Search Results - "Celkan, T T"

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders by PEYVANDI, F., PALLA, R., MENEGATTI, M., SIBONI, S. M., HALIMEH, S., FAESER, B., PERGANTOU, H., PLATOKOUKI, H., GIANGRANDE, P., PEERLINCK, K., CELKAN, T., OZDEMIR, N., BIDLINGMAIER, C., INGERSLEV, J., GIANSILY‐BLAIZOT, M., SCHVED, J. F., GILMORE, R., GADISSEUR, A., BENEDIK‐DOLNIČAR, M., KITANOVSKI, L., MIKOVIC, D., MUSALLAM, K. M., ROSENDAAL, F. R.

“…Background:  The European Network of Rare Bleeding Disorders (EN‐RBD) was established to bridge the gap between knowledge and practise in the care of patients…”
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Use of hyperbaric oxygen therapy of purpura fulminans in an extremely low birth weight preterm: A case report by Yılmaz, A, Kaya, N, Meriç, R, Bayramli, Z, Öroğlu, B, Celkan, T T, Vural, M, Perk, Y

“…Purpura fulminans (PF) is a rare and fatal complication of septic shock or diffuse intravascular coagulation (DIC) resulting in skin and soft tissue necrosis…”
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Langerhans Cell Histiocytosis: Single Center Experience of 25 Years by Tuysuz, G, Yildiz, I, Ozdemir, N, Adaletli, I, Kurugoglu, S, Apak, H, Dervisoglu, S, Bozkurt, S, Celkan, T

“…To review a single center outcome of patients with Langerhans Cell Histiocytosis diagnosed at a tertiary referral hospital from Turkey.Methods: The files…”
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Reduced early prophylaxis of children with haemophilia in a developing country, Turkey by CELKAN, T., ÖZDEMIR, N.

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Deregulated WNT signaling in childhood T-cell acute lymphoblastic leukemia by Ng, O H, Erbilgin, Y, Firtina, S, Celkan, T, Karakas, Z, Aydogan, G, Turkkan, E, Yildirmak, Y, Timur, C, Zengin, E, van Dongen, J J M, Staal, F J T, Ozbek, U, Sayitoglu, M

“…WNT signaling has been implicated in the regulation of hematopoietic stem cells and plays an important role during T-cell development in thymus. Here we…”
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253 Management of Hemangiomas: A Single Center Experience by Tuysuz, G, Ozdemir, N, Kutlubay, B, Celkan, T

“…Aim To share our experience of 185 (F/M: 2.4) patients with hemangiomas followed between 2003–2011 at Cerrahpasa Medical Faculty, Istanbul. Results…”
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753 The Association of Zinc Deficiency with Iron Deficiency by Arcagok, B, Celkan, T, Ozdemir, N, Yildiz, I

“…Aim The aim of this study is to determine whether iron deficiency is associated with zinc deficiency. Methods Ninety-eight patients with ID and/or IDA and 100…”
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746 Glazmann Thrombasthenia: Single Center Experience by Kutlubay, B, Ozdemir, N, Tuysuz, G, Apak, H, Celkan, T

“…Aim Glazmann thrombasthenia is a rare autosomal recessive disease characterized by defect in platelet aggregation. Here we report the management of children…”
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Late effects of childhood ALL treatment on body mass index and serum leptin levels by Karaman, S, Ercan, O, Yildiz, I, Bolayirli, M, Celkan, T, Apak, H, Ozkan, A, Onal, H, Canbolat, A

“…It is well known that survivors of acute lymphoblastic leukemia (ALL) show a tendency to become overweight. Cranial irradiation (CRT), is considered to be the…”
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A new family with hereditary hyperferritinemia cataract syndrome by Tuysuz, G, Ozdemir, N, Sonmez, E, Kannengiesser, C, Celkan, T

“…Hereditary hyperferritinemia cataract syndrome (HHCS) is a rare disorder with an autosomal dominant trait. The disease is defined with early onset cataract and…”
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Low-dose immune tolerance induction for paediatric haemophilia patients with factor VIII inhibitors by UNUVAR, A., KAVAKLI, K., BAYTAN, B., KAZANCI, E., SAYLI, T., OREN, H., CELKAN, T., GURSEL, T.

“…The development of an inhibitor against factor VIII (FVIII) is a serious complication in children with haemophilia A. Immune tolerance induction (ITI) therapy…”
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Blue rubber bleb nevus syndrome associated with consumption coagulopathy: treatment with interferon by Apak, H, Celkan, T, Ozkan, A, Yildiz, I, Aydemir, E H, Ozdil, S, Kuruoglu, S

“…The blue rubber bleb nevus syndrome (BRBNS) is a rare vascular malformation syndrome with cutaneous and visceral lesions frequently associated with serious,…”
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Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey by Toksoy, Güven, Uludağ Alkaya, Dilek, Bagirova, Gülendam, Avcı, Şahin, Aghayev, Agharza, Günes, Nilay, Altunoğlu, Umut, Alanay, Yasemin, Başaran, Seher, Berkay, Ezgi G., Karaman, Birsen, Celkan, Tiraje T., Apak, Hilmi, Kayserili, Hülya, Tüysüz, Beyhan, Uyguner, Zehra O.

“…Fanconi anemia (FA) is a rare multigenic chromosomal instability syndrome that predisposes patients to life-threatening bone marrow failure, congenital…”
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Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N by BERBER, E., FIDANCI, I. D., UN, C., EL-MAARRI, O., AKTUGLU, G., GURGEY, A., CELKAN, T., MERAL, A., OLDENBURG, J., GRAW, J., AKAR, N., CAGLAYAN, H.

“…The most common cause for severe cases of hemophilia A is the homologous recombination involving intron 22 and related sequences outside the F8 gene. F8 coding…”
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Bacteremia in Childhood Cancer by Celkan, Tiraje, Ozkan, Alp, Apak, Hilmi, Diren, Suküfe, Can, Günay, Yuksel, Lebriz, Yildiz, Inci

“…Infection‐related mortality affects the overall survival rates of children who are receiving treatment for cancer. The leading cause of mortality is bacteremia…”
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Severe factor X deficiency treated with heparin-added prothrombin complex concentrate by Apak, H, Celkan, T, Ozkan, A, Yüksel, L, Bilgi, Z, Yildiz, I

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Defective cytotoxic lymphocyte degranulation in syntaxin-11–deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients by Bryceson, Yenan T., Rudd, Eva, Zheng, Chengyun, Edner, Josefine, Ma, Daoxin, Wood, Stephanie M., Bechensteen, Anne Grete, Boelens, Jaap J., Celkan, Tiraje, Farah, Roula A., Hultenby, Kjell, Winiarski, Jacek, Roche, Paul A., Nordenskjöld, Magnus, Henter, Jan-Inge, Long, Eric O., Ljunggren, Hans-Gustaf

“…Familial hemophagocytic lymphohistiocytosis (FHL) is typically an early onset, fatal disease characterized by a sepsislike illness with cytopenia,…”
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Tropisetron (Navoban®) in the Control of Nausea and Vomiting Induced by Combined Cancer Chemotherapy in Children by Özkan, Alp, Yildiz, Inci, Yüksel, Lebriz, Apak, Hilmi, Celkan, Tiraje

“…Background: We aimed to assess the potency and efficacy of tropisetron, a 5-HT3 receptor antagonist, in the prevention of nausea and emesis observed in the…”
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Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry by Yılmaz Karapınar, Deniz, Patıroğlu, Türkan, Metin, Ayşe, Çalışkan, Ümran, Celkan, Tiraje, Yılmaz, Barış, Karakaş, Zeynep, Karapınar, Tuba H., Akıncı, Burcu, Özkınay, Ferda, Onay, Hüseyin, Yeşilipek, Mehmet Akif, Akar, Himmet Haluk, Tüysüz, Gülen, Tokgöz, Hüseyin, Özdemir, Gül Nihal, Aslan Kıykım, Ayça, Karaman, Serap, Kılınç, Yurdanur, Oymak, Yeşim, Küpesiz, Alphan, Olcay, Lale, Keskin Yıldırım, Zuhal, Aydoğan, Gönül, Gökçe, Müge, İleri, Talia, Aral, Yusuf Ziya, Bay, Ali, Atabay, Berna, Kaya, Zuhre, Söker, Murat, Özdemir Karadaş, Nihal, Özbek, Uğur, Özsait Selçuk, Bilge, Özdemir, Hamiyet Hekimci, Uygun, Vedat, Tezcan Karasu, Gülsün, Yılmaz, Şebnem

“…Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in…”
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OC 50.3 Inhibitor Development Upon Switch After 50 EDs from Plasma-Derived to Recombinant FVIII in Pups with Severe Haemophilia A: The PUP-SWITCH Study Results by Miri, S., Rosendaal, F., Kavakli, K., Eshghi, P., Mohammadi Moghaddam, S., Elalfy, M., Halimeh, S., Gürlek Gökçebay, D., Özbek, N., Celkan, T., Mohammadi, A., Karimi, M., Yılmaz, B., Albayrak, C., Tatli Güneş, B., Kaya, Z., Ay, Y., Akbayram, S., Ören, H., Peyvandi, F.

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