Volume 7, Issue 3
مرور بر اساس
ارسال های اخیر
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Chondroectodermal dysplasia (Ellis-Van Creveld syndrome: A case report
(Iranian Society of Dermatology, 2004-04-01)Ellis-Van Creveld syndrome is a very rare congenital disorder which its principal features are polysyndactyly, chondrodysplasia, cardiac abnormalities and ectodermal dysplasia. We report a 10-year-old girl with major ...
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Identification of Mycobacteria species in cutaneous lesions of Sarcoidosis by PCR-Restriction Ragment Length Polymorphism (PCR-RFLP) method
(Iranian Society of Dermatology, 2004-04-01)Background: Sarcoidosis is a granulomatous multisystem disease of unknown etiology. It has recently been tired to detect Mycobacteria genome in biopsy specimens of patients with sarcoidosis by Polymorphism chain reaction ...
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Coexistence of Sezary syndrome with Kaposi's sarcoma: Report of a case with concurrent generalized dermatophyte infection
(Iranian Society of Dermatology, 2004-04-01)Immunosuppression is known to be associated with increased rate of malignancies and widespread dermatophytosis in the patients with sezary syndrome and this may account for the occurrence of Kaposi's sarcoma and ...
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Serum antibody levels to Helicobacter Pylori in patients with recurrent Aphthous Stomatitis
(Iranian Society of Dermatology, 2004-04-01)Background: Recurrent aphthous stomatitis (RAS) is a common disease, which several etiologic factors have been considered for it. The infectious agents and immunological factors are the most suspected causes. Recently a ...
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Anatomical location of basal cell carcinoma in relation to histopathological subtypes: Analysis of 189 cases in Hamadan Sina Hospital during 1997-99
(Iranian Society of Dermatology, 2004-04-01)Background: Basal cell carcinoma (BCC) is the most common skin cancer in whites. Objective: Determination of anatomical localization of BCC in relation to histological subtypes of this tumor. Patients and methods: ...
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P53 antigen expression in cutaneous Melanoma and its relation to tumor thickness
(Iranian Society of Dermatology, 2004-04-01)Background: P53 tumor suppressor gene mutation is one of the most common genetic alterations in human malignancies. The mutated from of the gene is stable and can be detected with immunohistochemistry methods. There is ...



