Prenatal diagnosis of methylmalonic aciduria by analysis of organic acids and total homocysteine in amniotic fluid-Reference-Cited by-同舟云学术

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Prenatal diagnosis of methylmalonic aciduria by analysis of organic acids and total homocysteine in amniotic fluid

Published:2008-02 Issue:3 Volume:121 Page:216-219
ISSN:0366-6999
Container-title:Chinese Medical Journal
language:en
Short-container-title:Chinese Medical Journal

Author:

ZHANG Yao,YANG Yan-ling,HASEGAWA Yuki,YAMAGUCHI Seiji,SHI Chun-yan,SONG Jin-qing,SAYAMI Sujan,LIU Ping,YAN Rong,DONG Jin-hua,QIN Jiong

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference15 articles.

1. Clinical and Biochemical Studies on Chinese Patients With Methylmalonic Aciduria

2. Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening

3. Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC)

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case report: An asymptomatic mother with an inborn error of cobalamin metabolism (cblC) detected through high homocysteine levels during prenatal diagnosis;Frontiers in Nutrition;2023-05-12

2. Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduria;PLOS ONE;2022-03-31

3. Prenatal Diagnosis of Two Common Inborn Errors of Metabolism by Genetic and Mass Spectrometric Analysis of Amniotic Fluid;Frontiers in Pediatrics;2022-02-09

4. Noninvasive Prenatal Testing of Methylmalonic Acidemia cblC Type Using the cSMART Assay for MMACHC Gene Mutations;Frontiers in Genetics;2022-01-07

5. Inherited defects of cobalamin metabolism;Vitamins and Hormones;2022

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