Search Results - "Prenatal Diagnosis/methods"
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1
Authors: et al.
Source: Ultrasound Obstet Gynecol
Rode, L, Wright, A, Wright, D, Overgaard, M, Sperling, L, Sandager, P, Nørgaard, P, Jørgensen, F S, Zingenberg, H, Riishede, I, Tabor, A, Ekelund, C K & the PRESIDE Study Group 2025, ' Screening for pre-eclampsia using pregnancy-associated plasma protein-A or placental growth factor measurements in blood samples collected at 8–14 weeks' gestation ', Ultrasound in Obstetrics and Gynecology, vol. 65, no. 5, pp. 567-574 . https://doi.org/10.1002/uog.29204
the PRESIDE Study Group 2025, 'Screening for pre-eclampsia using pregnancy-associated plasma protein-A or placental growth factor measurements in blood samples collected at 8–14 weeks' gestation', Ultrasound in Obstetrics and Gynecology, vol. 65, no. 5, pp. 567-574. https://doi.org/10.1002/uog.29204Subject Terms: Adult, placental growth factor, pre-eclampsia, competing-risks model, Denmark, Pre-Eclampsia/diagnosis, Gestational Age, First/blood, pregnancy-associated plasma protein-a, Pre-Eclampsia, Prenatal Diagnosis/methods, Pregnancy, Predictive Value of Tests, Prenatal Diagnosis, Humans, Pregnancy-Associated Plasma Protein-A, Prospective Studies, Placenta Growth Factor, Original Paper, screening, Placenta Growth Factor/blood, Pregnancy Trimester, First, Pregnancy-Associated Plasma Protein-A/analysis, Female, Pregnancy Trimester, Fetal Medicine Foundation, first trimester, Biomarkers/blood, Biomarkers
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/40127386
https://curis.ku.dk/ws/files/450868170/Ultrasound_in_Obstet_Gyne_-_2025_-_Rode_-_Screening_for_pre_eclampsia_using_pregnancy_associated_plasma_protein_A_or.pdf
https://portal.findresearcher.sdu.dk/da/publications/1793d418-5386-4d1a-a4e3-66b27e3ccf71
https://doi.org/10.1002/uog.29204 -
2
Authors: et al.
Source: Prenatal diagnosis, vol. 44, no. 12, pp. 1526-1529
Subject Terms: Adult, Heterozygote, Fetal Growth Retardation, DNA Helicases, Nervous System Malformations, Ultrasonography, Prenatal, DEAD-box RNA Helicases, Pregnancy, Prenatal Diagnosis, Exome Sequencing, Microcephaly, Humans, Female, Abnormalities, Multiple, DEAD-box RNA Helicases/genetics, Fetal Growth Retardation/genetics, Fetal Growth Retardation/diagnosis, Fetal Growth Retardation/diagnostic imaging, Microcephaly/genetics, Microcephaly/diagnosis, Microcephaly/diagnostic imaging, DNA Helicases/genetics, Abnormalities, Multiple/genetics, Abnormalities, Multiple/diagnosis, Abnormalities, Multiple/diagnostic imaging, Nervous System Malformations/genetics, Nervous System Malformations/diagnosis, Nervous System Malformations/diagnostic imaging, Prenatal Diagnosis/methods, DDX11, Warsaw Breakage Syndrome, cerebellar vermis hypoplasia, cohesinopathy, delayed sulcation, exome sequencing, intrahepatic portal‐systemic shunt, microcephaly, short corpus callosum
File Description: application/pdf
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3
Authors: Cengisiz, Cengiz
Subject Terms: Prenatal Diagnosis/nursing, Maternal Behavior/ethnology, Prenatal Care/history, Perinatal Care/history, Paternal Behavior/history, Prenatal Injuries/diagnosis, Perinatal Care/ethics, Prenatal Care/ethics, Prenatal Diagnosis/methods, Prenatal Diagnosis, Maternal Behavior/physiology, Prenatal Care/trends, Maternal Behavior, Perinatal Mortality, Prenatal Care/methods, Maternal Behavior/psychology, Prenatal Care, Perinatal Care/trends, Perinatal Care/standards, Perinatal Care, Perinatal Care/methods, Prenatal Diagnosis/mortality, Prenatal Diagnosis/history, Prenatal Diagnosis/trends, Prenatal Care/psychology, Maternal Behavior/history
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4
Authors: et al.
