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Research 91–120 of 145
- Serum biotin levels in women complaining of hair loss
- The Hair Cycle and Its Relation to Nutrition
- Nutritional Disorders of the Hair and Their Management
- Retinoids in Hair Loss
- Ernährungsstörungen des Haares und deren Management
- Transport of Biotin in Human Keratinocytes
- 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
- 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
- Biotinidase Enzyme Deficiency ( Case Report )
- A Rare Case of Biotinidase Deficiancy
- Biotinidase Deficiency: A Treatable Neurometabolic Disorder- A Case Report
- Biotinidase Deficiency and Seizures
- Ocular aspects in biotinidase deficiency Clinical and genetic original studies
- Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency
- Rethinking biotin therapy for hair, nail, and skin disorders
- Inborn Errors of Biotin Metabolism
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Biotin deficiency in an infant fed with amino acid formula and hypoallergenic rice
- Inborn errors of biotin metabolism
- Hair abnormalities and neurological disease
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Skin signs of nutritional disorders.
- Quantification of biotin in plasma samples by column switching liquid chromatography – tandem mass spectrometry
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Hair Loss After Sleeve Gastrectomy and Effect of Biotin Supplements
- 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