用于检测遗传性和获得性氨基酸病的快速筛查方法。 - Suppr

Suppr

超能文献

Rapid screening methods for the detection of inherited and acquired aminoacidopathies.

作者信息

Saifer A

出版信息

Adv Clin Chem. 1971;14:145-218. doi: 10.1016/s0065-2423(08)60146-8.

DOI:10.1016/s0065-2423(08)60146-8

PMID:4109903

Abstract

摘要

相似文献

Rapid screening methods for the detection of inherited and acquired aminoacidopathies.

Adv Clin Chem. 1971;14:145-218. doi: 10.1016/s0065-2423(08)60146-8.

[Chromatographic analysis in the diagnosis of metabolic aminoacidopathies].

Minerva Pediatr. 1971 Dec 22;23(51):2125-8.

[Diagnostic methods for the detection of amino acid metabolism disorders].

Monatsschr Kinderheilkd (1902). 1973 May;121(5):184-9.

[Our preliminary experiences with a unidimensional paper-chromatographic technic for the study of aminoacidopathies and pathological infantile aminoacidurias].

Clin Pediatr (Bologna). 1967 May;49(5):246-56.

Aminoacidopathies in mental retardation.

Monogr Hum Genet. 1972;6:146-7.

Diagnosis and mangement of inherited aminoacidopathies in the newborn and the unborn.

Clin Endocrinol Metab. 1974 Mar;3(1):145-52. doi: 10.1016/s0300-595x(74)80030-7.

[Areas of applicability of thin-layer chromatography. Practical mass screening; data on intestinal mucosa lesions].

Padiatr Padol. 1983;18(2):105-11.

[Amino acid analysis in clinical chemistry].

Z Klin Chem Klin Biochem. 1970 Sep 8;7(5):404-26.

The effect of desalting on the determination of amino acids in urine by thin-layer chromatography.

Clin Chim Acta. 1971 May;32(3):457-63. doi: 10.1016/0009-8981(71)90448-7.

[A simple thin layer chromatography screening test for the detection of hyperaminoacidemias].

Z Klin Chem Klin Biochem. 1970 Sep 8;7(5):521-4.

引用本文的文献

Why is the Sensory Response of Organic Probes within a Polymer Film Different in Solution and in the Solid-State? Evidence and Application to the Detection of Amino Acids in Human Chronic Wounds.

Polymers (Basel). 2020 May 29;12(6):1249. doi: 10.3390/polym12061249.

Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria.

J Inherit Metab Dis. 1980;3(3):85-6. doi: 10.1007/BF02312533.

Inherited defect in hereditary pancreatitis.

Am J Dig Dis. 1977 Nov;22(11):999-1004. doi: 10.1007/BF01076200.

Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet.

J Inherit Metab Dis. 1978;1(3):95-7. doi: 10.1007/BF01805680.

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