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Research 30 of 105
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- Mechanism of Vitamin D Receptor Action
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- Vitamin D resistance
- 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
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- 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
- Multiple endocrine defects in adult-onset Sprouty1/2/4 triple knockout mice
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- Some Clues and Pitfalls in the Diagnosis of Acromegaly
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Polyglandular Syndrome Type 1 Complicated with Dilated Cardiomyopathy: A Case Report
- Patient‐Level Adverse Event Patterns in a Single‐Institution Study of the Multi‐Kinase Inhibitor Sorafenib
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Clinical development and management of adverse events associated with FGFR inhibitors
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- E-Poster
- Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy
- Abstracts Pt.30
- Medical complications of anorexia nervosa and bulimia nervosa
- The clinical spectrum of parathyroid disease
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Clinical Aspects and Spectrum of Illness of TSS: Overview
- THE DISEASE SPECTRUM, EPIDEMIOLOGY, AND ETIOLOGY OF TOXIC-SHOCK SYNDROME