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1
Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient: A case report
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Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient: A case report

Medicine (Baltimore), 2020-07, Vol.99 (28), p.e20813-e20813 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020813 ;PMID: 32664073

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2
Epidemiology of microvascular complications of diabetes in South Asians and comparison with other ethnicities
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Epidemiology of microvascular complications of diabetes in South Asians and comparison with other ethnicities

Journal of diabetes, 2016-07, Vol.8 (4), p.470-482 [Peer Reviewed Journal]

2016 Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd ;2016 Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. ;ISSN: 1753-0393 ;EISSN: 1753-0407 ;DOI: 10.1111/1753-0407.12378 ;PMID: 26781344

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3
Acupuncture and weight loss in Asians: A PRISMA-compliant systematic review and meta-analysis
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Acupuncture and weight loss in Asians: A PRISMA-compliant systematic review and meta-analysis

Medicine (Baltimore), 2019-08, Vol.98 (33), p.e16815-e16815 [Peer Reviewed Journal]

Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000016815 ;PMID: 31415397

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4
Generational perspective on asthma self‐management in the Bangladeshi and Pakistani community in the United Kingdom: A qualitative study
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Generational perspective on asthma self‐management in the Bangladeshi and Pakistani community in the United Kingdom: A qualitative study

Health expectations : an international journal of public participation in health care and health policy, 2022-10, Vol.25 (5), p.2534-2547 [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd. ;COPYRIGHT 2022 John Wiley & Sons, Inc. ;2022. 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. ;ISSN: 1369-6513 ;EISSN: 1369-7625 ;DOI: 10.1111/hex.13579 ;PMID: 35999685

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5
Cell cycle-related lncRNAs and mRNAs in osteoarthritis chondrocytes in a Northwest Chinese Han Population
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Cell cycle-related lncRNAs and mRNAs in osteoarthritis chondrocytes in a Northwest Chinese Han Population

Medicine (Baltimore), 2020-06, Vol.99 (24), p.e19905-e19905 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;ISSN: 1536-5964 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000019905 ;PMID: 32541446

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6
Type 2 diabetes in South Asians compared to Europeans: Higher risk and earlier development of major cardiovascular events irrespective of the presence and degree of retinopathy. Results from The HinDu The Hague Diabetes Study
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Type 2 diabetes in South Asians compared to Europeans: Higher risk and earlier development of major cardiovascular events irrespective of the presence and degree of retinopathy. Results from The HinDu The Hague Diabetes Study

Endocrinology, diabetes & metabolism, 2021-07, Vol.4 (3), p.e00242-n/a [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Ltd. ;2021 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. ;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. ;ISSN: 2398-9238 ;EISSN: 2398-9238 ;DOI: 10.1002/edm2.242 ;PMID: 34277967

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7
Role of mitochondria DNA A10398G polymorphism on development of Parkinson's disease: A PRISMA‐compliant meta‐analysis
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Role of mitochondria DNA A10398G polymorphism on development of Parkinson's disease: A PRISMA‐compliant meta‐analysis

Journal of clinical laboratory analysis, 2022-03, Vol.36 (3), p.e24274-n/a [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC. ;2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. ;2022. 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. ;ISSN: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.24274 ;PMID: 35146807

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8
Racial/Ethnic Differences in COVID-19 Vaccine Hesitancy Among Health Care Workers in 2 Large Academic Hospitals
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Racial/Ethnic Differences in COVID-19 Vaccine Hesitancy Among Health Care Workers in 2 Large Academic Hospitals

JAMA Network Open, 2021-08, Vol.4 (8), p.e2121931 [Peer Reviewed Journal]

2021. This work is published under https://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. ;Copyright 2021 Momplaisir FM et al. . ;ISSN: 2574-3805 ;EISSN: 2574-3805 ;DOI: 10.1001/jamanetworkopen.2021.21931 ;PMID: 34459907

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9
Preeclampsia Prevalence, Risk Factors, and Pregnancy Outcomes in Sweden and China
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Preeclampsia Prevalence, Risk Factors, and Pregnancy Outcomes in Sweden and China

JAMA Network Open, 2021-05, Vol.4 (5), p.e218401-e218401 [Peer Reviewed Journal]

2021. This work is published under https://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. ;Copyright 2021 Yang Y et al. . ;ISSN: 2574-3805 ;EISSN: 2574-3805 ;DOI: 10.1001/jamanetworkopen.2021.8401 ;PMID: 33970258

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10
A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy
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A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy

Medicine (Baltimore), 2020-10, Vol.99 (41), p.e22663 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000022663 ;PMID: 33031330

