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1985 2
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1998 4
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Page 1
Biotin: biochemical, physiological and clinical aspects.
Said HM. Said HM. Subcell Biochem. 2012;56:1-19. doi: 10.1007/978-94-007-2199-9_1. Subcell Biochem. 2012. PMID: 22116691 Review.
This is underscored by the serious clinical abnormalities that occur in conditions of biotin deficiency, which include, among other things, growth retardation, neurological disorders, and dermatological abnormalities (reviewed in 1). Studies in animals have also shown that …
This is underscored by the serious clinical abnormalities that occur in conditions of biotin deficiency, which include, among other t …
Biotin: overview of the treatment of diseases of cutaneous appendages and of hyperseborrhea.
Piraccini BM, Berardesca E, Fabbrocini G, Micali G, Tosti A. Piraccini BM, et al. G Ital Dermatol Venereol. 2019 Oct;154(5):557-566. doi: 10.23736/S0392-0488.19.06434-4. G Ital Dermatol Venereol. 2019. PMID: 31638351 Review.
One of the most common micronutrient deficiencies with cutaneous findings is the vitamin B, also known as biotin, deficiency. Biotin deficiency may be due to congenital lack of biotinidase, or acquired following some conditions that interfere with its absorpt …
One of the most common micronutrient deficiencies with cutaneous findings is the vitamin B, also known as biotin, deficiency. Biotin …
Ataxia.
Winchester S, Singh PK, Mikati MA. Winchester S, et al. Handb Clin Neurol. 2013;112:1213-7. doi: 10.1016/B978-0-444-52910-7.00043-X. Handb Clin Neurol. 2013. PMID: 23622331 Review.
., Kawasaki), metabolic etiologies (e.g., maple syrup urine disease, pyruvate dehydrogenase deficiency, ornithine transcarbamylase deficiency, biotinidase deficiency, Hartnup disease, and argininosuccinic aciduria), migraine, migraine equivalents (beni …
., Kawasaki), metabolic etiologies (e.g., maple syrup urine disease, pyruvate dehydrogenase deficiency, ornithine transcarbamylase …
Biotinidase deficiency and our champagne legacy.
Wolf B. Wolf B. Gene. 2016 Sep 10;589(2):142-50. doi: 10.1016/j.gene.2015.10.010. Epub 2015 Oct 9. Gene. 2016. PMID: 26456103 Review.
Biotinidase deficiency is an autosomal recessively inherited metabolic disorder. If untreated, individuals with biotinidase deficiency usually develop neurological and cutaneous symptoms that can result in coma or death. ...
Biotinidase deficiency is an autosomal recessively inherited metabolic disorder. If untreated, individuals with biotinidase …
Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without and vision loss.
Wolf B. Wolf B. Mol Genet Metab. 2015 Nov;116(3):113-8. doi: 10.1016/j.ymgme.2015.08.012. Epub 2015 Sep 3. Mol Genet Metab. 2015. PMID: 26358973 Review.
Multiple symptomatic children with biotinidase deficiency have exhibited spastic para- or tetraplegia due to myelopathy with and without vision loss. ...Many of these children have gone weeks to months before they were correctly diagnosed with biotinidase …
Multiple symptomatic children with biotinidase deficiency have exhibited spastic para- or tetraplegia due to myelopathy with a …
The neurology of biotinidase deficiency.
Wolf B. Wolf B. Mol Genet Metab. 2011 Sep-Oct;104(1-2):27-34. doi: 10.1016/j.ymgme.2011.06.001. Epub 2011 Jun 12. Mol Genet Metab. 2011. PMID: 21696988 Review.
Biotinidase deficiency is an autosomal recessively inherited metabolic disorder in which the enzyme, biotinidase, is defective and the vitamin, biotin, is not recycled. Individuals with biotinidase deficiency, if not treated with biotin, usually …
Biotinidase deficiency is an autosomal recessively inherited metabolic disorder in which the enzyme, biotinidase, is de …
Biotinidase: its role in biotinidase deficiency and biotin metabolism.
Wolf B. Wolf B. J Nutr Biochem. 2005 Jul;16(7):441-5. doi: 10.1016/j.jnutbio.2005.03.024. J Nutr Biochem. 2005. PMID: 15992688 Review.
Renewed interest in biotinidase, the enzyme responsible for recycling the vitamin biotin, initially came from the discovery of biotinidase deficiency in 1982. ...Biotinidase may have an important regulatory role(s) in chromatin/DNA function....
Renewed interest in biotinidase, the enzyme responsible for recycling the vitamin biotin, initially came from the discovery of bio …
Biotinidase deficiency presenting as recurrent myelopathy in a 7-year-old boy and a review of the literature.
Raha S, Udani V. Raha S, et al. Pediatr Neurol. 2011 Oct;45(4):261-4. doi: 10.1016/j.pediatrneurol.2011.06.010. Pediatr Neurol. 2011. PMID: 21907891 Review.
Biotinidase deficiency may produce variable neurologic manifestations. ...Severe biotinidase deficiency was established, and the patient demonstrated complete recovery with biotin supplementation. ...
Biotinidase deficiency may produce variable neurologic manifestations. ...Severe biotinidase deficiency was esta …
71 results