Hypermethioninemia in Campania: Results from 10 years of newborn screening-Reference-Cited by-同舟云学术

Hypermethioninemia in Campania: Results from 10 years of newborn screening

Published:2019-12 Issue: Volume:21 Page:100520
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Villani Guglielmo R.D.,Albano Lucia,Caterino Marianna,Crisci Daniela,Di Tommaso Silvia,Fecarotta Simona,Fisco Maria Grazia,Frisso Giulia,Gallo Giovanna,Mazzaccara Cristina,Marchese Emanuela,Nolano Antonio,Parenti Giancarlo,Pecce Rita,Redi Adriana,Salvatore Francesco,Strisciuglio Pietro,Turturo Maria Grazia,Vallone Fabiana,Ruoppolo Margherita

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

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5. Elevated plasma total homocysteine in severe methionineadenosyltransferase I/III deficiency;Stabler;Metabolism.,2002

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1. Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature;Children;2023-02-17

2. Chemical hypermethioninemia in young mice: oxidative damage and reduction of antioxidant enzyme activity in brain, kidney, and liver;Metabolic Brain Disease;2022-10-29

3. Genomic analysis of 9 infants with hypermethioninemia by whole-exome sequencing among in Henan, China;Clinica Chimica Acta;2022-08