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Item Metadata only Acquired bilateral nevoid telangiectasia syndrome with gastrointestinal involvement(John Libbey Eurotext, 2011) Turan, Hakan; Turan, Aysegul; Sarıcaoğlu, Hayriye; Başkan, Emel Bülbül; Keskin, Murat; Adım, Saduman Balaban; Tunalı, Şükran; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Gastroenteroloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.; 0000-0002-0144-3263; AAH-1388-2021; 14055302400; 6603722836; 6602518817; 23050640000; 14046617400; 7004191748Item Metadata only Acroangiodermatitis in a below-knee amputation stump(Wiley, 2011-07) Turan, Hakan; Başkan, Emel Bülbül; Adım, Şaduman Balaban; Sarıcaoğlu, Hayriye; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.; 0000-0002-0144-3263; AAH-1388-2021; 6602518817; 15730076300; 6603722836Item Metadata only Acute multiple cranial neuropathy in a patient with neurosarcoidosis(Springer-Verlag, 2010-12) Erer, Sevda Özbek; Bora, İbrahim Hakkı; Yurtoğullar, Şükran; Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı.; 25635370800; 6602914249; 35605270600Item Open Access Ailevi akdeniz ateşi ilişkili spondiloartropati ile ankilozan spondilit ayrımı(Türk Romatizma Derneği, 2012-09) Mengi, Gönen; Bingöl, Ümit; Kücükçakır, Nurten; Uludağ Üniversitesi/Tıp Fakültesi/Fiziksel Tıp ve Rehabilitasyon Anabilim Dalı.; 36570700500; 6507727900; 37117057300Item Metadata only Amniotic band syndrome associated with sacral meningocele and anal atresia(Wiley, 2010-06) Büyükyavuz, İlker; Ayata, Ali; Eren, Erdal; Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.; 0000-0002-1684-1053; AAM-1734-2020; 36113153400Item Open Access Analysis of p53 gene mutations in parapsoriasis(Wiley, 2006) Başkan, Emel Bülbül; Tunca, Berrin; Çeçener, Gülşah; Tunalı, S.; Egeli, Ünal; Sarıcaoğlu, H.; Adım, Şadıman Balaban; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.; 0000-0002-0144-3263; 0000-0001-7904-883X; 0000-0002-1619-6680; AAH-1388-2021; AAH-1420-2021; ABI-6078-2020; 6602518817; 9280090300; 49762870600; 7004191748; 49762749200; 6603722836; 49762661900The histological diagnosis of the initial stages of Mycosis Fungoides (MF) have not yet been established by exact morphological criteria.1 The borderline between parapsoriasis and MF is not clear due to non-specific changes in the early stages of MF. The underlying molecular changes which may occur during progression or transition from parapsoriasis and early MF to advanced stages have not yet been clarified either.2 However, abnormalities of cell cycle control genes and well-defined tumour suppressor genes may contribute to the disease pathogenesis and progression. The p53 gene plays an important role in the control of cell death and proliferation, inducing cell cycle arrest and/ or apoptosis in response to various cellular stress, and alterations of the p53 gene are commonly associated with malignant transformation.3 The p53 gene mutations, one of the most common genetic alterations in human cancers, have been described in several types of haemato logic malignancies.4 By contrast, only a few studies have focused on p53 abnormalities in various categories of T-cell lymphomas and to the best of our knowledge, parasoriasis has not been studied so far.5–10 Studies of p53 protein expression in primary cutaneous T-cell lymphoma have shown to be increased in the late stages of the dis ease. This prompted us to investigate the incidence of p53 gene mutations in parapsoriasis and its role in the pathogenesis.Item Open Access Antioxidant treatment in dialysis patients - importance of ferritin(Oxford Univ Press, 2006) Ersoy, Alpaslan; Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji Anabilim Dalı.; 0000-0002-0710-0923; AAH-5054-2021; 35612977100Sir, Cardiovascular disease remains one of the leading causes of mortality in haemodialysis (HD) patients. Abnormal oxidative stress and impaired antioxidant defence may contribute to accelerated atherogenesis associated with uraemia. I read with interest the article by Fumeron et al. [1], reporting that short-term oral vitamin C supplementation did not modify well-defined oxidative/antioxidative stress and inflammation markers in HD patients. As stated, they did not evaluate the effect of long-term intravenous vitamin C supplementation with lower or higher doses on oxidative stress, nor the efficacy of co-administration of vitamin E. Iron is a powerful oxidizing substance. Ferritin may have other