Yazar "Yaman, Yöntem" için listeleme
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A child with a severe headache: Answers
Telhan, Leyla; Beğenik, Murat; Yaman, Yöntem; Yavaşcan, Önder (Springer Science and Business Media Deutschland GmbH, 2021)1) What is your suspected diagnosis of acute severe headache in this patient? We report here an adolescent girl who presented with severe headache while receiving acute sinusitis treatment and was found to have bilateral ... -
A child with a severe headache: Questions
Telhan, Leyla; Beğenik, Murat; Yaman, Yöntem; Yavaşcan, Önder (Springer, 2021)A 12-year-old girl presented with complaint of severe headache lasting 10 days, nausea and vomiting for 1 day. The headache was localized in the right fronto-occipital region with spread to the neck and shoulders. In her ... -
Chronic neutropenia in childhood: Laboratory and clinical features
Nepesov, Serdar; Yaman, Yöntem; Elli, Murat; Bayram, Nihan; Özdilli, Kürşat; Ayaz, Akif; Anak, Sema (Springer India, 2022)Objectives To describe the clinical characteristics of patients with chronic neutropenia. Methods Data of 36 patients with chronic neutropenia, who were followed up in the authors' clinic between May 2013 and May 2020, ... -
Clinical efficacy of ruxolitinib monotherapy and haploidentical hematopoeitic stem cell transplantation in a child with philadelphia chromosome-like relapsed/refractory acute lymphoblastic leukemia
Bayram, Nihan; Yaman, Yöntem; Özdilli, Kürşat; Telhan, Leyla; Nepesov, Serdar; Bilgen, Hülya; Elli, Murat; Behar, Sude Sema; Anak, Sema (Wiley, 2021)Introduction (Ph-like) ALL is a subset of leukemia which has a gene expression profile similar to Ph+disease, but without the presence of BCR-ABL1 translocation. Case description We reported an exceptional case of a ... -
Clinical, genetic, and outcome characteristics of pediatric patients with primary hemophagocytic lymphohistiocytosis
Nepesov, Serdar; Yaman, Yöntem; Elli, Murat; Bayram, Nihan; Özdilli, Kürşat; Kıykım, Ayça; Çakır, Deniz; Kılıç, Betül; Aydın, Kürşad; Ayaz, Akif; Telhan, Leyla; Anak, Sema (AVES, 2022)Objectİive: In this study, we sought to describe the clinical, laboratory, and genetic characteristics of patients diagnosed with primary hemophagocytic lymphohistiocytosis. Thus, we aimed to evaluate the early diagnosis ... -
Different kinetics and risk factors for isolated extramedullary relapse after allogeneic hematopoietic stem cell transplantation in children with acute leukemia
Hazar, Volkan; Öztürk, Gülyüz; Yalçın, Koray; Uygun, Vedat; Aksoylar, Serap; Küpesiz, Alphan; Ok Bozkaya, İkbal; Karagün, Barbaros Şahin; Bozkurt, Ceyhun; İleri, Talia; Atay, Didem; Koçak, Ülker; Tezcan Karasu, Gülsün; Yeşilipek, Akif; Gökçe, Müge; Kansoy, Savaş; Tüysüz Kintrup, Gülen; Karakükcü, Musa; Okur, Fatma Visal; Ertem, Mehmet; Kaya, Zühre; Gürsel, Orhan; Yaman, Yöntem; Özbek, Namık; Antmen, Bülent; Tüfekçi, Özlem; Albayrak, Canan; Adaklı Aksoy, Başak; Sezgin, Gülay; Albayrak, Davut; Sezgin Evim, Melike; Zengin, Emine; Pekpak, Esra (Elsevier Science Inc., 2021)Relapse after allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the most frequent cause of post-transplantation mortality. Isolated extramedullary (EM) relapse (iEMR) after HSCT is relatively rare and ... -
Durable remissions in TCF3-HLF positive acute lymphoblastic leukemia with blinatumomab and stem cell transplantation
Mouttet, Brice; Vinti, Luciana; Ancliff, Philip; Bodmer, Nicole; Brethon, Benoit; Cario, Gunnar; Chen-Santel, Christiane; Elitzur, Sarah; Hazar, Volkan; Kunz, Joachim; Moericke, Anja; Stein, Jerry; Vora, Ajay; Yaman, Yöntem; Schrappe, Martin; Anak, Sema; Baruchel, Andre; Locatelli, Franco; von Stackelberg, Arend; Stanulla, Martin; Bourquin, Jean-Pierre (Ferrata Storti Foundaition, 2019)TCF3-HLF-positive leukemia represents a rare subtypeof childhood acute lymphoblastic leukemia (ALL), characterized by a high rate of treatment failure despite treatment intensification and allogeneic stem cell transplantation ... -
Eltrombopag for treatment of thrombocytopenia after allogeneic hematopoietic cell transplantation in children: Single-centre experience
Yaman, Yöntem; Elli, Murat; Şahin, Şifa; Özdilli, Kürşat; Bilgen, Hülya; Bayram, Nihan; Nepesov, Serdar; Anak, Sema (Wiley, 2021)Delayed recovery of thrombocytopenia is a well-known complication after allogeneic HSCT. Eltrombopag (ELT), a thrombopoietin receptor agonist (TRAs), induces platelet maturation and release. Mostly conducted in adults, ... -
Eltrombopag use for post hematopoetic stem cell transplantation thrombocytopenia in pediatric patients
Elli, Murat; Yaman, Yöntem; Özdilli, Kürşat; Bilgen, Hülya; Çakır, Aslı; Şahin, Şifa; Anak, Sema (Nature Publishing Group, 2019)... -
Evaluation of the demographic and clinical findings of pediatric patients that developed acute graft-versus-host disease after allogeneic hematopoietic stem cell
Yüksel, Mavişe; Yaman, Yöntem; Elli, Murat (2020)Aim: Acute graft-versus-host disease (GVHD) is an complication after allogeneic hematopoietic stem cell transplantation (alloHSCT), manifesting with an erythematous maculopapular rash followed by liver disease and dysfunctions ... -
Graft-versus-host disease in a child with neuroblastoma after autologous stem cell transplantation
Yaman, Yöntem; Baysoy, Gökhan; Keleşoğlu, Emre; Özdilli, Kürşat; Çakır, Aslı; Genç, Dildar Bahar; Elli, Murat; Anak, Sema (Termedia Publishing House Ltd, 2019)In the pediatric population, hematopoietic stem cell transplantation (HSCT) is used to treat a wide variety of diseases, both malignant and nonmalignant. For many of these diseases, HSCT is a well-established treatment. ... -
Hematopoietic stem cell transplantation in patients with severe combined immunodeficiency: A single-center experience
Nepesov, Serdar; Yaman, Yöntem; Elli, Murat; Bayram, Nihan; Özdilli, Kürşat; Kıykım, Ayça; Anak, Sema (Istanbul University, 2022)Objective: The aim of this study was to determine the factors affecting outcomes in patients who underwent hematopoietic stem cell transplantation (HSCT) with the diagnosis of severe combined immunodeficiency (SCID). ... -
HLA - matched related donor hematopoietic stem cell transplantation in a patient with polynucleotide kinase 3-phosphatase mutation developed acute myeloid leukemia
Bayram, Nihan; Yaman, Yöntem; Elli, Murat; Özdilli, Kürşat; Nepesov, Serdar; Doğan, Mehmet Sait; Ayaz, Akif; Anak, Sema (Wiley, 2022)Background PNPK gene mutations result in DNA repair disorders and have a spectrum of neurodevelopmental manifestations. To date, cancer predisposition has not been described in patients with PNKP mutations. Observation ... -
Hodgkin lenfoma nüks ve/veya kemoterapi dirençli olgularda hematopoetik kök hücre nakli ve yüksek doz kemoterapi: Tek merkez deneyimi
Yaman, Yöntem; Elli, Murat; Özdilli, Kürşat; Telhan, Leyla; Bayram, Nihan; Hazar, Volkan; Tuprul Sarıbeyoğlu, Ebru; Şahin, Şifa; Anak, Sema (İstanbul Üniversitesi, 2021)Giriş: Standart tedavi alan Hodgkin Lymphoma (HL) hastalarının yaklaşık %20’sinde hastalık dirençli seyredebilir veya tekrar edebilir. Tekrar eden/ dirençli HL’da standart tedavi yüksek doz kemoterapi ve takip eden otolog ... -
Inflammatory bowel disease and guillain barre syndrome in FCHO1 deficiency
Aydemir, Sezin; İşlek, Ali; Nepesov, Serdar; Yaman, Yöntem; Baysoy, Gökhan; Beşer, Ömer Faruk; Çullu Çokuğraş, Fügen; Barış, Safa; Karakoç Aydıner, Elif; Çokuğraş, Haluk; Hubrack, Satanay Z.; Kendir Demirkol, Yasemin; Lo, Bernice; Kıykım, Ayça; Özen, Ahmet (Springer, 2021)To the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, ... -
Investigation of beta globin gene mutations in Syrian refugee patients with thalassemia major
Çevirici, Hatice; Acıpayam, Can; Yenilmez, Ebru Dündar; Belen, Fatma Burcu; Pekpak, Esra; Yaman, Yöntem; Tuli, Abdullah (De Gruyter, 2019)Objectives: This study, detection of beta globin gene mutations in thalassemia major patients who migrated from Syria to Kahramanmaraş region were planned. Materials and methods: The study included 35 Syrian national beta ... -
Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: A rare case report
Yaman, Yöntem; Köker, Sultan Aydın; Ayhan, Fahri Yüce; Genel, Ferah; Acıpayam, Can; Oymak, Yeşim; Sarıbeyoǧlu, Ebru Tuǧrul; Vergin, Canan Raziye (Termedia Publishing House Ltd., 2019)Leukocyte adhesion deficiency type II (LAD II) is a rare, autosomal, recessive inherited immunodeficiency disease that induces frequent and recurrent infections, persistent leukocytosis, severe mental and growth retardation, ... -
Mesenchymal stem cell therapy for steroid refractory acute graft versus host disease
Anak, Sema; Yaman, Yöntem; Özdilli, Kürşat; Bilgen, Hülya; Sarıbeyoğlu, Ebru Tuğrul; Hazar, Volkan; Ayman, Fatma Nur; Elli, Murat (Nature Publishing Group, 2019)...