Abstract Aim: A variety of methods are used to determine biotinidase activity (BA), such as different substrates, biological samples, and analytical techniques. In this study, we aimed to discuss the specificity and sensitivity of the fluorometric method used in the measurement of biotinidase activity in the newborn screening program (NSP) in Turkey. Material and Methods: Medical records of 164 patients who were referred to our clinic with the diagnosis of biotinidase deficiency (BD) from primary health care institutions were evaluated retrospectively. According to this classification, those with normal BA were included in the negative group and those with partial or profound BD were included in the positive group. Results: Four patients ha...
INTRODUÇÃO: A deficiência de biotinidase é um erro inato do metabolismo caracterizado principalmente...
Four children with biotinidase deficiency were identified during the first year of a neonatal screen...
Health-associated reference values are universally needed in clinical chemistry. The aim of this stu...
Biotinidase activity assay is included in most newborn screening protocols, and the positive results...
Background Biotin, a water-soluble vitamin, is used as a co-factor by enzymes involved in carboxylat...
We describe a method for neonatal screening for biotinidase (EC 3.5.1.12) deficiency. Biotinidase ac...
Biotinidase deficiency is an inherited metabolic disorder characterized by neurological and cutaneou...
Biotinidase deficiency is an inherited metabolic disorder characterized by neurological and cutaneou...
INTRODUÇÃO: A deficiência de biotinidase é um erro inato do metabolismo caracterizado principalmente...
Biotinidase deficiency is an inherited metabolic disorder that, if untreated, can result in neurolog...
Biotinidase deficiency is a rare inherited metabolic disorder that can cause severe neurological sym...
Biotinidase deficiency is a rare inherited metabolic disorder that can cause severe neurological sym...
Biotinidase deficiency is an autosomal recessive metabolic disease that causes biotin deficiency. Th...
Biotinidase deficiency is a hereditary disorder of biotin metabolism. The incidence of biotinidase d...
All worldwide newborn screening (NBS) for lysosomal storage diseases (LSDs) is performed as a first-...
INTRODUÇÃO: A deficiência de biotinidase é um erro inato do metabolismo caracterizado principalmente...
Four children with biotinidase deficiency were identified during the first year of a neonatal screen...
Health-associated reference values are universally needed in clinical chemistry. The aim of this stu...
Biotinidase activity assay is included in most newborn screening protocols, and the positive results...
Background Biotin, a water-soluble vitamin, is used as a co-factor by enzymes involved in carboxylat...
We describe a method for neonatal screening for biotinidase (EC 3.5.1.12) deficiency. Biotinidase ac...
Biotinidase deficiency is an inherited metabolic disorder characterized by neurological and cutaneou...
Biotinidase deficiency is an inherited metabolic disorder characterized by neurological and cutaneou...
INTRODUÇÃO: A deficiência de biotinidase é um erro inato do metabolismo caracterizado principalmente...
Biotinidase deficiency is an inherited metabolic disorder that, if untreated, can result in neurolog...
Biotinidase deficiency is a rare inherited metabolic disorder that can cause severe neurological sym...
Biotinidase deficiency is a rare inherited metabolic disorder that can cause severe neurological sym...
Biotinidase deficiency is an autosomal recessive metabolic disease that causes biotin deficiency. Th...
Biotinidase deficiency is a hereditary disorder of biotin metabolism. The incidence of biotinidase d...
All worldwide newborn screening (NBS) for lysosomal storage diseases (LSDs) is performed as a first-...
INTRODUÇÃO: A deficiência de biotinidase é um erro inato do metabolismo caracterizado principalmente...
Four children with biotinidase deficiency were identified during the first year of a neonatal screen...
Health-associated reference values are universally needed in clinical chemistry. The aim of this stu...