Molecular prenatal diagnosis of 3-hydroxy−3-methylglutaryl coa lyase deficiency-Reference-Cited by-同舟云学术

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Molecular prenatal diagnosis of 3-hydroxy−3-methylglutaryl coa lyase deficiency

Published:1995-08 Issue:8 Volume:15 Page:725-729
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Mitchell Grant A.,Jakobs Cornelis,Gebson K. Michael,Robert Marie-France,Burlina Alberto,Dionisi-Vici Carlo,Dallaire Louis

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference18 articles.

1. Measurement of 3-hydroxy-3-methylglutaryl-CoA lyase activity in amniotic cells and in chorionic villi

2. First Trimester Prenatal Diagnosis of 3-Hydroxy-3-Methylglutaric Aciduria

3. Prenatal diagnosis of 3-Hydroxy-3-methylglutaric aciduria by GC-MS and enzymology on cultured amniocytes and chorionic villi

4. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients

Cited by 34 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. Disorders of Metabolism of Amino Acids and Related Compounds;Genetic Disorders and the Fetus;2021-04-20

2. Prevention by L-carnitine of DNA damage induced by 3-hydroxy-3-methylglutaric and 3-methylglutaric acids and experimental evidence of lipid and DNA damage in patients with 3-hydroxy-3-methylglutaric aciduria;Archives of Biochemistry and Biophysics;2019-06

3. Disorders of Metabolism of Amino Acids and Related Compounds;Genetic Disorders and the Fetus;2015-11-23

4. Induction of a Proinflammatory Response in Cortical Astrocytes by the Major Metabolites Accumulating in HMG-CoA Lyase Deficiency: the Role of ERK Signaling Pathway in Cytokine Release;Molecular Neurobiology;2015-06-23

5. Increased oxidative stress in patients with 3-hydroxy-3-methylglutaric aciduria;Molecular and Cellular Biochemistry;2015-01-04

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