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Volumn 49, Issue 3, 2001, Pages 396-400

Neurological and neuropathologic heterogeneity in two brothers with cobalamin C deficiency

Author keywords

[No Author keywords available]

Indexed keywords

COBALAMIN DERIVATIVE;

EID: 0035091599     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.78     Document Type: Article
Times cited : (54)

References (18)
  • 2
    • 0001904134 scopus 로고    scopus 로고
    • Nutritional and metabolic disorders
    • Graham DI, Lantos PL, eds. Greenfield's neuropathology, 6th ed. London: Anold
    • (1997) , pp. 621-624
    • Harper, C.1    Butterworth, R.2
  • 3
    • 0000526332 scopus 로고
    • Inherited disorders of cobalamin transport and metabolism
    • Scriver CR, Beaudet AL Sly WS, Valle D, eds. The metabolic and molecular bases of inherited disease, 7th ed. New York: McGraw-Hill
    • (1995) , pp. 3129-3149
    • Fenton, W.A.1    Rosenberg, L.E.2
  • 5
    • 0029165415 scopus 로고
    • Neurological complications of acquired cobalamin deficiency: Clinical aspects
    • Wickramasinghe SN, ed. Baillière's clinical haematology: international practice and research. Megaloblastic anaemia. London: Bailliere Tindall
    • (1995) , vol.8 , pp. 657-678
    • Savage, D.G.1    Lindenbaum, J.2
  • 8
    • 0033938389 scopus 로고    scopus 로고
    • Complementation studies in the cbLA class of inborn error of cobalamin metabolism: Evidence for interallelic complementation and for a new complementation class (cblH)
    • (2000) J Med Genet , vol.37 , pp. 510-513
    • Watkins, D.1    Matiaszuk, N.2    Rosenblatt, D.S.3
  • 10
    • 0016169197 scopus 로고
    • 12 metabolism associated with cellular deficiency of coenzyme forms of the vitamin; pathological and neurochemical findings in one case
    • (1974) J Neurol Sci , vol.23 , pp. 117-128
    • Davan, A.D.1    Ramsey, R.B.2
  • 11
    • 0021615191 scopus 로고
    • Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence: A treatable cause of dementia and myelopathy
    • (1984) N Engl J Med , vol.311 , pp. 451-454
    • Shinnar, S.1    Singer, H.S.2
  • 15
    • 0000443712 scopus 로고
    • Inherited disorders of folate transport and metabolism
    • Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic and molecular bases of inherited disease, 7th ed. New York: McGraw-Hill
    • (1995) , pp. 3111-3128
    • Rosenblatt, D.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.