Einloggen

Thematische Bibliographien / Prenatal diagnosis / Dissertationen

Um die anderen Arten von Veröffentlichungen zu diesem Thema anzuzeigen, folgen Sie diesem Link: Prenatal diagnosis.

Dissertationen zum Thema „Prenatal diagnosis“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 25. Juli 2025

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit Top-50 Dissertationen für die Forschung zum Thema "Prenatal diagnosis" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Sehen Sie die Dissertationen für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.

1

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

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

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.

Der volle Inhalt der Quelle

Annotation:

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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

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.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

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.

Der volle Inhalt der Quelle

Annotation:

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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

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/.

Der volle Inhalt der Quelle

Annotation:

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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

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

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

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.

Der volle Inhalt der Quelle

Annotation:

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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

8

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.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

9

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.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

10

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.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

11

Tedgård, Ulf. "Prenatal diagnosis of haemophilia psychological, social and ethical aspects /." Malmö : Dept. of Pediatrics, University Hospital of Malmö, University of Lund, 1999. http://catalog.hathitrust.org/api/volumes/oclc/57455671.html.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

12

McDougall, Christopher W. "Uncertain risks, responsibilities & regulations : the ethics & control of PGD in Canada." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33915.

Der volle Inhalt der Quelle

Annotation:

The current state of preimplantation genetic diagnosis technology is presented, as are the biological principles and medical procedures that make it possible. The arguments of both proponents and those with social and ethical reservations about the broader implications of the technique are carefully reviewed, and the limitations of the dominant medical model approach to the technique are exposed. A discussion of reproductive autonomy in light of emerging testing applications of PGD not directly related to the avoidance of serious genetic abnormalities in the resulting child demonstrates the co

APA, Harvard, Vancouver, ISO und andere Zitierweisen

13

Lo, Yuk-Ming Dennis. "Genetic analysis of fetal cells in maternal blood." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359448.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

14

Jafri, Syed Hussain. "Attitudes toward prenatal diagnosis and termination of pregnancy in Pakistan." Thesis, University of Leeds, 2017. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713499.

Der volle Inhalt der Quelle

Annotation:

Introduction: Prenatal diagnosis for genetic conditions has been available in Pakistan since 1994, however very little is known about this population's attitudes toward prenatal diagnosis or termination of affected pregnancies for different conditions. Advances in molecular biology mean it is possible to offer prenatal diagnosis for an increasing number of conditions and therefore, it is important to assess these attitudes. Objective: To explore Pakistani parents' attitudes toward prenatal diagnosis and termination of affected pregnancies for a range of conditions and the factors that contribu

APA, Harvard, Vancouver, ISO und andere Zitierweisen

15

Morrigan, Viviane School of History &amp Philosophy of Science UNSW. "An ethics of reproductive choice : genetic counselling and prenatal diagnosis." Awarded by:University of New South Wales. School of History & Philosophy of Science, 2002. http://handle.unsw.edu.au/1959.4/19396.

Der volle Inhalt der Quelle

Annotation:

For this project I describe the socio-historical development of a particular application of genetic prenatal diagnosis, in terms of changing social relations that govern an ethics of reproductive choice. I examine ways that medicine and government articulate prenatal diagnosis to problematise the maternal body and govern women's reproductive choices about chromosomal abnormality in the fetus. Since its introduction in the early 1970s, the major use of prenatal diagnosis has been to detect chromosomal abnormalities-in particular, Down syndrome-in the fetus. Medico-scientific knowledge claims ne

APA, Harvard, Vancouver, ISO und andere Zitierweisen

16

Saltvedt, Sissel. "Prenatal diagnosis in routine antenatal care : a randomised controlled trial /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-549-6/.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

17

Cederholm, Maria. "Consequences of amniocentesis and chorionic villus sampling for prenatal diagnosis." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2002. http://publications.uu.se/theses/91-554-5225-6/.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

18

Johansen, Marianne. "Trophoblast deportation : its relevance for pre-eclampsia and prenatal diagnosis." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337598.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

19

Smith, Marissa B. "A description of genetic counselors' views and current practice with regard to the use of array-CGH for prenatal diagnosis." Cleveland, Ohio : Case Western Reserve University, 2009. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1246977726.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

20

Strange, Heather. "Non-invasive prenatal diagnosis and testing : perspectives on the emergence and translation of a new prenatal testing technology." Thesis, Cardiff University, 2015. http://orca.cf.ac.uk/90887/.

