메뉴 건너뛰기




Volumn 21, Issue 1, 1998, Pages 17-22

The association of protein-losing enteropathy with cobalamin C defect

Author keywords

[No Author keywords available]

Indexed keywords

COBALAMIN; HYDROXOCOBALAMIN; MECOBALAMIN;

EID: 0031985809     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005303128904     Document Type: Article
Times cited : (12)

References (11)
  • 1
    • 0023830785 scopus 로고
    • Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria
    • Bartholomew DW, Batshaw ML, Allen RH, et al (1988) Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria. J Pediatr 112: 32-39.
    • (1988) J Pediatr , vol.112 , pp. 32-39
    • Bartholomew, D.W.1    Batshaw, M.L.2    Allen, R.H.3
  • 2
    • 0018690479 scopus 로고
    • Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. Case report and histopathology
    • Baumgartner ER, Wick H, Maurer R, Egli N, Steinmann B (1979) Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. Case report and histopathology. Helv Paediatr Acta 34: 465-482.
    • (1979) Helv Paediatr Acta , vol.34 , pp. 465-482
    • Baumgartner, E.R.1    Wick, H.2    Maurer, R.3    Egli, N.4    Steinmann, B.5
  • 3
    • 0000526332 scopus 로고
    • Inherited disorders of cobalamin transport and metabolism
    • Scriver CR, Beaudet AL, Sly WS, Valle D, eds. New York: McGraw-Hill
    • Fenton WA, Rosenberg LE (1995) Inherited disorders of cobalamin transport and metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill 3129-3149.
    • (1995) The Metabolic and Molecular Bases of Inherited Disease , pp. 3129-3149
    • Fenton, W.A.1    Rosenberg, L.E.2
  • 4
    • 0026594251 scopus 로고
    • Cobalamin C defect associated with haemolytic-uraemic syndrome
    • Geraghty MT, Periman E, Martin LS, et al (1992) Cobalamin C defect associated with haemolytic-uraemic syndrome. J Paediatr 120: 934-937.
    • (1992) J Paediatr , vol.120 , pp. 934-937
    • Geraghty, M.T.1    Periman, E.2    Martin, L.S.3
  • 5
    • 0014748026 scopus 로고
    • A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria
    • Levy HL, Mudd SH, Dreyfus PM, et al (1970) A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria. Am J Med 48: 390-397.
    • (1970) Am J Med , vol.48 , pp. 390-397
    • Levy, H.L.1    Mudd, S.H.2    Dreyfus, P.M.3
  • 6
    • 0015059956 scopus 로고
    • Postnatal changes in some red cell parameters
    • Matoth Y, Zaizov R, Varsanoa I (1971) Postnatal changes in some red cell parameters. Acta Pediatr Scand 60: 317-323.
    • (1971) Acta Pediatr Scand , vol.60 , pp. 317-323
    • Matoth, Y.1    Zaizov, R.2    Varsanoa, I.3
  • 7
    • 0014545138 scopus 로고
    • Vascular pathology of homocysteinemia: Implications for the pathogenesis of arterosclerosis
    • McCully KS (1969) Vascular pathology of homocysteinemia: implications for the pathogenesis of arterosclerosis. Am J Pathol 56: 111-123.
    • (1969) Am J Pathol , vol.56 , pp. 111-123
    • McCully, K.S.1
  • 8
    • 0022652473 scopus 로고
    • Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria
    • Mitchell GA, Watkins D, Melacon SB, et al (1980) Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria. J. Pediatr 108: 410-415.
    • (1980) J. Pediatr , vol.108 , pp. 410-415
    • Mitchell, G.A.1    Watkins, D.2    Melacon, S.B.3
  • 9
    • 0343441356 scopus 로고
    • Protein losing enteropathy
    • Walker WA, Durie PR, Hamilton JR, Walker-Smith JA, Watkins JB, eds. Toronto: Becker
    • Proujansky R (1991) Protein losing enteropathy. In Walker WA, Durie PR, Hamilton JR, Walker-Smith JA, Watkins JB, eds. Pediatric Gastrointestinal Disease. Toronto: Becker, 812-818.
    • (1991) Pediatric Gastrointestinal Disease , pp. 812-818
    • Proujansky, R.1
  • 10
    • 0025253512 scopus 로고
    • Methlymalonic aciduria with homomcystinuria: Biochemical studies, treatment, and clinical course of a Cbl-C patient
    • Ribes A, Briones P, Vilaseca MA, et al (1990) Methlymalonic aciduria with homomcystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patient. Eur J Pediatr 149: 412-415.
    • (1990) Eur J Pediatr , vol.149 , pp. 412-415
    • Ribes, A.1    Briones, P.2    Vilaseca, M.A.3
  • 11
    • 0026720833 scopus 로고
    • A congenital anomaly of vitamin B12 metabolism: A study of three cases
    • Russo P, Doyon J, Sonsino E, Ogier H, Saudubray J-M (1992) A congenital anomaly of vitamin B12 metabolism: a study of three cases. Hum Pathol 23(5): 504-512.
    • (1992) Hum Pathol , vol.23 , Issue.5 , pp. 504-512
    • Russo, P.1    Doyon, J.2    Sonsino, E.3    Ogier, H.4    Saudubray, J.-M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.