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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

3. Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement

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

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

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

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

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

11. Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis

13. Correction to: Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients

18. Two cases with undefined childhood interstitial lung disease: Can it be related to telomere variants?

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

21. Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country.

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

26. 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

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

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

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

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

34. First report of t(1;9)(q21;q34) in Fanconi anemia as a preceeding chromosomal aberration before leukemia development

38. 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))

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

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