Thematische Bibliographien / Fetal

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Auswahl der wissenschaftlichen Literatur zum Thema „Fetal“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 9. Juni 2025

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Zeitschriftenartikel zum Thema "Fetal"

Sweeney, Raymond W., Robert H. Whitlock, and Ann E. Rosenberger. "Mycobacterium paratuberculosis isolated from fetuses of infected cows not manifesting signs of the disease." American Journal of Veterinary Research 53, no. 4 (April 1, 1992): 477–80. http://dx.doi.org/10.2460/ajvr.1991.53.04.477.

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Summary Fetuses were obtained from 58 cows that were fecal culture-positive for Mycobacterium paratuberculosis, but were not manifesting signs of paratuberculosis. Fetal tissues from 5 of 58 cows were culture-positive for M paratuberculosis. All 5 culture-positive fetuses were from cows that were classified as heavy fecal shedders (5/28; 17.8%). Difference in prevalence of fetal infection between light (< 70 colonies/tube) and heavy fecal shedders was significant (Fisher's exact test, P < 0.05). Association was not evident between serologic status of the dam and prevalence of fetal infection. In infected cows without signs of paratuberculosis, fetal infection develops with lower frequency than previously reported for cows with clinical signs of the disease. In this study, fetal infection was found only in cows that were heavy fecal shedders.

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Heyborne, Kent. "Elevated Middle Cerebral Artery Peak Systolic Velocity in a Nonanemic Fetus with Alpha-Thalassemia Trait." Obstetrics and Gynecology International 2009 (2009): 1–2. http://dx.doi.org/10.1155/2009/819380.

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Background. Elevated middle cerebral artery peak systolic velocity (MCA-PSV) has been reported in nonanemic fetuses following fetal transfusion, and has been attributed to a major population of red blood cells (RBCs) with an adult mean corpuscular volume (MCV) in the fetal circulation. Reported here is an analogous case of elevated MCA-PSV with a normal fetal hematocrit and relative fetal microcytosis due to fetalα-thalassemia trait.Case. Ultrasound findings concerning for early hydrops prompted measurement of MCA-PSV, which was elevated. Cordocentesis revealed fetal microcytosis with a normal hematocrit which proved to be due to fetalα-thalassemia trait inherited from the mother.Conclusion. This case provides another example of elevated MCA-PSV with normal hematocrit and microcytosis, here due to fetalα-thalassemia trait. This finding provides support for the observation that MCA-PSV may be influenced by hematological indices other than the fetal hematocrit.

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Zhu, Mengni, and Liping Liu. "Fetal Heart Rate Extraction Based on Wavelet Transform to Prevent Fetal Distress In Utero." Journal of Healthcare Engineering 2021 (September 29, 2021): 1–7. http://dx.doi.org/10.1155/2021/7608785.

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In order to improve the effective extraction of fetal heart rate and prevent fetal distress in utero, a study of fetal heart rate feature extraction based on wavelet transform to prevent fetal distress in utero was proposed. This paper adopts a fetal heart rate detection method based on the maximum value of the binary wavelet transform modulus. The method is simulated by the Doppler fetal heart signal obtained from the clinic. Compared with the original curve, the transformed curve can roughly see the change rule of the original signal and identify the peak point of the signal, but due to the large disturbance of the peak point, the influence on the computer processing is also great. The periodicity of the transformed signal is greatly enhanced, making it easier to deal with the computation. A total of 300 pregnant women with full-term fetal heart monitoring from January 2018 to January 2020 were selected as the research subjects and divided into the observation group and the control group. The observation group consisted of 100 patients with abnormal fetal heart monitoring, and the control group consisted of 200 patients with normal fetal heart monitoring. The uterine contractions and fetal heart rate were recorded, and the incidence of fetal distress, cesarean section, neonatal asphyxia, and amniotic fluid and fecal contamination were observed. The incidence of fetal distress, cesarean section, neonatal asphyxia, and amniotic fluid fecal stain in the observation group were significantly higher than those in the control group. Fetal heart monitoring can accurately judge the situation of the fetus in pregnant women and timely diagnose the abnormal fetal heart rate, which has a better effect on the prognosis of perinatal infants and can reduce their mortality. It can effectively solve the problems existing in the autocorrelation algorithm and extract the fetal heart rate more accurately. It is an effective improved scheme of fetal heart rate extraction. It is very helpful in preventing fetal distress in utero.

