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- Non-nutritional rickets: Approach, precision medicine, and outcomes
- E-Poster
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- THE DISEASE SPECTRUM, EPIDEMIOLOGY, AND ETIOLOGY OF TOXIC-SHOCK SYNDROME
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Reporting on Adverse Clinical Events
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The clinical spectrum of parathyroid disease
- Endocrinology
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- FGF Family: From Drug Development to Clinical Application
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Mineral Deficiencies: A Root Cause for Reduced Longevity in Mammals
- Linking the brain and bone through fat
- Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy
- Follikelhormone
- The role of protein lactylation in skin diseases: from molecular mechanisms to potential therapeutics
- Abstracts Pt.30
- Vitamin D, Lipid Metabolism and Prostate Cancer
- The urine as a diagnostic key for a homozygous EGFR mutation
- Cutaneous Manifestations of Chronic Kidney Disease: A Narrative Review
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Nutritional Disorders of the Hair and Their Management
- Ernährungsstörungen des Haares und deren Management
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters