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Research 61–90 of 1000+
- Keratosis Pilaris Is a Keratinization of Hair Follicles
- Clinical and microscopic features of generalized discoid lupus erythematosus in dogs (10 cases)
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Lower prostate cancer risk in Swedish men with the androgen receptor E213 A-allele
- The Rotterdam Study: 2016 objectives and design update
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Differential diagnosis of the scalp hair folliculitis.
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- <i>WNT10A</i> , dermatology and dentistry
- Alopecia Areata and Alopecia Areata Incognita
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Hair regrowth in a patient with central centrifugal cicatricial alopecia after a 2-month trial of baricitinib
- Occipital Fibrosing Alopecia in a Young Male: A Case Report
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Genomic Analysis of Trichotillomania
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Frontal Fibrosing Alopecia
- Commentary on A New Subtype of Lichen Planopilaris Affecting Vellus Hairs and Clinically Mimicking Androgenetic Alopecia
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Trichostasis spinulosa: An overlooked entity
- Pediatric Lichen: Epidemiological and Clinical Characteristics in Children
- Clinical-Exome Sequencing Unveils the Genetic Landscape of Polycystic Ovarian Syndrome (PCOS) Focusing on Lean and Obese Phenotypes: Implications for Cost-Effective Diagnosis and Personalized Treatment