• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Slow progression of chronic renal failure in a woman of short stature and leg deformities: what is the link?

作者信息

Vanacker An, Segaert Marc, Verbanck Johan, Van Dorpe Jo, Poppe Bruce, Maes Bart

机构信息

Department of Nephrology, Heilig Hartziekenhuis Roeselare-Menen, B-8800 Roeselare.

Department of Pathology, Heilig Hartziekenhuis Roeselare-Menen, B-8800 Roeselare.

出版信息

NDT Plus. 2008 Aug;1(4):257-61. doi: 10.1093/ndtplus/sfn062. Epub 2008 Jun 3.

DOI:10.1093/ndtplus/sfn062
PMID:25983897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4421228/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/772190284a76/sfn062fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/f96539d36c47/sfn062fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/6386c6f48222/sfn062fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/e9815d7016da/sfn062fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/7c104a0af61c/sfn062fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/772190284a76/sfn062fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/f96539d36c47/sfn062fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/6386c6f48222/sfn062fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/e9815d7016da/sfn062fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/7c104a0af61c/sfn062fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/4421228/772190284a76/sfn062fig5.jpg

相似文献

1
Slow progression of chronic renal failure in a woman of short stature and leg deformities: what is the link?一名身材矮小且腿部畸形的女性慢性肾衰竭进展缓慢：其中有什么关联？
NDT Plus. 2008 Aug;1(4):257-61. doi: 10.1093/ndtplus/sfn062. Epub 2008 Jun 3.
2
Calcium metabolism and growth during early treatment of children with X-linked hypophosphataemic rickets.X连锁低磷性佝偻病患儿早期治疗期间的钙代谢与生长
Eur J Pediatr. 1998 Nov;157(11):894-900. doi: 10.1007/s004310050962.
3
Hereditary hypophosphatemic rickets with hypercalciuria: case report.遗传性低血磷性佝偻病伴高钙尿症：病例报告。
Nefrologia. 2012 Jul 17;32(4):529-34. doi: 10.3265/Nefrologia.pre2012.Apr.11321.
4
Familial hypophosphataemic rickets affecting a father and his two daughters: a case report.家族性低磷血症性佝偻病累及一位父亲及其两个女儿：病例报告
West Afr J Med. 2010 Jul-Aug;29(4):271-4.
5
Windswept lower limb deformities in patients with hypophosphataemic rickets.伴有低血磷性佝偻病的下肢风蚀样畸形。
Swiss Med Wkly. 2013 Dec 6;143:w13904. doi: 10.4414/smw.2013.13904. eCollection 2013.
6
Medullary nephrocalcinosis: sonographic findings in adult patients.
Bildgebung. 1995 Mar;62(1):18-22.
7
A case of X-linked hypophosphatemic rickets: complications and the therapeutic use of cinacalcet.一例X连锁低磷性佝偻病：并发症及西那卡塞的治疗应用
Eur J Endocrinol. 2008 Dec;159 Suppl 1:S101-5. doi: 10.1530/EJE-08-0383. Epub 2008 Sep 5.
8
Treatment of hypophosphataemic rickets in children remains a challenge.儿童低磷性佝偻病的治疗仍然是一项挑战。
Dan Med J. 2014 Jul;61(7):A4874.
9
Nephrocalcinosis, hyperparathyroidism, and renal failure in familial hypophosphatemic rickets.家族性低磷血症性佝偻病中的肾钙质沉着症、甲状旁腺功能亢进和肾衰竭。
Clin Pediatr (Phila). 1992 Mar;31(3):180-3. doi: 10.1177/000992289203100311.
10
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23.常染色体显性低磷性佝偻病与FGF23基因突变有关。
Nat Genet. 2000 Nov;26(3):345-8. doi: 10.1038/81664.

引用本文的文献

1
Burden of disease associated with X-linked hypophosphataemia in adults: a systematic literature review.成人X连锁低磷血症相关的疾病负担：一项系统文献综述
Osteoporos Int. 2021 Jan;32(1):7-22. doi: 10.1007/s00198-020-05548-0. Epub 2020 Jul 24.

本文引用的文献

1
Two novel PHEX mutations in Taiwanese patients with X-linked hypophosphatemic rickets.台湾X连锁低磷性佝偻病患者中的两种新型PHEX突变。
Nephron Physiol. 2006;103(4):p157-63. doi: 10.1159/000092916. Epub 2006 Apr 24.
2
Recombinant growth hormone therapy for X-linked hypophosphatemia in children.重组生长激素治疗儿童X连锁低磷血症
Cochrane Database Syst Rev. 2005 Jan 25(1):CD004447. doi: 10.1002/14651858.CD004447.pub2.
3
Prolonged high-dose phosphate treatment: a risk factor for tertiary hyperparathyroidism in X-linked hypophosphatemic rickets.
长期大剂量磷酸盐治疗：X连锁低磷性佝偻病患者发生三发性甲状旁腺功能亢进的一个危险因素。
Clin Endocrinol (Oxf). 2003 Feb;58(2):163-8. doi: 10.1046/j.1365-2265.2003.01685.x.
4
Thiazide diuretics arrest the progression of nephrocalcinosis in children with X-linked hypophosphatemia.噻嗪类利尿剂可阻止X连锁低磷血症患儿肾钙质沉着症的进展。
Pediatrics. 2001 Jul;108(1):E6. doi: 10.1542/peds.108.1.e6.
5
Effect of growth hormone treatment on final height, phosphate metabolism, and bone mineral density in children with X-linked hypophosphatemic rickets.生长激素治疗对X连锁低磷性佝偻病患儿最终身高、磷代谢及骨密度的影响。
J Pediatr. 2001 Feb;138(2):236-43. doi: 10.1067/mpd.2001.108955.
6
Tertiary hyperparathyroidism in X-linked hypophosphatemic rickets.
Intern Med. 2000 Jun;39(6):468-71. doi: 10.2169/internalmedicine.39.468.
7
PHEX gene and hypophosphatemia.PHEX基因与低磷血症
Kidney Int. 2000 Jan;57(1):9-18. doi: 10.1046/j.1523-1755.2000.00807.x.
8
X-linked hypophosphataemia: a homologous disorder in humans and mice.X连锁低磷血症：人类和小鼠中的一种同源性疾病。
Nephrol Dial Transplant. 1999 Feb;14(2):333-41. doi: 10.1093/ndt/14.2.333.
9
24,25 Dihydroxyvitamin D supplementation corrects hyperparathyroidism and improves skeletal abnormalities in X-linked hypophosphatemic rickets--a clinical research center study.补充24,25-二羟基维生素D可纠正X连锁低磷性佝偻病中的甲状旁腺功能亢进并改善骨骼异常——一项临床研究中心的研究
J Clin Endocrinol Metab. 1996 Jun;81(6):2381-8. doi: 10.1210/jcem.81.6.8964881.
10
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium.一种与内肽酶具有同源性的基因（PEX）在X连锁低磷血症性佝偻病患者中发生突变。HYP研究小组。
Nat Genet. 1995 Oct;11(2):130-6. doi: 10.1038/ng1095-130.