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4. 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 [Abstract] [Full Text] [Related]
5. [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 [Abstract] [Full Text] [Related]
7. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism. Baumgartner ER, Suormala T. Int J Vitam Nutr Res; 1997 Dec; 67(5):377-84. PubMed ID: 9350481 [Abstract] [Full Text] [Related]
8. [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]
9. [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 [Abstract] [Full Text] [Related]
16. [Multiple carboxylase deficiency]. Andersen JB, Haagerup A, Christensen E. Ugeskr Laeger; 1998 Feb 16; 160(8):1151-7. PubMed ID: 9492625 [Abstract] [Full Text] [Related]
17. [Diagnostic criteria in classical infantile subacute necrotizing encephalomyelopathy (Leigh's disease)]. Sperl W, Rumpl E, Rittinger F, Pillwein K, Wick H, Henn R, Plöchl E. Klin Padiatr; 1989 Feb 16; 201(2):86-92. PubMed ID: 2716238 [Abstract] [Full Text] [Related]
18. [Biotinidase deficiency--a progressive metabolic disease in children with seizures and ataxia]. Anger H, Lorenz K, Cobet G. Psychiatr Neurol Med Psychol (Leipz); 1990 Mar 16; 42(3):163-6. PubMed ID: 2356250 [Abstract] [Full Text] [Related]
19. Biotin-responsive encephalopathy with myoclonus, ataxia, and seizures. Bressman S, Fahn S, Eisenberg M, Brin M, Maltese W. Adv Neurol; 1986 Mar 16; 43():119-25. PubMed ID: 3946108 [Abstract] [Full Text] [Related]