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Bibliografias temáticas / Prenatal diagnosis

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Literatura científica selecionada sobre o tema "Prenatal diagnosis"

Autor: Grafiati

Publicado: 4 de junho de 2021

Última modificação: 25 de julho de 2025

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Artigos de revistas sobre o assunto "Prenatal diagnosis"

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Gorbunov, D. V., and L. S. Abikeeva. "Prenatal diagnosis of critical congenital heart defects in Kazakhstan: a single-center 8 years’ experience." Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 67, no. 5 (2022): 96–102. http://dx.doi.org/10.21508/1027-4065-2022-67-5-96-102.

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Purpose. To give a quantitative and qualitative assessment of the results of prenatal diagnosis of critical congenital heart defects in the Republic of Kazakhstan based on the treatment of newborns at the head cardiac surgery center.Methods. A retrospective analysis of the medical records of 511 newborns with critical congenital heart defects treated at the National Research Cardiac Surgery Center (NRCSC) in 2012–2019 was performed. The proportion of those operated on was 474/511 (92.8%). The studied parameters were the presence of prenatal diagnosis of critical congenital heart defects (yes/n

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ACAR, Züat, Işıl TURAN BAKIRCI, Deniz Kanber ACAR, and Helen BORNAUN. "Prenatal diagnosis and clinical outcomes of isolated interruption of the inferior vena cava: an analysis of 12 cases." Journal of Medicine and Palliative Care 4, no. 5 (2023): 530–34. http://dx.doi.org/10.47582/jompac.1358089.

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Objectives: This study aimed to comprehensively investigate the clinical manifestations and outcomes of prenatally diagnosed isolated interrupted inferior vena cava (IIVC) with azygos continuation to shed light on the significance of prenatal diagnosis.  Methods: A longitudinal study involved 12 fetuses prenatally diagnosed with IIVC and azygos continuation. Detailed fetal anomaly scans and echocardiography were performed, and pediatric cardiologists confirmed postnatal diagnoses. Genetic testing and extensive follow-ups were also performed.  Results: The study confirme

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DiLiberti, J. H., M. A. Greenstein, and S. S. Rosengren. "Prenatal Diagnosis." Pediatrics in Review 13, no. 9 (1992): 334–42. http://dx.doi.org/10.1542/pir.13-9-334.

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Begum, Rashida. "Prenatal Diagnosis." Bangladesh Journal of Obstetrics & Gynaecology 31, no. 2 (2017): 61–62. http://dx.doi.org/10.3329/bjog.v31i2.34211.

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Baumiller, Robert. "Prenatal Diagnosis." Ethics & Medics 20, no. 11 (1995): 3–4. http://dx.doi.org/10.5840/em1995201122.

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Hafner, Erich. "Prenatal diagnosis." Hamdan Medical Journal 5, no. 3 (2012): 213. http://dx.doi.org/10.7707/hmj.v5i3.196.

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DiLiberti, John H., Mark A. Greenstein, and Sally Shulman Rosengren. "Prenatal Diagnosis." Pediatrics In Review 13, no. 9 (1992): 334–42. http://dx.doi.org/10.1542/pir.13.9.334.

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The enormous progress witnessed in the field of prenatal diagnosis during the past two decades is likely to continue into the future. Improved imaging techniques are likely to enhance the resolution of noninvasively obtained fetal images considerably over their current excellent quality. Although this undoubtedly will be true for ultrasonography, the increased speed of magnetic resonance equipment may offer a new realm of imaging possibilities. Computerized image processing, analysis, and three-dimensional reconstructions all should make interpretation of fetal images easier and more understan

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Texler, K. C. "Prenatal diagnosis." Medical Journal of Australia 152, no. 3 (1990): 149. http://dx.doi.org/10.5694/j.1326-5377.1990.tb125125.x.

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Lippman, A. "Prenatal diagnosis." American Journal of Public Health 89, no. 10 (1999): 1592–93. http://dx.doi.org/10.2105/ajph.89.10.1592.

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WILLIAMSON, ROGER A. "PRENATAL DIAGNOSIS." Clinical Obstetrics and Gynecology 31, no. 2 (1988): 231. http://dx.doi.org/10.1097/00003081-198806000-00003.

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Teses / dissertações sobre o assunto "Prenatal diagnosis"

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Overton, Timothy Graeme. "Minimally invasive prenatal diagnosis." Thesis, Imperial College London, 2000. http://hdl.handle.net/10044/1/7869.

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Турова, Людмила Олександрівна, Людмила Александровна Турова, Liudmyla Oleksandrivna Turova, and W. A. Alsaedi. "New methods in prenatal diagnosis." Thesis, Сумський державний університет, 2013. http://essuir.sumdu.edu.ua/handle/123456789/32308.

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The development of genotyping and sequencing techniques has been dramatic during the recent years. Now it is possible to obtain a full view over an individual’ s genetic landscape in the form of a million common single-nucleotide polymorphisms (SNPs) in single and affordable experiments. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/32308

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Crang-Svalenius, Elizabeth. "The use of routine ultrasound in pregnancy with special reference to normal and abnormal foetal growth, information and informed choice and the womens' experiences of the prenatal diagnostic aspects /." Lund : Lund University, Dept. of Obstetrics and Gynaecology, University Hospital, 1997. http://catalog.hathitrust.org/api/volumes/oclc/39072830.html.

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Leung, Kwok-yin, та 梁國賢. "Prenatal ultrasound prediction of homozygous α⁰-thalassemia". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B47454039.

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Homozygous α0-thalassemia is a serious autosomal recessive disorder with poor fetal outcome and severe maternal complications. Conventionally, prenatal diagnosis is performed by an invasive test. A non-invasive approach using serial ultrasonography can effectively reduce the need for invasive tests in unaffected pregnancies. For two-dimensional ultrasound prediction, a total of 777 at-risk fetuses were studied from 12 to 20 weeks between 1995 and 2006. At 12–15 weeks’ gestation, the highest sensitivity (98.3%) was achieved by the combination of fetal cardiothoracic ratio (CTR) and/o

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Miller, Chloe Louise. "A comparison of attitudes towards prenatal diagnosis and pre-implantation genetic diagnosis." Thesis, University of Leeds, 2010. http://etheses.whiterose.ac.uk/1083/.

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Technological advances in prenatal screening and diagnosis mean that it is now possible to test for a wide range of congenital conditions (Hewison et al., 2007). Traditionally testing has been carried out during pregnancy (prenatal diagnosis, PND). However, advances in technology have made it possible for diagnosis of an embryo created through in vitro fertilisation, prior to implantation into the womb (pre-implantation genetic diagnosis, PGD). This means that women can avoid the birth of a child with a genetic condition without the stress of terminating a pregnancy. This raises questions abou

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Lee, Sansan. "Genetic counseling perspectives on prenatal array CGH testing." Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23259.

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Azri, Stephanie. "Prenatal Diagnosis and Psychosocial Support: A Study about the Impact of Psychosocial Support on Women’s Wellbeing Following an Adverse Prenatal Diagnosis." Thesis, Griffith University, 2017. http://hdl.handle.net/10072/366774.

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Prenatal diagnosis testing, whether a woman chooses to terminate her pregnancy or carry to term after an adverse prenatal diagnosis, comes with long term, complex implications which include psychiatric, emotional and social problems (Black & Sandelowski, 2010; Fonseca, Nazare & Canavarro, 2012; Howard, 2006, Korenromp, Christiaens, Bout, Mulder, Hunfeld & Bilardo, 2005; Lathrop & VandeVuss, 2011a; Taylor, 1998). A variety of strategies are utilised by professionals to support women prior to the decision-making process, at the point of decision-making and after the termination or birth followin

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LaPan, Amy C. "Prenatal testing, birth outcomes, and views of social workers." online access from Digital Dissertation Consortium, 2005. http://libweb.cityu.edu.hk/cgi-bin/er/db/ddcdiss.pl?3202790.

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Leung, Wing-cheong, and 梁永昌. "Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B4520553X.

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Paal, Andrea M. "Parents' Informational Needs Following Prenatal Diagnosis of Spina Bifida." University of Cincinnati / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1276976280.

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Livros sobre o assunto "Prenatal diagnosis"

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Hahn, Sinuhe, and Laird G. Jackson, eds. Prenatal Diagnosis. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-066-9.

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Levy, Brynn, ed. Prenatal Diagnosis. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-8889-1.

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Abramsky, Lenore, and Jean Chapple, eds. Prenatal Diagnosis. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9.

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I, Evans Mark, ed. Prenatal diagnosis. McGraw-Hill Medical Pub. Division, 2005.

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Sinuhe, Hahn, and Jackson Laird G, eds. Prenatal diagnosis. Humana Press, 2008.

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Jack, FitzSimmons, ed. Prenatal diagnosis. Elsevier, 1993.

