Biotidinaz eksikliği: Olgu Sunumu
Abstract
Keywords
References
- Wolf B, Heard GS, Weissbecker KA, et al. Biotinidase deficiency: initial clinical features and and rapid diagnosis. Ann Neurol, 1985;18:614-7.
- Rezvani I and Rosenblatt DS. Valine, leucine, isoleucine, and related organic acidemias. In: Behrman RE, Kleigman R, Jenson HB, editors. Nelson textbook of pediatrics 17th ed. Philadelphia: W.B. Saunders, 2003: p.409-18.
- Gulati S, Passi GR, Kumar A, et al. Biotinidase deficiency--a treatable entity. Indian J Pediatr, 2000;67(6):464-6.
- Wolf B. Biotinidase Deficiency: New Directions and Practical Concerns. Curr Treat Options Neurol, 2003;5(4):321-8.
- Baykal T, Huner G, Sarbat G, et al. Incidence of biotinidase deficiency in Turkish newborns. Acta Paediatr, 1998;87(10):1102-3.
- Hymes J, Stanley CM, Wolf B. Mutations in BTD causing biotinidase deficiency. Hum Mutat, 2001;18(5):375-81.
- Pomponio RJ, Coskun T, M Demirkol M, et al. Novel mutations cause biotinidase deficiency in Turkish children. J Inherit Metab Dis, 2000; 23(2):120-8.
- Lyon G, Adams RD, Kolodny EH. Neurology of hereditary metabolic diseases of children. Second ed. New York: McGraw-Hill, 1996:76-8.
Details
Primary Language
Turkish
Subjects
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Journal Section
-
Authors
Akın İşcan
This is me
İrfan Altıntaş
This is me
M Mansur Tatlı
This is me
A Himmet Karazeybek
This is me
Publication Date
August 1, 2004
Submission Date
-
Acceptance Date
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Published in Issue
Year 2004 Volume: 1 Number: 4