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Research 451–480 of 1000+
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- PA33 When bones speak through nails: insights from a paediatric case series
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Treatments of hereditary hair loss (alopecia)
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- [Androgenetic alopecia].
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Exploring the potential of herbal drugs for the treatment of hair loss
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Alopecia totalis in an infant
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Ugreelig hår
- Diagnosis dan Tata Laksana Graves’ Disease
- Pigmentary and Hair Disorders
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- Hair Transplantation
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Hyperadrenocorticism in Ferrets
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Combination of Netherton Syndrome and Hypopituitarism with Isolated Somatotropin Deficiency: Case Study
- Dermatomyositis Disease in Dogs
- Faculty Opinions recommendation of Hidradenitis suppurativa as a potential subtype of autoinflammatory keratinization disease.
- Netherton Syndrome
- Clinical Snippets
- Alopecias
- Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance