Search Results - "Hacisalihoglu, Şadan"

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  1. 1

    The Development of Chylothorax in a Child With T-cell Lymphoblastic Lymphoma and Ataxia Telangiectasia During Induction Therapy by Özyörük, Derya, Güzelküçük, Zeliha, Hacisalihoglu, Şadan, Cinel, Güzin

    Published in Journal of pediatric hematology/oncology (01-03-2022)
    “…Chylothorax is an unusual complication of childhood cancer. It causes to additional morbidity and mortality during management. It should be kept in mind that…”
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    Journal Article
  2. 2

    A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to Heat by Aksu, Tekin, Yarali, Neşe, Fermo, Elisa, Marcello, Anna, Hacisalihoğlu, Şadan, Bianchi, Paola, Özbek, Namik Y

    Published in Journal of pediatric hematology/oncology (01-10-2018)
    “…Pyruvate kinase (PK) deficiency is the most common defect of the glycolytic pathway leading to congenital hemolytic anemia. We present the case of an…”
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    The Development of Chylothorax in a Child With T-Cell Lymphoblastic Lymphoma and Ataxia Telangiectasia During Induction Therapy by Özyörük, Derya, Güzelküçük, Zeliha, Hacisalihoglu, Şadan, Cinel, Güzin

    Published in Journal of pediatric hematology/oncology (23-12-2020)
    “…Chylothorax is an unusual complication of childhood cancer. It causes to additional morbidity and mortality during management. It should be kept in mind that…”
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    Journal Article
  5. 5

    Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a tremendously huge mass over the face and paraneoplastic hypercalcemia-hyperleukocytosis by Emir, Suna, Hacısalihoğlu, Şadan, Özyörük, Derya, Kaçar, Dilek, Erdem, Arzu, Karakuş, Esra

    Published in Turkish journal of pediatrics (2017)
    “…Emir S, Hacısalihoğlu Ş, Özyörük D, Kaçar D, Erdem A, Karakuş E. Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a…”
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    Journal Article
  6. 6

    Assessment of tumors in children with tuberous sclerosis: a single centre's experience by Emir, Suna, Hacısalihoğlu, Şadan, Özyörük, Derya, Ekici, Filiz, Değerliyurt, Aydan, Güven, Alev, Çetin, İlker

    Published in Turk Pediatri Arsivi (01-03-2017)
    “…As a result of mutations in TSC1 (9q34) and TSC2 (16p13.3) tumor supressor genes, the mammalian target of the rapamycin (mTor) signaling pathway is…”
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    Journal Article
  7. 7

    Prevalence and genotype distribution of rotaviruses in children with gastroenteritis in Rize province by Dereci, Selim, Çopur Çiçek, Ayşegül, Savaş Acar, Sümeyra, Bakkaloğlu, Zekiye, Özkasap, Serdar, Kanber, Kadri, Hacisalihoğlu, Şadan, Albayrak, Yücehan, Durmaz, Rıza

    Published in Bosnian journal of basic medical sciences (01-08-2015)
    “…Determination of the distribution of rotavirus genotypes is essential for understanding the epidemiology of this virus responsible for nearly half a million of…”
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    Journal Article
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    Successful treatment of multiple relapsed–refractory Langerhans cell histiocytosis with cyclosporine by Özyörük, Derya, Yozgat, Ayça Koca, Kaçar, Dilek, Yazal Erdem, Arzu, Işık, Melek, Güzelküçük, Zeliha, Hacısalihoğlu, Şadan

    Published in Tumori (01-12-2021)
    “…Langerhans cell histiocytosis is a rare hematologic disorder and patients who fail first-line treatment have a poor prognosis, and require more intensive…”
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    Journal Article
  10. 10

    Is kiwifruit allergy a matter in kiwifruit‐cultivating regions? A population‐based study by Haktanir Abul, Mehtap, Dereci, Selim, Hacisalihoglu, Sadan, Orhan, Fazil

    Published in Pediatric allergy and immunology (01-02-2017)
    “…Background Although kiwifruit is known as a common cause of food allergy, population‐based studies concerning the prevalence of kiwifruit allergy do not exist…”
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  11. 11

    Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a tremendously huge mass over the face and paraneoplastic hypercalcemiahyperleukocytosis by Emir, Suna, Hacısalihoğlu, Şadan, Özyörük, Derya, Kaçar, Dilek, Erdem, Arzu, Karakuş, Esra

    Published in Turkish journal of pediatrics (01-11-2017)
    “…Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder that results from genetic defects in DNA repair and manifests with a marked hypersensivity to…”
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    Treatment of dyskeratosis congenita with granulocyte-macrophage colony-stimulating factor and erythropoietin by ERDURAN, Erol, HACISALIHOGLU, Sadan, OZORAN, Yavuz

    Published in Journal of pediatric hematology/oncology (01-04-2003)
    “…Dyskeratosis congenita (DC) is a rare inherited disorder characterized by reticulate skin pigmentation, nail dystrophy, mucosal leucoplakia, and bone marrow…”
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  16. 16

    IN VITRO DETERMINATION OF THE APOPTOTIC EFFECT OF HEPARIN ON LYMPHOBLASTS USING DNA ANALYSIS AND MEASUREMENTS OF Fas AND Bcl-2 PROTEINS BY FLOW CYTOMETRY by Erduran, Erol, Tekelioglu, Yavuz, Gedik, Yusuf, Bekta, smail, Hacisalihoglu, Sadan

    Published in Pediatric hematology and oncology (01-07-2004)
    “…Heparin has an apoptotic effect beside its anticoagulant, anti-inflammatory, antihypertensive, and antiproliferative effects. In this study, the authors…”
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