Repository of Research and Investigative Information

Repository of Research and Investigative Information

Zahedan University of Medical Sciences

Items where Author is "Alizadeh, S."

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Number of items: 32.

Article

(2019) Expression and CpG island methylation pattern of MMP-2 and MMP-9 genes in patients with congenital factor XIII deficiency and intracranial hemorrhage. Hematology. pp. 601-605. ISSN 1024-5332

(2018) 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. Int J Hematol Oncol Stem Cell Res. pp. 43-48. ISSN 2008-3009 (Print) 2008-2207

(2016) Childhood acute lymphoblastic leukemia: refusal and abandonment of treatment in the southeast of Iran. Turkish Journal of Medical Sciences. pp. 706-711. ISSN 1300-0144

(2016) DETERMINATION OF FACTOR II CODONS GENOTYPE IN SOUTH EAST IRANIAN PATIENTS WITH HEREDITARY DEFICIENCY OF FACTOR II. Thrombosis Research. S36-S36. ISSN 0049-3848

(2016) DETERMINATION OF FACTOR X CODONS GENOTYPE IN PATIENTS WITH HEREDITARY DEFICIENCY OF FACTOR X IN SOUTH EAST IRANIAN POPULATION. Thrombosis Research. S36-S36. ISSN 0049-3848

(2016) Establishment of a prenatal diagnosis schedule as part of a prophylaxis program of factor XIII deficiency in the southeast of Iran. Blood Coagulation & Fibrinolysis. pp. 97-100. ISSN 0957-5235

(2015) Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiency. Hematology. pp. 487-492. ISSN 1024-5332

(2015) Central nervous system bleeding in pediatric patients with factor XIII deficiency: A study on 23 new cases. Hematology. pp. 112-118. ISSN 1024-5332

(2015) Congenital Factor V Deficiency: Comparison of the Severity of Clinical Presentations among Patients with Rare Bleeding Disorders. Acta Haematologica. pp. 148-154. ISSN 0001-5792

(2015) Congenital combined deficiency of coagulation factors: a study of seven patients. Blood Coagulation & Fibrinolysis. pp. 59-62. ISSN 0957-5235

(2015) Effect of Social Factors on the Highest Global Incidence of Congenital Factor XIII Deficiency in Southeast of Iran. Archives of Iranian Medicine. p. 331. ISSN 1029-2977

(2015) Factor XIII Deficiency in Iran: A Comprehensive Review of the Literature. Seminars in Thrombosis and Hemostasis. pp. 323-329. ISSN 0094-6176

(2015) First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran. Blood Coagulation & Fibrinolysis. pp. 908-911. ISSN 0957-5235

(2015) Inhibition of factor XIIa, a new approach in management of thrombosis. Ann Transl Med. S20. ISSN 2305-5839 (Print) 2305-5839

(2015) Long Term Prophylaxis in Patients with Severe Congenital Factor XIII Deficiency is Not Complicated With Inhibitor Formation. Haemophilia. p. 23. ISSN 1351-8216

(2015) Prophylaxis Refusal And Life Threatening Complications In Patients With Severe Factor XIII Deficiency In South East Of Iran. Haemophilia. p. 74. ISSN 1351-8216

(2014) Assessment the quality of life in children with factor XIII deficiency in Southeast of Iran. Haemophilia. p. 87. ISSN 1351-8216

(2014) Clinical Manifestations and Bleeding Episodes Among Heterozygote Individuals of Factor XIII Deficiency, a Short Term Prospective Study. Blood. p. 3. ISSN 0006-4971

(2014) Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency. International Journal of Hematology. pp. 437-443. ISSN 0925-5710

(2014) Clinical manifestations and therapeutic response to recombinant factor VII in patients with glanzmann thrombasthenia. Haemophilia. pp. 83-84. ISSN 1351-8216

(2014) Congenital factor V deficiency, comparison the severity of clinical presentations among patients with rare bleeding disorders. Haemophilia. p. 107. ISSN 1351-8216

(2014) Long term two central follow up study on a large group of patients with congenital factor XIII deficiency treated prophylactically with Fibrogammin P (R). Haemophilia. p. 107. ISSN 1351-8216

(2014) Molecular analysis, clinical manifestations and management of factor XIII deficiency in Southeast of Iran. Haemophilia. p. 108. ISSN 1351-8216

(2014) Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency. Haemophilia. E89-E92. ISSN 1351-8216

(2014) Public Health Problems related to factor V deficiency in southeast of Iran. Med J Islam Repub Iran. p. 27. ISSN 1016-1430 (Print) 1016-1430

(2014) This Is a Title : Long Term succsesfull Prophylaxis in 190 Patients with Severe Congenital Factor XIII Deficiency, a Four Years Experience. Here Is the Sub-Title: Succsefull Prophylaxis in Factor XIII Deficiency. Blood. p. 3. ISSN 0006-4971

(2013) Anemia and thrombocytopenia in acute and chronic renal failure. Int J Hematol Oncol Stem Cell Res. pp. 34-9. ISSN 2008-3009 (Print) 2008-2207

(2013) Effect of social factors on high prevalence of factor XIII deficiency in southeast Iran. Journal of Thrombosis and Haemostasis. pp. 1161-1162. ISSN 1538-7933

(2013) POLYMORPHISM OF THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR AND RISK OF INTRACRANIAL HEMORRHAGE IN FACTOR XIII DEFICIENCY. Haematologica. p. 743. ISSN 0390-6078

(2013) A Prospective Study of Tubular Dysfunction in Pediatric Patients with Beta Thalassemia Major Receiving Deferasirox. Pediatric Hematology and Oncology. pp. 748-754. ISSN 0888-0018

(2013) Safety of human blood products in rare bleeding disorders in southeast of Iran. Haemophilia. e90-e92. ISSN 1351-8216

(2012) Prophylactic Program in fxiii Deficient Patients From Iran. Blood. p. 1. ISSN 0006-4971

This list was generated on Sun Mar 29 16:06:06 2020 +0430.