Subject Terms: Postnatal Care/standards, diagnostic techniques, Postnatal Care/ethics, prenetal diagnosis, Maternal Welfare/psychology, Perinatal Care/history, Postnatal Care/methods, Obstetricians/psychology, Prenatal Care, Prenatal Diagnosis/psychology, Perinatal Care, Perinatal Care/methods, Maternal Welfare/ethics, Prenatal Diagnosis/methods, Postnatal Care/trends, Prenatal Diagnosis/history, Prenatal Diagnosis/ethics, Prenatal Diagnosis/trends, postnatal care, Postnatal Care/psychology, Prenatal Care/trends, Maternal Welfare, Perinatal Mortality, perintal death, Maternal Welfare/trends
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5
Authors: et al.
Source: Thomsen, S H, Hjortshøj, T D, Barbosa, M, Laursen, L, Larsen, M, Hvidbjerg, M S, Tørring, P, Sperling, L, Lund, I C B, Andreasen, L, Ernst, A, Sunde, L, Balslev-Harder, M, Petersen, O B, Lou, S, Becher, N & Vogel, I 2025, 'Genetik i føtalmedicin', Ugeskrift for Læger, bind 187, nr. 18. https://doi.org/10.61409/V12240853
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6
Authors: et al.
Source: Jensen, L N, Hvingel, B H, Kamper, C H, Nørgaard, P, Martens, P C, Thorup, M B, Langkilde, A R, Larsen, V A & Sandager, P 2025, 'Prænatal diagnostik af misdannelser i centralnervesystemet', Ugeskrift for Læger, bind 187, nr. 18. https://doi.org/10.61409/V11240764
Subject Terms: Nervous System Malformations/diagnostic imaging, Neural Tube Defects/diagnostic imaging, Pregnancy, Prenatal Diagnosis/methods, Humans, Female, Genetic Testing, Magnetic Resonance Imaging, Ultrasonography, Prenatal
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7
Authors: et al.
Subject Terms: Male, Sex Determination Analysis, Practical recommendation, Sex Determination Analysis/methods, Noninvasive Prenatal Testing, Disorders of Sex Development, Diagnostic algorithm, Genetics & genetic processes, Génétique & processus génétiques, Pregnancy, Prenatal Diagnosis/methods, Prenatal Diagnosis, Disorders of Sex Development/diagnosis, Humans, Variation in sex differentiation, Medicine (all), Decision Trees, Infant, Newborn, Life sciences, Fetal sex discordance, Noninvasive Prenatal Testing/methods, Sciences du vivant, Female, NIPT, Algorithms, Disorders of Sex Development/genetics
Access URL: https://hdl.handle.net/2268/331695
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8
Authors: et al.
Source: Childs Nerv Syst
Subject Terms: Infant, Newborn [MeSH], Female [MeSH], Prenatally diagnosed complex arachnoid cysts, Arachnoid cysts, Humans [MeSH], Mini Review, Neurosurgery, MRI, Arachnoid Cysts/surgery [MeSH], Neurosurgical Procedures/methods [MeSH], Arachnoid Cysts/diagnostic imaging [MeSH], Pregnancy [MeSH], Prenatal Diagnosis/methods [MeSH], Infant, Newborn, Neurosurgical Procedures, Arachnoid Cysts, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, Prenatal Diagnosis, Humans, Female
File Description: application/pdf
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9
Authors: et al.
Source: Matern Child Health J
MATERNAL AND CHILD HEALTH JOURNAL
r-FISABIO. Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)Subject Terms: Male, Prenatal diagnosis, Congenital diaphragmatic hernia, Gestational Age, Congenital Abnormalities/mortality, Article, Europe/epidemiology, Congenital Abnormalities, Cohort Studies, Gastroschisis/mortality, Prenatal Diagnosis/methods, Pregnancy, Prenatal Diagnosis, Infant Mortality, Humans, Registries, Child, Preschool, Spina bifida, Hernias, Gastroschisis, 2. Zero hunger, Congenital/mortality, Congenital diaphragmatic hernia · Gastroschisis · Prenatal diagnosis · Spina bifida · Transposition of greatarteries, Infant, Newborn, Infant, Infant Mortality/trends, Length of Stay, Newborn, Transposition of great arteries, 3. Good health, Europe, Survival Rate, Length of Stay/statistics & numerical data, Child, Preschool, Morbidity/trends, Female, Morbidity, Hernias, Diaphragmatic, Congenital, Diaphragmatic
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/38438690
https://fisabio.portalinvestigacion.com/publicaciones/17662
https://link.springer.com/content/pdf/10.1007/s10995-024-03911-9.pdf
https://doi.org/10.1007/s10995-024-03911-9
https://cronfa.swan.ac.uk/Record/cronfa65965/Download/65965__29929__2e8a82e670a248c68e7ce3e67babcc8c.pdf -
10
Decoding 22q11.2: prenatal profiling and first‐trimester risk assessment in Danish nationwide cohort
Authors: et al.
