Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Taregh Bamedi"'
Autor:
Taregh Bamedi, Ghazaleh Dadashizadeh, Afsaneh Sarabandi, Shadi Tabibian, Mahmood Shams, Akbar Dorgalaleh
Publikováno v:
Journal of Cellular and Molecular Anesthesia, Vol 2, Iss 1, Pp 19-23 (2017)
Inhibitor development is a lifelong challenge for patients with bleeding disorders who received replacement therapy. Most commonly, inhibitor formation was observed in hemophilia A patients but patients with rare bleeding disorders (RBD) especially p
Externí odkaz:
https://doaj.org/article/800f8c9838ef4ea7aa59302ac4d5f5d3
Autor:
Akbar Dorgalaleh, Mohammad Mahmudi, Shadi Tabibian, Zahra Kashani Khatib, Gholam Hossein Tamaddon, Esmaeil Sanei Moghaddam, Taregh Bamedi, Shaban Alizadeh, Eshagh Moradi
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 7, Iss 4 (2013)
Background: 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 water homeostasis. When this impairment is prolonged and entered chronic phase
Externí odkaz:
https://doaj.org/article/9673b4b03f1b44768df67af215363034
Publikováno v:
Hematology. 21:300-310
Hemophilia A (HA) and B (HB) are common bleeding disorders, Iran having the ninth largest such population in the world. A considerable number of studies have been performed on different aspects of their disorder.The aim of the study was to gather all
Autor:
Shadi Tabibian, Majid Naderi, Akbar Dorgalaleh, Shaban Alizadeh, Soudabeh Hosseini, Morteza Shamsizadeh, Taregh Bamedi
Publikováno v:
International Journal of Hematology. 100:443-449
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 molecular characteristics, clinical manifestations and management of life-threatening diathesi
Autor:
Zahra Kashani Khatib, Taregh Bamedi, Shadi Tabibian, Farhad Zaker, Akbar Dorgalaleh, Ahmad Kazemi, Majid Naderi, Shaban Alizadeh
Publikováno v:
Hematology. 20:112-118
Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder, which has the highest incidence in Sistan and Baluchistan Province in Iran, compared to its overall incidence around the world. This disorder has different clinical manifestations
Autor:
Dorgalaleh Akbar, Hosseini Shamsabadi Rozita, Kalantar Ebrahim, Hosseini Soudabeh, Taregh Bamedi, Hooman Nakisa
Publikováno v:
Central-European Journal of Immunology
Background: atypical hemolytic uremic syndrome (aHus), a rare disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, and acute renal failure, is associated with mutations and polymorphisms in various components and regulators
Autor:
Masumeh Jalalvand, Shadi Tabibian, Eshagh Moradi, Mansour Asadi, Sayed Ezatolla Rafiee Alavi, Morteza Shamsizadeh, Shahrzad Soori, Taregh Bamedi, Akbar Dorgalaleh
Publikováno v:
Hematology (Amsterdam, Netherlands). 22(4)
Rare bleeding disorders (RBDs) are heterogeneous disorders, mostly inherited in an autosomal recessive pattern. Iran is a Mideast country with a high rate of consanguinity that has a high rate of RBDs.In this study, we present prevalence and clinical
Autor:
Soudabeh Hosseini, Akbar Dorgalaleh, Shadi Tabibian, Aziz Rahimizadeh, Taregh Bamedi, Sharif Ebrahimi, Khanagha Tavakol, Bijan Varmaghani, Morteza Shamsizadeh, Majid Naderi, Shaban Alizadeh
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 26(8)
Factor XIII deficiency (FXIIID) is an extremely rare bleeding disorder with the highest global incidence in southeast of Iran. Southwestern Afghanistan (Nimruz Province) is located near the border with Iran in the vicinity of Sistan and Baluchestan P
Autor:
Akbar Dorgalaleh, Shaban Alizadeh, Shadi Tabibian, Peyman Eshghi, Taregh Bamedi, Majid Naderi
Publikováno v:
Gene, Cell and Tissue. 1
1Genetic Researcher Center in Non-Communicable Disease, Zahedan University of Medical Sciences, Zahedan, IR Iran2Department of Hematology, Allied Medical School, Tehran University of Medical Sciences, Tehran, IR Iran3Pediatric Congenital Hematologic
Autor:
Saeed Dorgalaleh, Shaban Alizadeh, Shadi Tabibian, Hosnie Hosseini, Meysam Kashiri, Taregh Bamedi, Esmaeil Sanei Moghaddam, Samira Esmaeili Reykande, Akbar Dorgalaleh
Publikováno v:
Thrita. 3
Background: The presence of interfering substances is the most common preanalytic factor that can affect the precision and accuracy of Blood Cell Count results. These clinical laboratory interferences are difficult to determine and are largely undere