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Research 211–240 of 1000+
- Cosmetic Dermatology: Principles and Practice.
- A rare case of woolly hair with unusual associations
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Assessing the Efficacy of Multimodal Therapy in Nonsurgical Hair Restoration for Noncicatricial Alopecia: A Retrospective Study
- The Skin Microenvironment: A Dynamic Regulator of Hair Follicle Development, Cycling and Disease
- The Excesses of Cosmetic Medicine
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Pincer Nails – A Rare Manifestation of Systemic Lupus Erythematosus
- A clinical study of Geriatric dermatoses at Tertiary care center in South India
- Proteins in Scalp Hair of Preschool Children
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Letters to the Editors
- Overexpression of Bcl-2 Protects from Ultraviolet B-Induced Apoptosis but Promotes Hair Follicle Regression and Chemotherapy-Induced Alopecia
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Limonin, a Component of Immature Citrus Fruits, Activates Anagen Signaling in Dermal Papilla Cells
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- Keratin expression by corneal and limbal stem cells during development
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Going Beyond Hair: Seven Simple Actions We Can Take to Help Prevent Major Illness in Our Hair Transplant Patients
- Psychological Dimensions of Hair Transplantation: A Narrative Review of Current Evidence
- The Wonder Tool Platelet Rich Plasma in Cosmetic Dermatology, Trichology and Hair Transplant