Source: Gadsbøll, K, Vogel, I, Pedersen, L H, Kristensen, S E, Steffensen, E H, Wright, A, Wright, D, Hyett, J, Petersen, O B & Danish Cytogenetic Central Registry Study Group 2024, ' Decoding 22q11.2 : prenatal profiling and first-trimester risk assessment from a Danish nationwide cohort ', Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, vol. 63, no. 1, pp. 34-43 . https://doi.org/10.1002/uog.27466
Danish Cytogenetic Central Registry Study Group 2024, 'Decoding 22q11.2 : prenatal profiling and first-trimester risk assessment in Danish nationwide cohort', Ultrasound in Obstetrics & Gynecology, vol. 63, no. 1, pp. 34-43. https://doi.org/10.1002/uog.27466
Gadsbøll, K, Vogel, I, Pedersen, L H, Kristensen, S E, Steffensen, E H, Wright, A, Wright, D, Hyett, J & Petersen, O B 2024, ' Decoding 22q11.2 : prenatal profiling and first-trimester risk assessment in Danish nationwide cohort ', Ultrasound in Obstetrics and Gynecology, vol. 63, no. 1, pp. 34-43 . https://doi.org/10.1002/uog.27466Subject Terms: Denmark, CNV, 22q11.2, cFTS, Risk Assessment, Cohort Studies, Prenatal Diagnosis/methods, Pregnancy, Prenatal Diagnosis, XXXXXX - Unknown, Humans, Pregnancy-Associated Plasma Protein-A, Chorionic Gonadotropin, beta Subunit, Human, DiGeorge syndrome, combined first-trimester screening, Down Syndrome/diagnostic imaging, atypical chromosomal anomaly, Denmark/epidemiology, 3. Good health, Pregnancy Trimester, First, copy-number variation, prenatal screening, Female, Down Syndrome, Nuchal Translucency Measurement, Biomarkers
File Description: application/pdf; print
Access URL: https://pubmed.ncbi.nlm.nih.gov/37643358
https://curis.ku.dk/ws/files/379167210/Ultrasound_in_Obstet_Gyne_2023_Gadsb_ll_Decoding_22q11_2_prenatal_profiling_and_first_trimester_risk_assessment_in.pdf
https://pure.au.dk/portal/en/publications/d952bcc1-db32-4200-b3c2-2f8f0525a9ab
https://doi.org/10.1002/uog.27466
http://www.scopus.com/inward/record.url?scp=85181449403&partnerID=8YFLogxK
https://pure.au.dk/portal/en/publications/e2dc1007-fe13-45c3-b12a-1e929db809c8
https://doi.org/10.1002/uog.27466 -
11
Authors: et al.
Subject Terms: Perinatal Mortality, Perinatal Care, Perinatal Care/history, Perinatal Care/methods, Prenatal Care, Prenatal Care/trends, perintal death, Postnatal Care/psychology, Postnatal Care/ethics, Postnatal Care/methods, Postnatal Care/standards, Postnatal Care/trends, postnatal care, Prenatal Diagnosis/history, Prenatal Diagnosis/methods, Prenatal Diagnosis/trends, Prenatal Diagnosis/ethics, Prenatal Diagnosis/psychology, prenetal diagnosis, Maternal Welfare, Maternal Welfare/ethics, Maternal Welfare/trends, Maternal Welfare/psychology, Obstetricians/psychology, diagnostic techniques
Relation: https://zenodo.org/records/15307822; oai:zenodo.org:15307822; https://doi.org/10.5281/zenodo.15307822
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12
Authors: et al.
Source: ISSN: 1470-0328 ; BJOG, vol. 132, no. 6 (2025) p. 805-815.
Subject Terms: Cost utility, Cytomegalovirus, Prenatal screening, Humans, Female, Pregnancy, Cytomegalovirus Infections / economics, Cytomegalovirus Infections / diagnosis, Cytomegalovirus Infections / prevention & control, Cytomegalovirus Infections / congenital, Cost-Benefit Analysis, Pregnancy Complications, Infectious / diagnosis, Infectious / economics, Quality-Adjusted Life Years, Prenatal Diagnosis / economics, Prenatal Diagnosis / methods, Canada, Pregnancy Trimester, First, Antiviral Agents / therapeutic use, Antiviral Agents / economics, Infectious Disease Transmission, Vertical / prevention & control, Vertical / economics, Infant, Newborn
Relation: info:eu-repo/semantics/altIdentifier/pmid/39895506; unige:188863
Availability: https://archive-ouverte.unige.ch/unige:188863
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13
Authors: et al.
