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Research 61–90 of 1000+
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Hair loss in children.
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- An Update of Congenital Adrenal Hyperplasia
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Sleep quality and its clinical associations in trichotillomania and skin picking disorder
- In Search of Predictive Models for Inhibitors of 5-alpha Reductase 2 Based on the Integration of Bioactivity and Molecular Descriptors Data.
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Androgenic Effects on Ventricular Repolarization
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- Hair loss
- What does acne genetics teach us about disease pathogenesis?
- Prevalence and Clinical Spectrum of Dermatologic Conditions in Renal Transplant Recipients: A 10-Year Retrospective Cross-Sectional Study
- Hair and Scalp Variation Related to Gender
- Learning from nudity: lessons from the nude phenotype
- Melanocyte stem cells: a melanocyte reservoir in hair follicles for hair and skin pigmentation
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Nonclassic adrenal hyperplasia
- Acquired scalp alopecia. Part I: A review
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Zebrafish Model of Hereditary Pigmentary Disorders