Der volle Inhalt der Quelle

Annotation:

This thesis presents findings from a qualitative study of the emergence and early clinical translation of non-invasive prenatal diagnosis (NIPD) in the UK. Drawing from interviews with a range of experts and users I track the enrolment and translation of this new prenatal testing technology across a variety of clinical and social spaces. I show how encounters with NIPD prompt deep critical examination of the moral, social and political implications - not only of the technology - but of the established clinical practices (routine and specialised prenatal testing) and specific policy contexts (p

APA, Harvard, Vancouver, ISO und andere Zitierweisen

21

McCormack, Michael James. "Development of prenatal diagnosis of metabolic disorders using chorionic villus sampling." Thesis, Queen's University Belfast, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317449.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

22

Liu, David T. Y. "Development of transcervical chorion villus sampling for first trimester prenatal diagnosis." Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293186.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

23

Sconyers, Emma (Emma G. ). "I carry you in my heart : facing an incurable prenatal diagnosis." Thesis, Massachusetts Institute of Technology, 2014. http://hdl.handle.net/1721.1/92632.

Der volle Inhalt der Quelle

Annotation:

Thesis: S.M. in Science Writing, Massachusetts Institute of Technology, Department of Humanities, Graduate Program in Science Writing, 2014.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references (pages 38-40).<br>Prenatal diagnosis has given doctors the ability to predict problems before a child is even born. But what happens when the information gleaned from these tests is that the child is fatally sick? Doctors call these "futile" pregnancies. The increasing sophistication and prevalence of prenatal diagnostic tests means that prospective parents and their doctors a

APA, Harvard, Vancouver, ISO und andere Zitierweisen

24

Alsulaiman, Ayman. "Attitudes toward prenatal diagnosis and termination of pregnancy in Saudi Arabia." Thesis, University of Leeds, 2004. http://etheses.whiterose.ac.uk/536/.

Der volle Inhalt der Quelle

Annotation:

INTRODUCTION: Advances in molecular biology will soon make it possible to offer parents prenatal testing for a large number of different genetic disorders. The tests that have been offered to date are available because of technology, not because of the burden or prevalence of the condition. Parents' attitudes to different genetic disorders need to be evaluated, because little is known about how people's attitudes to testing for one disorder relate to their views on testing for other disorders. AIMS: To assess the attitudes of Saudi parents with and without an affected child, towards prenatal d

APA, Harvard, Vancouver, ISO und andere Zitierweisen

25

Bridle, Lisa. "Stories of choice : mothers of children with Down syndrome and the ethics of prenatal diagnosis /." [St. Lucia, Qld.], 2004. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe18304.pdf.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

26

Yeoh, S. C. "The isolation and identification of fetal leucocytes in the maternal circulation." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.256745.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

27

Hui, Pui-wah, and 許佩華. "Nuchal translucency in pregnancies conceived after assisted reproduction technology." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2003. http://hub.hku.hk/bib/B31971040.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

28

Hui, Pui-wah, and 許佩華. "Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/208518.