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ÖZLÜ, Onur. "Maternal-Fetal Anesthesia/Analgesia in Fetal Interferences: Traditional Review." Turkiye Klinikleri Journal of Anesthesiology Reanimation 19, no. 3 (2021): 140–50. http://dx.doi.org/10.5336/anesthe.2021-85460.

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Patil, Alka, Nitin Kulkarni, and Richa Patel. "Fetal Macrosomia." Indian Journal of Maternal-Fetal & Neonatal Medicine 4, no. 2 (December 15, 2020): 201–5. http://dx.doi.org/10.21088/ijmfnm.2347.999x.4217.16.

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Preconceptional, conception, antenatal period and intrapartum period are in continuum. For successful obstetric outcome, prepregnancy weight and proper antenatal care are important factors. Newborn whose birthweight exceeds 40004500gms is labled as macrosomia. Prolong labour, arrest of labour, foetal distress, shoulder dystocia, instrumental delivery and increased incidence of cesarean section are associated with macrosomic fetuses. Early detection, watchfull expectancy active interventions are key factors for safe delivery of macrosomic fetuses.

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Kemal, Tolga Saracoglu. "Fetal Monitoring in Open Fetal Surgery." Global Journal of Anesthesiology 2, no. 2 (October 15, 2015): 053. https://doi.org/10.17352/2455-3476.000017.

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Open surgery and fetoscopic surgery are of the safest procedures, whilst the ex-utero intrapartum treatment (EXIT) procedure has lost its significance as a result of the severe complications experienced both by the mother and the fetus. While uteroplacental circulation maintains, the EXIT is performed before delivery. The fetus is to be delivered at the conclusion of the case. A neonatal resuscitation area and two operating rooms are needed. Significant uterine relaxation is required for open midge station surgery. The risk for rapid bleeding and hemodynamic instability are the common accompanying parts of this procedure. It still continues to be a process done in certain centers not only in United States but also in Europe [1].

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Mărginean, Claudiu, Lucian Pușcașiu, Varlam Claudiu Molnar, and Cosmin Rugină. "INFECȚIA MATERNĂ CU PARVOVIRUS B19 CAUZEAZĂ HIDROPS FETAL CU MOARTE INTRAUTERINĂ – PREZENTARE DE CAZ." Romanian Journal of Infectious Diseases 19, no. 3 (September 30, 2016): 119–22. http://dx.doi.org/10.37897/rjid.2016.3.11.

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Parvovirusul B19 aparține familiei Parvoviridae, genul Erythrovirus și prezintă citotoxicitate asupra liniei eritroblastice umane ducând la anemie severă. Prezentăm cazul unei paciente în vârsta de 35 de ani, aflată la a 3-a sarcină, cu un avort spontan de prim trimestru în antecedente și o naștere fiziologică, care s-a prezentat la controlul de specialitate la 20 de săptămâni gestaționale, asociind semnele unei viroze respiratorii și fără alte patologii până la această vârstă gestațională. Analizele de laborator și ecografia fetală nu au evidențiat nimic patologic, astfel că pacienta a fost trimisă la domiciliu cu recomandarea de a reveni peste 2 săptămâni pentru reevaluare, moment în care ecografia fetală a evidențiat hidrops fetal și anemie severă, iar la 24 de ore asistolie fetală. Serologia maternă a pus în evidență infecția recentă cu Parvovirus B19. Particularitatea acestui caz constă în apariția unei infecții fetale relativ rare în trimestrul doi, în cazul unei sarcini fiziologice, monitorizate, cu prognostic nefavorabil și evoluție fulminantă spre moarte intrauterină.

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Westgren, M., and O. Ringden. "Fetal to fetal transplantation." Acta Obstetricia et Gynecologica Scandinavica 73, no. 5 (January 1994): 371–72. http://dx.doi.org/10.3109/00016349409006245.

