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1
High-grade endometrial stromal sarcoma presenting in a 28-year-old woman during pregnancy: a case report
High-grade endometrial stromal sarcoma presenting in a 28-year-old woman during pregnancy: a case report
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High-grade endometrial stromal sarcoma presenting in a 28-year-old woman during pregnancy: a case report

Journal of medical case reports, 2010-08, Vol.4 (1), p.243-243, Article 243 [Peer Reviewed Journal]

COPYRIGHT 2010 BioMed Central Ltd. ;Copyright ©2010 Amant et al; licensee BioMed Central Ltd. 2010 Amant et al; licensee BioMed Central Ltd. ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/1752-1947-4-243 ;PMID: 20684773

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2
Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth
Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth
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Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth

BMC women's health, 2024-01, Vol.24 (1), p.42-12, Article 42 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;ISSN: 1472-6874 ;EISSN: 1472-6874 ;DOI: 10.1186/s12905-023-02856-5 ;PMID: 38225596

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3
Pregnancy and cardiovascular risk for women with Turner syndrome
Pregnancy and cardiovascular risk for women with Turner syndrome
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Pregnancy and cardiovascular risk for women with Turner syndrome

Women's Health, 2014-07, Vol.10 (4), p.469-476 [Peer Reviewed Journal]

2014 SAGE Publications ;2015 INIST-CNRS ;COPYRIGHT 2014 Sage Publications Ltd. (UK) ;2014 Future Medicine Ltd ;ISSN: 1745-5057 ;ISSN: 1745-5065 ;EISSN: 1745-5065 ;DOI: 10.2217/whe.14.34 ;PMID: 25259906

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4
Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014-2020
Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014-2020
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Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014-2020

Orphanet journal of rare diseases, 2022-12, Vol.17 (1), p.446-446, Article 446 [Peer Reviewed Journal]

2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-022-02594-1 ;PMID: 36550515

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5
Antenatal depression and its potential causal mechanisms among pregnant mothers in Gondar town: application of structural equation model
Antenatal depression and its potential causal mechanisms among pregnant mothers in Gondar town: application of structural equation model
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Antenatal depression and its potential causal mechanisms among pregnant mothers in Gondar town: application of structural equation model

BMC pregnancy and childbirth, 2020-03, Vol.20 (1), p.168-168, Article 168 [Peer Reviewed Journal]

2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-020-02859-2 ;PMID: 32183726

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6
A partial molar pregnancy associated with a fetus with intrauterine growth restriction delivered at 31 weeks: a case report
A partial molar pregnancy associated with a fetus with intrauterine growth restriction delivered at 31 weeks: a case report
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A partial molar pregnancy associated with a fetus with intrauterine growth restriction delivered at 31 weeks: a case report

Journal of medical case reports, 2019-07, Vol.13 (1), p.204-204, Article 204 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/s13256-019-2150-4 ;PMID: 31269962

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7
The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women
The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women
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The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women

Genetic testing and molecular biomarkers, 2011-10, Vol.15 (10), p.701-707 [Peer Reviewed Journal]

COPYRIGHT 2011 Mary Ann Liebert, Inc. ;COPYRIGHT 2011 Mary Ann Liebert, Inc. ;ISSN: 1945-0265 ;EISSN: 1945-0257 ;DOI: 10.1089/gtmb.2010.0171 ;PMID: 21699408

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8
Triploidy and Routine Combined First Trimester Pregnancy Screening
Triploidy and Routine Combined First Trimester Pregnancy Screening
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Triploidy and Routine Combined First Trimester Pregnancy Screening

Avicenna journal of medical biotechnology, 2019-01, Vol.11 (1), p.124-126 [Peer Reviewed Journal]

COPYRIGHT 2019 Avicenna Research Institute ;Copyright© 2019 Avicenna Research Institute 2019 ;ISSN: 2008-2835 ;EISSN: 2008-4625 ;PMID: 30800253

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9
Circulating nucleic acids in plasma and serum: applications in diagnostic techniques for noninvasive prenatal diagnosis
Circulating nucleic acids in plasma and serum: applications in diagnostic techniques for noninvasive prenatal diagnosis
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Circulating nucleic acids in plasma and serum: applications in diagnostic techniques for noninvasive prenatal diagnosis

International journal of women's health, 2013-01, Vol.5 (default), p.177-186 [Peer Reviewed Journal]

COPYRIGHT 2013 Dove Medical Press Limited ;COPYRIGHT 2013 Dove Medical Press Limited ;2013. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2013 Gahan, publisher and licensee Dove Medical Press Ltd 2013 ;ISSN: 1179-1411 ;EISSN: 1179-1411 ;DOI: 10.2147/IJWH.S34442 ;PMID: 23637563

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10
Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination
Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination
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Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination

Diagnostics (Basel), 2023-11, Vol.13 (23), p.3576 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 2075-4418 ;EISSN: 2075-4418 ;DOI: 10.3390/diagnostics13233576 ;PMID: 38066817

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11
Risks of pregnancy for women with Turner syndrome
Risks of pregnancy for women with Turner syndrome
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Risks of pregnancy for women with Turner syndrome

Expert Review of Obstetrics & Gynecology, 2011-03, Vol.6 (2), p.217-227 [Peer Reviewed Journal]

Expert Reviews Ltd 2011 ;COPYRIGHT 2011 Expert Reviews Ltd. ;ISSN: 1747-4108 ;EISSN: 1747-4116 ;DOI: 10.1586/eog.11.7

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12
Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
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Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

BMC medical genomics, 2012-12, Vol.5 (1), p.57-57, Article 57 [Peer Reviewed Journal]

COPYRIGHT 2012 BioMed Central Ltd. ;COPYRIGHT 2012 BioMed Central Ltd. ;2012 Jiang et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2012 Jiang et al.; licensee BioMed Central Ltd. 2012 Jiang et al.; licensee BioMed Central Ltd. ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/1755-8794-5-57 ;PMID: 23198897

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13
Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results
Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results
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Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results

BMC pregnancy and childbirth, 2022-11, Vol.22 (1), p.1-813, Article 813 [Peer Reviewed Journal]

2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-022-05139-3 ;PMID: 36333674

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14
Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study
Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study
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Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study

BMC pregnancy and childbirth, 2024-01, Vol.24 (1), p.93-93, Article 93 [Peer Reviewed Journal]

2024. The Author(s). ;2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-024-06275-8 ;PMID: 38297236

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15
Gestational diabetes is associated with the risk of offspring’s congenital anomalies: a register-based cohort study
Gestational diabetes is associated with the risk of offspring’s congenital anomalies: a register-based cohort study
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Gestational diabetes is associated with the risk of offspring’s congenital anomalies: a register-based cohort study

BMC pregnancy and childbirth, 2023-10, Vol.23 (1), p.1-708, Article 708 [Peer Reviewed Journal]

2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;BioMed Central Ltd., part of Springer Nature 2023 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-023-05996-6 ;PMID: 37789251

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16
Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test
Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test
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Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test

Molecular cytogenetics, 2019-07, Vol.12 (1), p.34-34, Article 34 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s). 2019 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-019-0446-0 ;PMID: 31338126

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17
Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review
Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review
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Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review

BMC pregnancy and childbirth, 2019-10, Vol.19 (1), p.385-385, Article 385 [Peer Reviewed Journal]

The Author(s). 2019 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-019-2518-x ;PMID: 31660889

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18
Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients
Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients
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Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients

BMC medical genomics, 2022-04, Vol.15 (1), p.90-90, Article 90 [Peer Reviewed Journal]

2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-022-01240-w ;PMID: 35436901

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19
Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior
Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior
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Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior

Italian journal of pediatrics, 2012-10, Vol.38 (1), p.52-52 [Peer Reviewed Journal]

2012 Lalatta et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2012 Lalatta et al.; licensee BioMed Central Ltd. 2012 Lalatta et al.; licensee BioMed Central Ltd. ;ISSN: 1824-7288 ;ISSN: 1720-8424 ;EISSN: 1824-7288 ;DOI: 10.1186/1824-7288-38-52 ;PMID: 23034220

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20
Nonendocrine mechanisms of sex bias in rheumatic diseases
Nonendocrine mechanisms of sex bias in rheumatic diseases
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Nonendocrine mechanisms of sex bias in rheumatic diseases

Nature reviews. Rheumatology, 2019-11, Vol.15 (11), p.673-686 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2019 ;ISSN: 1759-4790 ;EISSN: 1759-4804 ;DOI: 10.1038/s41584-019-0307-6 ;PMID: 31597952

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