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Research 31–60 of 1000+
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- Genetic Disorders and Defects in Vitamin D Action
- Molecular Genetics of Alopecias
- Coat Problems
- Current Genetics in Hair Diseases
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Hereditary Chorea Associated With and Aggravated by Systemic Lupus Erythematosus
- Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis].
- CUTANEOUS MANIFESTATIONS OF POLYCYSTIC OVARIAN DISEASE
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- What does acne genetics teach us about disease pathogenesis?
- Case Study: Hereditary Cancer Genetic Testing in Unaffected Patients May Allow for Early Intervention and Aggressive Management
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Consecuencias civiles en el impago de la primera prima o sucesivas de la póliza de seguro en los juicios penales por accidente de tráfico: ¿tiene cobertura por la aseguradora el conductor?
- Leukokoria sebagai Tanda Peringatan Penyakit Coats dan Gangguan Retina Lainnya
- Clinical cases of Darier-White follicular dyskeratosis
- Alopecia Areata: A Case Report
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Familial patterns of alopecia areata: A systematic review and meta-analysis
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals