A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency-Reference-Cited by-同舟云学术

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A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency

Published:2008-04 Issue:4 Volume:93 Page:363-370
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Arnold Georgianne L.,Koeberl Dwight D.,Matern Dietrich,Barshop Bruce,Braverman Nancy,Burton Barbara,Cederbaum Stephen,Fiegenbaum Annette,Garganta Cheryl,Gibson James

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 60 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. Newborn screening and genetic diagnosis of 3-methylcrotonyl-CoA carboxylase deficiency in Quanzhou,China;Molecular Genetics and Metabolism Reports;2024-09

2. An asymptomatic father diagnosed with 3-methylcrotonyl-CoA carboxylase deficiency following his son newborn screening test;Molecular Genetics and Metabolism Reports;2024-09

3. Host–microbe interactions rewire metabolism in a C. elegans model of leucine breakdown deficiency;Nature Metabolism;2024-08-08

4. Surgical Repair of Atrial Septal Defect in a Patient with 3-Methylcrotonyl-CoA Carboxylase Deficiency;Heart Views;2024-01

5. Consensus recommendations for the treatment and management of patients with Fabry disease on migalastat: a modified Delphi study;Frontiers in Medicine;2023-09-01

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