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Lakhno, I. V. "THE MODERN APPROACHES FOR THE ASSESSMENT OF FETAL WELL-BEING." Reproductive health of woman 1(41) (July 31, 2020): 19–21. https://doi.org/10.30841/2708-8731.1.2020.471247.

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Fetal growth restriction is known as an intrauterine pathological condition that is associated with some diseases in a further lifetime. Fetal distress is a satellite of fetal growth restriction. Timely and true diagnosing of fetal distress is still an issue in perinatology. This case study showed that non-invasive fetal electrocardiography could contribute to better diagnosing of fetal distress. The variables of beat-to-beat variations, fetal heart rate variability and fetal autonomic brain age score should be investigated as the biophysical markers of fetal deterioration.

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Kelekçi, Sefa, Emre Ekmekçi, Seçil Kurtulmuş, and Savaş Demirpençe. "An unexpected temporary fetal acid reason: rupture of fetal ovarian cyst." Perinatal Journal 23, no. 2 (August 1, 2015): 105–8. http://dx.doi.org/10.2399/prn.15.0232002.

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Dissertationen zum Thema "Fetal"

Cohen, Doron. "Human fetal phonocardiography and the detection of fetal activity." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235812.

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Antepartum detection of the fetus at risk of death or damage in-utero remains a major challenge in modern obstetrics. Ultrasonic monitoring of individual fetal biophysical activities (such as fetal heart rate, fetal breathing or fetal body movements) has become widely applied as a method for evaluating fetal well-being. The combined assessment of these fetal activities and the relations between them, however, may well be more useful both in predicting imminent fetal death and in preventing it. The results of ultrasound studies, however, are hampered (e.g. from a safety viewpoint) by the natural periodicity of fetal activities. Fetal phonocardiographic techniques, on the other hand, can be easily used over long time periods and there can be no doubt of their safety. Furthermore, the fetal phonocardiogram may contain more information that fetal heart rate alone. This thesis describes the design and development of a new high-fidelity fetal phono-sensor, based on a piezo-electric PVDF transducer, which offers a completely non-invasive and reliable method of assessing the fetus over the long term. This sensor has been optimised to record faithfully the acoustic output of the fetus and to maximise the signal energy transfer across the maternal abdominal wall, where hitherto this has not been achieved. This is done by matching the compliance of the sensor to that of the maternal abdominal wall. Using a purpose built measuring device, abdominal wall compliance was measured clinically as 3.5 mm/N (averaged over 76 patients). Theoretical and experimental techniques were used to adjust the sensor's compliance to match that of the maternal abdominal wall [to within 4:1], as well as to minimise noise and maximise signal capture. The sensor's force and displacement senstivities were measured as 2183 V/N and 2480 mm/N (much greater than for any present or past phono-sensors). Using a new experimental rig developed to simulate the transmission of the fetal phono-signals through the maternal abdominal wall, the dynamic performance and frequency response of the sensor were also optimised. Clinical studies on 18 patients from 28-41 weeks gestation, showed that the fetal phonocardiogram contains not only fetal heart rate information, but also information about fetal breathing movements (FBM) and fetal body movements (FM), as well as detailed beat-to-beat heart sound interval information. By comparison with real-time ultrasound, various phono-signal patterns were shown to be caused by the fetal activities: regular and cyclic for FBM; and intermittent and noise-like for FM. By using new computerised signal processing techniques in the time domain (such as template-matching and zero-crossing functions), these recorded fetal activities were detected automatically (in over 80% of the time) and their timing periodicities analysed. Frequency domain analysis (using techniques such as the Hilbert transform and cepstral analysis) of the timing periodicities of the fetal heart sounds, showed that diastolic and beat-to-beat time intervals (as wll as their variabilities) are significantly increased during FBM. Fetal heart rate is also decreased [from 147 to 141 bpm] during FBM episodes. Fetal body movements, on the other hand, are associated with significant decreases in systolic, diastolic and beat-to-beat time intervals, whilst their variabilities are increased. Fetal heart rate, in this case, is found to increase [from 144 to 157 bpm]. Although these techniques do not run in real-time at present, they would be capable of doing so if transferred onto fast computers (or transputers). As a result of this work, one is now perhaps in a better position to envisage an automatic real-time fetal phono-based monitoring system for the routine clinical assessment of fetal well-being.

