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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1989
[Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H]J Nothjunge, I Krägeloh-Mann, T M Suormala, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1988
Quantitative determination of biocytin in urine of patients with biotinidase deficiency using high-performance liquid chromatography (HPLC)T M Suormala, E R Baumgartner, J Bausch, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Comparison of patients with complete and partial biotinidase deficiency: biochemical studiesT M Suormala, E R Baumgartner, H Wick, et al.
Archives of Disease in Childhood|January 1, 1992
A biotinidase Km variant causing late onset bilateral optic neuropathyV T Ramaekers, T M Suormala, M Brab, et al.
Pediatric Research|September 1, 1989
Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcomeE R Baumgartner, T M Suormala, H Wick, et al.
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