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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 2
1986 2
1987 1
1988 1
1989 3
1991 2
1992 1
1993 1
1994 1
1996 2
1997 1
1998 4
1999 2
2000 1
2001 2
2002 4
2003 2
2004 1
2005 5
2006 4
2008 1
2009 1
2010 1
2011 4
2012 2
2013 3
2014 1
2015 6
2016 3
2017 1
2019 3
2021 1
2022 3
2023 0

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69 results

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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 …
Regulation of immunological and inflammatory functions by biotin.
Kuroishi T. Kuroishi T. Can J Physiol Pharmacol. 2015 Dec;93(12):1091-6. doi: 10.1139/cjpp-2014-0460. Epub 2015 Mar 26. Can J Physiol Pharmacol. 2015. PMID: 26168302 Review.
Holocarboxylase synthetase (HLCS) catalyzes the biotinylation of carboxylases and other proteins, whereas biotinidase catalyzes the release of biotin from biotinylated peptides. Previous studies have reported that nutritional biotin deficiency and genetic defects in …
Holocarboxylase synthetase (HLCS) catalyzes the biotinylation of carboxylases and other proteins, whereas biotinidase catalyzes the r …
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 …
Effect of ultraviolet radiation, smoking and nutrition on hair.
Trüeb RM. Trüeb RM. Curr Probl Dermatol. 2015;47:107-20. doi: 10.1159/000369411. Epub 2015 Feb 20. Curr Probl Dermatol. 2015. PMID: 26370649 Review.
Ultimately, important commercial interest lies in the question of whether increasing the content of an already adequate diet with specific amino acids, vitamins and/or trace elements may further promote hair growth. Unless the hair is impaired due to nutritional deficiency …
Ultimately, important commercial interest lies in the question of whether increasing the content of an already adequate diet with specific a …
Biotin interference in immunoassays based on biotin-strept(avidin) chemistry: An emerging threat.
Luong JHT, Male KB, Glennon JD. Luong JHT, et al. Biotechnol Adv. 2019 Sep-Oct;37(5):634-641. doi: 10.1016/j.biotechadv.2019.03.007. Epub 2019 Mar 11. Biotechnol Adv. 2019. PMID: 30872068 Review.
However, this scenario is not considered for patients in emergency situations or those with biotinidase deficiency, mitochondrial metabolic disorders or multiple sclerosis. ...
However, this scenario is not considered for patients in emergency situations or those with biotinidase deficiency, mitochondr …
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.
Wolf B, Heard GS. Wolf B, et al. Adv Pediatr. 1991;38:1-21. Adv Pediatr. 1991. PMID: 1927696 Review. No abstract available.
69 results