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List of works by Majid Naderi

A Comparison of Efficacy Between Recombinant Activated Factor VII (Aryoseven) and Novoseven in Patients With Hereditary FVIII Deficiency With Inhibitor.

scientific article published on 24 October 2014

A comparison between recombinant activated factor VII (Aryoseven) and Novoseven in patients with congenital factor VII deficiency

scientific article published on 19 March 2014

A large case series on surgical outcomes in congenital factor XIII deficiency patients in Iran.

scientific article

A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasirox

scientific article published in November 2013

Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.

scientific article published on 06 December 2011

Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiency

scientific article published on 29 December 2014

Association of functional polymorphism at the miR-502-binding site in the 3' untranslated region of the SETD8 gene with risk of childhood acute lymphoblastic leukemia, a preliminary report.

scientific article published on 23 July 2014

Association of lnc-LAMC2-1:1 rs2147578 and CASC8 rs10505477 Polymorphisms with Risk of Childhood Acute Lymphoblastic Leukemia

scientific article published on November 2016

Central nervous system bleeding in pediatric patients with factor XIII deficiency: a study on 23 new cases

scientific article

Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran

scientific article published on 23 June 2015

Childhood acute lymphoblastic leukemia: refusal and abandonmentof treatment in the southeast of Iran.

scientific article published on 19 April 2016

Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency.

scientific article published on 18 September 2014

Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases

scientific article

Congenital combined deficiency of coagulation factors: a study of seven patients

scientific article published in January 2015

Congenital factor V deficiency: comparison of the severity of clinical presentations among patients with rare bleeding disorders

scientific article published on 26 September 2014

DROSHA rs642321 Polymorphism Influence Susceptibility to Childhood Acute Lymphoblastic Leukemia: A Preliminary Report

scientific article published in October 2017

Diabetes as the cause of end-stage renal disease affects the pattern of post kidney transplant rehospitalizations

scientific article published on 01 May 2007

Diagnosis of factor XIII deficiency

scientific article published on 30 March 2016

Disseminated intravascular coagulation with positive D-dimer: a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran.

scientific article

Effects of a subdermal levonorgestrel contraceptive implant (Norplant) on serum cholesterol, triglycerides, ALT and AST in Iranian women.

scientific article published on 26 August 2005

Establishment of a prenatal diagnosis schedule as part of a prophylaxis program of factor XIII deficiency in the southeast of Iran.

scientific article published on January 2016

Evaluation of functional RAGE gene polymorphisms in childhood acute lymphoblastic leukemia-A case-control study from Iran

scientific article published on 3 January 2017

Evaluation of the FXIII deficiency prophylaxis intervals in large number of FXIII deficiency patients from Iran.

scientific article

Expression and CpG island methylation pattern of MMP-2 and MMP-9 genes in patients with congenital factor XIII deficiency and intracranial hemorrhage

scientific article published on 01 December 2019

FHIT promoter DNA methylation and expression analysis in childhood acute lymphoblastic leukemia

scientific article published on 23 August 2017

Factor XIII deficiency diagnosis: Challenges and tools

scientific article published on 13 October 2017

Factor XIII deficiency in Iran: a comprehensive review of the literature.

scientific article

First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran.

scientific article published on 29 July 2015

IKZF1 gene polymorphisms increased the risk of childhood acute lymphoblastic leukemia in an Iranian population

scientific article published on 21 January 2016

Intracranial hemorrhage in congenital bleeding disorders

scientific article published on 9 September 2017

Intracranial hemorrhage pattern in the patients with factor XIII deficiency

scientific article published on 23 October 2013

Long non-coding RNA PAX8-AS1 polymorphisms increase the risk of childhood acute lymphoblastic leukemia

scientific article published on 13 December 2017

Long-term prophylaxis in patients with severe congenital factor XIII deficiency is not complicated by inhibitor formation.

scientific article published on 14 June 2016

Marital Status and Fertility in Adult Iranian Patients with β-Thalassemia Major.

scientific article published on 7 February 2015

Minimal factor XIII activity level to prevent major spontaneous bleeds: comment.

scientific article published on 4 September 2017

Miscarriage and recurrent miscarriage in patients with congenital factor V deficiency: a report of six cases in Iran

scientific article

Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran

scientific article published in June 2016

Molecular basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran

scientific article published on 21 June 2011

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

scientific article

Molecular diagnosis of factor XIII deficiency, data from comprehensive coagulation laboratory in Iran.

scientific article

Molecular genetic analysis of ten unrelated Iranian patients with congenital factor XIII deficiency.

scientific article published on 25 December 2016

Morbidity and mortality in a large number of Iranian patients with severe congenital factor XIII deficiency.

scientific article published on 22 December 2015

Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency.

scientific article published on 31 October 2013

Post-traumatic stress disorder and related factors in parents of children with cancer in South-East of iran

scientific article published on 6 December 2012

Pri-miR-34b/c rs4938723 polymorphism is associated with the risk of childhood acute lymphoblastic leukemia

scientific article published on 30 September 2016

Prolonged rehospitalizations following renal transplantation: causes, risk factors, and outcomes

scientific article published on 01 May 2007

Safety of human blood products in rare bleeding disorders in southeast of Iran ⬇️

scientific article published on December 6, 2012

The burden and management of FXIII deficiency

scientific article published on 17 July 2014

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