Yazar "Devecioglu, C" seçeneğine göre listele

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    Chemotherapy-induced bullous acral erythema in a subject with B-cell lymphoma
    (European Acad Dermatology & Venereology, 2001) Soker, M; Akdeniz, S; Devecioglu, C; Haspolat, K
    [Abstract Not Available]
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    Henna-induced hemolytic anemia and acute renal failure
    (Turkish J Pediatrics, 2001) Devecioglu, C; Katar, S; Dogru, Ö; Tas, MA
    Henna is a traditional cosmetic agent ana is used worldwide, especially in the Middle East. Its active agent is lawsone (2-hydroxy-1,4-naphthoquinone). Henna is not only applied to hands or hair as a cosmetic agent in traditional ceremonies, but is also applied to the body on lesions in the treatment of seborrheic dermatitis or fungal infections. However, its application over the body or in newborns is rare. Here we report a 27-day-old boy who developed hemolytic anemia and acute renal failure following topical application of henna to his abdomen, intertriginous region and legs to treat diaper rash.
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    Interferon-? treatment as a possible cause of relapse in a child with precursor B acute lymphoblastic leukemia
    (Lippincott Williams & Wilkins, 2001) Söker, M; Dikici, Bünyamin; Devecioglu, C; Ece, A; Haspolat, K
    [Abstract Not Available]
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    Non-African Burkitt's lymphoma manifesting at the jaw and as a right orbital mass in a child
    (Slack Inc, 2003) Çakmak, SS; Söker, M; Ayyildiz, O; Devecioglu, C; Söker, SI
    [Abstract Not Available]
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    Prevalence of factor V Leiden and prothrombin G20210A gene mutation
    (Saudi Med J, 2005) Irdem, A; Devecioglu, C; Batun, S; Soker, M; Sucakli, IA
    Objectives: To determine the prevalence of factor V Leiden (FVL) and prothrombin gene (PG) 20210A mutations in patients who attended the outpatient clinic and do not have a family history of thrombosis. Methods: We researched FVL and PG20210A mutations in 151 outpatients (92 males and 59 females) who attended the Pediatrics Polyclinic, Medical Faculty, Dicle University, Turkey between May 2002 and July 2002. Peripheral venous bloods (2 cc) with ethylenediaminetetraacetic acid were used to isolate DNA by high pure polymerase chain reaction (PCR). Later, by using light-cycler FVL (Roche) and prothrombin mutation detection kit (Roche) and light-cycler equipment, FVL and PG20210A gene mutations were determined from the samples in the glass capillary tubes by PCR specific adaptation. For active protein C (APC) resistance, STA-STACLOT APC-R Detection Kit was used. Expected values were evaluated with STA equipment and using STA-STACLOT APC-R procedure. Results: The prevalence of heterozygote mutations of FVL was 4.6% and PG20210A was 0.7%. The FVL mutation frequency obtained in our study is lower than the other studies in Turkey, but in correlation with the results of the other Caucasian populations throughout the world. Active protein C resistance in patients carrying heterozygote mutation of FVL has been found in low rates. Factor V Leiden and PG20210A were confronted in high prevalences in patients who suffer venous thrombosis (VT). Conclusion: Scanning of FVL and PG20210A gene mutations may be recommended in high risk groups such as relatives of FVL and PG20210A carriers and relatives of patients with VT, and in during pregnancy, the use of oral contraceptives and before surgery. Routine scanning of FVL and PG20210A gene mutations is not recommended in people who do not have risk factors for VT.
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    Spontaneous humerus fracture and osteoporosis
    (Lippincott Williams & Wilkins, 2000) Söker, M; Devecioglu, C; Gürkan, F; Haspolat, K
    [Abstract Not Available]
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    Treatment of subdural empyema by burr hole
    (Israel Journal Med Sciences, 1996) Ak, HE; Ozkan, U; Devecioglu, C; Kemaloglu, MS
    Subdural empyema, a collection of pus in the space between the dura and arachnoid, is a rare type of intracranial infection. We report on 23 patients, aged 8 months to 70 years, with subdural empyema who were treated in our clinic between 1989 and 1994. The sources of subdural empyemas were meningitis in five patients, middle ear in five, trauma in four, paranasal sinus in three, complications of surgery and subdural tap in four, and unknown in two patients. The common presentations were headache, focal neurologic deficit, fever, vomiting, seizures, and neck stiffness. Diagnosis was achieved by computerized tomography and neurologic examinations in all cases. Treatment was effected by burr hole or small craniotomy with catheter drainage, and antibiotics were administered to all patients. The mortality rate was 8.7%; the remaining patients made a good recovery without sequelae. We therefore recommend burr hole with catheter drainage plus antibiotics as a method of treating subdural empyema.