Medicine and Dentistry
Biotinidase Deficiency
77%
Spinal Cord Disease
44%
Child
44%
Spinal Cord
44%
Diagnosis
22%
Biotinidase
22%
Pediatric Neurology
22%
Magnetic Resonance Imaging
11%
Enzyme Activity
11%
Nutritional Deficiency
11%
Infancy
11%
Intractable Epilepsy
11%
Autosomal Recessive Inheritance
11%
Gene Sequence
11%
Paracetamol
11%
Depletion
11%
Hypotonia
11%
Biotin
11%
Dimemorfan Phosphate
11%
Feeding
11%
Inborn Error of Metabolism
11%
Lethargy
11%
Thinking
11%
Symptom
11%
Demyelination
11%
Multiple Carboxylase Deficiency
11%
Therapeutic Procedure
11%
Brain
11%
Patient
11%
Recognition
11%
Female
11%
Marker
11%
Childhood
11%
Early Diagnosis
11%
Neuroscience
Biotinidase
100%
Spinal Cord Disease
44%
Magnetic Resonance Imaging
33%
Seizure
11%
Enzyme Activity
11%
Hypotonia
11%
Gene Sequence
11%
Carboxylase
11%
Biotin
11%
Brain Injury
11%
Recognition
11%
Feeding Behavior
11%
Psychology
Biotinidase Deficiency
77%
Children
44%
Spinal Cord
22%
Depletion
11%
Hypotonia
11%
Feeding Problem
11%
Treatment
11%
Regression
11%
Sequencing
11%
Seizures
11%
Multiple Carboxylase Deficiency
11%
Respiratory Problem
11%
Biochemistry, Genetics and Molecular Biology
Biotinidase
100%
Mutation
11%
Enzyme Activity
11%
Inborn Error of Metabolism
11%
Autosomal Recessive Inheritance
11%
Gene Sequence
11%
Infancy
11%
Recognition
11%
thought
11%
Childhood
11%
Biotin
11%