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Research 781–810 of 1000+
- Weight Changes Are Linked to Adipose Tissue Genes in Overweight Women with Polycystic Ovary Syndrome
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- LB943 Tofacitinib treatment of inflammatory skin conditions in patients with Down Syndrome
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- A different approach to PCOS: evaluation of spermiogram results in male patients with a family history of PCOS
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Male pattern hair loss
- Primary High‐Grade Ovarian Sertoli–Leydig Cell Tumor With Bilateral Adnexal Involvement in a Patient Diagnosed With Peutz–Jeghers Syndrome
- Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives
- The Impact of Gender Affirming Hormone Therapy on Physical Performance
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Turner's syndrome associated with psoriasis and alopecia areata
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome
- Dermoscopy: A rapid bedside tool to assess monilethrix
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Efficacy and safety of ritlecitinib in Asian patients with alopecia areata: A subgroup analysis of the ALLEGRO phase 2b/3 trial
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Beta Human Papillomavirus and Merkel Cell Polyomavirus in Skin Neoplasms
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Cell Therapy for Androgenetic Alopecia: Elixir or Trick?
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital