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Volumn 32, Issue 3, 2009, Pages 400-402

Autism: Is there a folate connection?

Author keywords

[No Author keywords available]

Indexed keywords

DIHYDROFOLATE REDUCTASE; DIHYDROPTERIDINE REDUCTASE; DNA; FOLIC ACID; METHOTREXATE;

EID: 67349181029     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-009-1093-0     Document Type: Conference Paper
Times cited : (17)

References (6)
  • 1
    • 34447643277 scopus 로고    scopus 로고
    • Preliminary evidence for involvement of the folate gene polymorphism 19 bp deletion-DHFR in occurrence of autism
    • Adams M, Lucock M, Stuart J, Fardell S, Baker K, Ng X (2007) Preliminary evidence for involvement of the folate gene polymorphism 19 bp deletion-DHFR in occurrence of autism. Neurosci Lett 422: 24-29.
    • (2007) Neurosci Lett , vol.422 , pp. 24-29
    • Adams, M.1    Lucock, M.2    Stuart, J.3    Fardell, S.4    Baker, K.5    Ng, X.6
  • 2
    • 33845438146 scopus 로고    scopus 로고
    • Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism
    • James SJ, Melnyk S, Jernigan S, et al (2006) Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism. Am J Med Genet B Neuropsychiatr Genet 14: 947-996.
    • (2006) Am J Med Genet B Neuropsychiatr Genet , vol.14 , pp. 947-996
    • James, S.J.1    Melnyk, S.2    Jernigan, S.3
  • 4
    • 44349142821 scopus 로고    scopus 로고
    • Folate receptor autoimmunity and cerebral folate deficiency in low functioning autism with neurological deficits
    • Ramaekers VT, Blau N, Sequeira JM, Nassogne MC, Quadros EV (2007) Folate receptor autoimmunity and cerebral folate deficiency in low functioning autism with neurological deficits. Neuropediatrics 38: 276-281.
    • (2007) Neuropediatrics , vol.38 , pp. 276-281
    • Ramaekers, V.T.1    Blau, N.2    Sequeira, J.M.3    Nassogne, M.C.4    Quadros, E.V.5
  • 5
    • 0029990539 scopus 로고    scopus 로고
    • Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei
    • Rodier PM, Ingram JI, Tisdale B, Nelson S, Ramano J (1996) Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei. J Comp Neurol 370: 247-261.
    • (1996) J Comp Neurol , vol.370 , pp. 247-261
    • Rodier, P.M.1    Ingram, J.I.2    Tisdale, B.3    Nelson, S.4    Ramano, J.5
  • 6
    • 0021800607 scopus 로고
    • Clinical role of pteridine therapy in tetrahydrobiopterin deficiency
    • Smith I, Hyland K, Kendall B, Leeming RJ (1985) Clinical role of pteridine therapy in tetrahydrobiopterin deficiency. J Inherit Metab Dis 8: 39-45.
    • (1985) J Inherit Metab Dis , vol.8 , pp. 39-45
    • Smith, I.1    Hyland, K.2    Kendall, B.3    Leeming, R.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.