Study title: Nothjunge-J, Krageloh-Mann-I, Suormala-T-M, Baumgartner-E-R. Abteilung Allgemeine Padiatrie, Universitats-Kinderklinik, Tubingen, Germany. Biotinidase deficiency: A hereditary metabolic disorder successfully treated with biotin. Monatsschrift fur Kinderheilkunde {MONATSSCHR-KINDERHEILKD}, 1989, Vol/Iss/Pg. 137/11 (737-740), ISSN: 0026-9298.Nothjunge-J, Krageloh-Mann-I, Suormala-T-M, Baumgartner-E-R. Abteilung Allgemeine Padiatrie, Universitats-Kinderklinik, Tubingen, Germany. Biotinidase deficiency: A hereditary metabolic disorder successfully treated with biotin. Monatsschrift fur Kinderheilkunde {MONATSSCHR-KINDERHEILKD}, 1989, Vol/Iss/Pg. 137/11 (737-740), ISSN: 0026-9298.
| Type of medicine: Medicines containing chemical active substances | |||||
| Therapeutic area: Nutritional and Metabolic Diseases [C18] | |||||
| Brands: Please see report | |||||
| MAH holders: Please see report | |||||
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| Active substance: BIOTIN | |||||
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| Scope of study: Clinical | |||||
| Population of study subjects: | Preterm newborn Infants | Newborn infants (1 to 27 days) | Infants and toddlers (28 days to 24 months) | Children (2 to 11 years) | Adolescents (12 to 18 years) |
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