Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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21 |
Material Type: Article
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P608 Simpleprobe PCR assay for detection of mutations associated with macrolide resistance in mycoplasma genitalium samplesSexually transmitted infections, 2019-07, Vol.95 (Suppl 1), p.A269 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1368-4973 ;EISSN: 1472-3263 ;DOI: 10.1136/sextrans-2019-sti.676Full text available |
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22 |
Material Type: Article
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P243 High prevalence of Ureaplasma spp. in women visiting an STI clinic although no azithromycin resistance was discoveredSexually transmitted infections, 2019-07, Vol.95 (Suppl 1), p.A149 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1368-4973 ;EISSN: 1472-3263 ;DOI: 10.1136/sextrans-2019-sti.377Full text available |
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23 |
Material Type: Article
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P597 Comparison of assays and specimen types for the diagnosis of mycoplasma genitalium and macrolide resistant mutationsSexually transmitted infections, 2019-07, Vol.95 (Suppl 1), p.A265 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1368-4973 ;EISSN: 1472-3263 ;DOI: 10.1136/sextrans-2019-sti.666Full text available |
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24 |
Material Type: Article
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ReplyAmerican journal of ophthalmology, 2018-02, Vol.186, p.170 [Peer Reviewed Journal]Copyright Elsevier Limited Feb 2018 ;ISSN: 0002-9394 ;EISSN: 1879-1891 ;DOI: 10.1016/j.ajo.2017.11.005Full text available |
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25 |
Material Type: Article
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PO180 Mosaicism in neurofibromatosis type 2: a case reportJournal of neurology, neurosurgery and psychiatry, 2017-12, Vol.88 (Suppl 1), p.A59-A59 [Peer Reviewed Journal]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 ;Copyright: 2017 © 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 ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2017-ABN.202Full text available |
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26 |
Material Type: Article
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PO186 Hereditary leukoencephalopathy (hls) and csf1r heterogeneityJournal of neurology, neurosurgery and psychiatry, 2017-12, Vol.88 (Suppl 1), p.A60-A60 [Peer Reviewed Journal]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 ;Copyright: 2017 © 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 ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2017-ABN.207Full text available |
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27 |
Material Type: Article
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PO202 Natural history study in hereditary sensory neuropathy type 1Journal of neurology, neurosurgery and psychiatry, 2017-12, Vol.88 (Suppl 1), p.A65-A65 [Peer Reviewed Journal]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 ;Copyright: 2017 © 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 ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2017-ABN.223Full text available |
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28 |
Material Type: Article
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CORRIGENDUMGenetics (Austin), 2019-07, Vol.212 (3), p.953-953 [Peer Reviewed Journal]Copyright Genetics Society of America Jul 2019 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.119.302298Full text available |
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29 |
Material Type: Article
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Abstract 49: A single centre experience on nodular adrenocortical cushings syndromeIndian journal of endocrinology and metabolism, 2022-12, Vol.26 (8), p.21-21 [Peer Reviewed Journal]COPYRIGHT 2022 Medknow Publications and Media Pvt. Ltd. ;2022. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2230-8210 ;EISSN: 2230-9500 ;DOI: 10.4103/2230-8210.363736Full text available |
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30 |
Material Type: Article
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Correction: Association of SMAD4 mutation with patient demographics, tumor characteristics, and clinical outcomes in colorectal cancerPloS one, 2017-05, Vol.12 (5), p.e0178275-e0178275 [Peer Reviewed Journal]COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 The PLOS ONE Staff. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017 The PLOS ONE Staff 2017 The PLOS ONE Staff ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0178275 ;PMID: 28545046Full text available |
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31 |
Material Type: Article
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Correction: A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Unique Predisposing Mutations in JapanPloS one, 2017-05, Vol.12 (5), p.e0178015-e0178015 [Peer Reviewed Journal]COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 Yoshida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017 Yoshida et al 2017 Yoshida et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0178015 ;PMID: 28520790Full text available |
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32 |
Material Type: Article
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A44 INTERVENTIONAL PULMONARY: CASE REPORTS: C.1309c/t Endoglin (eng) Gene Mutation Associated Multiple Pulmonary Arteriovenous Malformations Successfully Treated By Endovascular Coiling And Vascular PlugsAmerican journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970Full text available |
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33 |
Material Type: Article
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C25 NON-TUBERCULOUS MYCOBACTERIA: FROM BENCH TO CLINIC: A Bna-Pcr Based Rapid Identification System For The Detection Of Macrolide Resistant Mycobacterium Avium-Intracellulare ComplexAmerican journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970Full text available |
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34 |
Material Type: Article
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C80-J THORACIC ONCOLOGY CASE REPORTS IV: Histologic Transformation From Non-Small Cell Lung Cancer (nsclc) Adenocarcinoma With EGFR-Mutant Exons 20(s768i) And 21(l858r) To Small Cell Lung Carcinoma (sclc): Case ReportAmerican journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970Full text available |
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35 |
Material Type: Article
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CORRECTIONNature (London), 2018-11, Vol.563 (7732), p.E27-E27 [Peer Reviewed Journal]Copyright Nature Publishing Group Nov 22, 2018 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-018-0580-6Full text available |
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36 |
Material Type: Article
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Genotype/Phenotype Correlation of Cases with PTPN11 Gene Mutation: Eastern Black Sea ExperienceAnkara Ueniversitesi Tip Fakültesi mecmuasi, 2022-10, Vol.75 (3), p.368-372 [Peer Reviewed Journal]2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1307-5608 ;ISSN: 0365-8104 ;EISSN: 1307-5608 ;DOI: 10.4274/atfm.galenos.2022.06978Full text available |
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37 |
Material Type: Article
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The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XVBone research, 2021-11, Vol.9 (1), p.48-48 [Peer Reviewed Journal]The Author(s) 2021. 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) 2021 ;ISSN: 2095-4700 ;EISSN: 2095-6231 ;DOI: 10.1038/s41413-021-00170-0 ;PMID: 34759273Full text available |
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38 |
Material Type: Article
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Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancerNature genetics, 2016-05, Vol.48 (6), p.700-700 [Peer Reviewed Journal]ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng0616-700a ;PMID: 27230686Full text available |
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39 |
Material Type: Article
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Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital CataractPloS one, 2015-05, Vol.10 (5), p.e0125949-e0125949 [Peer Reviewed Journal]COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Zhu et al 2015 Zhu et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0125949 ;PMID: 25970271Full text available |
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40 |
Material Type: Article
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The landscape of genomic alterations across childhood cancersNature (London), 2018-03, Vol.555 (7696), p.321-327 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Mar 15, 2018 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature25480 ;PMID: 29489754Full text available |