Source: American journal of medical genetics. Part A, vol. 197, no. 3, pp. e63920
Subject Terms: Humans, Nuchal Translucency Measurement, Female, Pregnancy, Adult, Mutation/genetics, Aneuploidy, Fetus/diagnostic imaging, Fetus/abnormalities, Prenatal Diagnosis/methods, Phenotype, NUP107, Galloway‐Mowat syndrome, nuchal translucency, steroid‐resistant nephrotic syndrome, whole exome sequencing, whole genome sequencing
File Description: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/39473271; info:eu-repo/semantics/altIdentifier/eissn/1552-4833; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_979716B8A5906; https://serval.unil.ch/notice/serval:BIB_979716B8A590; https://serval.unil.ch/resource/serval:BIB_979716B8A590.P001/REF.pdf
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14
Authors: et al.
Contributors: et al.
Source: ISSN: 0197-3851.
Subject Terms: prenatal medicine, whole exome sequencing, ultrasonography fetal anomaly findings, ethics, MESH: Exome Sequencing* / ethics, MESH: Exome Sequencing* / methods, MESH: Female, MESH: France, MESH: Genetic Testing / ethics, MESH: Humans, MESH: Pregnancy, MESH: Prenatal Diagnosis* / ethics, MESH: Prenatal Diagnosis* / methods, [SDV]Life Sciences [q-bio], [SDV.ETH]Life Sciences [q-bio]/Ethics, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, [SHS.DROIT]Humanities and Social Sciences/Law
Relation: info:eu-repo/semantics/altIdentifier/pmid/39532683; PUBMED: 39532683; PUBMEDCENTRAL: PMC11893516
Availability: https://hal.science/hal-04882188
https://hal.science/hal-04882188v1/document
https://hal.science/hal-04882188v1/file/Prenatal%20Diagnosis%20-%202024%20-%20Cogan%20-%20Use%20of%20Prenatal%20Exome%20Sequencing%20Opinion%20Statement%20of%20the%20French%20Federation%20of%20Human.pdf
https://doi.org/10.1002/pd.6692 -
15
Authors: et al.
Contributors: et al.
Source: Birth Defects Res
Birth defects research, vol. 116, no. 11, pp. e2414Subject Terms: Male, 0301 basic medicine, congenital ocular anomalies, descriptive epidemiological study, epidemiology, Europe, ocular defect, Infant, Newborn, Gestational Age, Humans, Europe/epidemiology, Prevalence, Eye Abnormalities/epidemiology, Female, Pregnancy, Registries, Prenatal Diagnosis/methods, [SDV] Life Sciences [q-bio], 03 medical and health sciences, 0302 clinical medicine, Prenatal Diagnosis, Eye Abnormalities, Research Article
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/39582415
https://research.rug.nl/en/publications/114cf24a-4089-4412-a9a0-434bfb314558
https://doi.org/10.1002/bdr2.2414
https://hdl.handle.net/11370/114cf24a-4089-4412-a9a0-434bfb314558
https://cronfa.swan.ac.uk/Record/cronfa68870
https://cronfa.swan.ac.uk/Record/cronfa68370/Download/68370__32992__ba9ddac9eafa4e0580ea48c2250fba98.pdf
https://serval.unil.ch/notice/serval:BIB_C2CBC5D9581F
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C2CBC5D9581F6
https://serval.unil.ch/resource/serval:BIB_C2CBC5D9581F.P001/REF.pdf -
16
Authors: et al.
Source: Clinical Genetics. 104:505-515
Subject Terms: 576.5, Genotype, Noninvasive Prenatal Testing, DNA, 3. Good health, Consanguinity, Fetal DNA, Pregnancy, Prenatal Diagnosis, DNA / genetics, Prenatal Diagnosis / methods, Humans, Female, Monogenic disease, Cell-free circulating DNA, Noninvasive prenatal diagnosis
File Description: application/pdf
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17
Authors: et al.
Contributors: et al.
