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Research 31–60 of 49
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- Vitamin D deficiency in non-scarring and scarring alopecias: a systematic review and meta-analysis
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers
- 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
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Hereditary vitamin D rickets: a case series in a family
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- 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
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- 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
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Genetic Disorders and Defects in Vitamin D Action
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Type II Vitamin D Dependent Rickets: A Case Report
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia