Search
for
Sort by
Research 211–240 of 1000+
- Obsessive-compulsive skin disorders: a novel classification based on degree of insight
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Prognostic factors that affect the response to topical treatment in patchy alopecia areata
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome
- Nail Matrix Pathology in Cronkhite–Canada Syndrome: The First Case Report
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- A Case of Cronkhite-Canada Syndrome Involving the Entire Gastrointestinal Tract
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Olmsted syndrome
- Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- 1503 Prostaglandin E2 prevents radiotherapy-induced alopecia by attenuating transit amplifying cell apoptosis through promoting G1 arrest
- Clouston’s syndrome: a rare case report
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- A patient with Cronkhite-Canada syndrome whose entire digestive tracts was examined endoscopically
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Comparison of Young and Adult Rat Models of Chemotherapy-Induced Alopecia
- Trichothiodystrophy
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Apremilast and tofacitinib exert differential effects in the humanized mouse model of alopecia areata
- 516 Possible role of ILC1 in the pathogenesis of alopecia areata (AA)
- Author response: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Decision letter: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- 431 Innate lymphoid cells type 1 may be new, non-antigen-specific player in the pathogenesis of alopecia areata
- Innate lymphoid cells type 1 may be new, non-antigen-specific player in the pathogenesis of alopecia areata
- Alex de la Iglesia: "Todos somos perversos"
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings