Search Results - "Dorgalaleh, Akbar"

Blood Coagulation Factor XIII and Factor XIII Deficiency by Dorgalaleh, Akbar, Rashidpanah, Jamal

“…Abstract Factor XIII (FXIII) is a multifunctional pro-γ-transglutaminase that, in addition to its well-known role in haemostasis, has a crucial role in…”
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Intracranial hemorrhage in congenital bleeding disorders by Tabibian, Shadi, Motlagh, Hoda, Naderi, Majid, Dorgalaleh, Akbar

“…Intracranial hemorrhage (ICH), as a life-threatening bleeding among all kinds of congenital bleeding disorders (CBDs), is a rare manifestation except in factor…”
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Guidelines for laboratory diagnosis of factor XIII deficiency by Dorgalaleh, Akbar, Tabibian, Shadi, Hosseini, Soudabeh, Shamsizadeh, Morteza

“…Factor XIII (FXIII) deficiency is an extremely rare hemorrhagic disorder with an approximate worldwide incidence of one per two million. With current tests,…”
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Molecular Basis of Congenital Factor XIII Deficiency in Iran by Dorgalaleh, Akbar, Assadollahi, Vahideh, Tabibian, Shadi, Shamsizadeh, Morteza

“…Factor XIII deficiency (FXIIID) is an extremely rare autosomal recessive disorder that has the highest incidence in Iran. The FXIIID is primarily due to…”
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Mining of mortality-related findings in rare bleeding disorders: a retrospective study from two centers by Rafieemehr, Hassan, Dorgalaleh, Akbar, Mansouritorghabeh, Hassan

“…Rare bleeding disorders include inherited coagulation disorders except for von Willebrand disease and hemophilia A and B. These disorders affect both men and…”
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Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency by Naderi, Majid, Dorgalaleh, Akbar, Alizadeh, Shaban, Tabibian, Shadi, Hosseini, Soudabeh, Shamsizadeh, Morteza, Bamedi, Taregh

“…Factor XIII (FXIII) deficiency is a rare hemorrhagic disorder for which the highest incidence occurs in southeast Iran. The aim of this study was to assess…”
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First-time Blood Donors Are Double-edged Swords for Blood Transfusion Centers: A Retrospective Study in Southwest Iran by Niazkar, Hamid Reza, Dorgalaleh, Akbar, Rad, Fariba

“…First-time blood donors are the most common group of blood donors. They usually have different motivations for blood donation, some of which provoke the donors…”
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Prevalence of Acute Complications of Transfusion in Children with β-thalassemia Major in Southeast Iran: A Prospective Study by Ghasem Miri-Aliabad, Leila Asgarzadeh, Akbar Dorgalaleh, Mehran Bahraini

“…Background: Acute complications of transfusion are among leading causes of morbidity and mortality in chronically transfused patients. One of the main goals of…”
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Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience by Rassoulzadegan, Maryam, Ala, Fereydoun, Jazebi, Mohammad, Enayat, Mohammad Said, Tabibian, Shadi, Shams, Mahmood, Bahraini, Mehran, Dorgalaleh, Akbar

“…Type 2 von Willebrand disease (VWD) is the most common congenital bleeding disorder, with variable bleeding tendency and a complex laboratory phenotype. In the…”
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Miscarriage and recurrent miscarriage in patients with congenital factor V deficiency: a report of six cases in Iran by Naderi, Majid, Tabibian, Shadi, Shamsizadeh, Morteza, Dorgalaleh, Akbar

“…Miscarriage and recurrent miscarriage have not been reported in women with congenital factor V (FV) deficiency. Here we describe cases of both miscarriage and…”
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Bleeding and Bleeding Risk in COVID-19 by Dorgalaleh, Akbar

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The History of Factor XIII Deficiency by Dorgalaleh, Akbar

“…Despite the early discovery of factor XIII (FXIII) in 1944, the diagnosis of FXIII deficiency was not made until 1960, after all the other coagulation factor…”
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Novel Insights into Heterozygous Factor XIII Deficiency by Dorgalaleh, Akbar

“…The prevalence and clinical significance of heterozygous factor XIII (FXIII) deficiency has long been debated, with controversial reports emerging since 1988…”
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Laboratory Diagnosis of Factor XIII Deficiency in Developing Countries: An Iranian Experience by Dorgalaleh, Akbar, Tabibian, Shadi, Shams, Mahmood, Tavasoli, Behnaz, Gheidishahran, Maryam, Shamsizadeh, Morteza

“…Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with an approximately 12-times higher than the rest of the world. The International…”
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How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency by Shahraki, Hojat, Dorgalaleh, Akbar, Fathi, Majid, Tabibian, Shadi, Teimourian, Shahram, Mollanoori, Hasan, Khiabani, Alireza, Zaker, Farhad

“…Congenital factor XIII (FXIII) deficiency is an extremely rare bleeding disorder (RBD) with estimated prevalence of one per 2 million in the general…”
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The Impact of SARS-CoV-2 Infection on Blood Coagulation and Fibrinolytic Pathways: A Review of Prothrombotic Changes Caused by COVID-19 by Bahraini, Mehran, Dorgalaleh, Akbar

“…The cardinal pathology of coronavirus disease 2019 (COVID-19) is a primary infection of pulmonary tract cells by severe acute respiratory syndrome coronavirus…”
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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 by Naderi, Majid, Habibpour, Manizheh, Alizadeh, Shaban, Kashani Khatib, Zahra, Dorgalaleh, Akbar, Issah, Mohammed Awal, Naadali, Fatemeh

“…Glanzmann Thrombasthenia (GT) is a rare autosomal disease. HPA (Human Platelet Alloantigen) is a surface polymorphic alloantigen of platelets. This study was…”
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Severe Congenital Deficiency of Factor XIII: A Brief Report of Morbidity and Mortality Rates of Severe Congenital Deficiency of Factor 13 in Iran by Dorgalaleh, Akbar, Esmaeili Reykandeh, Samira, Shamsizadeh, Moreza, Tavasoli, Behnaz, Moradi, Eshagh

“…Background: Factor XIII (FXIII) deficiency is a bleeding disorder and it inherited in an autosomal recessive manner. in areas where consanguineous marriage is…”
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Anemia and thrombocytopenia in acute and chronic renal failure by Dorgalaleh, Akbar, Mahmudi, Mohammad, Tabibian, Shadi, Khatib, Zahra Kashani, Tamaddon, Gholam Hossein, Moghaddam, Esmaeil Sanei, Bamedi, Taregh, Alizadeh, Shaban, Moradi, Eshagh

“…Acute renal failure describes as a syndrome by rapid decline in the ability of the kidney to eliminate waste products, regulate acid-base balance, and manage…”
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Bilateral Maxillary, Sphenoid Sinuses and Lumbosacral Spinal Cord Extramedullary Relapse of CML Following Allogeneic Stem Cell Transplant by Hosseini, Soudabeh, Ansari, Shahla, Vosough, Parvaneh, Bahoush, Gholamreza, Hamidieh, Amir Ali, Chahardouli, Bahram, Shamsizadeh, Morteza, Mehrazma, Mitra, Dorgalaleh, Akbar

“…Isolated extramedullary relapse of chronic myelogenous leukemia (CML) after allogeneic stem cell transplant is rare. There is a case report of a child who…”
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