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
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Therapeutic area: Nutritional and Metabolic Diseases [C18]
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Brands: Please see report |
MAH holders: Please see report |
Assessment: |
Active substance: BIOTIN |
ATC code: |
Document link:
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Document date:
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Study number: |
EudraCT number:
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Scope of study: Clinical |
Population of study subjects:
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Preterm newborn Infants
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Newborn infants
(1 to 27 days)
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Infants and toddlers
(28 days to 24 months)
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Children
(2 to 11 years)
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Adolescents
(12 to 18 years)
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Y
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