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Research 121–150 of 1000+
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Gut–ovary axis and multiomic insights into PCOS in a DHEA-induced rat model
- Biology and Genetics of Hair
- Marie-unna hereditary hypotrichosis
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Substance P in keratosis follicularis spinulosa decalvans
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Exploring the Relationship Between Immune Cells and Non-Scarring Hair Loss: A Mendelian Randomization Study
- Genetics of Diabetes in Childhood
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- The clinical spectrum of parathyroid disease
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Lifestyle Diseases and the Hair Growth Cycle: A multidisciplinary approach using Nourkrin® with Marilex®, a proteoglycan replacement therapy, for anagen induction and maintenance
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Secondary cicatricial and other permanent alopecias
- Hair Shaft Dysplasias
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Alopecia areata
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered