Search
for
Sort by
Research 481–510 of 1000+
- Hereditary, Congenital, and Acquired Alopecias
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Hereditary Androgenetic Alopecia and Minoxidil
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Topical Minoxidil Therapy in Hereditary Androgenetic Alopecia
- Monilethrix: A rare hereditary condition
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Treatments of hereditary hair loss (alopecia)
- Quantitative image analysis for hereditary hair disorders
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Case Study: Hereditary Cancer Genetic Testing in Unaffected Patients May Allow for Early Intervention and Aggressive Management
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- 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
- IMMUNOLOGICAL AND GENETIC ASPECTS OF HEREDITARY ANTIBODY DEFICIENCIES
- Testosterone stimulates proliferation and inhibits interleukin‐6 production of normal and hereditary gingival fibromatosis fibroblasts
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Multiple, hereditary dome-shaped papules and acrochordons. Birt-Hogg-Dube syndrome
- Editorial: Vitamin D 1α-Hydroxylase Knockout Mice as a Hereditary Rickets Animal Model
- Real-World Outcomes and Healthcare Utilization of Lanadelumab in Spain: Insights from First Cohort of Difficult-to-Treat Hereditary Angioedema Cases
- 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
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Hair Loss, Insulin Resistance, and Heredity in Middle-aged Women. a Population-based Study
- The human keratins: biology and pathology
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Keratins of the Human Hair Follicle