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Research 271–300 of 1000+
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Frontal Fibrosing Alopecia: A Review
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Familial Frontal Fibrosing Alopecia
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Inherited Epidermolysis Bullosa: A Clinical Case
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Microneedling plus topical dutasteride solution for androgenetic alopecia: a randomized placebo‐controlled study
- A study of the Geheimratsacken angle as predictor for early diagnosis of androgenetic alopecia in adolescent population
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- The Hair Shedding Visual Scale: A Quick Tool to Assess Hair Loss in Women
- Diagnostic approach to low‐renin hypertension
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Nonclassic adrenal hyperplasia
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Ectodermal Dysplasia: Variable Expressions
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Hair Anomalies in a 6-Year-Old Girl
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center
- Targeting integrin pathways: mechanisms and advances in therapy
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Bioengineering the Hair Follicle
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome