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Journal Abstract Search

370 related items for PubMed ID: 3318710

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  • 3. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism.
    Baumgartner ER, Suormala T.
    Int J Vitam Nutr Res; 1997; 67(5):377-84. PubMed ID: 9350481
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  • 4. [Importance of biotin metabolism].
    Rodríguez Meléndez R.
    Rev Invest Clin; 2000; 52(2):194-9. PubMed ID: 10846444
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  • 8. Biotinidase deficiency.
    Wolf B, Heard GS.
    Adv Pediatr; 1991; 38():1-21. PubMed ID: 1927696
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  • 10. [Biotinidase deficiency. Its form of presentation and response to treatment].
    Campistol J, Vilaseca MA, Ribes A, Riudor E.
    An Esp Pediatr; 1996 Apr; 44(4):389-92. PubMed ID: 8796946
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  • 12. [Biotinidase deficiency. Progressive encephalopathy curable with biotin].
    Héron B, Gautier A, Dulac O, Ponsot G.
    Arch Fr Pediatr; 1993 Dec; 50(10):875-8. PubMed ID: 8053766
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  • 13. Skin manifestations of biotin deficiency.
    Mock DM.
    Semin Dermatol; 1991 Dec; 10(4):296-302. PubMed ID: 1764357
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  • 15. Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities.
    Holme E, Jacobson CE, Kristiansson B.
    J Inherit Metab Dis; 1988 Dec; 11(3):270-6. PubMed ID: 3148068
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  • 17. [Biotinidase deficiency: disease with mainly neurocutaneous manifestations responding to biotin].
    Marandian MH, Soltanabadi A, Lessani M, Kouchanfar A, Fallah A.
    Ann Pediatr (Paris); 1987 Nov; 34(9):725-8. PubMed ID: 3426084
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