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Volumn 29, Issue 1, 2003, Pages 56-58

Biotinidase deficiency: Clinical and MRI findings consistent with myelopathy

Author keywords

[No Author keywords available]

Indexed keywords

BIOTIN;

EID: 0141790229     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(03)00042-0     Document Type: Article
Times cited : (24)

References (14)
  • 1
    • 0025987716 scopus 로고
    • Biotinidase deficiency
    • Wolf B., Heard G.S. Biotinidase deficiency. Adv Pediatr. 38:1991;1-21.
    • (1991) Adv Pediatr , vol.38 , pp. 1-21
    • Wolf, B.1    Heard, G.S.2
  • 2
    • 0020513116 scopus 로고
    • Phenotypic variation in biotinidase deficiency
    • Wolf B., Grier R.E., Allen R.J., et al. Phenotypic variation in biotinidase deficiency. J Pediatr. 103:1983;233-237.
    • (1983) J Pediatr , vol.103 , pp. 233-237
    • Wolf, B.1    Grier, R.E.2    Allen, R.J.3
  • 7
    • 0031449290 scopus 로고    scopus 로고
    • Late presentation of biotinidase deficiency with acute visual loss and gait disturbance
    • Rahman S., Standing S., Dalton R.N., Pike M.G. Late presentation of biotinidase deficiency with acute visual loss and gait disturbance. Dev Med Child Neurol. 39:1997;830-831.
    • (1997) Dev Med Child Neurol , vol.39 , pp. 830-831
    • Rahman, S.1    Standing, S.2    Dalton, R.N.3    Pike, M.G.4
  • 8
    • 0030853668 scopus 로고    scopus 로고
    • Biotinidase deficiency with neurologic features resembling multiple sclerosis
    • Tokatli A., Coskun T., Ozalp I. Biotinidase deficiency with neurologic features resembling multiple sclerosis. J Inher Metab Dis. 20:1997;707-708.
    • (1997) J Inher Metab Dis , vol.20 , pp. 707-708
    • Tokatli, A.1    Coskun, T.2    Ozalp, I.3
  • 9
    • 0031890445 scopus 로고    scopus 로고
    • Delayed-onset profound biotinidase deficiency
    • Wolf B., Pomponio R.J., Norrgard K.J., et al. Delayed-onset profound biotinidase deficiency. J Pediatr. 132:1998;362-365.
    • (1998) J Pediatr , vol.132 , pp. 362-365
    • Wolf, B.1    Pomponio, R.J.2    Norrgard, K.J.3
  • 10
    • 0024457140 scopus 로고
    • Biotinidase deficiency: A cause of subacute necrotizing encephalomyelopathy (Leigh Syndrome). Report of a case with lethal outcome
    • Baumgartner E.R., Suormala T.M., Wick H., et al. Biotinidase deficiency A cause of subacute necrotizing encephalomyelopathy (Leigh Syndrome). Report of a case with lethal outcome . Pediatr Res. 26:1989;260-266.
    • (1989) Pediatr Res , vol.26 , pp. 260-266
    • Baumgartner, E.R.1    Suormala, T.M.2    Wick, H.3
  • 14
    • 0019191766 scopus 로고
    • Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: A biotin-responsive disorder
    • Sander J.E., Malamud N., Cowan M.J., Packman S., Amman A.J., Wara D.W. Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies A biotin-responsive disorder . Ann Neurol. 8:1980;544-547.
    • (1980) Ann Neurol , vol.8 , pp. 544-547
    • Sander, J.E.1    Malamud, N.2    Cowan, M.J.3    Packman, S.4    Amman, A.J.5    Wara, D.W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.