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263 results on '"Unal, Sule"'

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1. Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia.

2. Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

4. HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia

5. A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

6. Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy

7. Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients

11. Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

12. Edoxaban for Thromboembolism Prevention in Pediatric Patients With Cardiac Disease

13. Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

14. Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

16. HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia

17. HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia

18. HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia

19. Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients

20. Erratum: Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy (The American Journal of Human Genetics (2021) 108(7) (1301–1317), (S0002929721001877), (10.1016/j.ajhg.2021.05.003))

25. Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients

26. Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients—A Single-Center Experience in Genetic Diagnosis

28. Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

34. Double-Blind, Randomized Study of Canakinumab Treatment in Pediatric and Young Adult Patients with Sickle Cell Anemia

36. Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

37. The European Hematology Association Roadmap for European Hematology Research: a consensus document

41. Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias

43. Diamond-Blackfan Anemia Phenotype Caused By Deficiency of Adenosine Deaminase 2

47. Infant Lymphoblastic Leukemia: A Single Center Experience

48. THE GLYCOCALYX AND TRAUMA

49. Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1.

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