Wide metabolite coverage LC-MS/MS assay for the diagnosis of inherited metabolic disorders in urine-Reference-Cited by-同舟云学术

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Wide metabolite coverage LC-MS/MS assay for the diagnosis of inherited metabolic disorders in urine

Published:2024-05 Issue: Volume:271 Page:125699
ISSN:0039-9140
Container-title:Talanta
language:en
Short-container-title:Talanta

Author:

Ivanovová Eliška^ORCID,Piskláková Barbora^ORCID,Dobešová Dana^ORCID,Janečková Hana^ORCID,Foltenová Hana^ORCID,Kvasnička Aleš^ORCID,Prídavok Matúš,Bouchalová Kateřina^ORCID,de Sousa Julie^ORCID,Friedecký David^ORCID

Funder

Agentura Pro Zdravotnický Výzkum České Republiky

Ministry of Health

Ministry of Health of the Czech Republic

Palacky University Olomouc

Publisher

Elsevier BV

Reference28 articles.

1. A proposed nosology of inborn errors of metabolism;Ferreira;Genet. Med.,2019

2. Inherited metabolic rare disease;Pampols;Rare Diseases Epidemiology,2010

3. Inborn Metabolic Diseases: Diagnosis and Treatment;Saudubray,2016

4. Advances in inborn errors of metabolism;Fukao;J. Hum. Genet.,2019

5. Novel LC-MS tools for diagnosing inborn errors of metabolism;Ivanovova;Microchem. J.,2021

Cited by 1 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. Serum metabolomics reveals the effectiveness of human placental mesenchymal stem cell therapy for Crohn's disease;Talanta;2024-09

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