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Research 961–990 of 1000+
- A rare case of woolly hair with unusual associations
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- Nail Matrix Pathology in Cronkhite–Canada Syndrome: The First Case Report
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Somatization in the dermatology patient: Some sociocultural perspectives
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Elkonyxis associated with habit-tic deformity: Two case reports
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A Case of Cronkhite-Canada Syndrome Involving the Entire Gastrointestinal Tract
- The Future of Aesthetic Medicine: Patient‐Centered Trends and Technologies with Dr. Face and Dr. Slim
- Is Every Patient of Hair Loss a Candidate for Hair Transplant?—Deciding Surgical Candidacy in Pattern Hair Loss
- A Case of Cronkhite-Canada Syndrome Presenting with Hematochezia
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Practice and Educational Gaps in Dermatology
- Olmsted syndrome
- The Coexistence of Trachyonychia and Mucocutaneous Lichen Planus: A Case Report
- Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations
- Lifestyle Drugs in Old Age – A Mini-Review
- Scalpel, Toxin, and Performance Pressure: Metabolic, Psychiatric, and Psychosocial Aspects of Aesthetic Medicine in Competitive and Physique Athletes
- Psychological Dimensions of Hair Transplantation: A Narrative Review of Current Evidence
- PA33 When bones speak through nails: insights from a paediatric case series
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Pincer Nails – A Rare Manifestation of Systemic Lupus Erythematosus
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Polyglandular Syndrome Type 1 Complicated with Dilated Cardiomyopathy: A Case Report
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- 1503 Prostaglandin E2 prevents radiotherapy-induced alopecia by attenuating transit amplifying cell apoptosis through promoting G1 arrest
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome