Isolated and Combined Remethylation Disorders-Reference-Cited by-同舟云学术

Isolated and Combined Remethylation Disorders

Published:2017-01 Issue: Volume:5 Page:232640981668573
ISSN:2326-4098
Container-title:Journal of Inborn Errors of Metabolism and Screening
language:en
Short-container-title:Journal of Inborn Errors of Metabolism and Screening

Author:

Richard Eva¹²³,Brasil Sandra¹²³,Leal Fátima¹²³,Navarrete Rosa¹²³,Vega Ana¹²³,Ecay María Jesús¹²³,Desviat Lourdes R.¹²³,Pérez-Cerda Celia¹²³,Ugarte Magdalena¹²³,Merinero Begoña¹²³,Pérez Belén¹²³

Affiliation:

1. Centro de Diagnóstico de Enfermedades Moleculares, Centro de Biología Molecular-SO UAM-CSIC, Universidad Autónoma de Madrid, Madrid, Spain

2. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain

3. IdiPAZ, Madrid, Spain

Publisher

FapUNIFESP (SciELO)

Subject

Genetics(clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/2326409816685732

Reference75 articles.

1. Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects

2. Homocysteine and DNA methylation: A review of animal and human literature

3. Hyperhomocysteinemia: Related genetic diseases and congenital defects, abnormal DNA methylation and newborn screening issues

4. Inborn errors of cobalamin absorption and metabolism

5. Cobalamin‐dependent methionine synthase

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1. A Five-Year Cohort Study of Iraqi Patients with Homocysteine Remethylation Disorders in a Tertiary Pediatric Center;2024

2. Importance of homocysteine determination in differential diagnosis of rare causes of macrocytic anaemia;Biologia;2022-01-19

3. Subcutaneous vitamin B12 administration using a portable infusion pump in cobalamin-related remethylation disorders: a gentle and easy to use alternative to intramuscular injections;Orphanet Journal of Rare Diseases;2021-05-12

4. Molecular and biochemical investigations of inborn errors of metabolism-altered redox homeostasis in branched-chain amino acid disorders, organic acidurias, and homocystinuria;Free Radical Research;2021-01-27