Author:
Colmenero Isabel,Molho-Pessach Vered,Torrelo Antonio,Zlotogorski Abraham,Requena Luis
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Dermatology,General Medicine,Pathology and Forensic Medicine
Reference12 articles.
1. . The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.;Molho-Pessach;J Am Acad Dermatol,2008
2. . The H syndrome is caused by mutations in the nucleoside transporter hENT3.;Molho-Pessach;Am J Hum Genet,2008
3. . H syndrome: recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases.;Doviner;Am J Dermatopathol,2010
4. . A case of H syndrome showing immunophenotype similarities to Rosai-Dorfman disease.;Avitan-Hersh;Am J Dermatopathol,2011
5. . Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.;Morgan;PLoS Genet,2010
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