Search Results - "Özdemir, Hamiyet Hekimci"

Aplastic Anemia Frequency and Management in Pediatric Liver Transplantations Due to Non-A-E Hepatitis by Kıran Taşcı, Ezgi, Karakoyun, Miray, Özdemir Karadaş, Nihal, Hekimci Özdemir, Hamiyet, Yılmaz Karapınar, Deniz, Karaca, Can, Çetin, Funda, Aydoğdu, Sema

“…Hepatitis-associated aplastic anemia (HAAA) is a rare complication that presented with bone marrow failure after acute hepatitis. HAAA usually occurs in…”
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Congenital Neutropenia Patient With Hypomorphic Biallelic CSF3R Mutation Responding to GCSF by Yilmaz Karapinar, Deniz, Akinci, Burcu, Şahin Yaşar, Akkiz, Hekimci Özdemir, Hamiyet, Önder Siviş, Zuhal, Onay, Hüseyin, Özkinay, Ferda

“…Congenital neutropenia (CN) is a rare disorder, and the most common gene responsible for CN is ELANE. Furthermore, the mutations of HAX1, G6PC3, and JAGN1…”
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Extranodal Ocular Adnexal Marginal Zone Lymphoma in a Ten-Year-Old Child by Çetingül, Nazan, Palamar, Melis, Hacıkara, Şükriye, Kamer, Serra, Hekimci Özdemir, Hamiyet, Ataseven, Eda, Barut Selver, Özlem, Hekimgil, Mine

“…A 10-year-old girl was brought to the clinic with the complaint of a salmon-colored conjunctival lesion for 1 month. With the aid of histopathological…”
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Fertility in Patients with Thalassemia and Outcome of Pregnancies: A Turkish Experience by Akıncı, Burcu, Yaşar, Akkız Şahin, Özdemir Karadaş, Nihal, Önder Siviş, Zuhal, Hekimci Özdemir, Hamiyet, Yılmaz Karapınar, Deniz, Balkan, Can, Kavaklı, Kaan, Aydınok, Yeşim

“…In recent years, the rates of marriage and pregnancy are increasing in patients with thalassemia major. The aim of the present study was to investigate the…”
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Retrospective Evaluation of Childhood Cutaneous Mastocytosis Cases by Akinci, Burcu, Ozdemir, Hamiyet Hekimci, Karadas, Niha L. Ozdemir, Yasar, Akkiz Sahin, Sivis, Zuha L. Onder, Aydinok, Yesim, KavakLi, Kaan, Balkan, Can, Karapinar, Deniz YiLmaz

“…Aim: Mastocytosis is a rare disease characterized by clonal mast cell proliferation in one or more organs. It can lead to different clinical manifestations and…”
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Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study by Demir, Derya, Hekimgil, Mine, Karaca, Emin, Ulusoy, Yusuf, Özdemir, Hamiyet Hekimci, Saydam, Güray, Durmaz, Burak, Akın, Haluk, Çetingül, Nazan, Tombuloğlu, Murat, Özsan, Nazan

“…Myeloid sarcoma (MS) is a rare tumour comprising myeloid blasts occurring at an anatomical site other than the bone marrow. We sought to investigate both…”
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Therapeutic plasma exchange in critically ill children: A single center experience by Yazici Özkaya, Pinar, Koç, Gülizar, Ersayoğlu, İrem, Cebeci, Kübra, Hekimci Özdemir, Hamiyet, Karadas, Nihal, Yilmaz Karapinar, Deniz, Karapinar, Bülent

“…Introduction Therapeutic plasma exchange (TPE) is used in a wide spectrum of diseases in critically ill pediatric patients. We aim to review the indications,…”
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The effect of chemotherapy on symptoms and nutritional status in children with cancer by Özalp Gerçeker, Gülçin, Yildirim, Büşra Güliz, Arıcıoğlu Sülün, Ayşe, Bektaş, Murat, Hekimci Özdemir, Hamiyet, Malbora, Barış

