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Research 61–90 of 136
- Biotinidase Deficiency: A Treatable Neurometabolic Disorder- A Case Report
- Biotinidase Deficiency and Seizures
- Inborn Errors of Biotin Metabolism
- Inborn errors of biotin metabolism
- Biotin deficiency complicating parenteral alimentation: Diagnosis, metabolic repercussions, and treatment
- Is the Addition of Oral Biotin to PRP More Beneficial for Treating Male Pattern Hair Loss Compared to PRP Alone? A Randomized Control Trial
- Quantification of biotin in plasma samples by column switching liquid chromatography – tandem mass spectrometry
- Analytical interference of biotin
- Biotin: A friend or foe in hair loss
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- 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
- 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
- Biotinidase Deficiency Accompanying Hair Changes and Periorificial Lesions: A Case Report
- Possible involvement of partial biotinidase deficiency in alopecia areata
- P447: Late onset biotinidase deficiency misdiagnosed as neuromyelitis optica: A case report and review of diagnostic challenges
- A Rare Case of Biotinidase Deficiancy
- Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency
- Rethinking biotin therapy for hair, nail, and skin disorders
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Biotin deficiency in an infant fed with amino acid formula and hypoallergenic rice