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Items: 1 to 20 of 97

1.

Oxidative stress-related biomarkers in autism: systematic review and meta-analyses.

Frustaci A, Neri M, Cesario A, Adams JB, Domenici E, Dalla Bernardina B, Bonassi S.

Free Radic Biol Med. 2012 May 15;52(10):2128-41. doi: 10.1016/j.freeradbiomed.2012.03.011. Epub 2012 Apr 18. Review.

2.

Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism.

James SJ, Cutler P, Melnyk S, Jernigan S, Janak L, Gaylor DW, Neubrander JA.

Am J Clin Nutr. 2004 Dec;80(6):1611-7.

3.

Redox metabolism abnormalities in autistic children associated with mitochondrial disease.

Frye RE, Delatorre R, Taylor H, Slattery J, Melnyk S, Chowdhury N, James SJ.

Transl Psychiatry. 2013 Jun 18;3:e273. doi: 10.1038/tp.2013.51.

4.

One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders.

Paşca SP, Dronca E, Kaucsár T, Craciun EC, Endreffy E, Ferencz BK, Iftene F, Benga I, Cornean R, Banerjee R, Dronca M.

J Cell Mol Med. 2009 Oct;13(10):4229-38. doi: 10.1111/j.1582-4934.2008.00463.x.

5.

Congenital heart defects and maternal biomarkers of oxidative stress.

Hobbs CA, Cleves MA, Zhao W, Melnyk S, James SJ.

Am J Clin Nutr. 2005 Sep;82(3):598-604.

6.

Plasma homocysteine, serum folic acid, serum vitamin B12, serum vitamin B6, MTHFR and risk of pseudoexfoliation glaucoma: a meta-analysis.

Xu F, Zhang L, Li M.

Graefes Arch Clin Exp Ophthalmol. 2012 Jul;250(7):1067-74. doi: 10.1007/s00417-011-1877-4. Epub 2011 Dec 2.

PMID:
22134713
7.

Blood oxidative stress markers in Gaucher disease patients.

Roversi FM, Galdieri LC, Grego BH, Souza FG, Micheletti C, Martins AM, D'Almeida V.

Clin Chim Acta. 2006 Feb;364(1-2):316-20. Epub 2005 Aug 24.

PMID:
16125160
8.

A prospective study of transsulfuration biomarkers in autistic disorders.

Geier DA, Kern JK, Garver CR, Adams JB, Audhya T, Geier MR.

Neurochem Res. 2009 Feb;34(2):386-93. doi: 10.1007/s11064-008-9782-x. Epub 2008 Jul 9. Erratum in: Neurochem Res. 2009 Feb;34(2):394.

PMID:
18612812
9.

Peripheral arterial disease and methylenetetrahydrofolate reductase (MTHFR) C677T mutations: A case-control study and meta-analysis.

Khandanpour N, Willis G, Meyer FJ, Armon MP, Loke YK, Wright AJ, Finglas PM, Jennings BA.

J Vasc Surg. 2009 Mar;49(3):711-8. doi: 10.1016/j.jvs.2008.10.004. Epub 2009 Jan 21. Review.

10.

The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.

Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W.

Kardiol Pol. 2003 Jul;59(7):17-26; discussion 26.

PMID:
14560345
12.

C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects.

Erdogan MO, Yildiz SH, Solak M, Eser O, Cosar E, Eser B, Koken R, Buyukbas S.

Genet Mol Res. 2010 Jun 22;9(2):1197-203. doi: 10.4238/vol9-2gmr816.

13.

Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms.

Fillon-Emery N, Chango A, Mircher C, Barbé F, Bléhaut H, Herbeth B, Rosenblatt DS, Réthoré MO, Lambert D, Nicolas JP.

Am J Clin Nutr. 2004 Dec;80(6):1551-7.

15.

Biomarkers of environmental toxicity and susceptibility in autism.

Geier DA, Kern JK, Garver CR, Adams JB, Audhya T, Nataf R, Geier MR.

J Neurol Sci. 2009 May 15;280(1-2):101-8. doi: 10.1016/j.jns.2008.08.021. Epub 2008 Sep 25.

PMID:
18817931
16.

[Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data].

Guilland JC, Favier A, Potier de Courcy G, Galan P, Hercberg S.

Pathol Biol (Paris). 2003 Mar;51(2):101-10. Review. French.

PMID:
12801808
17.

Metabolic biomarkers related to oxidative stress and antioxidant status in Saudi autistic children.

Al-Gadani Y, El-Ansary A, Attas O, Al-Ayadhi L.

Clin Biochem. 2009 Jul;42(10-11):1032-40. doi: 10.1016/j.clinbiochem.2009.03.011. Epub 2009 Mar 21.

PMID:
19306862
18.

Aberrations in folate metabolic pathway and altered susceptibility to autism.

Mohammad NS, Jain JM, Chintakindi KP, Singh RP, Naik U, Akella RR.

Psychiatr Genet. 2009 Aug;19(4):171-6. doi: 10.1097/YPG.0b013e32832cebd2.

PMID:
19440165
19.

Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida.

Perez AB, D'Almeida V, Vergani N, de Oliveira AC, de Lima FT, Brunoni D.

Am J Med Genet A. 2003 May 15;119A(1):20-5.

PMID:
12707953
20.

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