Homocystinuria-Megaloblastic Anemia
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1757-1
Reference12 articles.
1. Bowron A, Barton A, Scott J, Stansbie D (2005) Blood spot homocysteine: a feasibility and stability study. Clin Chem 51:257–258. https://doi.org/10.1373/clinchem.2004.041640
2. Huemer M et al (2015a) Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data. J Inherit Metab Dis 38:957–967. https://doi.org/10.1007/s10545-014-9803-7
3. Huemer M et al (2015b) Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines. J Inherit Metab Dis 38:1007–1019. https://doi.org/10.1007/s10545-015-9830-z
4. Huemer M et al (2017) Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency. J Inherit Metab Dis 40:21–48. https://doi.org/10.1007/s10545-016-9991-4
5. Kim J, Kim H, Roh H, Kwon Y (2018) Causes of hyperhomocysteinemia and its pathological significance. Arch Pharm Res 41:372–383. https://doi.org/10.1007/s12272-018-1016-4
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