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冼世源 and Sai-yuen Sin. "Fetal cardiac function predicting fetal compromise: a prospective study." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31969823.

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Sin, Sai-yuen. "Fetal cardiac function predicting fetal compromise : a prospective study /." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21903566.

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Jaishankar, Gayatri. "Fetal Alcohol Syndrome." Digital Commons @ East Tennessee State University, 1995. https://dc.etsu.edu/etsu-works/8867.

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Barreira, Ana Raquel Matos Alves. "Hidrópsia fetal imune." Master's thesis, Faculdade de Medicina da Universidade do Porto, 2010. http://hdl.handle.net/10216/61128.

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Proniaiev, D. V. "Fetal uterus anatomy." Thesis, БДМУ, 2022. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/19329.

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Barreira, Ana Raquel Matos Alves. "Hidrópsia fetal imune." Dissertação, Faculdade de Medicina da Universidade do Porto, 2010. http://hdl.handle.net/10216/61128.

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Damodaram, Mellisa. "Brain development in fetal growth restriction : a volumetric approach using fetal MRI." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9853.

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Fetal growth restriction is the failure of a fetus to achieve its full growth potential, resulting in a neonate that is small for its gestational age. The aetiology of fetal growth restriction is varied and fetal growth restriction secondary to placental insufficiency is attributed to a failure of trophoblast invasion leading to under perfusion of the uteroplacental bed. In response to the adverse conditions in-utero, fetuses tend to compensate by increasing blood flow to the essential organs such as the brain, heart, and adrenals, at the expense of other organs (cerebral redistribution). As a consequence, growth tends to be asymmetric, with maintenance of the head growth velocity while the other growth parameters tail off; an effect which is also known as the ‘brain sparing effect’. Despite this apparent brain sparing effect, children who were growth restricted in utero are at increased risk of developmental delay and behavioural problems. 30 growth restricted and 48 normally grown fetuses were recruited into this study and were imaged using both conventional ultrasound with Doppler assessment, as well as fetal MRI with ssFSE sequences through the feto-placental unit and fetal brain. A dynamic approach was taken when imaging the fetal brain to compensate for the presence of fetal motion. MR imaging of the feto-placental unit detected significant differences in placental appearance, significantly smaller volumes of intra-abdominal and intra-thoracic organs, and significantly smaller regional brain growth among growth restricted fetuses. MR studies of the placenta in fetal growth restriction demonstrated a placental phenotype in growth restricted pregnancies that is characterised by smaller placental volumes, a significant increase in the placental volume affected by apparent pathology on MRI and a thickened, globular placenta. Although placental volume increased with gestation in both groups, the placental volume remained significantly smaller in the growth restricted fetuses (p = 0.003). There was also a significant correlation between the percentage of placental volume affected by abnormal heterogeneity and the severity of fetal growth restriction (r = 0.82, p < 0.001), and an increase in the maximal placental thickness to placental volume ratio above the 95th centile for gestational age was associated with fetal and early neonatal mortality (relative risk = 7, 95%CI = 2.96 – 16.55, p < 0.001) (figure 3.6) MR studies of fetal intra-thoracic and intra-abdominal volumes showed that although the volume of the intra-thoracic and intra-abdonimal organs (heart, lungs, thymus, liver and kidney) increased as gestation increased in both groups, the volumes of all three structures remained smaller in growth restricted fetuses (p < 0.01) (Figures 4.7 - 4.9) compared with normally grown fetuses. MR studies of the fetal brain demonstrated smaller intracranial volume, total brain volume and cerebellar volume in growth restricted fetuses. In addition, growth restricted fetuses with early onset fetal growth restriction demonstrated smaller vermis height and a corresponding increase in the tegmento-vermian angle. Growth restricted fetuses also demonstrated a disproportionate decrease in extra- and intra-cerebral fluid. This thesis showed evidence of changes in regional and global organ growth in growth restricted fetuses using high resolution fetal MRI. It is hoped that future imaging studies could offer useful insights into the origins and clinical significance of these findings and its consequences for later neurodevelopment.