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1946-, Filkins Karen, and Russo Joseph F. 1945-, eds. Human prenatal diagnosis. M. Dekker, 1985.

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1946-, Filkins Karen, and Russo Joseph F. 1945-, eds. Human prenatal diagnosis. 2nd ed. M. Dekker, 1990.

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Paley Galst, Joann, and Marion S. Verp, eds. Prenatal and Preimplantation Diagnosis. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18911-6.

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1943-, Simpson Joe Leigh, and Elias Sherman, eds. Essentials of prenatal diagnosis. Churchill Livingstone, 1993.

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Capítulos de livros sobre o assunto "Prenatal diagnosis"

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Atkinson, H. Glenn, and Alan Handyside. "Preimplantation diagnosis." In Prenatal Diagnosis. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_8.

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Kleijer, W. J. "Prenatal Diagnosis." In Inborn Metabolic Diseases. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-662-02613-7_54.

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Kardon, Nataline, and Lisa Edelmann. "Prenatal Diagnosis." In Molecular Genetic Pathology. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-405-6_17.

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Peña, Alberto, and Andrea Bischoff. "Prenatal Diagnosis." In Surgical Treatment of Colorectal Problems in Children. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-14989-9_3.

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Eady, R. A. J. "Prenatal Diagnosis." In Dermatology in Five Continents. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-83360-1_18.

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Jackson, John F. "Prenatal Diagnosis." In Genetics and You. Humana Press, 1996. http://dx.doi.org/10.1007/978-1-4612-0227-1_3.

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Zuckerwise, Lisa C., Karen Archabald, and Joshua Copel. "Prenatal diagnosis." In Evidence-based Obstetrics and Gynecology. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119072980.ch21.

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Rothman, Barbara Katz. "Prenatal Diagnosis." In Biomedical Ethics Reviews. Humana Press, 1991. http://dx.doi.org/10.1007/978-1-59259-445-0_9.

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Milunsky, Aubrey. "Prenatal Diagnosis." In Genetics and the Law III. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4952-5_24.

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Thomas, David F. M., and Robert H. Whitaker. "Prenatal Diagnosis." In Clinical Practice in Urology. Springer London, 1989. http://dx.doi.org/10.1007/978-1-4471-1712-4_5.

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Trabalhos de conferências sobre o assunto "Prenatal diagnosis"

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Li, Haonan, Mengke Chen, and Jiyue Zhang. "Research Progress on the Application of AI in Prenatal Diagnosis and Fetal Growth and Development." In 2024 3rd International Conference on Health Big Data and Intelligent Healthcare (ICHIH). IEEE, 2024. https://doi.org/10.1109/ichih63459.2024.11064905.

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Forestier, F., F. Daffos, C. Kaplan, and P. Champeix. "PRENATAL DIAGNOSIS OF HEMORRHAGIC DISORDERS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644270.

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Utilizing an easy and safe procedure for fetal blood sampling in utero. we have studied 123 fetuses for congenital oracquire hemorrhagic disorders.Usually, the diagnosis is performed at the 18th week of gestation. To date, no fetal less or premature labor has beenattributed to these fetal samplings. Theduration of the procedure was less than 10 minutes in 90 % of the cases. Direct blood sampling with a needle guided by ultrasound is safer for fetuses and simpler for the patients than fetoscopy. Among the 1.465 samplings the mortality rateis 0.2 %. We have established the basis values for fetal

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Oseji, Ogochukwu, Felipe Mercado Olivares, Torri Anderson, et al. "Prenatal Diagnosis of Gastroschisis." In 13th Philadelphia Prenatal Virtual Conference—Selected Abstracts. Thieme Medical Publishers, Inc., 2021. http://dx.doi.org/10.1055/s-0041-1735769.

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Oseji, Ogochukwu, Felipe Mercado Olivares, Torri Anderson, et al. "Prenatal Diagnosis of Gastroschisis." In 13th Philadelphia Prenatal Virtual Conference—Selected Abstracts. Thieme Medical Publishers, Inc., 2021. http://dx.doi.org/10.1055/s-0041-1735769.

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Olivares, Felipe Mercado, Ogochukwu Oseji, Israel Benjamin, et al. "Prenatal Diagnosis of Ocular Anomalies." In 13th Philadelphia Prenatal Virtual Conference—Selected Abstracts. Thieme Medical Publishers, Inc., 2021. http://dx.doi.org/10.1055/s-0041-1735771.

