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Research 361–390 of 1000+
- 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
- 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
- Ectodermal Dysplasia: Variable Expressions
- 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
- 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
- Role of caffeine in the management of androgenetic alopecia
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.