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Research 511–540 of 1000+
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Nonclassic adrenal hyperplasia
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- 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
- 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
- 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
- Management of CAH during pregnancy
- Role of caffeine in the management of androgenetic alopecia
- 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
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- 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
- Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology