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Research 211–240 of 1000+
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Genomic Characterization of Quality Wool Traits in Spanish Merino Sheep
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Ectodermal Dysplasia: Variable Expressions
- Difficult and rare forms of acne
- Hair Anomalies in a 6-Year-Old Girl
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Androgen sensitivity gateway to COVID‐19 disease severity
- Ehlers-Danlos syndrome: From bedside to bench
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center
- Targeting integrin pathways: mechanisms and advances in therapy
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Role of caffeine in the management of androgenetic alopecia
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>