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Research 91–120 of 802
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Lichen Planopilaris As Part of Multiple Autoimmune Syndrome: A Case Report of New Association
- Parry Romberg Syndrome: When the Diagnosis of a Rare Disease Is Made in the Primary Care Setting
- Diagnostic dilemma: Multiple Autoimmune Syndrome versus incomplete Graham-Little-Piccardi-Lassueur Syndrome overlap mixed connective tissue disease
- IL6 is correlated with metabolic syndrome parameters in oral lichen planus
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Dermatologic Manifestations in Patients with Metabolic Syndrome in Brazil
- Dermatolojik Problemler ve COVID-19
- Mucocutaneous reactions to chemotherapy
- Severe cutaneous adverse reactions to drugs
- Endocrine-skin interactions
- Eosinophilic Fasciitis Associated With Tryptophan Ingestion
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- En Coup de Sabre in a Pediatric Patient Treated With Calcipotriene
- Ischemic onycholysis of the hands
- Nutrition and hair
- Werner′s syndrome
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Multiple Autoimmune Syndrome With Alopecia Universalis and Immune Thrombocytopenic Purpura
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Treatment of Scleroderma-Related Microstomia Using Hyaluronic Acid: An Interventional Study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Immunosuppressive therapy in autoimmune disease — A review