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Graves' disease and Gitelman syndrome.

作者信息

Mizokami Tetsuya, Hishinuma Akira, Kogai Takahiko, Hamada Katsuhiko, Maruta Tetsushi, Higashi Kiichiro, Tajiri Junichi

机构信息

Tajiri Thyroid Clinic, Kumamoto, Japan.

Department of Infection Control and Clinical Laboratory Medicine, Dokkyo Medical University, Tochigi, Japan.

出版信息

Clin Endocrinol (Oxf). 2016 Jan;84(1):149-50. doi: 10.1111/cen.12829. Epub 2015 Jul 3.

DOI:10.1111/cen.12829
PMID:26041598
Abstract
摘要

相似文献

1
Graves' disease and Gitelman syndrome.格雷夫斯病和吉特曼综合征。
Clin Endocrinol (Oxf). 2016 Jan;84(1):149-50. doi: 10.1111/cen.12829. Epub 2015 Jul 3.
2
Coexistence of Graves' Disease in a 14-year-old young girl with Gitelman Syndrome.一名14岁患有吉特曼综合征的年轻女孩同时患有格雷夫斯病。
Clin Endocrinol (Oxf). 2015 Dec;83(6):995-7. doi: 10.1111/cen.12800. Epub 2015 May 7.
3
[A case of Gitelman syndrome with Graves disease as initial diagnosis].以格雷夫斯病初诊的吉特曼综合征1例
Zhonghua Nei Ke Za Zhi. 2020 May 1;59(5):382-384. doi: 10.3760/cma.j.cn112138-20190509-00356.
4
Perioperative considerations in patients with Gitelman syndrome: a case series.Gitelman 综合征患者的围手术期注意事项:病例系列。
J Clin Anesth. 2012 Feb;24(1):14-8. doi: 10.1016/j.jclinane.2011.04.009.
5
Graves' immune reconstitution inflammatory syndrome in childhood.儿童格雷夫斯氏免疫重建炎症综合征。
Thyroid. 2013 Aug;23(8):1010-4. doi: 10.1089/thy.2012.0618.
6
Clinical and genetic analyses of Chinese patients with Gitelman syndrome.中国吉特曼综合征患者的临床与基因分析
Genet Mol Res. 2016 May 6;15(2):gmr7859. doi: 10.4238/gmr.15027859.
7
Gitelman syndrome: an analysis of the underlying pathophysiologic mechanisms of acid-base and electrolyte abnormalities.格替曼综合征:酸碱电解质异常的潜在病理生理机制分析。
Int Urol Nephrol. 2018 Jan;50(1):91-96. doi: 10.1007/s11255-017-1653-4. Epub 2017 Jul 25.
8
Course of depression in Cushing's syndrome: response to treatment and comparison with Graves' disease.库欣综合征中抑郁症的病程:对治疗的反应及与格雷夫斯病的比较。
Horm Res. 1993;39(5-6):202-6. doi: 10.1159/000182736.
9
Bilateral carpal tunnel syndrome caused by Graves' disease.格雷夫斯病引起的双侧腕管综合征
Arch Intern Med. 1985 Feb;145(2):345-6.
10
Gitelman Syndrome: Presenting During Pregnancy with Adverse Foetal Outcome.吉特曼综合征:孕期出现并伴有不良胎儿结局
J Assoc Physicians India. 2016 Oct;64(10):104-105.

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RNA-binding proteins regulate immune-related alternative splicing in inherited salt-losing tubulopathies.RNA结合蛋白在遗传性失盐性肾小管病中调节免疫相关的可变剪接。
Orphanet J Rare Dis. 2025 Aug 9;20(1):416. doi: 10.1186/s13023-025-03972-1.
2
A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature.一个新的 SLC12A3 基因突变导致 Gitelman 综合征合并自身免疫性甲状腺炎:病例报告及文献复习。
CEN Case Rep. 2024 Oct;13(5):330-338. doi: 10.1007/s13730-023-00845-z. Epub 2024 Feb 3.
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Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.
Gitelman 综合征合并 Graves 病致横纹肌溶解症 1 例报告并文献复习
BMC Nephrol. 2023 May 2;24(1):123. doi: 10.1186/s12882-023-03180-8.
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Novel compound heterozygous mutation of in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review.吉特曼综合征中新型复合杂合突变与甲状腺功能亢进并存:一例报告及文献复习
World J Clin Cases. 2022 Jul 26;10(21):7483-7494. doi: 10.12998/wjcc.v10.i21.7483.
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Concurrent Gitelman Syndrome-like Tubulopathy and Grave's Disease.并发吉特曼综合征样肾小管病和格雷夫斯病。
Indian J Nephrol. 2022 May-Jun;32(3):275-278. doi: 10.4103/ijn.IJN_532_20. Epub 2022 May 20.
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Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes.鉴定一个中国 Gitelman 综合征家系中 SLC12A3 基因突变的复合杂合子,该家系表现出 Bartter 综合征样表型。
BMC Nephrol. 2020 Aug 5;21(1):328. doi: 10.1186/s12882-020-01996-2.
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Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review.复杂型 Gitelman 综合征合并自身免疫性甲状腺疾病:一例新的 SLC12A3 基因突变纯合子病例报告及文献复习。
BMC Endocr Disord. 2018 Nov 8;18(1):82. doi: 10.1186/s12902-018-0298-3.