• 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

Familial hypomagnesaemia with secondary hypocalcaemia--autosomal or X-linked inheritance?

作者信息

Pronicka E, Gruszczyńska B

机构信息

Department of Metabolic Diseases, Memorial Child Health Centre, Warsaw, Poland.

出版信息

J Inherit Metab Dis. 1991;14(3):397-9. doi: 10.1007/BF01811713.

DOI:10.1007/BF01811713
PMID:1770801
Abstract
摘要

相似文献

1
Familial hypomagnesaemia with secondary hypocalcaemia--autosomal or X-linked inheritance?家族性低镁血症伴继发性低钙血症——常染色体遗传还是X连锁遗传?
J Inherit Metab Dis. 1991;14(3):397-9. doi: 10.1007/BF01811713.
2
Afebrile seizures in infants: Never forget magnesium!
J Paediatr Child Health. 2018 Apr;54(4):446-448. doi: 10.1111/jpc.13854. Epub 2018 Feb 7.
3
Familial hypomagnesaemia with secondary hypocalcaemia: a new case that indicates autosomal recessive inheritance.家族性低镁血症伴继发性低钙血症:提示常染色体隐性遗传的一例新病例。
J Inherit Metab Dis. 2001 Dec;24(8):875-6. doi: 10.1023/a:1013952510698.
4
Familial hypomagnesaemia--hypercalciuria leading to end-stage renal failure.
Pediatr Nephrol. 1995 Feb;9(1):74-6. doi: 10.1007/BF00858976.
5
Primary hypomagnesaemia with secondary hypocalcaemia in an infant.
Lancet. 1967 Apr 1;1(7492):703-5. doi: 10.1016/s0140-6736(67)92181-2.
6
Primary infantile hypomagnesaemia.原发性婴儿低镁血症。
Proc R Soc Med. 1974 Aug;67(8):759-60. doi: 10.1177/003591577406700836.
7
Primary hypomagnesaemia with secondary hypocalcaemia in an infant.
Med J Aust. 1969 Aug 2;2(5):242-4. doi: 10.5694/j.1326-5377.1969.tb114672.x.
8
Isolated familial hypomagnesaemia with novel neurological features: causal link or chance concurrence?
Eur J Neurol. 2001 Sep;8(5):495-9. doi: 10.1046/j.1468-1331.2001.00274.x.
9
Hereditary isolated renal magnesium loss maps to chromosome 11q23.遗传性孤立性肾镁丢失定位于染色体11q23。
Am J Hum Genet. 1999 Jan;64(1):180-8. doi: 10.1086/302199.
10
Hypomagnesaemia and hypocalcaemia in a patient with ovarian carcinoma.一名卵巢癌患者出现低镁血症和低钙血症。
Postgrad Med J. 1993 Jul;69(813):583-5. doi: 10.1136/pgmj.69.813.583.

本文引用的文献

1
Parathyroid hormone secretion and responsiveness to parathyroid hormone in primary hypomagnesemia.原发性低镁血症中甲状旁腺激素的分泌及对甲状旁腺激素的反应性
Isr J Med Sci. 1983 Apr;19(4):345-8.
2
[Magnesium deficiency in children].[儿童镁缺乏症]
Arch Fr Pediatr. 1982 Dec;39(10):837-44.
3
Primary hypomagnesaemia, an autosomal recessive inherited disease?原发性低镁血症,一种常染色体隐性遗传病?
Lancet. 1983 Apr 23;1(8330):927. doi: 10.1016/s0140-6736(83)91352-1.
4
Primary hypomagnesaemia, an X-borne allele?
Lancet. 1983 Mar 26;1(8326 Pt 1):701. doi: 10.1016/s0140-6736(83)91986-4.
5
Primary infantile hypomagnesaemia; report of two cases and review of literature.原发性婴儿低镁血症:两例报告及文献复习
Eur J Pediatr. 1989 Feb;148(5):459-61. doi: 10.1007/BF00595914.
6
Gene mapping of mineral metabolic disorders.矿物质代谢紊乱的基因定位
J Inherit Metab Dis. 1989;12 Suppl 1:231-46. doi: 10.1007/BF01799298.
7
[Primary hypomagnesemia. Clinical, diagnostic and therapeutic studies in three children (author's transl)].
Monatsschr Kinderheilkd (1902). 1979 Jan;127(1):37-42.