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Price, Robin Owen. "Maternal health and fetal brain development : altered fetal neurogenesis following maternal inflammation /." May be available electronically:, 2009. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.

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Beckett, Cynthia Diane. "Navajo children and families living with fetal alcohol syndrome/fetal alcohol effects." Diss., The University of Arizona, 2002. http://hdl.handle.net/10150/280150.

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The aim of the study was to develop a culturally sensitive Grounded Theory of Navajo parenting for families who are living with Fetal Alcohol Syndrome (FAS)/Fetal Alcohol Effects (FAE). The research question was: What are the social and cultural factors and processes that Navajo families use to mange care for a child with FAS/FAE? The philosophical perspectives that guided the study were: the Navajo philosophy, or view of life; resilience (middle range theory); the Family Stress Theory; and the Resiliency Mode of Family Stress, Adjustment, and Adaptation. Resilience was used as the over arching conceptual perspective for the study. A Grounded Theory of Navajo Parenting emerged from the data. Key categories to support the emerging theory were identified. The core category was Versatility through Transcendence. The supporting categories were: Strategies for Managing Challenges; Transcendence in Parenting; Intergenerational Alcohol Abuse, Violence and Suffering; and Knowledge/Acquisition of Needs. The families described their stories of transcendence through substance abuse, suffering, and violence to be able to parent their children who were living with the primary and secondary challenges of prenatal alcohol exposures. Further research is needed to test and expand this emerging theory of Navajo parenting of children with FAS/FAE. The challenges that were related to FAS/FAE were more easily managed with patterns of resilience within the families. Factors that influenced family's abilities to parent will be disseminated to assist other families who are managing the problems associated with FAS/FAE.

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Bücher zum Thema "Fetal"

Prayer, Daniela. Fetal MRI. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

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Simpson, John, Vita Zidere, and Owen I. Miller, eds. Fetal Cardiology. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77461-9.

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Prayer, Daniela, ed. Fetal MRI. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-540-73271-6.

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Schumacher, Reinhard, Laurie H. Seaver, and Jürgen Spranger. Fetal Radiology. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-05374-4.

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Kumar, Bid, and Zarko Alfirevic, eds. Fetal Medicine. Cambridge: Cambridge University Press, 2016. http://dx.doi.org/10.1017/cbo9781107585843.

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Kilby, Mark D., Anthony Johnson, and Dick Oepkes, eds. Fetal Therapy. Cambridge: Cambridge University Press, 2012. http://dx.doi.org/10.1017/cbo9780511997778.

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Reissland, Nadja, and Barbara S. Kisilevsky, eds. Fetal Development. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-22023-9.

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Sharp, F., R. B. Fraser, and R. D. B. Milner, eds. Fetal Growth. London: Springer London, 1989. http://dx.doi.org/10.1007/978-1-4471-1707-0.

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Schumacher, Reinhard, Laurie H. Seaver, and Jürgen Spranger. Fetal Radiology. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-03560-9.

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Ratha, Chinmayee, and Ashok Khurana. Fetal Medicine. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-6099-4.

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Buchteile zum Thema "Fetal"

León, María I. Martínez, Juan E. Gutiérrez, and Luisa Ceres Ruiz. "Fetal." In Learning Pediatric Imaging, 219–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-16892-5_10.

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Howsepian, A. A. "Fetal Pains and Fetal Brains." In Philosophy and Medicine, 187–210. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1602-5_10.

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Buck, Matthew V., and Michael G. Richardson. "Fetal Monitoring." In Monitoring Technologies in Acute Care Environments, 355–66. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8557-5_42.

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Gardiner, Helena M. "Fetal Treatment." In Pediatric Cardiovascular Medicine, 248–53. Oxford, UK: Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781444398786.ch16.

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deRegnier, Raye-Ann, and Shivani Desai. "Fetal Development." In The Wiley-Blackwell Handbook of Infant Development, 9–32. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444327588.ch1.

