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  • 1
    Electronic Resource
    Electronic Resource
    Granuloma annulare associated with prostate carcinoma (2003)
    Oxford, UK : Blackwell Science Ltd
    Journal of the European Academy of Dermatology and Venereology 17 (2003), S. 0 
    Details
    ISSN: 1468-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Granuloma annulare occurs as an idiopathic and benign condition, although it may be associated with some neoplasms. We describe a 60-year-old man with granuloma annulare on dorsal hands who developed prostate carcinoma. To the best of our knowledge, this is the first case report of granuloma annulare with prostate carcinoma. Granuloma annulare, especially in older age groups, may be classified as a sign of various carcinomas.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1046/j.1468-3083.2003.00800.x
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  • 2
    Electronic Resource
    Electronic Resource
    SCE frequency of herpes simplex virus type I infected cells
    Amsterdam : Elsevier
    Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 306 (1994), S. 81-83 
    Details
    ISSN: 0027-5107
    Keywords: Herpes simplex virus type I ; Peripheral blood lymphocytes ; Sister-chromatid exchange
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/0027-5107(94)90169-4
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  • 3
    Electronic Resource
    Electronic Resource
    A case of an enterorenal fistula and pyelonephritis with air in the renal pelvis (1995)
    Springer
    Pediatric radiology 25 (1995), S. 229-230 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report on a 10-year-old boy with recurrent urinary tract infection. Renal ultrasound demonstrated the presence of air in the collecting system of the right kidney. The patient was examined radiologically and an enterorenal fistula was diagnosed. The case serves as a reminder that, although entero-renal fistulas are rare, they should be included in the differential diagnosis of recurrent urinary tract infections, especially if air is observed in the collecting system.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02021544
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  • 4
    Electronic Resource
    Electronic Resource
    Treatment of tacrolimus-related adverse effects by conversion to cyclosporine in liver transplant recipients (2000)
    Springer
    Transplant international 13 (2000), S. 73-78 
    Details
    ISSN: 1432-2277
    Keywords: Key words Tacrolimus toxicity ; Liver transplantation ; Cyclosporine conversion ; Immunosuppression side effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract When tacrolimus side effects persist despite dose reduction, conversion to cyclosporine-based immunosuppression (CyA) is necessary. We characterized tacrolimus side effects that warranted discontinuation of the drug, and outcomes after conversion. Of 388 liver recipients who received tacrolimus as primary immunosuppression, 70 required conversion to CyA. We recorded indication for conversion, whether conversion was early or late after transplantation, tacrolimus dose and trough blood level at conversion, and incidence of rejection after conversion. Conversion was early in 29 patients (41.4 %) and late in 41 (58.6 %). Indications for early conversion were neurotoxicity (20), (insulin-dependent) diabetes mellitus (IDDM) (5), nephrotoxicity (3), gastrointestinal (GI) toxicity (6), and cardiomyopathy (1), and for late conversion were neurotoxicity (15), IDDM (12), nephrotoxicity (3), GI toxicity (5), hepatotoxicity (6), post-transplant lmphoproliferate disease (PTLD) (2), cardiomyopathy (1), hemolytic anemia (1), and pruritis (1). All early-conversion patients showed improvement/resolution of symptoms. Among late-conversion patients, 37 (90.2 %) had improvement/resolution; in 4 (9.8 %), adverse effects persisted. The overall rejection rate was 30 %. Sixty-two patients (88.6 %) are alive with functioning grafts 686 ± 362 days (range, 154–1433 days) after conversion. When tacrolimus side effects are unresponsive to dose reduction, conversion to CyA can be accomplished safely, with no increased risk of rejection and excellent long-term outcome.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s001470050012
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  • 5
    Electronic Resource
    Electronic Resource
    Hemostatic problems and thromboembolic complications in nephrotic children (2000)
    Springer
    Pediatric nephrology 14 (2000), S. 138-142 
    Details
    ISSN: 1432-198X
    Keywords: Key words Nephrotic syndrome ; Antithrombin III ; Thromboembolism ; Hypercoagulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  A hypercoagulable state and the risk of thromboembolism in both arterial and venous circulation is a relatively frequent and serious feature of nephrotic syndrome (NS) in children and adults. The aim of this study was to evaluate the coagulation states of children with NS before and after corticosteroid (CS) therapy and to compare the results with a healthy control group. The first group consisted of 49 nephrotic children (30 boys and 19 girls) with a mean age of 6.5±4.9 years (range 1–16 years). The control group included 17 healthy children (9 boys and 8 girls). At the time of admission, all patients were evaluated for the presence of clinical thromboembolism, hematological and biochemical indicators of a hypercoagulative state, and renal disease. This was repeated after CS treatment. Deep vein thrombosis was observed in 2 nephrotic patients who had very low plasma antithrombin III (AT III) levels and fibrinogen levels above 750 mg/dl. Thus, the prevalence of thromboembolism was 4% in our pediatric nephrotic population. The mean AT III level of the study group was 68.2±23.4% at the onset of the disease, which was significantly lower than the level of the control group (84.0±7.6%). Plasma AT III levels increased to 74.4±15.3% after CS treatment, which correlated with the serum albumin levels. However, there was no correlation with urinary protein excretion. Protein C levels were higher than controls during all stages of the disease in both steroid-responsive and -unresponsive patients. The mean protein S level was similar in both groups. Plasma fibrinogen and cholesterol levels were significantly higher in the study group but decreased to within normal limits with remission. Our study suggests that thromboembolic complications are not infrequent in children with NS, and may be related to low plasma AT III and albumin and high fibrinogen and cholesterol levels.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004670050029
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  • 6
    Electronic Resource
    Electronic Resource
    Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children (2000)
    Springer
    Pediatric nephrology 14 (2000), S. 1111-1114 
    Details
    ISSN: 1432-198X
    Keywords: Key words Turner syndrome ; Renal malformation ; Ultrasonography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  We evaluated the frequency of renal malformations in relation to nonmosaic 45,X (group A, 45 patients, 54.9%) and mosaic/structural abnormalities of X (group B, 37 patients, 45.1%) in 82 Turkish patients with Turner syndrome (TS). Ultrasonography of the kidneys and collecting system was performed in all patients. Of the 82 patients, 31 had different renal malformations (37.8%). Horse-shoe kidney was observed in 9 (29.0%) of the 31 patients, and 17 patients (54.8%) had various collecting system malformations, while 5 (16.2%) had malrotation and other positional abnormalities. The prevalence of renal malformations was significantly higher in group A (51.1%) than group B (21.6%) (2:7.94, P〈0.05). Although 8 of the 9 patients with horse-shoe kidney had the 45,X karyotype, collecting system malformations were observed more frequently in group B. Recurrent urinary tract infections (UTIs) were detected during follow-up in 7 patients, and hypertension developed in 3 patients. In patients who had a normal baseline nephrological evaluation, no problem suggesting renal disease developed during follow-up. We conclude that all forms of TS should have routine nephrological screening on diagnosis, since structural malformations of the kidney occur more frequently in nonmosaic 45,X TS, while collecting system malformations are mostly seen in mosaic/structural X forms. Those included in the group for nephrological follow-up had an increased risk for hypertension and/or UTI.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004670000315
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  • 7
    Electronic Resource
    Electronic Resource
    Analysis of three mutations in Turkish children with Gaucher disease (1999)
    Springer
    Journal of inherited metabolic disease 22 (1999), S. 947-948 
    Details
    ISSN: 1573-2665
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1005668230365
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