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Research 391–420 of 1000+
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- First Symposium of Ichthyosis Experts
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Risk factors and comorbidities associated with central centrifugal cicatricial alopecia
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Abstracts
- Tissue Resident Foxp3+ Regulatory T Cells: Sentinels and Saboteurs in Health and Disease
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Intrinsic factors in the pathogenesis of hidradenitis suppurativa: Genetics, hormones, and the microbiome
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Mendelian randomization analysis of the causal relationship between low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and androgenic alopecia
- Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- How I Do It: Galenic Lotions for Topical Use to Cure Hair Thinning in Males and Females
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Dermal T cell immunity and key regulatory signaling pathways: Implications in immune-mediated alopecia and hair regeneration