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Research 31–60 of 1000+
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Rickets and Alopecia with Resistance to 1,25-Dihydroxyvitamin D: Two Different Clinical Courses with Two Different Cellular Defects*
- Genetic Disorders and Defects in Vitamin D Action
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The role of vitamin D receptor mutations in the development of alopecia
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Calcitriol-Resistant Rickets With Alopecia
- Calcitriol-resistant rickets with alopecia
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- 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
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- Dental manifestations in Vitamin D dependent rickets Type II with Alopecia: a short pictorial case report
- VITAMIN D DEPENDENT RICKETS TYPE II (VDR-11). RESPONSE TO PROLONGED THERAPY WITH NOCTURNAL CALCIUM INFUSIONS
- Vitamin D-dependent Rickets Type II
- Effect of calcium supplementation on bone deformity and histopathological findings of skin papules in a pediatric patient with vitamin D–dependent rickets type 2A: a case report
- A rare case of Vitamin D dependent rickets type II: a case report
- Type II Vitamin D Dependent Rickets: A Case Report
- Hair Loss in Paediatric and Adolescent Age Group: A Clinico-Pathological Analysis in a Tertiary Health Care Centre
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Rickets with alopecia: An inborn error of vitaminD metabolism
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- Vitamin D-dependent rickets type II. Defective induction of 25-hydroxyvitamin D3-24-hydroxylase by 1,25-dihydroxyvitamin D3 in cultured skin fibroblasts.
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- 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