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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study

Orphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 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: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-018-0976-2 ;PMID: 30642344

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2
Is the prevalence of Klinefelter syndrome increasing?
Is the prevalence of Klinefelter syndrome increasing?
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Is the prevalence of Klinefelter syndrome increasing?

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.163-170 [Peer Reviewed Journal]

2008 INIST-CNRS ;Copyright Nature Publishing Group Feb 2008 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201956 ;PMID: 18000523

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3
Emergence and evolution of internationally disseminated cephalosporin-resistant Neisseria gonorrhoeae clones from 1995 to 2005 in Japan
Emergence and evolution of internationally disseminated cephalosporin-resistant Neisseria gonorrhoeae clones from 1995 to 2005 in Japan
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Emergence and evolution of internationally disseminated cephalosporin-resistant Neisseria gonorrhoeae clones from 1995 to 2005 in Japan

BMC infectious diseases, 2015-09, Vol.15 (1), p.378-378, Article 378 [Peer Reviewed Journal]

COPYRIGHT 2015 BioMed Central Ltd. ;COPYRIGHT 2015 BioMed Central Ltd. ;Shimuta et al. 2015 ;ISSN: 1471-2334 ;EISSN: 1471-2334 ;DOI: 10.1186/s12879-015-1110-x ;PMID: 26381611

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4
Etiology and clinical presentation of birth defects: population based study
Etiology and clinical presentation of birth defects: population based study
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Etiology and clinical presentation of birth defects: population based study

BMJ (Online), 2017-05, Vol.357, p.j2249 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Copyright: 2017 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to 2017 BMJ ;ISSN: 0959-8138 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.j2249 ;PMID: 28559234

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5
Non-alcoholic fatty liver disease: an emerging driving force in chronic kidney disease
Non-alcoholic fatty liver disease: an emerging driving force in chronic kidney disease
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Non-alcoholic fatty liver disease: an emerging driving force in chronic kidney disease

Nature reviews. Nephrology, 2017-05, Vol.13 (5), p.297-310 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group May 2017 ;ISSN: 1759-5061 ;EISSN: 1759-507X ;DOI: 10.1038/nrneph.2017.16 ;PMID: 28218263

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6
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
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Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.521-526 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group May 2012 ;Copyright © 2012 Macmillan Publishers Limited 2012 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2011.246 ;PMID: 22234154

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7
Multiple genetic origins of histidine-rich protein 2 gene deletion in Plasmodium falciparum parasites from Peru
Multiple genetic origins of histidine-rich protein 2 gene deletion in Plasmodium falciparum parasites from Peru
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Multiple genetic origins of histidine-rich protein 2 gene deletion in Plasmodium falciparum parasites from Peru

Scientific reports, 2013-09, Vol.3 (1), p.2797, Article 2797 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2013 ;Copyright © 2013, Macmillan Publishers Limited. All rights reserved 2013 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep02797 ;PMID: 24077522

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8
Seroprevalence and risk factors for Toxoplasma gondii in sheep in Grosseto district, Tuscany, Italy
Seroprevalence and risk factors for Toxoplasma gondii in sheep in Grosseto district, Tuscany, Italy
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Seroprevalence and risk factors for Toxoplasma gondii in sheep in Grosseto district, Tuscany, Italy

BMC veterinary research, 2013-02, Vol.9 (1), p.25-25 [Peer Reviewed Journal]

2013 Cenci-Goga 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 ©2013 Cenci-Goga et al.; licensee BioMed Central Ltd. 2013 Cenci-Goga et al.; licensee BioMed Central Ltd. ;ISSN: 1746-6148 ;EISSN: 1746-6148 ;DOI: 10.1186/1746-6148-9-25 ;PMID: 23391299

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9
A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated?
A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated?
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A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated?

Journal of Medical Genetics, 2012-08, Vol.49 (8), p.490-498 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;2015 INIST-CNRS ;Copyright: 2012 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2012-101013 ;PMID: 22889852 ;CODEN: JMDGAE

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10
Uremic pericarditis, pericardial effusion, and constrictive pericarditis in end‐stage renal disease: Insights and pathophysiology
Uremic pericarditis, pericardial effusion, and constrictive pericarditis in end‐stage renal disease: Insights and pathophysiology
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Uremic pericarditis, pericardial effusion, and constrictive pericarditis in end‐stage renal disease: Insights and pathophysiology

Clinical cardiology (Mahwah, N.J.), 2017-10, Vol.40 (10), p.839-846 [Peer Reviewed Journal]

