Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient: A case reportMedicine (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: 32664073Full text available |
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2 |
Material Type: Article
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Acupuncture and weight loss in Asians: A PRISMA-compliant systematic review and meta-analysisMedicine (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: 31415397Full text available |
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3 |
Material Type: Article
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Cell cycle-related lncRNAs and mRNAs in osteoarthritis chondrocytes in a Northwest Chinese Han PopulationMedicine (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: 32541446Full text available |
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4 |
Material Type: Article
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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 myopathyMedicine (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: 33031330Full text available |
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5 |
Material Type: Article
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Identification of RET fusions in a Chinese multicancer retrospective analysis by next‐generation sequencingCancer science, 2022-01, Vol.113 (1), p.308-318 [Peer Reviewed Journal]2021 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2022. 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: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/cas.15181 ;PMID: 34710947Full text available |
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6 |
Material Type: Article
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CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesiaMedicine (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: 34941110Full text available |
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7 |
Material Type: Article
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Association of the VEGFR2 single nucleotide polymorphism rs2305948 with glioma riskMedicine (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: 35029892Full text available |
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8 |
Material Type: Article
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Osimertinib in Japanese patients with EGFR T790M mutation‐positive advanced non‐small‐cell lung cancer: AURA3 trialCancer science, 2018-06, Vol.109 (6), p.1930-1938 [Peer Reviewed Journal]2018 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;ISSN: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/cas.13623 ;PMID: 29697876Full text available |
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9 |
Material Type: Article
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The association between 5, 10 - methylenetetrahydrofolate reductase and the risk of unexplained recurrent pregnancy loss in China: A Meta-analysisMedicine (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: 33907097Full text available |
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10 |
Material Type: Article
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Total cholesterol and mortality from ischemic heart disease and overall cardiovascular disease in Korean adultsMedicine (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: 31490384Full text available |
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11 |
Material Type: Article
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Age-specific reference values for the 5th generation cardiac troponin T assay in Chinese childrenMedicine (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: 35356945Full text available |
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12 |
Material Type: Article
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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 AsiansMedicine (Baltimore), 2020-05, Vol.99 (18), p.e20000-e20000 [Peer Reviewed Journal]ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020000 ;PMID: 32358377Full text available |
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13 |
Material Type: Article
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The role of p.Val444Ala variant in the ABCB11 gene and susceptibility to biliary atresia in Vietnamese patientsMedicine (Baltimore), 2021-11, Vol.100 (47), p.e28011-e28011 [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.0000000000028011 ;PMID: 34964797Full text available |
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14 |
Material Type: Article
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Mycophenolate mofetil in the treatment of Chinese patients with lupus nephritis: A PRISMA-compliant meta-analysisMedicine (Baltimore), 2020-08, Vol.99 (33), p.e21121 [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.0000000000021121 ;PMID: 32871981Full text available |
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15 |
Material Type: Article
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Pulmonary artery intimal sarcoma mimicking pulmonary thromboembolism: A case reportMedicine (Baltimore), 2021-02, Vol.100 (6), p.e24699-e24699 [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.0000000000024699 ;PMID: 33578605Full text available |
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16 |
Material Type: Article
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Identification of a novel X-linked arginine-vasopressin receptor 2 mutation in nephrogenic diabetes insipidus: Case report and pedigree analysisMedicine (Baltimore), 2019-10, Vol.98 (40), p.e17359-e17359 [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.0000000000017359 ;PMID: 31577731Full text available |
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17 |
Material Type: Article
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Wiedemann-steiner syndrome with a de novo mutation in KMT2A: A case reportMedicine (Baltimore), 2020-04, Vol.99 (16), p.e19813-e19813 [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.0000000000019813 ;PMID: 32311999Full text available |
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18 |
Material Type: Article
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Identification of a novel mutation in pseudohypoparathyroidism type Ia in a Chinese family: A case reportMedicine (Baltimore), 2020-05, Vol.99 (21), p.e19965-e19965 [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.0000000000019965 ;PMID: 32481259Full text available |
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19 |
Material Type: Article
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Targeted next-generation sequencing identifies a novel nonsense mutation in SPTB for hereditary spherocytosis: A case report of a Korean familyMedicine (Baltimore), 2018-01, Vol.97 (3), p.e9677-e9677 [Peer Reviewed Journal]Copyright © 2017 The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved. ;Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. 2018 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000009677 ;PMID: 29505016Full text available |
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20 |
Material Type: Article
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De-differentiation of papillary thyroid carcinoma into squamous cell carcinoma in an elderly patient: A case reportMedicine (Baltimore), 2020-04, Vol.99 (16), p.e19892-e19892 [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.0000000000019892 ;PMID: 32312017Full text available |