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Olivares, Felipe Mercado, Ogochukwu Oseji, Israel Benjamin, et al. "Prenatal Diagnosis of Ocular Anomalies." In 13th Philadelphia Prenatal Virtual Conference—Selected Abstracts. Thieme Medical Publishers, Inc., 2021. http://dx.doi.org/10.1055/s-0041-1735771.

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Benjamin, Israel, Rochelle Johns, Giovanni Sisti, et al. "Prenatal Diagnosis of Cleft Lip + Palate." In 13th Philadelphia Prenatal Virtual Conference—Selected Abstracts. Thieme Medical Publishers, Inc., 2021. http://dx.doi.org/10.1055/s-0041-1735768.

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Benjamin, Israel, Rochelle Johns, Giovanni Sisti, et al. "Prenatal Diagnosis of Cleft Lip + Palate." In 13th Philadelphia Prenatal Virtual Conference—Selected Abstracts. Thieme Medical Publishers, Inc., 2021. http://dx.doi.org/10.1055/s-0041-1735768.

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Moodie, P., I. R. Peake, M. B. Liddell, and A. L. Bloom. "CARRIER DETECTION AND PRENATAL DIAGNOSIS IN HAEMOPHILIA A BY GENE ANALYSIS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644007.

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Restriction fragment length polymorphism (RFLP) analysis has been used to perform family studies, including prenatal diagnosis, in 21 haemophilia A kindred.Two intragenomic RFLPs were studied in conjunction with one linked RFLP. The intragenomic BgII RFLP,situation 3' to exon 26 was detected with cDNA probe C (Genetics Institute) giving bands of 20kb (17% of X chromosomes) and 5kb (83%), and the intragenomic Bell RFLP, situated 3' to exon 18, was detected with the genomic DNA probe pi 14.12 from Genentech. The frequency of this RFLP in the local population was 23% (1.1 kb allele) and 77% (0.88

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Mladenović, Tamara. "FUNDAMENTAL LEGAL ASPECTS OF THE PRENATAL GENETIC DIAGNOSIS." In International scientific conference challenges and open issues of service law. Vol. 1. University of Kragujevac, Faculty of law, 2024. http://dx.doi.org/10.46793/xxmajsko1.395m.

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he field of genetic services within the legal system of the Republic of Serbia was initially regulated in 2015 with the enactment of the Law on Prevention and Diagnosis of Genetic Diseases, Genetically Conditioned Anomalies, and Rare Diseases. This law, commonly known as “Zoja’s Law”, was prompted by the advocacy of parents whose daughter suffered from a rare disease and was denied access to healthcare due to the inability to obtain a diagnosis in Serbia. As a result, the law was introduced to the public with significant attention and is recognized as one of the most modern legal frameworks in

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Relatórios de organizações sobre o assunto "Prenatal diagnosis"

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Bolkcom, Bridget. Etiology, Diagnosis, and Treatments of Ventral Wall Defects and Acess to Prenatal Care. Iowa State University, 2022. http://dx.doi.org/10.31274/cc-20240624-640.

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Feng, Zhichao, Zhimin Yan, and Qianyun Liu. MRI Signs for Prenatal Prediction of Placenta Accreta Spectrum Disorders and Invasiveness in High-risk Pregnant Women: A Systematic Review and Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.11.0003.

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Review question / Objective: This meta-analysis aimed to identify the significant MRI signs for placenta accreta spectrum in high-risk pregnant women and to determine their diagnostic value. Condition being studied: Placenta accreta spectrum (PAS) is a dangerous complication in pregnancies with increasing incidence worldwide, in which the villous tissue adheres or invades the uterine wall. Eligibility criteria: Articles assessing the diagnostic performance of MRI signs for PAS and/or placenta percreta in high-risk pregnant women underwent full-text review. Included studies required confirmatio

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Marchionni, Enrica, Daniele Guadagnolo, Gioia Mastromoro, and Antonio Pizzuti. Diagnostic yield of prenatal Exome Sequencing in fetal Central Nervous System Anomalies: systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.5.0003.

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Review question / Objective: The aim of this study is to assess the incremental diagnostic yield of prenatal exome sequencing analysis after inconclusive result of karyotype and Chromosomal Microarray Analysis in Central Nervous System fetal anomalies detected by ultrasound. Eligibility criteria: Inclusion criteria: papers describing fetuses with the indication to perform genome-wide sequencing studies based on prenatal imaging findings who underwent previous inconclusive karyotype and Chromosomal Microarray Analyses. The diagnostic yields of prenatal exome sequencing analysis OR prenatal geno

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