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Research 31–60 of 1000+
- Actualités du SOPK
- Mucocutaneous manifestations of acquired hypoparathyroidism: An observational study
- Stratum-Specific Expression of Human Transferrin Receptor Increases Iron in Mouse Epidermis
- Mineral Deficiencies: A Root Cause for Reduced Longevity in Mammals
- Iron–Skin Axis: Exploring the Interplay between Iron Homeostasis and Skin Disorders
- Pancreatogenic type 3C diabetes
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Iron Deficiency in Immune-Mediated Inflammatory Skin Diseases: A Missing Link Between Systemic Inflammation, Immunometabolism, and Disease Burden
- The Case Files
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Topical minoxidil therapy in hereditary androgenetic alopecia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- A Comparative Study of a New Food Supplement, ViviScal®, with Fish Extract for the Treatment of Hereditary Androgenic Alopecia in Young Males
- Topical minoxidil therapy for hereditary male pattern alopecia.
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene