Deniz YILMAZ KARAPINAR
Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı
Araştırma alanları: Sağlık Bilimleri, Tıp, Dahili Tıp Bilimleri, Çocuk Sağlığı ve Hastalıkları, İç Hastalıkları, Hematoloji, Pediatrik Hematoloji, Onkoloji, Tıbbi Genetik, Temel Bilimler
Yayınlar
- Real-world outcomes and safety of colistin therapy in children with multidrug-resistant gram-negative infections: a nine-year experience (2026)
- Comparison of Left Atrial Strain Parameters After Doxorubicin Therapy in Pediatric Patients With Leukemia and Healthy Children: A Cross-Sectional Case–Control Study (2026)
- Transfusional Iron Overload in Children With Leukemia (2026)
- The silent struggle of nurses caring for children battling leukemia: An in-depth examination of compassion fatigue (2026)
- Shifting Towards Empagliflozin First‐Line Therapy in Glycogen Storage Disease Type Ib: A Nationwide Real‐World Study (2026)
- Outcomes of down syndrome-related myeloid leukemia in Turkiye: a multicenter retrospective observational cohort study by the Turkish Pediatric Hematology Association (2026)
- A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency (2025)
- Severe hypercholesterolemia in a pediatric cohort: Familial homozygous and autosomal recessive hypercholesterolemia (2025)
- Konjenital Nötropeni ve Periodontal Hastalıklar: Bağlantılar, Riskler ve Yönetim (2025)
- Sequential serum galactomannan as outcome marker for invasive aspergillosis—An exploratory study from the FungiScope registry (2025)
- MALIGNANCY IN FANCONI APLASTIC ANEMIA; SINGLE CENTER EXPERIENCE (2025)
- A FAMILY WITH MYSM1 MUTATION (2025)
- False Positive Peripheral Blood Cultures in Children with Leukaemia: A Descriptive Retrospective Prevalence Study (2025)
- A Multicenter, Retrospective Study Comparing Immunosuppressive Therapy Combined with Eltrombopag to Immunosuppressive Therapy Alone as Front-Line Treatment for Pediatric Severe Aplastic Anemia (2025)
- Therapeutic plasma exchange in critically ill children: A single center experience (2024)
- Protein Network Alterations in G‐CSF Treated Severe Congenital Neutropenia Patients and Beneficial Effects of Oral Health Intervention (2024)
- Evaluation of thrombosis and bleeding events in the children with left ventricular assist device (L-VAD) (2024)
- COVID ‐19 disease in patients with chronic neutropenia: The experience from the European Network for Innovative Diagnosis and Treatment of Chronic Neutropenias (2024)
- Family Knowledge, Attitudes, and Practices Toward Severe Congenital Neutropenia (2023)
- Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections (2023)
- Invasive Fungal Infections in Children With Acute Myeloid Leukemia: A Single-center Experience Over 19 Years (2023)
- The Diagnostic Accuracy of Serum Galactomannan Assay in Children with Acute Myeloid Leukemia: Effect of the Revised EORTC/MSGERC 2020 Criteria (2023)
- Central nervous system thrombosis in pediatric acute lymphoblastic leukemia in Turkey: A multicenter study (2023)
- P779: LONG-TERM COURSE OF HAX1-RELATED CONGENITAL NEUTROPENIA: AN ANALYSIS OF THE EUROPEAN SEVERE CHRONIC NEUTROPENIA INTERNATIONAL REGISTRY (SCNIR) (2023)
- Primary Mold-Active Antifungal Prophylaxis Decreases the Need for Chest Computed Tomography Scans in Patients with Acute Lymphoblastic Leukemia (2023)
- Diagnostic Accuracy of Serum Galactomannan Assay in Children with Acute Myeloid Leukemia: Effect of the Revised EORTC/ MSGERC 2020 Criteria (2023)
- Current childhood chronic myeloid leukemia management under tyrosine kinase inhibitor treatment (2022)
- Akut Miyeloid Lösemili Çocuklarda Serum Galactomannan Testinin Tanısal Doğruluğu: Revize Edilmiş EORTC/MSGERC 2020 Kriterlerinin Etkinliği (2022)
- Modern Iron Chelation Management of Thalassemia Major Patients Guided by MRI techniques: Real-world Data From a Long-term Cohort Study (2022)
- Correction to: Modern management of iron overload in thalassemia major patients guided by MRI techniques: real‑world data from a long‑term cohort study (2022)
- Central Nervous System Fungal Infections in Children With Leukemia and Undergoing Hematopoietic Stem Cell Transplantation: A Retrospective Multicenter Study (2022)
- Clinical features and prognostic factors of Magnusiomyces (Saprochaete) infections in haematology. A multicentre study of SEIFEM/Fungiscope (2022)
- Hematuria in Patients with Congenital Coagulation Factor Deficiencies (2022)
- Assessment of Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia: A Multicenter Study From Turkey (2022)
- ÇOCUKLUK ÇAĞINDA OLGULARLA AKUT LÖSEMİLER (2021)
- ÇOCUK HEMATOLOJİ VE ONKOLOJİDE NUTRİSYON BÜLTENİ (2021)
- Lösemiye Sekonder Hemofagositik Lenfohistiyositoz ve Sonrasında AML Geliştiren Bir Olgu (2021)
- Akut Lenfoblastik Lösemide Nadir Bir Komplikasyon; Korsakoff Sendromu (2021)
- FUSARİUM ENFKSİYONU GELİŞEN AML TANILI BİR OLGU (2021)
- FUSARİUM ENFKSİYONU GELİŞEN AML TANILI BİR OLGU (2021)
- LÖSEMİLİ ÇOCUKTA NUTRİSYONEL YAKLAŞIM (2021)
- Antifungal prophylaxis with voriconazole significantly decreases the need for chest ct evaluation in patients with Acute Lymphoblastic Leukemi?a: single center experience (2021)
- A novel ganciclovir desensitization protocol for a pediatric patient: A case report (2021)
- Is Monitoring of Cytomegalovirus Disease Required in Nontransplant Pediatric Acute Lymphoblastic Leukemia? (2021)
- ÇOCUKLUK ÇAĞINDA OLGULARLA AKUT LÖSEMİLER (2021)
- ÇOCUKLUK ÇAĞINDA OLGULARLA AKUT LÖSEMİLER (2021)
- VORICONAZOLE PROPHYLAXIS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA (2021)
- THE EVALUATION OF CONGENITAL NEUTROPENIA PATIENTS (2021)
- TALASEMİ MAJORDA SERUM FERRİTİN EĞİLİMLERİ VE MR İLE DOKU DEMİR DİNAMİKLERİ İLİŞKİSİNİN UZUN SÜRELİ İZLEMİ (2021)
- Familyal Hemofagositik Lenfohistiyositoz Olgularının Değerlendirilmesi: Türk Pediatrik Hematoloji Derneği Histiyositoz Alt Çalışma Grubu Çok Merkezli Çalışması (2021)
- TREATMENT OF CHRONIC MYELOID LEUKEMIA IN CHILDREN WITH TYROSIN KINASE INHIBITORS (2021)
- Families’ Knowledge, Attitudes and Practices Toward Severe Congenital Neutropenia (2021)
- Hepatitis-Associated Aplastic Anemia: Etiology, Clinical Characteristics and Outcome (2021)
- Kronik Myeloid Lösemide Tirozin Kinaz İnhibitörünün Kesilmesi Mümkün Mü? (2021)
- Akut Myeloblastik Lösemi Hastalarının Değerlendirilmesi (2021)
- A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia. (2021)
- Is Monitoring of Cytomegalovirus Disease Required in Nontransplant Pediatric Acute Lymphoblastic Leukemia? (2021)
- Cerebral sinovenous thrombosis in children: A single-center experience (2021)
- Aplastic Anemia Frequency and Management in Pediatric Liver Transplantations Due to Non-A-E Hepatitis (2021)
- Çocukluk çağı akut lenfoblastik lösemide FISH yöntemi ile kromozomal yeniden düzenlenmelerin tespiti (2020)
- Is Normal Growth and Development Achieved By Current Management Approaches to Thalassemia Major in the New Era? (2020)
- Management of a Patient With Congenital Biallelic CSF3R Mutation With GM-CSF (2020)
- Retrospective Evaluation of Childhood Cutaneous Mastocytosis Cases (2020)
