一种葡萄糖和氨基酸的家族性肾小管吸收缺陷 - Suppr

Suppr

超能文献

A Familial Tubular Absorption Defect of Glucose and Amino Acids.

作者信息

Sheldon W, Luder J, Webb B

出版信息

Arch Dis Child. 1961 Feb;36(185):90-5. doi: 10.1136/adc.36.185.90.

DOI:10.1136/adc.36.185.90

PMID:21032379

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2012676/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b278/2012676/db427212e2e3/archdisch01598-0094-a.jpg

相似文献

A Familial Tubular Absorption Defect of Glucose and Amino Acids.一种葡萄糖和氨基酸的家族性肾小管吸收缺陷

Arch Dis Child. 1961 Feb;36(185):90-5. doi: 10.1136/adc.36.185.90.

A familial tubular absorption defect of glucose and amino acids.一种家族性葡萄糖和氨基酸肾小管吸收缺陷。

Arch Dis Child. 1955 Apr;30(150):160-4. doi: 10.1136/adc.30.150.160.

Tubular reabsorption delay of amino acids in the rabbit kidney.兔肾中氨基酸的肾小管重吸收延迟

Am J Physiol. 1985 Dec;249(6 Pt 2):F878-83. doi: 10.1152/ajprenal.1985.249.6.F878.

Familial hypouricaemia due to an isolated tubular defect of urate reabsorption.由于尿酸盐重吸收的孤立肾小管缺陷导致的家族性低尿酸血症。

Pediatr Nephrol. 1993 Feb;7(1):83-5. doi: 10.1007/BF00861582.

Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".伴有甘氨酸和亚氨基酸肠道吸收正常的家族性亚氨基甘氨酸尿症，与严重智力迟钝相关，一种可能的“脑表型”。

Helv Paediatr Acta. 1976 Aug;31(2):173-82.

Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samples.基于随机尿样评估钠、葡萄糖、磷酸盐和氨基酸的肾小管重吸收情况。

Acta Paediatr. 1994 Dec;83(12):1282-6. doi: 10.1111/j.1651-2227.1994.tb13017.x.

Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids.家族性高甘氨酸尿症。肾小管对甘氨酸和亚氨基酸转运的新缺陷。

Am J Med. 1973 Feb;54(2):265-71. doi: 10.1016/0002-9343(73)90232-5.

Tubular handling of amino acids after intravenous infusion of amino acids in healthy humans.健康人体静脉输注氨基酸后氨基酸的肾小管处理情况。

Nephrol Dial Transplant. 1992;7(6):493-500.

Facilitating effect of amino acids on fructose and sorbitol absorption in children.氨基酸对儿童果糖和山梨醇吸收的促进作用。

J Pediatr Gastroenterol Nutr. 1996 Aug;23(2):118-24. doi: 10.1097/00005176-199608000-00004.

Hyperdibasicaminoaciduria and hyperammonemia in familial protein intolerance.家族性蛋白质不耐受中的高双氨基酸尿症和高氨血症。

Am J Dis Child. 1976 Dec;130(12):1340-4. doi: 10.1001/archpedi.1976.02120130046010.

引用本文的文献

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.甘氨酸氨甲酰基转移酶（GATM）、肾范可尼综合征和肾衰竭。

J Am Soc Nephrol. 2018 Jul;29(7):1849-1858. doi: 10.1681/ASN.2017111179. Epub 2018 Apr 13.

An Acadian variant of Fanconi syndrome.范科尼综合征的一种阿卡迪亚变体。

Pediatr Nephrol. 2007 Oct;22(10):1711-5. doi: 10.1007/s00467-007-0553-8. Epub 2007 Aug 10.

The adult presenting idiopathic Fanconi syndrome.成年患者出现特发性范科尼综合征。

J Inherit Metab Dis. 1981;4(4):211-5. doi: 10.1007/BF02263654.

[Debré-De Toni-Fanconi syndrome with glycogenosis of the liver].[伴有肝糖原贮积症的德布雷-德托尼-范科尼综合征]

Klin Wochenschr. 1968 Mar 15;46(6):317-28. doi: 10.1007/BF01738691.

Idiopathic Fanconi syndrome with progressive renal failure: a case report and discussion.伴有进行性肾衰竭的特发性范科尼综合征：一例病例报告及讨论

Yale J Biol Med. 1990 Jan-Feb;63(1):15-28.

本文引用的文献

A familial tubular absorption defect of glucose and amino acids.一种家族性葡萄糖和氨基酸肾小管吸收缺陷。

Arch Dis Child. 1955 Apr;30(150):160-4. doi: 10.1136/adc.30.150.160.

The proteinuria of renal tubular disorders.肾小管疾病的蛋白尿

Lancet. 1958 Nov 8;2(7054):978-80. doi: 10.1016/s0140-6736(58)90473-2.

A method for estimating Tm for phosphate in man.一种估算人体磷酸盐Tm值的方法。

J Physiol. 1955 Nov 28;130(2):268-77. doi: 10.1113/jphysiol.1955.sp005409.

Amino-acid metabolism.氨基酸代谢

Br Med Bull. 1954;10(3):247-50. doi: 10.1093/oxfordjournals.bmb.a069430.

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