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Moradian, Maryam. "Fetal Circulation." In Comprehensive Approach to Adult Congenital Heart Disease, 13–17. London: Springer London, 2014. http://dx.doi.org/10.1007/978-1-4471-6383-1_3.

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Nagy, Anita, and Roger D. G. Malcomson. "Fetal Hydrops." In Keeling’s Fetal and Neonatal Pathology, 299–328. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19207-9_12.

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Bhattacharya, Niranjan, and Phillip G. Stubblefield. "Fetal Growth." In Human Fetal Growth and Development, 3–9. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-14874-8_1.

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Kumar, Sailesh. "Fetal Anomalies." In Dewhurst's Textbook of Obstetrics & Gynaecology, 254–67. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119211457.ch20.

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Olive, Aliza M., Aimee G. Kim, and Alan W. Flake. "Fetal Surgery." In Pediatric Surgery, 115–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/978-3-662-43588-5_7.

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Konferenzberichte zum Thema "Fetal"

P, Archana, Tanushree D, Vamshika M J, Varsha B C, and Varshini G. "Fetal Health Prediction." In 2024 Second International Conference on Advances in Information Technology (ICAIT), 1–5. IEEE, 2024. http://dx.doi.org/10.1109/icait61638.2024.10690588.

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Samjeed, Amna, Maisam Wahbah, and Ahsan H. Khandoker. "Estimation of Fetal Autonomic Age By Considering Fetal Behavioural States." In 2024 46th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), 1–4. IEEE, 2024. https://doi.org/10.1109/embc53108.2024.10782057.

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Tang, Weitao, Nhi Tran, Nasim Katebi, Reza Sameni, Gari D. Clifford, David Walker, Vaishnavi Horlali, Callum Taylor, Robert Galinsky, and Faezeh Marzbanrad. "Advancing Fetal Surveillance with Physiological Sensing: Detecting Hypoxia in Fetal Sheep." In 2024 IEEE SENSORS, 1–4. IEEE, 2024. https://doi.org/10.1109/sensors60989.2024.10784962.

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Pham, Ha-Hieu, Le Tran Quoc Khanh, Hoang-Thien Nguyen, Nguyen Lan Vi Vu, Quang-Vinh Dinh, Thanh-Huy Nguyen, Xingjian Li, and Min Xu. "Fetal-BCP: Addressing Empirical Distribution Gap in Semi-Supervised Fetal Ultrasound Segmentation." In 2025 IEEE 22nd International Symposium on Biomedical Imaging (ISBI), 1–4. IEEE, 2025. https://doi.org/10.1109/isbi60581.2025.10980925.

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Yulistiani, Risma, and Felix Indra Kurniadi. "Catboost in Fetal Health Classification." In 2024 International Conference on ICT for Smart Society (ICISS), 1–4. IEEE, 2024. http://dx.doi.org/10.1109/iciss62896.2024.10751585.

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Pavel, Md Saidur Rahman, Md Rafi Islam, and Asif Mohammed Siddiqee. "Fetal Arrhythmia Detection Using Fetal ECG Signal." In 2019 IEEE International Conference on Telecommunications and Photonics (ICTP). IEEE, 2019. http://dx.doi.org/10.1109/ictp48844.2019.9041789.

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Lincender-Cvijetić, Lidija. "FETAL MRI." In Međunarodni naučni simpozij FETALNA MEDICINA: OD LEONARDA DA VINCIJA DO DANAS. Akademija nauka i umjetnosti Bosne i Hercegovine, 2015. http://dx.doi.org/10.5644/pi2015-159.06.

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Sazali, Amirul Ridhwan, and Rania Al-Ashwal. "Fetal Movement Simulator for Fetal Monitoring System Testing." In 2018 IEEE-EMBS Conference on Biomedical Engineering and Sciences (IECBES). IEEE, 2018. http://dx.doi.org/10.1109/iecbes.2018.8626644.

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Fong, Daniel D., Kourosh Vali, and Soheil Ghiasi. "Contextually-aware Fetal Sensing in Transabdominal Fetal Pulse Oximetry." In 2020 ACM/IEEE 11th International Conference on Cyber-Physical Systems (ICCPS). IEEE, 2020. http://dx.doi.org/10.1109/iccps48487.2020.00019.

