Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Başak Kandi Coşkun"'
Publikováno v:
Journal of Cutaneous Pathology. 32:629-633
The incidence of tuberculosis in Western countries is rising, and continued vigilance together with an awareness of its protean manifestations is essential. Cutaneous tuberculosis is a relatively rare manifestation of the disease, accounting for only
Publikováno v:
The Tohoku Journal of Experimental Medicine. 206:305-312
Recurrent aphthous ulceration (RAU) is a common oral mucosal disorder characterized by recurrent, painful oral aphthae. Although the exact cause of RAU is not known, local trauma, microorganisms, nutritional deficiencies, hormonal changes, genetics,
Publikováno v:
The Journal of Dermatology. 31:666-670
We report a case of benign form of Degos' disease, a rare condition often characterized by multisystemic vasculopathy, and discuss the case by the light of the limited literature available. A 34-year-old male patient was admitted to our clinic with l
Publikováno v:
International Journal of Psychiatry in Clinical Practice. 9:52-54
Aim To investigate, retrospectively, psychiatric consultation results of inpatients staying in Fırat University Dermatology Clinic. Materials and method Records of 520 inpatients who were treated in Fırat University Dermatology Clinic between May 2
Publikováno v:
International Journal of Clinical Practice. 59:69-71
Summary Erythema nodosum (EN)-like lesions and superficial thrombophlebitis (ST) are skin symptoms that are frequently observed in Behcet's disease. In most of the patients, skin symptoms precede serious visceral involvement. The study included 78 pa
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 19:87-89
We present a case of Reiter syndrome (RS) associated with Terry nail in a 32-year-old male patient who also had subungual keratosis and onycholysis. The case had all the characteristic findings of complete RS including urethritis, conjunctivitis, art
Publikováno v:
Journal of Dermatological Treatment. 15:333-335
Granulomatous cheilitis (GC) is a chronic edema which frequently affects the upper lip due to granulomatous inflammation. Its etiology is currently unknown. This rare disease is generally accompanied by Melkersson-Rosenthal syndrome (MRS), characteri
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 48(6)
Background: The present study was aimed to define the gender ratio, familial occurrence, age of onset, precipitating factors, clinical types, nail and joint involvement of psoriasis in childhood and adolescence in Turkey. Methods: A total of 61 child
Publikováno v:
American journal of clinical dermatology. 6(6)
Monilethrix is a rare hereditary disorder that affects the hair and is characterized by shaft anomaly. There is no known treatment that successfully cures the condition. In this report we present a case of monilethrix in a 7-year-old girl treated wit
Publikováno v:
Clinical rheumatology. 25(3)