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- Treatment of cutaneous leiomyomas with botulinum toxin. Case report and review of literature
- Gender aspects in skin diseases
- Subject Index
- Index
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin
- Acne Syndromes and Mosaicism
- Update From 2017 Embracing the World of Dermatology Convention
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- 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