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Research 391–420 of 699
- Nosological profile of dermatological diseases in primary health care and dermatology secondary care in Florianópolis (2016–2017)
- An Update on Scalp Psoriasis
- Stem Cells and their Niches
- Structure and Function of the Skin
- A cross sectional study on geriatric dermatosis in patients attending a tertiary care hospital
- Amelioration of psoriasis-like skin lesions by human amniotic mesenchymal stem cells: insights from multiomics profiling in mice
- Do Dermatoses Trigger Neurodegenerative Diseases? A Retrospective Observational Study
- Swastyayanam of Bhela indriya Sthana - an explorative study
- Pharmacology of Glycyrrhiza glabra (Mulhatti): The grandfather of herbs
- A clinical study of geriatric dermatoses in Dharmapuri district, Tamil Nadu, India
- Table of Contents
- British Society for Dermatopathology
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Molecular Genetics of Human Hair Diseases
- The Immunological Intersection of Psoriasis and Autoimmune Diseases: Shared Pathways and Clinical Implications
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Ischemia-modified albumin as a possible marker of oxidative stress in patients with telogen effluvium
- Bipolar Patients and Bullous Pemphigoid after Risperidone Long-Acting Injectable: A Case Report and a Review of the Literature
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Clinical Evaluation Including Trichoscopy and Photography
- Bullous Lichen Planus treated with Oral Minipulse Therapy: A Rare Case Report
- Validation of <i>International Classification of Diseases</i> Codes for Dermatologic Conditions
- New Frontiers of Non‐Invasive Detection in Scalp and Hair Diseases: A Review of the Application of Novel Detection Techniques
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Cell death in the skin
- An Update on Medical Treatment Options for Hidradenitis Suppurativa