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Volumn 152, Issue 7, 1998, Pages 707-708

Picture of the month

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; ISOLEUCINE; METHYLMALONIC ACID; METHYLMALONYL COENZYME A MUTASE;

EID: 0032129047     PISSN: 10724710     EISSN: None     Source Type: Journal    
DOI: 10.1001/archpedi.152.7.707     Document Type: Article
Times cited : (3)

References (7)
  • 1
    • 0001362219 scopus 로고
    • Disorders of propionate and methylmalonate metabolism
    • Scriver CR, Beaudet AL, Sly WS. Valle D, eds. New York, NY: McGraw-Hill Book Co Inc
    • Fenton WA, Rosenberg LE. Disorders of propionate and methylmalonate metabolism. In: Scriver CR, Beaudet AL, Sly WS. Valle D, eds. The Metabolic Basis of Inherited Disease. New York, NY: McGraw-Hill Book Co Inc; 1995:1423-1449.
    • (1995) The Metabolic Basis of Inherited Disease , pp. 1423-1449
    • Fenton, W.A.1    Rosenberg, L.E.2
  • 2
    • 0025348714 scopus 로고
    • Cutaneous manifestations of methylmalonic acidemia
    • Koopman RJJ, Happle R. Cutaneous manifestations of methylmalonic acidemia. Arch Dermatol Res. 1990;282:272-273.
    • (1990) Arch Dermatol Res. , vol.282 , pp. 272-273
    • Koopman, R.J.J.1    Happle, R.2
  • 3
    • 0028314890 scopus 로고
    • Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria
    • De Raeve L, De Meirleir L, Ramet J, Vandenplas Y, Gerlo E. Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria. J Pediatr. 1994;124:416-420.
    • (1994) J Pediatr. , vol.124 , pp. 416-420
    • De Raeve, L.1    De Meirleir, L.2    Ramet, J.3    Vandenplas, Y.4    Gerlo, E.5
  • 4
    • 0001013319 scopus 로고
    • Peri-orificial dermatitis secondary to deficiency of isoleucine in treated infants with maple syrup urine disease
    • Spraker MK, Helminski MA, Elsas LJ. Peri-orificial dermatitis secondary to deficiency of isoleucine in treated infants with maple syrup urine disease [abstract]. J Invest Dermatol. 1986;4:508.
    • (1986) J Invest Dermatol. , vol.4 , pp. 508
    • Spraker, M.K.1    Helminski, M.A.2    Elsas, L.J.3
  • 5
    • 0027531692 scopus 로고
    • Exfoliative erythroderma resulting from inadequate intake of branched-chain amino acids in infants with maple syrup urine disease
    • Northrup H, Sigman ES, Hebert AA. Exfoliative erythroderma resulting from inadequate intake of branched-chain amino acids in infants with maple syrup urine disease. Arch Dermatol. 1993;129:384-385.
    • (1993) Arch Dermatol. , vol.129 , pp. 384-385
    • Northrup, H.1    Sigman, E.S.2    Hebert, A.A.3
  • 6
    • 0027282667 scopus 로고
    • Acrodermatitis enteropathica-like syndrome secondary to isoleucine deficiency during treatment of maple syrup urine disease
    • Giacoia GP, Berry GT. Acrodermatitis enteropathica-like syndrome secondary to isoleucine deficiency during treatment of maple syrup urine disease. AJDC. 1993; 147:954-956.
    • (1993) AJDC , vol.147 , pp. 954-956
    • Giacoia, G.P.1    Berry, G.T.2
  • 7
    • 0022632725 scopus 로고
    • Neonatal citrullinemia associated with cutaneous manifestations and arginine deficiency
    • Goldblum OM, Brusilow SW, Maldonado YA, Farmer ER. Neonatal citrullinemia associated with cutaneous manifestations and arginine deficiency. J Am Acad Dermatol. 1986;14:321-326.
    • (1986) J Am Acad Dermatol. , vol.14 , pp. 321-326
    • Goldblum, O.M.1    Brusilow, S.W.2    Maldonado, Y.A.3    Farmer, E.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.