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Research 421–450 of 680
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Evaluation of Sleep Quality, Restless Legs Syndrome, Anxiety and Depression in Polycystic Ovary Syndrome
- Treatment of female sexual dysfunction in postmenopausal women—What is the evidence?
- The Arrector Pili Muscle and the Follicular Unit of the Scalp
- Can gut flora changes be new biomarkers for depression?
- Biomaterials for dermal substitutes
- Hair Loss Dysmorphic Disorder – a Frequently Encountered and Often Neglected Disorder
- Microneedles meet photomedicine: emerging strategies for diagnosis and therapy of skin diseases
- Life Events Preceding Alopecia Areata Onset—a Descriptive Retrospective Cohort Study Focusing on Strain
- TỈ LỆ RỐI LOẠN LO ÂU Ở BỆNH NHÂN RỤNG TÓC TẠI BỆNH VIỆN DA LIỄU THÀNH PHỐ CẦN THƠ
- The Relationship Between Depression Levels and Suicide Risk in Pediatric Patients with Alopecia Areata and the Oxidant-Antioxidant Balance
- Formulation and evaluation of beta-sitosterol enriched herbal scalp serum
- Trichotillomania in a Male Patient With Depression: A Case Report
- Parenting Styles and Psychological Effects on Children with Alopecia Areata: Exploring Family Dynamics, Anxiety, and Depression
- Evaluating the Disease-Related Experiences of TikTok Users With Lupus Erythematosus: Qualitative and Content Analysis
- A comparative analysis of three explanatory models of mental disorder and a preferred focus of explanation
- Complications in Esthetic Surgery
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- First Symposium of Ichthyosis Experts
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Causes and Management of Hypertrichosis
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- FGF5 is a crucial regulator of hair length in humans