Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Abdolreza, Afrasiabi"'
Autor:
Ahmad Akbari, Sezaneh Haghpanah, Hamide Barzegar, Amin Shahsavani, Abdolreza Afrasiabi, Shirin Parand, Mehran Karimi
Publikováno v:
Heliyon, Vol 7, Iss 8, Pp e07734- (2021)
Background and aim: Thromboembolic events mainly occur in older age is related with high morbidity and mortality, and considerable health-care costs particularly in developing countries. Both arterial and venous thromboembolism has known risk factors
Externí odkaz:
https://doaj.org/article/60f7c10a85984fcaa855acb5fc72d896
Autor:
Javad Dehbozorgian, Abdolreza Afrasiabi, Majid Yavarian, Golam Reza Panahandeh Shahraki, Mehran Karimi, Mohammadreza Bordbar, Pier M. Mannucci
Publikováno v:
Iranian Journal of Medical Sciences, Vol 34, Iss 2, Pp 137-140 (2009)
Normal hemostasis requires balanced regulation of prothromboticand antithrombotic factors. Inherited alteration of factor Vand prothrombin gene, the G20210A mutation, increases the resistanceof factor V to degradation and booster production ofprothro
Externí odkaz:
https://doaj.org/article/2298cf8b0a234ec6af6fcc1e76235518
Autor:
Abdolreza Afrasiabi, Shirin Parand, Hamide Barzegar, Mehran Karimi, Amin Shahsavani, Sezaneh Haghpanah, Ahmad Akbari
Publikováno v:
Heliyon
Heliyon, Vol 7, Iss 8, Pp e07734-(2021)
Heliyon, Vol 7, Iss 8, Pp e07734-(2021)
Background and aim Thromboembolic events mainly occur in older age is related with high morbidity and mortality, and considerable health-care costs particularly in developing countries. Both arterial and venous thromboembolism has known risk factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eabd9ba63d8768126a28e0d590b329d
http://europepmc.org/articles/PMC8361253
http://europepmc.org/articles/PMC8361253
Publikováno v:
Journal of Family and Reproductive Health, Vol 6, Iss 3 (2012)
Objective: Pre-natal diagnosis is the most effected way to prevent genetic diseases in a society. The aim of this research was to show the prevention level of the birth of the children with major thalassemia disorder and the demographic condition of
Externí odkaz:
https://doaj.org/article/988e955b23be421fa6ef8adf655c3540
Autor:
Roberta Palla, Silvia Lavoretano, Rossana Lombardi, Isabella Garagiola, Mehran Karimi, Abdolreza Afrasiabi, Mani Ramzi, Raimondo De Cristofaro, Flora Peyvandi
Publikováno v:
Haematologica, Vol 94, Iss 2 (2009)
The inherited deficiency of ADAMTS13 is usually associated with severe forms of thrombotic thrombocytopenic purpura. Among the mutations identified in the ADAMTS13 gene, none have been described on the TSP1-6 repeat domain. We investigated an Iranian
Externí odkaz:
https://doaj.org/article/7e2bfe6d5f9547d8add3becb4e46b0ee
Autor:
Claudia Dall'Osso, Ilaria Guella, Stefano Duga, Nadia Locatelli, Elvezia Maria Paraboschi, Marta Spreafico, Abdolreza Afrasiabi, Christoph Pechlaner, Flora Peyvandi, Maria Luisa Tenchini, Rosanna Asselta
Publikováno v:
Haematologica, Vol 93, Iss 10 (2008)
Background Factor V deficiency is a rare autosomal recessive hemorrhagic disorder, associated with bleeding manifestations of variable severity. In the present study, we investigated the molecular basis of factor V deficiency in three patients, and p
Externí odkaz:
https://doaj.org/article/d710d9bb0a49475c84e52b8e27b3daa8
Publikováno v:
Haematologica, Vol 93, Iss 6 (2008)
Factor X deficiency is a severe rare hemorrhagic condition inherited as an autosomal recessive trait. It is one of the most severe recessive inherited coagulation disorders. We analyzed the clinical manifestations, laboratory phenotype and genotype i
Externí odkaz:
https://doaj.org/article/a1026022fd9248e29cd78e13adc402e6
Publikováno v:
Biosciences, Biotechnology Research Asia. 13:1259-1264
Thalassemias are heterogeneous group of inherited anemias caused by various mutations in the genes encoding the synthesis of α or β-chains of hemoglobin. It seems that there are some aspects in thalassemia that protect minor thalassemic patients fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6123436038cf19f13fe97597d52a1391
https://doi.org/10.13005/bbra/2161
https://doi.org/10.13005/bbra/2161
Autor:
Javad Dehbozorgian, Elham Javanmardi, Mohamad Moghadam, Abdolreza Afrasiabi, Seyed Javad Dehghani, Jaber Imanifard, Nazila Morshedi, Mehran Karimi, Azizollah Amiri, Somaye Montazeri, Rahimeh Asadzade, Fatemosadat Sotodegan, Zahra Saghatoleslam
Publikováno v:
Prenatal Diagnosis. 35:1238-1242
Aim The aim of this study was to evaluate the effectiveness of prenatal diagnosis (PND) for the prevention of thalassemia in Southern Iran. Methods From 2004 to 2012 1346 couples with β-thalassemia minor were referred to our center. Mutation analyse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fa74c4d1748a17c74ed131b0553a187
https://doi.org/10.1002/pd.4684
https://doi.org/10.1002/pd.4684
Autor:
Manuela Platé, Stefano Duga, M. Robusto, Flora Peyvandi, Marzia Menegatti, Ilaria Guella, Abdolreza Afrasiabi, Tahir Shamsi, Munira Borhany, Giulia Soldà, Rosanna Asselta
Publikováno v:
Thrombosis and Haemostasis. 113:567-576
SummaryFibrinogen is a plasma glycoprotein mainly synthesised by hepatocytes and circulating as a 340-kDa hexamer consisting of two sets of three different polypeptide chains (Aα, Bβ, and γ, encoded by the FGA, FGB, and FGG gene, respectively). Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::549abd0faf43f684dcf183eb4fb6371c
https://doi.org/10.1160/th14-07-0629
https://doi.org/10.1160/th14-07-0629