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Research 631–660 of 1000+
- A Newborn With Hair Loss
- The SAHA Syndrome
- The Hair Follicle: A Paradoxical Androgen Target Organ
- Neuroimmunoregulation of Androgens in the Adrenal Gland and the Skin
- Apparent Cortisone Reductase Deficiency: A Rare Cause of Hyperandrogenemia and Hypercortisolism
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Nonclassic Congenital Adrenal Hyperplasia
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- Hereditary vitamin D rickets: a case series in a family
- Hair Loss in an Adolescent
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Clinical Quiz
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- A Neonate with Unexplained Hair Loss
- HIV infection mimicking autoimmune disorder
- Inherited Acrodermatitis Enteropathica
- Trichorrhexis Invaginata in Tinea Capitis: A Rare Occurence
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Zinc Spray for Treatment of Acrodermatitis Enteropathica: A Case Report
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Hyperandrogenism in a set of triplets with modification of clinical course by hyperthyroidism
- Questions and answers for clinical insights
- Phenotypic variation in biotinidase deficiency
- Congenital atrichia with papular lesions
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Non-nutritional rickets: Approach, precision medicine, and outcomes