Der volle Inhalt der Quelle

Annotation:

Assisted reproduction technology is increasingly used for treatment of couples with subfertility. These women are usually of more advanced maternal age and carry a higher risk of fetal Down syndrome. Results from early publications showed that biochemical markers for screening of fetal Down syndrome in the second trimester were different between pregnancies from in vitro fertilization (IVF) and natural conception. This could potentially increase the false positive rate and result in unnecessary invasive diagnostic procedures. Questions were raised as to whether the alterations were related to

APA, Harvard, Vancouver, ISO und andere Zitierweisen

29

Ager, R. P. "Studies on some biochemical methods for the prenatal diagnosis of Down's syndrome." Thesis, University of Salford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381649.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

30

Elfarawi, Hunaydah. "Alobar Holoprosencephaly: Parental Perspectives on Prenatal Decision-making, Prenatal Provider Prognostication, and Quality of Life." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1617108856885634.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

31

Varawalla, Nermeen Y. "Molecular genetics of beta thalassaemia in Asian Indians : basis for prenatal diagnosis." Thesis, University of Oxford, 1992. http://ora.ox.ac.uk/objects/uuid:f3a2a0a7-3d14-4dcf-a6fc-616db75119bf.

Der volle Inhalt der Quelle

Annotation:

The primary aim of this thesis was to outline an approach for the prenatal diagnosis of β-thalassaemia in the Asian Indian population by DNA analysis. A polymerase chain reaction (PCR) based, nonradioactive and rapid technique, allele specific PCR, was successfully developed for the detection of β-thalassaemia mutations. A large sample of 656 unrelated carriers from seven different regions of the Indian subcontinent was studied by allele specific PCR and DNA sequence analysis. Sixteen different β-thalassaemia mutations were identified, two of which were new mutations. Of these five common muta

APA, Harvard, Vancouver, ISO und andere Zitierweisen

32

Zheng, Yun-Ling. "Rapid prenatal diagnosis of common fetal aneuploidies by fluorescence in situ hybridisation." Thesis, University of Cambridge, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318418.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

33

Pinto, Joana Isabel Monteiro. "Metabonomics of the blood of pregnant women for diagnosis of prenatal disorders." Master's thesis, Universidade de Aveiro, 2010. http://hdl.handle.net/10773/3156.

Der volle Inhalt der Quelle

Annotation:

Mestrado em Métodos biomoléculares<br>A aplicação da metabonómica na pesquisa de novos biomarcadores de doenças tem ganho um interesse crescente na investigação e desenvolvimento, tanto ao nível do processamento analítico como do tratamento de dados. Nomeadamente, a análise metabonómica usando espectroscopia de Ressonância Magnética Nuclear (NMR) fornece uma grande quantidade de dados de uma forma rápida e não invasiva sobre a composição de amostras complexas como o plasma sanguíneo. Uma vez que as doenças pré-natais têm um elevado impacto no metabolismo materno e fetal, sendo responsáveis por

APA, Harvard, Vancouver, ISO und andere Zitierweisen

34

Sutton, Erica J. "Prenatal testing and informed choice : the need for improved communication and understanding between health care professionals and pregnant women." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=19653.

Der volle Inhalt der Quelle

Annotation:

This research examines the many different ethical issues that emerge in the health care setting with regards to prenatal diagnostic testing. Identifying the areas of clinical practice and religious counselling in need of improvements, particularly physician-client communication, is important to ensure that competent pregnant women make informed, considered choices about prenatal testing. This paper investigates the many factors that contribute to pregnant women's decision-making processes surrounding the acceptance or refusal of the maternal serum alpha-fetoprotein screen, ultrasonography, amn

APA, Harvard, Vancouver, ISO und andere Zitierweisen

35

Sullivan, Amanda. "Genetic risk estimation and attendance for counselling among high-risk mothers-to-be." Thesis, University of Derby, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341401.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

36

Jiang, Sheng. "Application of nested PCR, whole genome amplification and comparative genomic hybridisation for single cell genetic analysis." Thesis, University of Glasgow, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366140.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

37

Chudleigh, Patricia Margaret. "The clinical significance of fetal renal pyelectasis as detected by routine ultrasound screening in the second trimester of pregnancy." Thesis, King's College London (University of London), 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327174.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

38

Buamah, P. K. "A study of biochemical methods for the prenatal diagnosis of neural tube defects." Thesis, University of Newcastle Upon Tyne, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370153.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

39

De, Blasio Miles Jonathon. "Placental restriction and endocrine control of postnatal growth." Title page, table of contents and abstract only, 2004. http://web4.library.adelaide.edu.au/theses/09PH/09phd2869.pdf.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

40

Wong, Hoi-hei Vera, and 王愷曦. "Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2015. http://hdl.handle.net/10722/208587.

