Lista de obras - Akbar Dorgalaleh - Dominio Público Uruguay

A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency

artículo científico publicado en 2019

A Unique Factor XIII Mutation in Southeastern Iran with an Unexpectedly High Prevalence: Khash Factor XIII

artículo científico publicado en 2019

A large deletion, spanning exons 1 to 25 of F8 gene, and a high-titer factor VIII inhibitor, in severe hemophilia A

artículo científico publicado en 2020

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

artículo científico publicado en 2013

A retrospective study on clinical manifestations of neonates with FXIII-A deficiency

artículo científico publicado en 2019

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

artículo científico publicado en 2014

Bilineal Acute Leukemia Associated With Fanconi Syndrome: The First Case Report

artículo científico publicado en 2016

Blood coagulation factor XIII and factor XIII deficiency

artículo científico publicado en 2016

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

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2014

Comparison of 2 Methods of Clot Solubility Testing in Detection of Factor XIII Deficiency.

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Correlation of bleeding score with frequency and severity of bleeding symptoms in FXIII deficiency assessing by the ISTH Bleeding Assessment Tool

scientific article published on 09 July 2019

Diagnosis of factor XIII deficiency

artículo científico publicado en 2016

Diagnosis, clinical manifestations and management of rare bleeding disorders in Iran.

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Do congenital bleeding disorders have a protective effect against COVID-19? A prospective study

artículo científico publicado en 2020

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

artículo científico publicado en 2016

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

Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation

artículo científico publicado en 2019

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

First-time Blood Donors Are Double-edged Swords for Blood Transfusion Centers: A Retrospective Study in Southwest Iran

scientific article published on 02 September 2019

Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19-A common clinical feature between a rare disorder and a new, common infection

artículo científico publicado en 2020

Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population

artículo científico publicado en 2015

Guidelines for laboratory diagnosis of factor XIII deficiency

artículo científico publicado en 2015

Hemophilia A in Afghanistan, the first report

artículo científico publicado en 2019

Hemophilia in Iran.

artículo científico publicado en 2016

Hemostasis critical values among Iranian clinical laboratories "National Survey of 157 Clinical Laboratories"

artículo científico publicado en 2019

Inherited Platelet Function Disorders (IPFDs).

artículo científico publicado en 2017

Inhibition of factor XIIa, a new approach in management of thrombosis

artículo científico publicado en 2015

Inhibitor development in patients with congenital factor VII deficiency, a study on 50 Iranian patients

artículo científico publicado en 2019

International Council for Standardization in Haematology (ICSH) laboratory guidance for the evaluation of haemostasis analyser-reagent test systems. Part 1: Instrument-specific issues and commonly used coagulation screening tests

artículo científico publicado en 2020

Intracranial Hemorrhage: A Devastating Outcome of Congenital Bleeding Disorders-Prevalence, Diagnosis, and Management, with a Special Focus on Congenital Factor XIII Deficiency.

artículo científico publicado en 2017

Intracranial hemorrhage in congenital bleeding disorders

artículo científico publicado en 2017

Laboratory Diagnosis of Factor XIII Deficiency in Developing Countries: An Iranian Experience

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Molecular Basis of Congenital Factor XIII Deficiency in Iran

artículo científico publicado en 2016

Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience

artículo científico publicado en 2020

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico

Persistent hiccups in a patient with mild congenital factor V deficiency and COVID-19; clinical and laboratory finding of a rare bleeding disorder

artículo científico publicado en 2020

Pharmacological management of rare coagulation factor deficiencies besides hemophilia

artículo científico publicado en 2020

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

artículo científico publicado en 2013

Prenatal diagnosis in rare bleeding disorders-An unresolved issue?

artículo científico publicado en 2018

Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.

artículo científico publicado en 2016

Standardization of Prothrombin Time/International Normalized Ratio (PT/INR)

scientific article published on 26 September 2020

The Effect of Demographic Factors and VKORC1 1639 G>A Genotypes on Estimated Warfarin Maintenance Dose in Iranian Patients Under Warfarin Therapy

scientific article published on 01 August 2018

Lista de obras de Akbar Dorgalaleh

A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency

A Unique Factor XIII Mutation in Southeastern Iran with an Unexpectedly High Prevalence: Khash Factor XIII

A large deletion, spanning exons 1 to 25 of F8 gene, and a high-titer factor VIII inhibitor, in severe hemophilia A

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

A retrospective study on clinical manifestations of neonates with FXIII-A deficiency

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

Bilineal Acute Leukemia Associated With Fanconi Syndrome: The First Case Report

Blood coagulation factor XIII and factor XIII deficiency

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

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

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

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

Comparison of 2 Methods of Clot Solubility Testing in Detection of Factor XIII Deficiency.

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

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

Correlation of bleeding score with frequency and severity of bleeding symptoms in FXIII deficiency assessing by the ISTH Bleeding Assessment Tool

Diagnosis of factor XIII deficiency

Diagnosis, clinical manifestations and management of rare bleeding disorders in Iran.

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

Do congenital bleeding disorders have a protective effect against COVID-19? A prospective study

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

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

Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation

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

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

First-time Blood Donors Are Double-edged Swords for Blood Transfusion Centers: A Retrospective Study in Southwest Iran

Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19-A common clinical feature between a rare disorder and a new, common infection

Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population

Guidelines for laboratory diagnosis of factor XIII deficiency

Hemophilia A in Afghanistan, the first report

Hemophilia in Iran.

Hemostasis critical values among Iranian clinical laboratories "National Survey of 157 Clinical Laboratories"

Inherited Platelet Function Disorders (IPFDs).

Inhibition of factor XIIa, a new approach in management of thrombosis

Inhibitor development in patients with congenital factor VII deficiency, a study on 50 Iranian patients

International Council for Standardization in Haematology (ICSH) laboratory guidance for the evaluation of haemostasis analyser-reagent test systems. Part 1: Instrument-specific issues and commonly used coagulation screening tests

Intracranial Hemorrhage: A Devastating Outcome of Congenital Bleeding Disorders-Prevalence, Diagnosis, and Management, with a Special Focus on Congenital Factor XIII Deficiency.

Intracranial hemorrhage in congenital bleeding disorders

Laboratory Diagnosis of Factor XIII Deficiency in Developing Countries: An Iranian Experience

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

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

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

Molecular Basis of Congenital Factor XIII Deficiency in Iran

Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience

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

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

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

Persistent hiccups in a patient with mild congenital factor V deficiency and COVID-19; clinical and laboratory finding of a rare bleeding disorder

Pharmacological management of rare coagulation factor deficiencies besides hemophilia

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

Prenatal diagnosis in rare bleeding disorders-An unresolved issue?

Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.

Standardization of Prothrombin Time/International Normalized Ratio (PT/INR)

The Effect of Demographic Factors and VKORC1 1639 G>A Genotypes on Estimated Warfarin Maintenance Dose in Iranian Patients Under Warfarin Therapy