1型原发性高草酸尿症在理解、诊断和治疗方面的最新进展。 - Suppr

Suppr

超能文献

Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

作者信息

Danpure C J

机构信息

MRC Clinical Research Centre, Harro, Middlesex, UK.

出版信息

J Inherit Metab Dis. 1989;12(2):210-24. doi: 10.1007/BF01800727.

DOI:10.1007/BF01800727

PMID:2502679

Abstract

摘要

相似文献

Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

J Inherit Metab Dis. 1989;12(2):210-24. doi: 10.1007/BF01800727.

Primary hyperoxaluria type I.

Eur J Pediatr. 1990 May;149(8):518-22. doi: 10.1007/BF01957682.

[Primary hyperoxaluria].

Ugeskr Laeger. 1989 Jul 17;151(29):1856-9.

Primary hyperoxaluria.

N Engl J Med. 2013 Aug 15;369(7):649-58. doi: 10.1056/NEJMra1301564.

Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1.

Prenat Diagn. 1989 Apr;9(4):271-81. doi: 10.1002/pd.1970090406.

Current approaches to the management of primary hyperoxaluria.

Arch Dis Child. 2000 Jun;82(6):470-3. doi: 10.1136/adc.82.6.470.

[Primary hyperoxaluria].

Nephrologie. 1995;16(6):399-406.

Prenatal exclusion of primary hyperoxaluria type 1.

Lancet. 1988 Feb 13;1(8581):367. doi: 10.1016/s0140-6736(88)91171-3.

Renal histology for the diagnosis of primary hyperoxaluria in patients with end-stage renal disease.

Nephron. 1989;53(1):81-2. doi: 10.1159/000185709.

Renal transplantation in primary hyperoxaluria/oxalosis: a report of two cases.

Transplant Proc. 1987 Aug;19(4):3431-2.

引用本文的文献

Primary hyperoxaluria type 1: diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT).

J Inherit Metab Dis. 1997 Sep;20(5):689-96. doi: 10.1023/a:1005326510239.

Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism.

J Inherit Metab Dis. 1994;17(1):27-40. doi: 10.1007/BF00735393.

Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.

J Inherit Metab Dis. 1994;17(4):487-99. doi: 10.1007/BF00711363.

Excessive urinary oxalate excretion after combined renal and hepatic transplantation for correction of hyperoxaluria type 1.

Eur J Pediatr. 1990 Nov;150(1):56-8. doi: 10.1007/BF01959482.

Clinical quiz. Primary hyperoxaluria (PH) type 1.

Pediatr Nephrol. 1991 May;5(3):365-7. doi: 10.1007/BF00867506.

Treatment of inherited metabolic disorders by liver transplantation.

J Inherit Metab Dis. 1991;14(4):604-18. doi: 10.1007/BF01797930.

Orthotopic liver transplantation in liver-based metabolic disorders.

Eur J Pediatr. 1992;151 Suppl 1:S32-8. doi: 10.1007/BF02125800.

本文引用的文献

The metabolism of glyoxylate by human- and rat-liver mitochondria.

Biochem J. 1962 Oct;85(1):163-71. doi: 10.1042/bj0850163.

Further observations on the genetic basis of primary hyperoxaluria.

Ann Hum Genet. 1959 Dec;23:367-81. doi: 10.1111/j.1469-1809.1959.tb01480.x.

Clinical manifestations of primary hyperoxaluria.

Arch Dis Child. 1960 Feb;35(179):108-12. doi: 10.1136/adc.35.179.108.

VITAMIN B6 AND OXALATE METABOLISM.

Vitam Horm. 1964;22:581-9.

PRIMARY HYPEROXALURIA.

Medicine (Baltimore). 1964 May;43:315-45. doi: 10.1097/00005792-196405000-00010.

STUDIES ON PRIMARY HYPEROXALURIA. I. IN VIVO DEMONSTRATION OF A DEFECT IN GLYOXYLATE METABOLISM.

N Engl J Med. 1963 Oct 17;269:821-9. doi: 10.1056/NEJM196310172691601.

Vitamin B6 deficiency and oxalate nephrocalcinosis in the cat.

Am J Med. 1959 Jul;27(1):72-80. doi: 10.1016/0002-9343(59)90062-2.

Observations on the possible genetic basis of primary hyperoxaluria.

Ann Hum Genet. 1958 Jul;22(4):373-9. doi: 10.1111/j.1469-1809.1958.tb01432.x.

Primary hyperoxaluria.

Lancet. 1957 Aug 17;273(6990):320-2. doi: 10.1016/s0140-6736(57)92210-9.

The organ distribution of human alanine-2-oxoglutarate aminotransferase and alanine-glyoxylate aminotransferase.

Biochem Med. 1980 Feb;23(1):25-34. doi: 10.1016/0006-2944(80)90051-4.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验