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Research 901–930 of 1000+
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- A guide to diagnosis and management of hypertrichosis
- Identification and characterization of genes for skin and hair disorders
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Central Centrifugal Cicatricial Alopecia
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center
- Can We Use Laser Hair Removal to Prevent the Formation of Trichoepithelioma Lesions?
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Solitary Nodular Lesion Over Face
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- Generalized Asymptomatic Cutaneous Pits and Comedones in a Young Woman
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- 1429 Proteomic analysis of cultured dermal papilla, dermal sheath and dermal fibroblast cells from female scalp highlights alterations in the cell populations with increasing age
- Pachyonychia congenita: Sporadic onset with mutation analysis