functions in addition to its well-described role in storing intracellular iron. Elevated ferritin levels are associated with an increased risk of atherosclerotic coronary artery disease and myocardial infarction. Recent proteomics and molecular biology studies have shown that ferritin levels in arteries are increased in diseased tissues [2]. Ferritin may be unregulated under particular physiological conditions and may act as a pro-oxidant. In the mammalian cell, iron stored in ferritin can participate in initiating lipid peroxidation [3]. High levels of serum ferritin may indicate iron overload. However, in many patients results may be elevated due to inflammation, even if iron stores are not increased. Limited evidence shows that elevated iron stores and high-dose intravenous iron therapy may increase morbidity and mortality in HD patients [4], and exacerbate increased oxidative stress in uraemic patients [5].Item Metadata only Ascaris-induced eosinophilic myocarditis presenting as acute ST elevation myocardial infarction and cardiogenic shock in a young woman(Lippincott Williams & Wilkins, 2012-03) Şentürk, Tunay; Özdemir, Bülent; Keçebaş, Mesut; Beşli, Feyzullah; Yeşilbursa, Dilek; Serdar, Osman Akın; Uludağ Üniversitesi/Tıp Fakültesi/Kardiyoloji Anabilim Dalı.; AAF-5116-2019; C-1517-2017; 8342098300; 7004168959; 36198369900; 35767335000; 6603558686; 6507416315Item Metadata only Awake intubation through the CTrach in the presence of an unstable cervical spine(Wiley, 2006-05) Bilgin, Hülya; Yılmaz, C.; Uludağ Üniversitesi/Tıp Fakültesi.; 0000-0001-6639-5533; A-7338-2016; 6701663354; 57225285006Item Metadata only A "biomarker biopsy" for the diagnosis of NASH: Promises from CK-18 fragments(Springer, 2008-11) Yılmaz, Yusuf; Ulukaya, Engin; Dolar, Enver; Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Gastroenteroloji Anabilim Dalı.; 0000-0003-4518-5283; AAG-9177-2021; K-5792-2018; K-6651-2012; 22936014300; 6602927353; 6602075084Item Metadata only Borrelial lymphocytoma cutis successfully treated with intralesional interferon-alpha-2A(Wiley, 2006-09) Aydoğan, Kenan; Karadoğan, S. Koran; Adım, Şaduman Balaban; Tunalı, S.; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.; 0000-0002-0193-1128; AAH-6216-2021; 9739755800; 14047086200; 14046617400; 7004191748Scrofuloderma is increasingly being recognized as themost common form of cutaneous tuberculosis in adults.2,3It results from contiguous involvement of the skinoverlying tuberculosis in a deeper structure, mostcommonly a lymph node, bone, joint or epididymis.2 Bothour patients had cervical glands disease, which is the mostcommon site of involvement in scrofuloderma.4 It haspreviously been suggested that cervical gland involve-ment in tuberculosis may be related to consumption ofunpasteurized milk, leading to infection of the tonsils andsubsequently of the cervical lymph glands by Mycobacte-rium bovis.5 Our patients admitted to boiling milk beforeconsumption.The incidence of systemic tuberculosis in children withcutaneous tuberculosis has been noted to be between21.2%5 and 26%.6 The incidence of systemic involvementin adults with scrofuloderma has been found to be as highas 35%.2 There was no evidence of systemic tuberculosisin our patients. DNA polymerase chain reaction andBACTEC are the ideal techniques for the diagnosis ofcutaneous tubercular infections, but their availability andcosts are major limitations.6 We failed to find any reportin literature indicating a particular genetic predispositionto cutaneous tuberculosis. But the occurrence of a specificform of cutaneous tuberculosis in these siblings mayindicate activity of a common genetically mediatedimmunological pathway.Item Metadata only Bortezomib and extramedullary disease in multiple myeloma: The shine and dark side of the moon(Pergamon-Elsevier Science, 2007-08) Ali, Rıdvan; Özkalemkaş, Fahir; Özkan, Atilla; Özkocaman, Vildan; Özçelik, Tülay; Ozan, Ülkü; Uludağ Üniversitesi/Tıp Fakültesi/Hematoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Radyasyon Onkoloji Anabilim Dalı.; AAG-8495-2021; AAH-1854-2021; 7201813027; 6601912387; 9250698600; 6603145040; 7005424333; 6507254632; 8843050600; 6602797853Item Metadata only Calcinosis cutis universalis with pediatric systemic lupus erythematosus(Springer, 2010-07) Dönmez, Osman; Durmaz, Oğuzhan; Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.; AAA-8778-2021; 19033971800; 14025426300Item Open Access Carcinoid tumor within