Source: Bronsgeest, K, Lust, E E R, Henneman, L, Crombag, N, Bilardo, C M, Stemkens, D, Galjaard, R-J H, Sikkel, E, van der Hout, S H, Bekker, M N & Haak, M C 2023, 'Current practice of first-trimester ultrasound screening for structural fetal anomalies in developed countries', Prenatal Diagnosis, vol. 43, no. 7, pp. 873-880. https://doi.org/10.1002/pd.6389
Prenatal Diagnosis, 43, 7, pp. 873-880Subject Terms: Developed Countries, 1. No poverty, Radboud University Medical Center, Ultrasonography, Prenatal, 3. Good health, Pregnancy Trimester, First, Prenatal Diagnosis/methods, Pregnancy, Prenatal Diagnosis, Journal Article, Radboudumc 0: Other Research Gynaecology, Humans, Female, Ultrasonography
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/37269059
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/294339
https://doi.org/10.1002/pd.6389
https://pure.eur.nl/en/publications/70c8fff7-846d-4f71-ac71-a45a907039f1
https://doi.org/10.1002/pd.6389
https://research.vumc.nl/en/publications/ec323d80-14b3-4b52-adb4-1328c1d63d3a
https://dspace.library.uu.nl/handle/1874/451125
https://pure.amsterdamumc.nl/en/publications/fd678348-0e77-4f78-b1f5-7969b2339171
https://doi.org/10.1002/pd.6389
https://hdl.handle.net/2066/294339
https://repository.ubn.ru.nl//bitstream/handle/2066/294339/294339.pdf
https://hdl.handle.net/1887/3728569 -
18
Authors: et al.
Source: Arch Gynecol Obstet
Subject Terms: Adult, Vesico-Ureteral Reflux, Kidney, Ultrasonography, Prenatal [MeSH], Exome sequencing, Urogenital Abnormalities/diagnosis [MeSH], PKD, WES, Detection rate, Horseshoe kidney, Urinary Tract/abnormalities [MeSH], Phenotype [MeSH], CAKUT, Kidney/abnormalities [MeSH], Prenatal Diagnosis/methods [MeSH], Female [MeSH], Urinary tract dilation, Adult [MeSH], Kidney/embryology [MeSH], Humans [MeSH], Retrospective Studies [MeSH], Exome Sequencing [MeSH], DSD, Kidney/diagnostic imaging [MeSH], Vesico-Ureteral Reflux [MeSH], Maternal-Fetal Medicine, Ectopic kidney, Polycystic kidney disease, Urogenital Abnormalities/genetics [MeSH], Pregnancy [MeSH], Ultrasonography, Prenatal, 3. Good health, Phenotype, Pregnancy, Urogenital Abnormalities, Prenatal Diagnosis, Exome Sequencing, Humans, Female, Urinary Tract, Retrospective Studies
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19
Authors: et al.
Source: Steffensen, E H, Skakkebaek, A, Gadsbøll, K, Petersen, O B, Westover, T, Strange, H, Vogel, I & NIPT-SCA-map Study Group 2023, 'Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA : A survey study', Prenatal Diagnosis, vol. 43, no. 2, pp. 144-155. https://doi.org/10.1002/pd.6322
The NIPT-SCA-map Study Group 2023, ' Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA : A survey study ', Prenatal Diagnosis, vol. 43, no. 2, pp. 144-155 . https://doi.org/10.1002/pd.6322Subject Terms: Sex Chromosomes, Noninvasive Prenatal Testing, Australia, Aneuploidy, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Prenatal Diagnosis/methods, Pregnancy, Prenatal Diagnosis, Surveys and Questionnaires, Humans, Hong Kong, Female, Sex Chromosome Aberrations
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/36703254
https://pure.au.dk/ws/files/306857058/Prenatal_Diagnosis_2023_Steffensen_Inclusion_of_sex_chromosomes_in_noninvasive_prenatal_testing_in_Asia_Australia_.pdf
https://curis.ku.dk/ws/files/359250216/Prenatal_Diagnosis_2023_Steffensen_Inclusion_of_sex_chromosomes_in_noninvasive_prenatal_testing_in_Asia_Australia_.pdf
https://pure.au.dk/ws/files/306857058/Prenatal_Diagnosis_2023_Steffensen_Inclusion_of_sex_chromosomes_in_noninvasive_prenatal_testing_in_Asia_Australia_.pdf
https://doi.org/10.1002/pd.6322
https://pure.au.dk/portal/en/publications/2818b8f8-389a-441a-85f2-eef5d5dd23b2 -
20
Authors:
Source: Swiss Medical Weekly, Vol 155, Iss 6 (2025)
Swiss medical weekly, vol. 155, pp. 4610Subject Terms: Female, Humans, Pregnancy, Noninvasive Prenatal Testing/methods, Pregnancy Trimester, First, Prenatal Diagnosis/methods, Switzerland, Trisomy/diagnosis, Ultrasonography, Prenatal, Medicine
File Description: application/pdf
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