2017 Wiley Periodicals, Inc. ;ISSN: 0160-9289 ;EISSN: 1932-8737 ;DOI: 10.1002/clc.22770 ;PMID: 28873222

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11
Genotypic Characterization of Non-O157 Shiga Toxin-Producing Escherichia coli in Beef Abattoirs of Argentina
Genotypic Characterization of Non-O157 Shiga Toxin-Producing Escherichia coli in Beef Abattoirs of Argentina
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Genotypic Characterization of Non-O157 Shiga Toxin-Producing Escherichia coli in Beef Abattoirs of Argentina

Journal of food protection, 2011-12, Vol.74 (12), p.2008-2017 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Allen Press Publishing Services Dec 2011 ;ISSN: 0362-028X ;EISSN: 1944-9097 ;DOI: 10.4315/0362-028x.jfp-11-189 ;PMID: 22186039 ;CODEN: JFPRDR

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12
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide
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Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide

Journal of community genetics, 2018-10, Vol.9 (4), p.377-386 [Peer Reviewed Journal]

The Author(s) 2017 ;ISSN: 1868-310X ;EISSN: 1868-6001 ;DOI: 10.1007/s12687-017-0336-2 ;PMID: 28948513

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13
Comparison of Dietary Micronutrient Intakes by Body Weight Status among Mexican-American and Non-Hispanic Black Women Aged 19-39 Years: An Analysis of NHANES 2003-2014
Comparison of Dietary Micronutrient Intakes by Body Weight Status among Mexican-American and Non-Hispanic Black Women Aged 19-39 Years: An Analysis of NHANES 2003-2014
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Comparison of Dietary Micronutrient Intakes by Body Weight Status among Mexican-American and Non-Hispanic Black Women Aged 19-39 Years: An Analysis of NHANES 2003-2014

Nutrients, 2019-11, Vol.11 (12), p.2846 [Peer Reviewed Journal]

2019. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 by the authors. 2019 ;ISSN: 2072-6643 ;EISSN: 2072-6643 ;DOI: 10.3390/nu11122846 ;PMID: 31757075

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14
Prevalence, Characteristics and Perinatal Outcome of Fetal Ventriculomegaly in 29,000 Pregnancies Followed at a Single Institution
Prevalence, Characteristics and Perinatal Outcome of Fetal Ventriculomegaly in 29,000 Pregnancies Followed at a Single Institution
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Prevalence, Characteristics and Perinatal Outcome of Fetal Ventriculomegaly in 29,000 Pregnancies Followed at a Single Institution

Fetal diagnosis and therapy, 2010-01, Vol.27 (3), p.142-148 [Peer Reviewed Journal]

2010 S. Karger AG, Basel ;2015 INIST-CNRS ;Copyright 2010 S. Karger AG, Basel. ;Copyright (c) 2010 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000304735 ;PMID: 20339298

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15
FRAXA and FRAXE: the results of a five year survey
FRAXA and FRAXE: the results of a five year survey
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FRAXA and FRAXE: the results of a five year survey

Journal of medical genetics, 2000-06, Vol.37 (6), p.415-421 [Peer Reviewed Journal]

Journal of Medical Genetics ;2000 INIST-CNRS ;Copyright: 2000 Journal of Medical Genetics ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.37.6.415 ;PMID: 10851251 ;CODEN: JMDGAE

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16
Prevalence, Distribution and Background Variables of Smooth-Bordered Tooth Wear in Teenagers in The Hague, The Netherlands
Prevalence, Distribution and Background Variables of Smooth-Bordered Tooth Wear in Teenagers in The Hague, The Netherlands
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Prevalence, Distribution and Background Variables of Smooth-Bordered Tooth Wear in Teenagers in The Hague, The Netherlands

Caries research, 2002-03, Vol.36 (2), p.147-154 [Peer Reviewed Journal]

2002 S. Karger AG, Basel ;Copyright 2002 S. Karger AG, Basel ;ISSN: 0008-6568 ;EISSN: 1421-976X ;DOI: 10.1159/000057874 ;PMID: 12037373

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17
Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?
Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?
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Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?

BMJ, 1994-07, Vol.309 (6948), p.158-162 [Peer Reviewed Journal]

1994 BMJ Publishing Group Ltd. ;Copyright 1994 British Medical Journal ;Copyright: 1994 (c) 1994 BMJ Publishing Group Ltd. ;ISSN: 0959-8138 ;EISSN: 1468-5833 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.309.6948.158 ;PMID: 8044094

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