“…This observational study carried out to determine the incidence of poor nutritional status and symptom burden in children undergoing chemotherapy treatment…”
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Current childhood chronic myeloid leukemia management under tyrosine kinase inhibitor treatment by Karadaş, Nihal, Göktepe, Şerife Şebnem Önen, Baş, İlke, Ece, Dilek, Özdemir, Hamiyet Hekimci, Balkan, Can, Kavaklı, Kaan, Aydinok, Yeşim, Karapinar, Deniz Yilmaz

“…Chronic myeloid leukemia (CML) is very rare during childhood. Tyrosine kinase inhibitors (TKI) provide very good results in terms of survival. The medical…”
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Management of a Patient With Congenital Biallelic CSF3R Mutation With GM-CSF by Yilmaz Karapinar, Deniz, Özdemir, Hamiyet Hekimci, Akinci, Burcu, Yaşar, Akkiz Şahin, Siviş, Zuhal Önder, Onay, Hüseyin, Özkinay, Ferda

“…Severe Congenital Neutropenia (SCN) is a rare inherited disease characterized by an absolute neutrophil count (ANC) lower than 500/μL. Genetic heterogeneity…”
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Primary Mold-Active Antifungal Prophylaxis Decreases the Need for Chest Computed Tomography Scans in Patients with Acute Lymphoblastic Leukemia by Karadaş, Nihal, Özdemir, Hamiyet Hekimci, Yilmaz, Yeşer, Göktepe, Şebnem Önen, Ece, Dilek, Karapinar, Deniz Yilmaz

“…Current guidelines recommend computed tomography (cCT) scans of the chest in children with leukemia following 96 h of the onset of idiopathic neutropenia to…”
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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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Influence of Paroxysmal Nocturnal Hemoglobinuria Clone Positivity on Outcome of Childhood Acquried Aplastic Anemia: A Multicenter Center Study by Unal Cangul, Sule, Yilmaz Karapinar, Deniz, Yazal Erdem, Arzu, Yarali, Husniye Nese, Hekimci Ozdemir, Hamiyet, Gumruk, Fatma, Cakmakli, Hasan Fatih, Unal Ince, Elif, Ozdemir, Gul Nihal Nihal, Gokce, Muge, Celkan, Tiraje, Bahadir, Aysenur, Bayhan, Turan, Oren, Hale, Gulen, Huseyin, Tayfun Kupesiz, Funda, Cetin, Mualla, Ozbek, Namik

“…Introduction: Paroxysmal nocturnal hemoglobinuria(PNH) in the classical hemolytic form is rare among childhood and children may present with aplastic anemia…”
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Immunodeficiency in a Child with Alström Syndrome by Ozdemir, Taha Resid, Karaca, Neslihan Edeer, Marshall, Jan Davis, Kutukculer, Necil, Aksu, Guzide, Ozgul, Riza Koksal, Ozanturk, Aysegul, Isik, Esra, Akgun, Bilcag, Ozdemir, Hamiyet Hekimci, Darcan, Sukran, Ozkinay, Ferda, Cogulu, Ozgur

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Hemofagositik lenfohistiyositoz hastalarında kraniyal MRG bulguları by ERASLAN, Cenk, AYDIN, Elçin, MAHARRAMOVA, Eltan, ŞAHİN, Akkız, HEKİMCİ ÖZDEMİR, Hamiyet, YILMAZ KARAPINAR, Deniz, ÇALLI, Cem, KİTİŞ, Ömer

“…Amaç: Hemofagositik lenfohistiyositoz (HLH) kontrolsüz immün yanıta yol açan hiperinflamasyonla karakterize klinik bir sendromdur. Etiyolojiye bağlı primer ve…”
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Immunodeficiency in a Child with Alström Syndrome by Ozdemir, Taha Resid, Karaca, Neslihan Edeer, Marshall, Jan Davis, Kutukculer, Necil, Aksu, Guzide, Ozgul, Riza Koksal, Ozanturk, Aysegul, Isik, Esra, Akgun, Bilcag, Ozdemir, Hamiyet Hekimci, Darcan, Sukran, Ozkinay, Ferda, Cogulu, Ozgur

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