Meckel's diverticulum causing gastrointestinal bleeding(Aves, 2009-06) Sözer, Muhsin; Horhorlu, Fevzi; Öztürk, Ersin; Altınel, Yüksel; Yılmazlar, Tuncay; Uludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı.; AAL-9231-2020; 35070171400; 26657125600; 6701800362The most common complications of Meckel’s diverticulum, which affects approximately 2% of the general population, are bleeding, intestinal obstruction and diverticulitis (1). Bleeding is usually the result of ileal mucosal ulceration that occurs due tumor occurring within a Meckel’s diverticulum is even more uncommon and is usually an incidental finding at surgery or autopsy (3, 4).Item Metadata only A case of advanced scalp angiosarcoma successfully treated with combination chemotherapy of adriamycin, cisplatin and ifosfamide(Elsevier, 2006-06) Özet, Ahmet; Ataergin, S.; Arpacı, F.; Özturk, Bülent; Arpacı, Fikret; Öztürk, M.; Komürcü, S.; Kuzhan, O.; Kanat, O.; Uludağ Üniversitesi/Tıp Fakültesi.; 6602187347Scalp angiosarcoma is a rare and highly malignant tumour originating from endothelial cells of vessels and occurring predominantly in elderly men. Its prognosis is poor and the 5-year survival rate of patients is reported to be 12–33% [1]. Complete surgical excision with wide margins remains the cornerstone of therapy for localised tumours. Additional radiotherapy may provide improved local control. Given the rarity of this tumour, an optimum chemotherapy regimen has not yet been defined for metastatic cases. Here we report a case of scalp angiosarcoma with local recurrence and distant metastases which was successfully treated with a combination chemotherapy consisting of adriamycin, cisplatin, ifosfamide and mesna (APIM). A 24-year-old man presented to a plastic surgeon in January 2005 with a painless nodule on the scalp measuring 3 cm in diameter. Surgical total excision of the nodule was carried out, providing a negative surgical margin (2 cm). The diagnosis of angiosarcoma was confirmed pathologically. An X-ray of the scull, magnetic resonance imaging of the brain and computed tomography of the neck, thorax and abdomen revealed no evidence of local or distant metastases at the time of diagnosis. The patient was not given any adjuvant therapy. Five months after the surgery, the patient developed two new angiosarcoma lesions (1.5 and 2 cm in diameter) on different sites of the scalp. In addition, computed tomography of the neck and chest revealed conglomerate lymph nodes on the left side of the neck and five small metastatic nodules, up to 1.5 cm greatest dimension in bilateral lung fields.Item Metadata only A case of generalized granuloma annulare with myelodysplastic syndrome: Successful treatment with systemic isotretinoin and topical pimecrolimus 1% cream combination(Wiley, 2007-05) Başkan, Emel Bülbül; Turan, Ayşegül; Tunalı, Şükran; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; 0000-0002-0144-3263; 6602518817; 14055302400; 7004191748Item Metadata only A case of granuloma annulare in a child following tetanus and diphtheria toxoid vaccination(Wiley, 2005-09) Başkan, Emel Bülbül; Tunalı, Şükran; Kaçar, Seval Doǧruk; Adım, Şaduman Balaban; Sarıcaoğlu, Hayriye; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.; 0000-0002-0144-3263; AAH-1388-2021; 6602518817; 7004191748; 55394051200; 15730076300; 9739878100Item Metadata only A case of partial facial duplication(Wiley, 2005) Kılıç, Nizamettin; Yavaşçaoğlu, Belgin; Yeşilyurt, A.; Doğruyol, Hasan; Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Anesteziyoloji ve Reanimasyon Anabilim Dalı.; AAI-7914-2021; AAI-3656-2021; 7005266570; 6602742300; 55763894700; 7003752033Item Metadata only A case of Sjogren-Larsson syndrome(Wiley, 1999) Sarıcaoğlu, Hayriye; Tunalı, Şükran; Bülbül, Emel; Alpakut, Şebnem; Özmen, Ahmet Tuncer; Okan, Mehmet; Palalı, Zeki; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Göz Hastalıkları Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Nöroloji Anabilim Dalı.; 6603722836; 7004191748; 6507149072; 6506017477; 57215467446; 6701707256; 6602430771Item Metadata only A case of syringocystadenoma papilliferum: An unusal localization on postoperative scar(Wiley, 2002-10-02) Sarıcaoğlu, Hayriye; Başkan, Emel Bülbül; Özuysal, Sema; Tunalı, Şükran; Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabiilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.; 0000-0002-0144-3263; AAH-1388-2021; 6603722836; 6602518817; 56616314600; 7004191748