Paper Details

Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Congenital Factor Xi Deficiency, Complete Genotype and Phenotype of Two Iranian Families

Zahra Kashanikhatib

Zahra Kashanikhatib

Assistant Professor of Laboratory Hematology and Blood Banking

Department Hematology

School of Allied Medical Sciences

Tehran University of Medical Sciences

Related Documents

1. Expression and Cpg Island Methylation Pattern of Mmp-2 and Mmp-9 Genes in Patients With Congenital Factor Xiii Deficiency and Intracranial Hemorrhage, Hematology (United Kingdom) (2019)

2. Central Nervous System Bleeding in Pediatric Patients With Factor Xiii Deficiency: A Study on 23 New Cases, Hematology (2015)

All Documents

1. Expression and Cpg Island Methylation Pattern of Mmp-2 and Mmp-9 Genes in Patients With Congenital Factor Xiii Deficiency and Intracranial Hemorrhage, Hematology (United Kingdom) (2019)

2. Study of the Relationship Between Hpa-1 and Hpa-5 Gene Polymorphisms and Refractory to Platelet Therapy and Recombinant Factor Vii in Glanzmann Thrombasthenia Patients in Southeast of Iran, International Journal of Hematology-Oncology and Stem Cell Research (2018)

3. Upregulation of Mir-210 Promotes Differentiation of Mesenchymal Stem Cells (Mscs) Into Osteoblasts, Bosnian Journal of Basic Medical Sciences (2018)

4. The Role of Micrornas in Myeloproliferative Neoplasia, International Journal of Hematology-Oncology and Stem Cell Research (2016)

5. Central Nervous System Bleeding in Pediatric Patients With Factor Xiii Deficiency: A Study on 23 New Cases, Hematology (2015)

6. Relationship Between the Matrix Metalloproteinases and the Occurrence of Central Nervous System Bleeding in Factor Xiii Deficiency, Journal of Isfahan Medical School (2015)