Recommendations for cancer screening and surveillance in patients with Werner syndrome.
作者信息
Aono Kazuto, Maezawa Yoshiro, Kato Hisaya, Kaneko Hiyori, Kubota Yoshitaka, Taniguchi Toshibumi, Oshitari Toshiyuki, Motegi Sei-Ichiro, Nakagami Hironori, Taniguchi Akira, Watanabe Kazuhisa, Takemoto Minoru, Koshizaka Masaya, Yokote Koutaro
机构信息
Department of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Division of Diabetes, Metabolism and Endocrinology, Chiba University Hospital, Chiba, Japan.
出版信息
Geriatr Gerontol Int. 2024 Oct;24(10):1085-1087. doi: 10.1111/ggi.14967. Epub 2024 Aug 24.
Abstract
摘要
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本文引用的文献
1
Renal dysfunction, malignant neoplasms, atherosclerotic cardiovascular diseases, and sarcopenia as key outcomes observed in a three-year follow-up study using the Werner Syndrome Registry.在一项为期三年的随访研究中，使用 Werner 综合征登记处观察到的肾功能障碍、恶性肿瘤、动脉粥样硬化性心血管疾病和肌肉减少症等主要结局。
Aging (Albany NY). 2023 May 1;15(9):3273-3294. doi: 10.18632/aging.204681.
2
Lifetime extension and the recent cause of death in Werner syndrome: a retrospective study from 2011 to 2020. Werner 综合征的寿命延长和近期死因：2011 年至 2020 年的回顾性研究。
Orphanet J Rare Dis. 2022 Jun 13;17(1):226. doi: 10.1186/s13023-022-02383-w.
3
Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.DNA修复障碍患儿癌症筛查与监测建议
Clin Cancer Res. 2017 Jun 1;23(11):e23-e31. doi: 10.1158/1078-0432.CCR-17-0465.
4
Spectrum and risk of neoplasia in Werner syndrome: a systematic review.沃纳综合征的肿瘤谱及风险：一项系统性回顾。
PLoS One. 2013;8(4):e59709. doi: 10.1371/journal.pone.0059709. Epub 2013 Apr 1.
5
Werner syndrome: a changing pattern of clinical manifestations in Japan (1917~2008). Werner 综合征：日本临床表现变化模式（1917~2008）。
Biosci Trends. 2013 Feb;7(1):13-22.
6
Japanese diabetic patients with Werner syndrome exhibit high incidence of cancer.患有沃纳综合征的日本糖尿病患者癌症发病率很高。
Acta Diabetol. 2012 Dec;49 Suppl 1:S259-60. doi: 10.1007/s00592-012-0424-z. Epub 2012 Aug 8.
7
Spontaneous and X-ray-induced chromosomal aberrations in Werner syndrome cells detected by FISH using chromosome-specific painting probes.使用染色体特异性涂染探针通过荧光原位杂交（FISH）检测沃纳综合征细胞中的自发及X射线诱导的染色体畸变。
Mutagenesis. 2000 Jul;15(4):303-10. doi: 10.1093/mutage/15.4.303.
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