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11
Associations between inflammasome‐related gene NLRP3 Polymorphisms (rs10754558 and rs35829419) and risk of bladder cancer in a Chinese population
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Associations between inflammasome‐related gene NLRP3 Polymorphisms (rs10754558 and rs35829419) and risk of bladder cancer in a Chinese population

Journal of clinical laboratory analysis, 2021-11, Vol.35 (11), p.e23973-n/a [Peer Reviewed Journal]

2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. ;2021. This work is published under http://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: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.23973 ;PMID: 34636069

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12
Effect of a Smartphone App on Weight Change and Metabolic Outcomes in Asian Adults With Type 2 Diabetes: A Randomized Clinical Trial
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Article
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Effect of a Smartphone App on Weight Change and Metabolic Outcomes in Asian Adults With Type 2 Diabetes: A Randomized Clinical Trial

JAMA Network Open, 2021-06, Vol.4 (6), p.e2112417-e2112417 [Peer Reviewed Journal]

2021. This work is published under https://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. ;Copyright 2021 Lim SL et al. . ;ISSN: 2574-3805 ;EISSN: 2574-3805 ;DOI: 10.1001/jamanetworkopen.2021.12417 ;PMID: 34081137

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13
Korean Genome Project: 1094 Korean personal genomes with clinical information
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Article
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Korean Genome Project: 1094 Korean personal genomes with clinical information

Science advances, 2020-05, Vol.6 (22), p.eaaz7835-eaaz7835 [Peer Reviewed Journal]

Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). ;Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). 2020 The Authors ;ISSN: 2375-2548 ;EISSN: 2375-2548 ;DOI: 10.1126/sciadv.aaz7835 ;PMID: 32766443

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14
CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia
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Article
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CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia

Medicine (Baltimore), 2021-12, Vol.100 (51), p.e28275-e28275 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000028275 ;PMID: 34941110

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15
Increased Mortality in Asians With Systemic Sclerosis in Northern California
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Article
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Increased Mortality in Asians With Systemic Sclerosis in Northern California

ACR open rheumatology, 2020-04, Vol.2 (4), p.197-206 [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals Inc on behalf of American College of Rheumatology. This article has been contributed to by US Government employees and their work is in the public domain in the USA. ;2020 The Authors. ACR Open Rheumatology published by Wiley Periodicals Inc on behalf of American College of Rheumatology. This article has been contributed to by US Government employees and their work is in the public domain in the USA. ;2020. This work is published under http://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: 2578-5745 ;EISSN: 2578-5745 ;DOI: 10.1002/acr2.11126 ;PMID: 32198914

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16
Association of the VEGFR2 single nucleotide polymorphism rs2305948 with glioma risk
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Article
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Association of the VEGFR2 single nucleotide polymorphism rs2305948 with glioma risk

Medicine (Baltimore), 2022-01, Vol.101 (1), p.e28454-e28454 [Peer Reviewed Journal]

Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000028454 ;PMID: 35029892

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17
The association between 5, 10 - methylenetetrahydrofolate reductase and the risk of unexplained recurrent pregnancy loss in China: A Meta-analysis
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Article
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The association between 5, 10 - methylenetetrahydrofolate reductase and the risk of unexplained recurrent pregnancy loss in China: A Meta-analysis

Medicine (Baltimore), 2021-04, Vol.100 (17), p.e25487-e25487 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000025487 ;PMID: 33907097

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18
Total cholesterol and mortality from ischemic heart disease and overall cardiovascular disease in Korean adults
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Article
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Total cholesterol and mortality from ischemic heart disease and overall cardiovascular disease in Korean adults

Medicine (Baltimore), 2019-09, Vol.98 (36), p.e17013 [Peer Reviewed Journal]

Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/md.0000000000017013 ;PMID: 31490384

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19
Age-specific reference values for the 5th generation cardiac troponin T assay in Chinese children
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Article
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Age-specific reference values for the 5th generation cardiac troponin T assay in Chinese children

Medicine (Baltimore), 2022-03, Vol.101 (11) [Peer Reviewed Journal]

Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000029101 ;PMID: 35356945

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20
A case report and literature review: Identification of a novel AIRE gene mutation associated with Autoimmune Polyendocrine Syndrome Type 1 in East Asians
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A case report and literature review: Identification of a novel AIRE gene mutation associated with Autoimmune Polyendocrine Syndrome Type 1 in East Asians

Medicine (Baltimore), 2020-05, Vol.99 (18), p.e20000-e20000 [Peer Reviewed Journal]

ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020000 ;PMID: 32358377

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