Der volle Inhalt der Quelle

Annotation:

There has been an increase in rates of chromosomal abnormalities in newborns as a result of reproductive aging. For the past decades, a lot of effort has been placed on identifying pregnancies at risk of genetic defects. Conventional prenatal genetic diagnosis is achieved by invasive procedures that have been associated with an increased risk of pregnancy loss. This has led the researchers to explore the use of non-/minimally invasive techniques for prenatal diagnosis. Trophoblasts are known to be shed from regressing chorionic villi into the lower uterine pole of pregnant women during the fi

APA, Harvard, Vancouver, ISO und andere Zitierweisen

41

Puszyk, William Matthew. "Epigenetics of cell-free plasma DNA for non-invasive prenatal diagnosis of fetal aneuploidies." Thesis, University of Warwick, 2008. http://wrap.warwick.ac.uk/1059/.

Der volle Inhalt der Quelle

Annotation:

Since the discovery of cell-free fetal DNA in the circulation of pregnant women fetal-specific DNA biomarkers for non-invasive prenatal diagnosis of fetal aneuploidy have been sought. A model system assessing the DNA methylation of placental DNA and adult peripheral leukocyte DNA has been developed previously to represent fetal and maternal plasma DNA. To use DNA methylation to detect specific DNA molecules it is desirable that cellfree plasma DNA maintains the methylation profile of its tissue source. Using the imprinted gene GNAS1, a test has been developed to assess, for the first time the

APA, Harvard, Vancouver, ISO und andere Zitierweisen

42

Yau, Hoi-ying Alice, and 邱凱盈. "Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B48079790.

Der volle Inhalt der Quelle

Annotation:

Risk is a crucial concept in healthcare communication. This is attested to by a large body of research on risk communication in psychology, sociology, and, more recently, discourse analysis. This previous research has primarily focused on how healthcare providers manage risk talk, whereas patients’ risk talk has received little attention. Where it has been researched, it has been presented in an oversimplified way, namely that the patients have been reported to perceive their risk in a simplified, ‘all-or-nothing manner’. Using theme-oriented discourse analysis (Roberts and Sarangi, 20

APA, Harvard, Vancouver, ISO und andere Zitierweisen

43

Lane, Jonnie A. "Evaluation of maternal serum triple screen as an identifier of trisomy 21 pregnancy." Morgantown, W. Va. : [West Virginia University Libraries], 2000. http://etd.wvu.edu/templates/showETD.cfm?recnum=1688.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

44

Corrochano, Fatule Mariana, Rodriguez Rodolfo Llanos, and Alcides Garcia. "Quiste de colédoco en una lactante de tres meses de edad: diagnóstico prenatal y manejo quirúrgico." Asociación Interciencia, 2014. http://hdl.handle.net/10757/333630.

Der volle Inhalt der Quelle

Annotation:

El quiste de colédoco es una patología poco común, diagnosticada generalmente después del nacimiento; pero en los últimos tiempos el diagnóstico prenatal ha tomado mayor importancia, pues permite una intervención precoz y brinda un mejor pronóstico a los pacientes. Se presenta el caso de una lactante que fue diagnosticada mediante ecografía obstétrica, a las 21 semanas de vida intrauterina; confirmándose luego el diagnóstico por medio de resonancia magnética. La paciente fue operada a los tres meses de vida, realizándosele una quistectomía, colecistectomía y derivación biliodigestiva

APA, Harvard, Vancouver, ISO und andere Zitierweisen

45

Emad, Ahmed Anwar Hasanin. "Development and assessment of strategies for non-invasive prenatal diagnosis using fetal cells in maternal blood." Thèse, Université de Sherbrooke, 2014. http://hdl.handle.net/11143/5855.

