:

Brabbing‐Goldstein, Dana;
Bazak, Lily;
Ruhrman‐Shahar, Noa;
Lidzbarsky, Gabriel Arie;
Orenstein, Naama;
Lifshiz‐Kalis, Marina;
Asia‐Batzir, Nurit;
Goldberg, Yael;
Basel‐Salmon, Lina

Publication type:

Article

Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use".

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1500, doi. 10.1002/pd.6656

By:

Vora, Neeta L.;
Langlois, Sylvie;
Chitty, Lyn S.

Publication type:

Article

Correspondence on "Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use".

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1498, doi. 10.1002/pd.6655

By:

Wynn, Julia;
Hoskovec, Jennifer

Publication type:

Article

Parental or Trio Magnetic Resonance Imaging to Improve Prenatal Counseling in Brain Anomalies.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1435, doi. 10.1002/pd.6653

By:

Rodó, Carlota;
Maiz, Nerea;
Vázquez, Élida;
Gómez‐Andrés, David;
Valenzuela, Irene;
Abulí, Anna;
Carreras, Elena

Publication type:

Article

Oral Abstracts of the ISPD 28th International Conference on Prenatal Diagnosis and Therapy, Boston, Massachusetts, United States, 7–10 July 2024.

Published in:: Prenatal Diagnosis, 2024, v. 44, p. 3, doi. 10.1002/pd.6665
Publication type:: Article

Uptake rate of carrier screening among consanguineous couples.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1470, doi. 10.1002/pd.6556

By:

Ricca, Julianne;
Brandt, Justin S.;
Jacob, Natalie;
Ashkinadze, Elena

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1421, doi. 10.1002/pd.6380
Publication type:: Article

Abstract Author Index of the ISPD 28th International Conference on Prenatal Diagnosis and Therapy, Boston, Massachusetts, United States, 7–10 July 2024.

Published in:: Prenatal Diagnosis, 2024, v. 44, p. 177, doi. 10.1002/pd.6667
Publication type:: Article

Poster Abstracts of the ISPD 28th International Conference on Prenatal Diagnosis and Therapy, Boston, Massachusetts, United States, 7–10 July 2024.

Published in:: Prenatal Diagnosis, 2024, v. 44, p. 23, doi. 10.1002/pd.6666
Publication type:: Article

Fetal Therapy for Congenital Pulmonary Malformations: A Prospective Population‐Based National Cohort Study.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1536, doi. 10.1002/pd.6646

By:

Weber, Mathilde;
Monier, Isabelle;
Rahshenas, Makan;
Salomon, Laurent J.;
Sananes, Nicolas;
Castaigne, Vanina;
Houfflin‐Debarge, Véronique;
Jouannic, Jean‐Marie;
Massardier, Jérôme;
Tsatsaris, Vassilis;
Khoshnood, Babak;
Lelong, Nathalie;
Delacourt, Christophe;
Benachi, Alexandra

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2024, v. 44, p. 1, doi. 10.1002/pd.6369
Publication type:: Article

Characterization of the Prenatal Ultrasound Phenotype Associated With 7q11.23 Microduplication Syndrome and Williams–Beuren Syndrome.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1398, doi. 10.1002/pd.6669

By:

Wang, Fengyang;
Peng, Huijuan;
Lou, Guiyu;
Ren, Yanxin;
Liao, Shixiu

Publication type:

Article

Reversal of Fetal Compromise Following In Utero Treatment of Vein of Galen Malformation Using Glue.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1367, doi. 10.1002/pd.6662

By:

Gowda, Mamatha;
Krishnaraj, Ariharan;
Ambalakkuthan, Murugesan;
Chinta, Navya;
Selvan, Tamil

Publication type:

Article

Lethal Skeletal Dysplasia in Fetus With Novel COL1A1 Variant.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1412, doi. 10.1002/pd.6652

By:

Wang, Michelle J.;
Schioppo, Davia;
Donovan, Bridget M.;
Febres‐Cordero, Daniela A.;
Connolly, Susan;
Robinson, Julian;
Duffy, Cassandra R.

Publication type:

Article

Imaging‐Based Prediction Parameters of Perinatal Morbidity and Mortality for Fetal Occipital Cephaloceles.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1327, doi. 10.1002/pd.6660

By:

Gaulden, Amber L.;
Nagaraj, Usha D.;
Emmert, A. Scott;
Vuong, Shawn M.;
Kline‐Fath, Beth M.;
Bierbrauer, Karin S.;
Patel, Smruti K.

Publication type:

Article

Agenesis of Corpus Callosum, Malformations of Cortical Development, Duodenal Atresia and Fetal Growth Restriction: Prenatal Markers for Zhu‐Tokita‐Takenouchi‐Kim Syndrome.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1416, doi. 10.1002/pd.6658

By:

Carmant, Laurence Sophie;
Miller, Elka;
Chong, Karen;
Chitayat, David;
Shinar, Shiri

Publication type:

Article

Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1296, doi. 10.1002/pd.6657

By:

Burnett, Brian;
Parobek, Christian;
Shanahan, Matthew;
Mitts, Matthew;
Albrecht, Kelly;
Munoz, Jessian L.;
Buskmiller, Cara;
Nassar, Ahmed A.;
Sanz Cortes, Magdalena;
Belfort, Michael A.;
Donepudi, Roopali V.

Publication type:

Article

The Conundrum of Mechanics Versus Genetics in Congenital Hydrocephalus and Its Implications for Fetal Therapy Approaches: A Scoping Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1354, doi. 10.1002/pd.6654

By:

Herzeg, Akos;
Borges, Beltran;
Diafos, Loukas N.;
Gupta, Nalin;
MacKenzie, Tippi C.;
Sanders, Stephan J.

Publication type:

Article

SNPscan Combined With CNVplex as a High‐Performance Diagnostic Method for Thalassemia.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1310, doi. 10.1002/pd.6661

By:

Wei, Xiaofeng;
Wang, Xingmin;
Xiong, Fu;
Zhang, Xinhua;
Liu, Dun;
Zhou, Wanjun;
He, Fei;
Shang, Xuan

Publication type:

Article

Maternal cell contamination in postnatal umbilical cord blood samples implies a low risk for genetic misdiagnoses.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1304, doi. 10.1002/pd.6595

By:

Smeekens, Sanne P.;
Leferink, Maike.;
Yntema, Helger G.;
Kamsteeg, Erik‐Jan

Publication type:

Article

Experimental Induction of Complex Gastroschisis in the Fetal Lamb: Systematic Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1372, doi. 10.1002/pd.6647

By:

Arai, Tomohiro;
Tianthong, Wasinee;
Russo, Francesca Maria;
Basurto, David;
Joyeux, Luc;
De Coppi, Paolo;
Deprest, Jan

Publication type:

Article