- Hyponatremia in Children with Acute Lymphoblastic Leukemia (2020)
- Rapid Detection of Specific Gram-negative Microorganisms Causing Bloodstream Infections in Children with the Microarray Method (2020)
- Çocukluk Çağı Lösemilerinde Geç Dönem Endokrin Komplikasyonlar (2019)
- Konjenital hemolitik anemi ve hipogammaglobulinemi ile prezente olan TRNT1 hastalığı (2019)
- Reflections of Yoga on Quality of Life Physical Status In Pediatric Oncology Nurses (2019)
- 2. Retrospektif analysis of thrombosisi and bleeding events in children with implanted ventricle assist device. Ulger Z, Elibol P, Karapınar DY. Engin C. 53rd Annual Meeting of the Association for European Paediatric and CongenitalCardiology (AEPC) Fibes–Conference and Exhibition Centre, Seville, Spain May 15–18, 2019. Cardiology in the Young Volume 29 supplement1. Page 89 (2019)
- Can Serial Measurement Enhance the Diagnostic Value of Procalcitonin as a Marker of Gram-negative Bacteremia in Children with Acute Leukemia? (2019)
- Hepatosplenic Fungal Infections in Children With Leukemia—Risk Factors and Outcome: A Multicentric Study (2019)
- Reflections of Yoga on Quality of LifePhysical Status In Pediatric Oncology Nurses (2019)
- Coexistence of Gaucher Disease and severe congenital neutropenia (2019)
- Venrikül Destek Cihazı Implante Edilen Çocuk Hastalarda Tromboz Ve Kanama Olaylarının Retrospektif Olarak Değerlendirilmesi. (2019)
- Congenital Neutropenia Patient With Hypomorphic Biallelic CSF3R Mutation Responding to GCSF (2019)
- 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 (2019)
- Epidemiology and survival of childhood cancers in Ege University Hospital (2019)
- Ege Üniversitesi Hastanesi çocukluk çağı tümörlerinde epidemiyoloji ve sağ kalım özellikleri (2019)
- Fertility in Patients with Thalassemia and Outcome of Pregnancies: a Turkish Experience (2019)
- Dilşah (2018)
- Shwachman-Diamond Sendromuna Neden Olan SBDS geni Mutasyon Spektrumu (2018)
- A Review of a Diagnostic Tool: Galactomannan (2018)
- AKUT LÖSEMİ OLGULARINDA C-KİT GEN MUTASYON SPEKTRUMU (2018)
- SHWACHMAN-DİAMOND SENDROMUNA NEDEN OLAN SBDSGENİ MUTASYON SPEKTRUMU (2018)
- Can Serial Measurement Enhance the Diagnostic Value of Procalcitonin as a Marker of Gram-Negative Bacteremia in Children with Acute Leukemia? (2018)
- Seronegatif Fulminan Hepatit Nedeniyle Karaciğer Nakli Yapılan Hastalarda Hepatit İlişkili Aplastik Anemi İnsidansı (2018)
- PEDİATRİK AKUT LÖSEMİLERDE FLT3 GEN ANALİZİNİN ÖNEMİ (2018)
- PEDİATRİK AKUT LÖSEMİLERDE FLT3 GEN ANALİZİN ÖNEMİ (2018)
- The management of menorrhagia in Von Willebrand Disease: Single center experience (2018)
- Stevens-Johnson Syndrome associated with methotrexate treatment for acutelymphoblastic leukemia: a case report (2018)
- Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndrome (2018)
- Hemofagositik lenfohistiyositoz hastalarında kraniyal MRG bulguları. (2018)
- LOW DOSE IMMUNE TOLERANCE INDUCTION APPROACH FOR HEMOPHILIA WITH INHIBITORS (2017)
- Anemik Hastaya Yaklaşım (2017)
- Lökomoid Reaksiyon Nedeniyle İzlenen 4 Olgu (2017)
- Pansitopeni ve Nötropeni (2017)
- LENFOPROLİFERATİF HASTALIK (2017)
- X’ e bağlı immün yetmezlik-poliendokrinopati (IPEX) fenotipinde başvuran ve yeni tanımlanan LRBA defekti saptanan 2 kardeş olgu (2017)
- X-LINKED IMMUNODEFICIENCY-POLYENDOCRINOPATHY-ENTEROPATHY (IPEX)-LIKE PHENOTYPE DUE TO LRBA MUTATIONS IN TWO SIBLINGS (2017)
- Treatment Options of Menorrhagia in Patients With Von Willebrand Disease (2017)