258 results on '"Ünal, Ekrem"'
Search Results
2. Evaluation of primary care physicians’ approaches to hemophilia and bleeding disorders: a questionnaire survey
3. 30 Years of Wilms Tumor Experience at One Center in Türkiye’s Central Anatolia Region
4. Hepatitis-associated aplastic anemia in pediatric patients: single center experience
5. A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant.
6. Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition
7. Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
8. The influence of RANKL/osteoprotegerin on the prognosis of childhood acute lymphoblastic leukemia
9. Microfluidic Chip based direct triple antibody immunoassay for monitoring patient comparative response to leukemia treatment
10. Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
11. Evaluation of primary care physicians’ approaches to hemophilia and bleeding disorders: a questionnaire survey
12. 30 Years of Wilms Tumor Experience at One Center in Türkiye's Central Anatolia Region.
13. Rare Coagulation Factor Deficiencies: Multicenter Experience With 188 Cases.
14. Inherited Bone Marrow Failure Syndromes in Children
15. Hepatosplenic Fungal Infections in Children With Leukemia—Risk Factors and Outcome: A Multicentric Study
16. Significance of CD49f in diagnosis of minimal residual disease in pediatric acute leukemia.
17. Etiological Factors of Opsoclonus Myoclonus Ataxia Syndrome: A Single Center Experience with Eight Children
18. Intracranial hemorrhage in children with hemophilia
19. Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment
20. A pilot study for treatment of severe COVID-19 pneumonia by aerosolized formulation of convalescent human immune plasma exosomes (ChipEXO™)
21. The Significance of soluble CD40 and CD40 ligand levels in childhood acute lymphoblastic leukemia patients
22. Triosephosphate isomerase deficiency in an infant
23. Comprehensive approach to hemophilia
24. A Novel Loss of Function Variant of SLC19A1 Presented with Immunodeficiency and Benefited from Folinic Acid Treatment
25. The effect of methylenetetrahydrofolate reductase polymorphisms on the methotrexate toxicity in children with acute lymphoblastic leukemia
26. Hemophagocytic lymphohistiocytosis: pouring gasoline on the cytokine storm
27. Social exclusion and behavior problems in adolescents with cancer and healthy counterparts
28. The Mutation of CD27 Deficiency Presented With Familial Hodgkin Lymphoma and a Review of the Literature
29. A Fatal Case of Familial Hemophagocytic Lymphohistiocytosis Associated with Fusarium Infection and Rare Mutation.
30. Novel variant detected in the FAS gene of a patient with Autoimmune Lymphoproliferative Syndrome
31. The Mutation of CD27 Deficiency Presented With Familial Hodgkin Lymphoma and a Review of the Literature
32. Nanopartikül İçermeyen Biyouyumlu Malzemelerle Yapılmış Kan İtici Süperhidrofobik Yüzeyler
33. EVALUATION OF CLINICAL AND LABORATORY CHARACTERISTICS OF CHILDREN WITH RHABDOID TUMOR: A MULTICENTER STUDY
34. Therapeutic effects of vitamin D and IL-22 on methotrexate-induced mucositis in mice
35. L-Asparaginase accociated acute pancreatitis in children with acute lymphoblastic leukemia
36. Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia
37. Transplantation for ultra high-risk neuroblastoma patients: effect of tandem autologous stem cell transplantation
38. The spectrum of underlying diseases in children with autoimmune hemolytic anemia
39. Single-center experience of childhood Hodgkin lymphoma treated without radiotherapy
40. Immunodeficiency associated with a novel functionally defective variant of SLC19A1benefits from folinic acid treatment
41. CHANGES IN MUCOSA-ASSOCIATED INVARIANT T CELLS (MAIT), ASSOCIATED CYTOKINES, AND MR-1+ CELL NUMBER AND PHENOTYPE IN THE PERIPHERAL BLOOD OF PEDIATRIC ITP PATIENTS WITH AND WITHOUT ELTROMBOPAG THERAPY
42. Type 2B Von Willebrand Disease Mimicking Autoimmune Thrombocytopenia in the Neonatal Period
43. Two pediatric cases of gastric adenocarcinoma and review of the literature
44. Type 2B Von Willebrand Disease MimickingAutoimmune Thrombocytopenia in the Neonatal Period
45. Impact of Intrauterine Growth Restriction Diseases on The Umbilical Cord Blood CD34+ Cell Counts
46. Turkish Pediatric Oncology Group Neuroblastoma 2009 Protocol Low Risk Group Treatment Results
47. Rare Diseases in Children Focusing on Pediatric Immunology & Neurology
48. Rare Diseases in Children: Focusing on Rare Diseases Pediatric Hematology, Oncology
49. Rare Diseases in Children: Focusing on Rare Diseases Pediatric Immunolgy, Neurology
50. Focusing on Rheumatology & Gastroenterology & General Pediatrics
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