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Research 121–150 of 1000+
- Physiology and Medical Treatments for Alopecia
- Genetic and molecular aspects of androgenetic alopecia
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Scalp whorls
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Hair Loss Diagnosis Using Artificial Neural Networks
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Genetic analysis of 5 α reductase type 2 enzyme in relation to oxidative stress in cases of androgenetic alopecia in a sample of egyptian population
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Two females with hair loss
- The inheritance of common baldness: Two B or not two B ?
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Stem Cells and the Niche: A Dynamic Duo
- Genetic Basis of Male Pattern Baldness
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- THE PATHOGENESIS OF ALOPECIA AREATA
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Ferreting out stem cells from their niches
- MENSTRUAL DISORDERS IN ADOLESCENTS
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS