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1
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
Mortality and incidence in women with 47,XXX and variants
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Mortality and incidence in women with 47,XXX and variants

American journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Peer Reviewed Journal]

Copyright © 2010 Wiley‐Liss, Inc. ;Copyright 2010 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.33214 ;PMID: 20101696

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3
VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo
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VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo

British journal of cancer, 2009-10, Vol.101 (7), p.1183 [Peer Reviewed Journal]

EISSN: 1532-1827 ;DOI: 10.1038/sj.bjc.6605249 ;PMID: 19707198

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4
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome

Journal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Peer Reviewed Journal]

Copyright 2002 Journal of Medical Genetics ;2002 INIST-CNRS ;COPYRIGHT 2002 BMJ Publishing Group Ltd. ;Copyright: 2002 Copyright 2002 Journal of Medical Genetics ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.39.3.217 ;PMID: 11897829 ;CODEN: JMDGAE

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5
Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee
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Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee

Clinical and experimental rheumatology, 2010-11, Vol.28 (6), p.803-805 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0392-856X ;EISSN: 1593-098X ;PMID: 21205458

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6
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events

Rheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Peer Reviewed Journal]

2005 INIST-CNRS ;Copyright Oxford University Press(England) Jul 2005 ;ISSN: 1462-0324 ;EISSN: 1462-0332 ;DOI: 10.1093/rheumatology/keh613 ;PMID: 15797975 ;CODEN: BJRHDF

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7
Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation
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Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation

American journal of transplantation, 2016-01, Vol.16 (1), p.213-220 [Peer Reviewed Journal]

Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons ;Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons. ;ISSN: 1600-6135 ;EISSN: 1600-6143 ;DOI: 10.1111/ajt.13434 ;PMID: 26317487

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8
Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases

Prenatal diagnosis, 2004-12, Vol.24 (12), p.1020-1021 [Peer Reviewed Journal]

Copyright © 2004 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1047 ;PMID: 15614873

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9
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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Doctors’ experiences of adverse events in secondary care: the professional and personal impact

Clinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Peer Reviewed Journal]

2014 © 2014 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;2015 INIST-CNRS ;2014 Royal College of Physicians 2014 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.14-6-585 ;PMID: 25468840

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10
47,XXX male: A clinical and molecular study
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47,XXX male: A clinical and molecular study

American journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Peer Reviewed Journal]

Copyright © 2001 Wiley‐Liss, Inc. ;2001 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/1096-8628(20010201)98:4<353::AID-AJMG1110>3.0.CO;2-D ;PMID: 11170081 ;CODEN: AJMGDA

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11
Malignant stromal tumour of the ovary with virilizing effects in an XXX female with streak ovaries. Clinical and pathological studies
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Malignant stromal tumour of the ovary with virilizing effects in an XXX female with streak ovaries. Clinical and pathological studies

Australian & New Zealand journal of obstetrics & gynaecology, 1980-05, Vol.20 (2), p.123-128 [Peer Reviewed Journal]

ISSN: 0004-8666 ;EISSN: 1479-828X ;DOI: 10.1111/j.1479-828X.1980.tb00110.x ;PMID: 6932203

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12
XXY son of a possibly XX-XXX mother
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XXY son of a possibly XX-XXX mother

The Lancet (British edition), 1972-03, Vol.1 (7752), p.697-698 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4125211

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13
Motor nerve conduction in 47, XXY and 48, XXYY males, and 47, XXX and 45, X females
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Motor nerve conduction in 47, XXY and 48, XXYY males, and 47, XXX and 45, X females

Clinical genetics, 1974-01, Vol.6 (3), p.205-215 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1974.tb00653.x ;PMID: 4426136

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14
CUTIS VERTICIS GYRATA IN A WOMAN WITH SUPERNUMERARY X CHROMOSOMES (46,XX/47,XXX/48,XXXX)
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CUTIS VERTICIS GYRATA IN A WOMAN WITH SUPERNUMERARY X CHROMOSOMES (46,XX/47,XXX/48,XXXX)

Acta psychiatrica Scandinavica, 1970-01, Vol.46 (2), p.120-125, Article 120 [Peer Reviewed Journal]

ISSN: 0001-690X ;ISSN: 0001-6314 ;EISSN: 1600-0447 ;EISSN: 1600-0404 ;DOI: 10.1111/j.1600-0447.1970.tb02107.x ;PMID: 5478539

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15
Mosaic Turner syndrome shows reduced penetrance in an adult population study
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Mosaic Turner syndrome shows reduced penetrance in an adult population study

Genetics in medicine, 2019-04, Vol.21 (4), p.877-886 [Peer Reviewed Journal]

2018. This work is published 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) 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0271-6 ;PMID: 30181606

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16
The impact of genetic polymorphisms, diltiazem, and demographic variables on everolimus trough concentrations in lung transplant recipients
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The impact of genetic polymorphisms, diltiazem, and demographic variables on everolimus trough concentrations in lung transplant recipients

Clinical transplantation, 2014-05, Vol.28 (5), p.590-597 [Peer Reviewed Journal]

2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd ;2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. ;ISSN: 0902-0063 ;EISSN: 1399-0012 ;DOI: 10.1111/ctr.12350 ;PMID: 24628014

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17
VEGF in the lung: a role for novel isoforms
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VEGF in the lung: a role for novel isoforms

American journal of physiology. Lung cellular and molecular physiology, 2010-06, Vol.298 (6), p.L768-L774 [Peer Reviewed Journal]

Copyright American Physiological Society Jun 2010 ;Copyright © 2010 the American Physiological Society ;ISSN: 1040-0605 ;EISSN: 1522-1504 ;DOI: 10.1152/ajplung.00353.2009 ;PMID: 20228180

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18
Brain-derived neurotrophic factor is not altered in the serum and cerebrospinal fluid of amyotrophic lateral sclerosis patients
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Brain-derived neurotrophic factor is not altered in the serum and cerebrospinal fluid of amyotrophic lateral sclerosis patients

Neurological sciences, 2002-03, Vol.22 (6), p.473-474 [Peer Reviewed Journal]

ISSN: 1590-1874 ;EISSN: 1590-3478 ;DOI: 10.1007/s100720200009 ;PMID: 11976981

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19
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

Nature communications, 2019-10, Vol.10 (1), p.4897-10, Article 4897 [Peer Reviewed Journal]

2019. This work is published 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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-12869-0 ;PMID: 31653860

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20
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
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Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience

BMC research notes, 2020-03, Vol.13 (1), p.167-167, Article 167 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;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: 1756-0500 ;EISSN: 1756-0500 ;DOI: 10.1186/s13104-020-05009-1 ;PMID: 32188487

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