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Vullings, R., C. H. L. Peters, M. Mischi, S. G. Oei, and J. W. M. Bergmans. "Fetal movement quantification by fetal vectorcardiography: A preliminary study." In 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2008. http://dx.doi.org/10.1109/iembs.2008.4649341.

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Berichte der Organisationen zum Thema "Fetal"

Gregory, Elizabeth, Claudia Valenzuela, and Donna Hoyert. Fetal Mortality: United States, 2019. National Center for Health Statistics (U.S.), October 2021. http://dx.doi.org/10.15620/cdc:109456.

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This report presents 2019 fetal mortality data by maternal race and Hispanic origin, age, tobacco use during pregnancy, and state of residence, as well as by plurality, sex, gestational age, birthweight, and selected causes of death. Trends in fetal mortality are also examined.

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Gregory C.W., Elizabeth, Claudia Valenzuela, and Donna Hoyert. Fetal Mortality: United States, 2020. National Center for Health Statistics (U.S.), August 2022. http://dx.doi.org/10.15620/cdc:118420.

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This report presents 2020 fetal mortality data by maternal race and Hispanic origin, age, tobacco use during pregnancy, and state of residence, as well as by plurality, sex, gestational age, birthweight, and selected causes of death. Trends in fetal mortality are also examined.

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Gregory, Elizabeth, Claudia Valenzuela, and Donna Hoyert. Fetal Mortality: United States, 2022. National Center Health Statistics (U.S.), September 2024. http://dx.doi.org/10.15620/cdc/158788.

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Gregory, Elizabeth, Claudia Valenzuela, and Donna Hoyert. Fetal Mortality: United States, 2023. National Center for Health Statistics (U.S., June 2025. https://doi.org/10.15620/cdc/174593.

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This report presents 2023 fetal mortality data by maternal race and Hispanic origin, age, tobacco use during pregnancy, and state of residence, as well as by plurality, sex, gestational age, birthweight, and selected causes of death. Trends in fetal mortality are also examined.

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Stovall, Marilyn, Charles Robert Blackwell, Jackson Cundiff, Devorah H. Novack, Jatinder R. Palta, Louis K. Wagner, Edward W. Webster, and Robert J. Shalek. Fetal Dose from Radiotherapy with Photon Beams. AAPM, 1995. http://dx.doi.org/10.37206/49.

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Hoyert, Donna, and Elizabeth Gregory C.W. Cause-of-death Data From the Fetal Death File, 2018–2020. National Center for Health Statistics (U.S.), October 2022. http://dx.doi.org/10.15620/cdc:120533.

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Paul, Satashree. Turning Back the Sickle Cell Disease: A New Drug into Play. Science Repository OÜ, May 2021. http://dx.doi.org/10.31487/sr.blog.38.

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Researchers at the Fulcrum Therapeutics developed a bioavailable drug candidate called FTX 6058 – (a novel small molecular fetal haemoglobin inducer for sickle cell disease) that can restore the body’s ability to produce fetal haemoglobin

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C.W., Elizabeth, Claudia Valenzuela, and Joyce Martin. Fetal Mortality in the United States: 2019–2020 and 2020–Provisional 2021. National Center for Health Statistics (U.S.), January 2023. http://dx.doi.org/10.15620/cdc:122291.

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This report describes changes between 2020 and 2021 in total, early, and late fetal mortality, as well as fetal mortality by maternal race and Hispanic origin and state of residence. Comparisons are made with findings for 2019 to 2020.

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Gregory C.W., Elizabeth, Claudia Valenzuela, and Joyce Martin. Fetal Mortality in the United States: 2019–2020 and 2020–Provisional 2021. National Center for Health Statistics (U.S.), January 2023. http://dx.doi.org/10.15620/cdc:122292.

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Stratton, Kalera. Fetal Stress and Neurogenesis in Thamnophis sirtalis parietalis. Portland State University Library, January 2016. http://dx.doi.org/10.15760/honors.330.

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