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Research 31–60 of 1000+
- Biotin: A friend or foe in hair loss
- Biotinidase Enzyme Deficiency ( Case Report )
- Biotin - facts and hopes
- Response to Falotico et al’s “Biotin beware: Perils of biotin supplementation”
- Evaluation of serum level of biotin and effect of biotin replacement therapy in patients with telegon effluvium
- Reply to: “Response to ‘Rethinking biotin therapy for hair, nail, and skin disorders’”
- Literature Review: Biotin and Hair Loss: Valuable or Just “In Vogue”?
- A Retrospective Evaluation of the Laboratory Findings of Dermatology Patients Whose Biotin Levels Were Checked
- Phenotypic variation in biotinidase deficiency
- Partial biotinidase deficiency: Clinical and biochemical features
- Biotinidase deficiency: a survey of 10 cases.
- Late presentation of biotinidase deficiency with acute visual loss and gait disturbance
- Vitamin Deficiency, Dependency, and Toxicity
- Biotinidase deficiency – clinching the diagnosis rapidly can make all the difference!
- Newborn screening for biotinidase deficiency: pilot study and follow-up of identified cases
- Possible involvement of partial biotinidase deficiency in alopecia areata
- Acrodermatitis enteropathica‐like skin eruption with neonatal seizures in a child with biotinidase deficiency
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Biotinidase Deficiency Accompanying Hair Changes and Periorificial Lesions: A Case Report
- Possible involvement of partial biotinidase deficiency in alopecia areata
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- P447: Late onset biotinidase deficiency misdiagnosed as neuromyelitis optica: A case report and review of diagnostic challenges
- A Rare Case of Biotinidase Deficiancy
- Biotinidase Deficiency: A Treatable Neurometabolic Disorder- A Case Report
- P175 The effects of biotin supplementation on alopecia in rats which were administrated to valproic acid
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Multiple Carboxylase Deficiency in an Infant Presenting With Severe Metabolic Acidosis and Sepsis‐Like Features: A Case Report and Literature Review
- MON-369 Treatment of Nonclassic 11-Hydroxylase Deficiency with "Hair, Skin, and Nails," an Over-the-Counter, Insulin Sensitizing Vitamin/Mineral Supplement
- Nutritional factors and hair loss
- Nutrition and hair