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Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without and vision loss
Barry Wolf
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Corresponding author for this work
Pediatrics
Research output
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Contribution to journal
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Review article
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peer-review
39
Scopus citations
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Dive into the research topics of 'Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without and vision loss'. Together they form a unique fingerprint.
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Keyphrases
Vision Loss
100%
Myelopathy
100%
Biotinidase Deficiency
100%
Spinal Cord
14%
Young children
14%
Neurological Injury
14%
Delayed Onset
14%
Hereditary Spastic Paraplegia
14%
Differential Diagnosis
14%
Clinical Features
14%
Newborn Screening
14%
Complete Recovery
14%
Neurological Symptoms
14%
Prompt Treatment
14%
Rapid Recognition
14%
Symptomatic children
14%
Spastic Tetraplegia
14%
Medicine and Dentistry
Visual Impairment
100%
Spinal Cord Disease
100%
Biotinidase Deficiency
100%
Diseases
14%
Differential Diagnosis
14%
Neurologic Disease
14%
Clinical Feature
14%
Newborn Screening
14%
Tetraplegia
14%
Spastic Paraplegia
14%
Neonatal Infant
14%
Toddlers
14%
Biochemistry, Genetics and Molecular Biology
Biotinidase
100%
Newborn Screening
14%