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Volumn 66, Issue 3, 2006, Pages 442-443

Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE;

EID: 33646185826     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000196491.42058.6f     Document Type: Article
Times cited : (14)

References (10)
  • 1
    • 0030860131 scopus 로고    scopus 로고
    • Adrenoleukodystrophy: Phenotype, genetics, pathogenesis and therapy
    • Moser HW. Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy. Brain 1997;120:1485-1508.
    • (1997) Brain , vol.120 , pp. 1485-1508
    • Moser, H.W.1
  • 2
    • 0026681106 scopus 로고
    • Adrenoleukodystrophy: Phenotypic variability and implications for therapy
    • Moser HW, Moser AB, Smith KD, et al. Adrenoleukodystrophy: phenotypic variability and implications for therapy. J Inherit Metab Dis 1992;15:645-664.
    • (1992) J Inherit Metab Dis , vol.15 , pp. 645-664
    • Moser, H.W.1    Moser, A.B.2    Smith, K.D.3
  • 3
    • 0035138765 scopus 로고    scopus 로고
    • Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy
    • van Geel BM, Bezman L, Loes DJ, Moser HW, Raymond GV. Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy. Ann Neurol 2001;49:186-194.
    • (2001) Ann Neurol , vol.49 , pp. 186-194
    • Van Geel, B.M.1    Bezman, L.2    Loes, D.J.3    Moser, H.W.4    Raymond, G.V.5
  • 4
    • 0029019620 scopus 로고
    • MR findings in adult-onset adrenoleukodystrophy
    • Kumar AJ, Köhler W, Kruse B, et al. MR findings in adult-onset adrenoleukodystrophy. AJNR Am J Neuroradiol 1995;16:1227-1237.
    • (1995) AJNR Am J Neuroradiol , vol.16 , pp. 1227-1237
    • Kumar, A.J.1    Köhler, W.2    Kruse, B.3
  • 7
    • 0029100208 scopus 로고
    • Mutational analysis of patients with X-linked adrenoleukodystrophy
    • Kok F, Neumann S, Sarde CO, et al. Mutational analysis of patients with X-linked adrenoleukodystrophy. Hum Mutat 1995;6:104-115.
    • (1995) Hum Mutat , vol.6 , pp. 104-115
    • Kok, F.1    Neumann, S.2    Sarde, C.O.3
  • 8
    • 20044384881 scopus 로고    scopus 로고
    • MTX-induced white matter changes are associated with polymorphisms of methionine-metabolism
    • Linnebank M, Pels H, Kleczar N, et al. MTX-induced white matter changes are associated with polymorphisms of methionine-metabolism. Neurology 2005;64:912-913.
    • (2005) Neurology , vol.64 , pp. 912-913
    • Linnebank, M.1    Pels, H.2    Kleczar, N.3
  • 10
    • 0026334413 scopus 로고
    • Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway
    • Surtees R, Leonard J, Austin S. Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway. Lancet 1991;338:1550-1554.
    • (1991) Lancet , vol.338 , pp. 1550-1554
    • Surtees, R.1    Leonard, J.2    Austin, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.