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Journal Abstract Search


182 related items for PubMed ID: 9616944

  • 1. [Biotinidase deficiency].
    Casado de Frías E.
    An R Acad Nac Med (Madr); 1997; 114(4):817-27; discussion 827-8. PubMed ID: 9616944
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  • 2. [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
    [No Abstract] [Full Text] [Related]

  • 3. Neurological deterioration and lactic acidemia in biotinidase deficiency. A treatable condition mimicking Leigh's disease.
    Mitchell G, Ogier H, Munnich A, Saudubray JM, Shirrer J, Charpentier C, Rocchiccioli F.
    Neuropediatrics; 1986 Aug; 17(3):129-31. PubMed ID: 3762868
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  • 4. Biotinidase deficiency.
    Wolf B, Heard GS.
    Adv Pediatr; 1991 Aug; 38():1-21. PubMed ID: 1927696
    [No Abstract] [Full Text] [Related]

  • 5. [Biotinidase deficiency (late-onset multiple carboxylase deficiency)].
    Sakamoto O, Narisawa K.
    Ryoikibetsu Shokogun Shirizu; 1998 Aug; (19 Pt 2):223-4. PubMed ID: 9645048
    [No Abstract] [Full Text] [Related]

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  • 7. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism.
    Baumgartner ER, Suormala T.
    Int J Vitam Nutr Res; 1997 Aug; 67(5):377-84. PubMed ID: 9350481
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  • 10. Inborn errors of biotin metabolism.
    Nyhan WL.
    Arch Dermatol; 1987 Dec; 123(12):1696-1698a. PubMed ID: 3318710
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  • 12. Multiple carboxylase deficiency.
    Nyhan WL.
    Int J Biochem; 1988 Dec; 20(4):363-70. PubMed ID: 3284772
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  • 15. [Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H].
    Nothjunge J, Krägeloh-Mann I, Suormala TM, Baumgartner ER.
    Monatsschr Kinderheilkd; 1989 Nov; 137(11):737-40. PubMed ID: 2608075
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  • 16. Biotinidase deficiency: early neurological presentation.
    Collins JE, Nicholson NS, Dalton N, Leonard JV.
    Dev Med Child Neurol; 1994 Mar; 36(3):268-70. PubMed ID: 8138076
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