液相色谱-串联质谱法定量氨基酸分析：对精氨琥珀酸尿症诊断的意义 - Suppr | 超能文献

相似文献

1

Quantitative amino acid analysis by liquid chromatography-tandem mass spectrometry: implications for the diagnosis of argininosuccinic aciduria.液相色谱-串联质谱法定量氨基酸分析：对精氨琥珀酸尿症诊断的意义

Clin Chim Acta. 2015 Mar 10;442:73-4. doi: 10.1016/j.cca.2015.01.008. Epub 2015 Jan 15.

2

Determination of amino acid profile for argininosuccinic aciduria disorder using High-Performance Liquid Chromatography with fluorescence detection.采用高效液相色谱-荧光检测法测定精氨琥珀酸尿症的氨基酸谱。

Acta Biochim Pol. 2020 Sep 14;67(3):347-351. doi: 10.18388/abp.2020_5164.

3

Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry.通过血清串联质谱法检测新生儿精氨琥珀酸裂解酶缺乏症

J Inherit Metab Dis. 2001 Jun;24(3):370-8. doi: 10.1023/a:1010560704092.

4

Argininosuccinic aciduria: clinical and biochemical phenotype findings in Malaysian children.精氨琥珀酸尿症：马来西亚儿童的临床和生化表型研究结果

Malays J Pathol. 2010 Dec;32(2):87-95.

5

A rapid, sensitive method for quantitative analysis of underivatized amino acids by liquid chromatography-tandem mass spectrometry (LC-MS/MS).一种快速、灵敏的液相色谱-串联质谱（LC-MS/MS）法，用于未衍生化氨基酸的定量分析。

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Jan 1;944:166-74. doi: 10.1016/j.jchromb.2013.11.017. Epub 2013 Nov 18.

6

Rhode Island metabolic newborn screening: the effect of early identification. A case report of argininosuccinic aciduria (ASA).

Med Health R I. 2011 May;94(5):121-3.

7

Argininosuccinic Aciduria-A Rare Indication for Liver Transplant: Report of Two Cases.精氨酸琥珀酸尿症——肝移植的罕见指征：两例报告

Exp Clin Transplant. 2017 Oct;15(5):581-584. doi: 10.6002/ect.2015.0078. Epub 2016 Jan 14.

8

Comparison of liquid chromatography with tandem mass spectrometry and ion-exchange chromatography by post-column ninhydrin derivatization for amino acid monitoring.高效液相色谱-串联质谱法与柱后茚三酮衍生-离子交换色谱法测定氨基酸的比较。

Clin Chim Acta. 2019 Aug;495:446-450. doi: 10.1016/j.cca.2019.05.007. Epub 2019 May 8.

9

Quantitative UPLC-MS/MS analysis of underivatised amino acids in body fluids is a reliable tool for the diagnosis and follow-up of patients with inborn errors of metabolism.体液中未衍生化氨基酸的定量超高效液相色谱-串联质谱分析是诊断和随访先天性代谢缺陷患者的可靠工具。

Clin Chim Acta. 2009 Sep;407(1-2):36-42. doi: 10.1016/j.cca.2009.06.023. Epub 2009 Jun 24.

10

Role of the clinical laboratory in evaluation of argininosuccinate lyase deficiency.

Clin Chem. 1991 Aug;37(8):1384-9.

引用本文的文献

1

Multi-dose enteral L-citrulline administration in premature infants at risk of developing pulmonary hypertension associated with bronchopulmonary dysplasia.多次经肠道给予早产儿 L-瓜氨酸以预防支气管肺发育不良相关肺动脉高压。

J Perinatol. 2024 Feb;44(2):280-287. doi: 10.1038/s41372-023-01809-y. Epub 2023 Oct 31.

2

Engineering At-Home Dilution and Filtration Methods to Enable Paper-Based Colorimetric Biosensing in Human Blood with Cell-Free Protein Synthesis.利用无细胞蛋白合成工程在家中进行稀释和过滤方法，以在人血中实现基于纸的比色生物传感。

Biosensors (Basel). 2023 Jan 6;13(1):104. doi: 10.3390/bios13010104.

3

Creatine metabolism in patients with urea cycle disorders.