High incidence of maternal vitamin B12 deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel-Reference-Cited by-同舟云学术

High incidence of maternal vitamin B12 deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel

Published:2018-06-15 Issue:5 Volume:14 Page:470-481
ISSN:1708-8569
Container-title:World Journal of Pediatrics
language:en
Short-container-title:World J Pediatr

Author:

Gramer Gwendolyn,Fang-Hoffmann Junmin,Feyh Patrik,Klinke Glynis,Monostori Peter,Okun Jürgen G.,Hoffmann Georg F.

Funder

Dietmar Hopp Stiftung

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/article/10.1007/s12519-018-0159-1/fulltext.html

Reference48 articles.

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2. Huemer M, Kozich V, Rinaldo P, Baumgartner MR, Merinero B, Pasquini E, et al. Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines. J Inherit Metab Dis. 2015;38:1007–19.

3. Wong D, Tortorelli S, Bishop L, Sellars EA, Schimmenti LA, Gallant N, et al. Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening. Genet Med. 2016;18:162–7.

4. El Bashir H, Dekair L, Mahmoud Y, Ben-Omran T. Neurodevelopmental and cognitive outcomes of classical homocystinuria: experience from qatar. JIMD Rep. 2015;21:89–95.

5. Whitehead VM. Acquired and inherited disorders of cobalamin and folate in children. Br J Haematol. 2006;134:125–36.

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