Format
Sort by
Items per page

Send to

Choose Destination

Best matches for methyltetrahydrofolate children:

Search results

Items: 1 to 20 of 266

1.

Mitochondrial DNA Deletion Syndromes.

Goldstein A, Falk MJ.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2003 Dec 17 [updated 2019 Jan 31].

2.

Association of a MiR-499 SNP and risk of congenital heart disease in a Chinese population.

Guo R, Feng Z, Yang Y, Xu H, Zhang J, Guo K, Bi Y.

Cell Mol Biol (Noisy-le-grand). 2018 Jul 30;64(10):108-112.

PMID:
30084801
3.

[Case-control study on the association between four single nucleotide polymorphisms in folate metabolism way and the risk of congenital heart disease].

Duan S, Li G, Qiu F, Zhao L, Zhao M, Wang L, Feng Z, Ma X.

Wei Sheng Yan Jiu. 2018 Jul;47(4):536-542. Chinese.

PMID:
30081977
4.

Altered methyltetrahydrofolate reductase gene polymorphism in mothers of children with attention deficit and hyperactivity disorder.

Baykal S, Batar B, Nalbantoğlu A, Albayrak Y, Hancı H, Potas N, Durankuş F, Beyazyüz M, Karabekiroğlu K.

Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jan 10;88:215-221. doi: 10.1016/j.pnpbp.2018.07.020. Epub 2018 Jul 24.

PMID:
30053573
5.

Genetically determined folate deficiency is associated with abnormal hepatic folate profiles in the spontaneously hypertensive rat.

Pravenec M, Leung KY, Zídek V, Mlejnek P, Šimáková M, Šilhavý J, Kožich V, Greene N.

Physiol Res. 2018 Jul 17;67(3):417-422.

6.

Effects of MTHFR A1298C polymorphism on peripheral blood folate concentration in healthy populations: a meta-analysis of observational studies.

Xin Y, Wu L, Lu X, Shangguan S, Wang Z, Chang S, Yin J, Piao W, Zhang T, Wang L.

Asia Pac J Clin Nutr. 2018;27(3):718-727. doi: 10.6133/apjcn.122017.02.

7.

Formate rescues neural tube defects caused by mutations in Slc25a32.

Kim J, Lei Y, Guo J, Kim SE, Wlodarczyk BJ, Cabrera RM, Lin YL, Nilsson TK, Zhang T, Ren A, Wang L, Yuan Z, Zheng YF, Wang HY, Finnell RH.

Proc Natl Acad Sci U S A. 2018 May 1;115(18):4690-4695. doi: 10.1073/pnas.1800138115. Epub 2018 Apr 16.

8.

Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems.

Saha T, Chatterjee M, Verma D, Ray A, Sinha S, Rajamma U, Mukhopadhyay K.

Prog Neuropsychopharmacol Biol Psychiatry. 2018 Jun 8;84(Pt A):1-10. doi: 10.1016/j.pnpbp.2018.01.016. Epub 2018 Jan 31.

PMID:
29407547
10.

Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis.

Komulainen-Ebrahim J, Saastamoinen E, Rahikkala E, Helander H, Hinttala R, Risteli L, Rantala H, Uusimaa J.

Neuropediatrics. 2017 Dec;48(6):467-472. doi: 10.1055/s-0037-1603976. Epub 2017 Jun 30. No abstract available.

PMID:
28666289
11.

Deleterious Effects of Chronic Folate Deficiency in the Ts65Dn Mouse Model of Down Syndrome.

Helm S, Blayney M, Whited T, Noroozi M, Lin S, Kern S, Green D, Salehi A.

Front Cell Neurosci. 2017 Jun 9;11:161. doi: 10.3389/fncel.2017.00161. eCollection 2017.

12.

On the relationship between head circumference, brain size, prenatal long-chain PUFA/5-methyltetrahydrofolate supplementation and cognitive abilities during childhood.

Catena A, Martínez-Zaldívar C, Diaz-Piedra C, Torres-Espínola FJ, Brandi P, Pérez-García M, Decsi T, Koletzko B, Campoy C.

Br J Nutr. 2017 Mar 29:1-9. doi: 10.1017/S0007114516004281. [Epub ahead of print]

PMID:
28351446
13.

L-Methylfolate supplementation in a child with autism and methyltetrahydrofolate reductase, enzyme gene C677TT allele.

Siscoe KS, Lohr WD.

Psychiatr Genet. 2017 Jun;27(3):116-119. doi: 10.1097/YPG.0000000000000170.

PMID:
28272116
14.

Analysis of methionine synthase (rs1805087) gene polymorphism in autism patients in Northern Iran.

Haghiri R, Mashayekhi F, Bidabadi E, Salehi Z.

Acta Neurobiol Exp (Wars). 2016;76(4):318-323.

15.

High dietary folate in pregnant mice leads to pseudo-MTHFR deficiency and altered methyl metabolism, with embryonic growth delay and short-term memory impairment in offspring.

Bahous RH, Jadavji NM, Deng L, Cosín-Tomás M, Lu J, Malysheva O, Leung KY, Ho MK, Pallàs M, Kaliman P, Greene NDE, Bedell BJ, Caudill MA, Rozen R.

Hum Mol Genet. 2017 Mar 1;26(5):888-900. doi: 10.1093/hmg/ddx004.

16.

Hemiretinal Artery Occlusion in an 11-Year-Old Child with Dextrocardia.

Arévalo Simental DE, Roig Melo-Granados EA, Cortés Quezada S, Páez Escamilla MA, Soria Orozco CL, Jacinto Buenrostro JE.

Case Rep Ophthalmol Med. 2016;2016:5104789. doi: 10.1155/2016/5104789. Epub 2016 Dec 6.

17.

Author response: CSF concentrations of 5-methyltetrahydrofolate in a cohort of young children with autism.

Shoffner J.

Neurology. 2017 Jan 3;88(1):111. doi: 10.1212/WNL.0000000000003475. No abstract available.

PMID:
28025402
18.

Letter re: CSF concentrations of 5-methyltetrahydrofolate in a cohort of young children with autism.

Barrett G.

Neurology. 2017 Jan 3;88(1):110-111. doi: 10.1212/WNL.0000000000003474. No abstract available.

PMID:
28025401
19.

Simultaneous measurement of monoamine metabolites and 5-methyltetrahydrofolate in the cerebrospinal fluid of children.

Akiyama T, Hayashi Y, Hanaoka Y, Shibata T, Akiyama M, Nakamura K, Tsuyusaki Y, Kubota M, Yoshinaga H, Kobayashi K.

Clin Chim Acta. 2017 Feb;465:5-10. doi: 10.1016/j.cca.2016.12.005. Epub 2016 Dec 7.

PMID:
27940130
20.

The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders.

Opladen T, Cortès-Saladelafont E, Mastrangelo M, Horvath G, Pons R, Lopez-Laso E, Fernández-Ramos JA, Honzik T, Pearson T, Friedman J, Scholl-Bürgi S, Wassenberg T, Jung-Klawitter S, Kuseyri O, Jeltsch K, Kurian MA, Garcia-Cazorla À; International Working Group on Neurotransmitter related disorders (iNTD).

Mol Genet Metab Rep. 2016 Oct 20;9:61-66. eCollection 2016 Dec.

Supplemental Content

Loading ...
Support Center