Der volle Inhalt der Quelle

Annotation:

Abstract : Current prenatal diagnosis depends on invasive procedures and is thus offered only to high-risk pregnancies. Development of non-invasive prenatal diagnosis (NIPD) would change the risk-benefit ratio and make it likely that more women would benefit from prenatal testing. Scientists have documented the presence of rare fetal cells in maternal blood and envisioned targeting them with specific markers and their use in NIPD. Considering their extremely low frequency in maternal blood, fetal cells have been difficult to retrieve and use in clinical practice. Therefore, there is a pressing

APA, Harvard, Vancouver, ISO und andere Zitierweisen

46

Rodríguez, Pérez Mª Ángeles. "Valoración ecográfica prenatal del cono medular fetal." Doctoral thesis, Universitat de Barcelona, 2016. http://hdl.handle.net/10803/397729.

Der volle Inhalt der Quelle

Annotation:

Con el término de disrafismos espinales se agrupan una serie heterogénea de malformaciones congénitas de la médula espinal definida por el defecto de la fusión de las estructuras neurales, óseas y mesenquimatosas de la línea media. Los disrafismos cerrados (espectro muy heterogéneo de anomalías: diastematomielia, lipomas, filum terminal engrosado, mielocistoceles, senos dérmicos), son más difíciles de diagnosticar intraútero debido a la ausencia de anomalías intracraneales. Frecuentemente se asocian a médula anclada, por lo que el cono medular (CM) se sitúa a un nivel más bajo de lo esperado,

APA, Harvard, Vancouver, ISO und andere Zitierweisen

47

Smolska, Andriana. "Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor." Thesis, Linköping University, Centre for Applied Ethics, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-6683.

Der volle Inhalt der Quelle

Annotation:

<p>The modern world is facing a revolutionary development in the clinical medicine and biomedical sciences. Due to the different life supporting systems, it is easily possible to keep patients with severe diseases alive. With organ transplantation a lot of people, who would otherwise die can live long and happy lives. In vitro fertilization allows a woman to bear the child that is not genetically related to her. Due to the possibility of contraception, safe abortions and prenatal diagnosis, women and couples can make preferable choices concerning their future child. Such medical developments a

APA, Harvard, Vancouver, ISO und andere Zitierweisen

48

Mamalis, Marios [Verfasser], and R. [Akademischer Betreuer] Axt-Fliedner. "Absent Pulmonary Valve Syndrome: Prenatal Diagnosis, Association and Outcome / Marios Mamalis ; Betreuer: R. Axt-Fliedner." Marburg : Philipps-Universität Marburg, 2019. http://d-nb.info/1178672042/34.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

49

Gardner, Patricia Emma. "Antibodies to secretory acetylcholinesterase : their possible role in the prenatal diagnosis of neural tube defects." Thesis, University of Bath, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.277120.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

50

Swarts, Elfriede. "The outcome of prenatal sonographic diagnosis of fetal talipes in the Cape Town Metro district." Master's thesis, University of Cape Town, 2017. http://hdl.handle.net/11427/27550.

Der volle Inhalt der Quelle

Annotation:

Background: Talipes equinovarus, also termed club foot, is a congenital deformity of the ankle joint. Despite its prevalence of approximately 1 per 1000 live births, fetal talipes is relatively poorly studied since the introduction of percutaneous tendo Achilles tenotomies. Objectives: To document the associations, outcomes and prognosis of patients with antenatally diagnosed fetal talipes. The study aims to examine the association between, and prevalence of, fetal talipes and other abnormalities, structural and chromosomal, as well as the outcome in relation to postnatal surgery. The accuracy

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!