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Autor:
Mohammad Jazebi, Seyedeh Somayeh Moazezi Nekoei Asl, F. Ala, Nazanin Baghaipour, Shadi Tabibian, Mohammad Reza Baghaipour, Gholam Reza Bahoush, Akbar Dorgalaleh, Mehran Bahraini
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 27(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2376c08c73b326737c2a642798e1c05
https://pubmed.ncbi.nlm.nih.gov/33550685
https://pubmed.ncbi.nlm.nih.gov/33550685
Autor:
Shadi Tabibian, Mahboobe Mohamadamini, Akbar Dorgalaleh, Gholam Reza Bahoush, Seyedeh Somayeh Moazezi Nekoei Asl, Mohammad Reza Baghaipour, Alireza Azizi Saraji, Tahmineh Salimi, F. Ala, Mohammad Jazebi
Publikováno v:
Transfusion and Apheresis Science. 60:103212
Background Prophylaxis the current standard care for patients with severe hemophilia should be planned to optimize the replacement therapy and minimize bleeding. We report our single-center experience of tailored prophylaxis in children affected by h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6247346aef95b9961e5269c9e9f6b998
https://doi.org/10.1016/j.transci.2021.103212
https://doi.org/10.1016/j.transci.2021.103212
Autor:
Gholamreza Bahoush, Shadi Tabibian, Mohammad Jazebi, Seyed Esmaeil Ahmadi, Mohammad Reza Baghaipour, F. Ala
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis
Congenital combined bleeding disorders (CBDs) are extremely rare disorders which mainly occur in regions with a high rate of consanguineous marriage. These disorders can present with a variety of symptoms ranging from mucocutaneous bleeding to life-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c444b6dc0ac8b4da71376e1bb87489a
https://doi.org/10.1177/1076029621996813
https://doi.org/10.1177/1076029621996813
Autor:
Noshahr, F. Ala1 fatemehala@rocketmail.com, Rafat, A.1
Publikováno v:
Iranian Journal of Applied Animal Science. Dec2014, Vol. 4 Issue 4, p887-890. 4p.
Autor:
Noshahr, F. Ala1 fatemehala@rocketmail.com, Rafat, A.1
Publikováno v:
Iranian Journal of Applied Animal Science. Jun2014, Vol. 4 Issue 2, p331-334. 4p.
Autor:
Reinhard Schneppenheim, Tobias Obser, U. Budde, Mohammad Jazebi, Sonja Schneppenheim, M. S. Enayat, F. Ala, M. Rassoulzadegan, S. Ravanbod
Publikováno v:
Haemophilia. 19:e261-e264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5571b08d34a7b4e981510b2b62e3af7c
https://doi.org/10.1111/hae.12161
https://doi.org/10.1111/hae.12161
Publikováno v:
Haemophilia. 18:e340-e346
In Haemophilia A (HA), the deficiency in coagulation factor VIII is caused by mutations in the F8 gene. In the past, HA carrier detection in Iran used to be carried out by tracking polymorphic DNA markers - a technical strategy with poor efficacy and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0c4af757cc56ef918a77ee96ec19ffb
https://doi.org/10.1111/j.1365-2516.2011.02708.x
https://doi.org/10.1111/j.1365-2516.2011.02708.x
Autor:
Akbar Dorgalaleh, Shadi Tabibian, Mahmood Shams, Behnaz Tavasoli, F. Ala, Rima Manafi, Gholamreza Bahoush, Mohammad Jazebi, Mohammad Reza Baghaipour
Publikováno v:
Annals of Blood. 3:4-4
von Willebrand disease (VWD) is the most common inherited bleeding disorder, and is classified into quantitative (type 1 and type 3) and qualitative (type 2) defects. The bleeding tendency is variable among affected patients, ranging from an asymptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::088a4d17af835302c1fc99051168b933
https://doi.org/10.21037/aob.2018.01.01
https://doi.org/10.21037/aob.2018.01.01
Publikováno v:
Haemophilia. 15:1097-1103
Summary. Hepatitis C virus (HCV) infection is a major cause of morbidity and mortality in patients with inherited bleeding disorders. The results of interferon and ribavirin combination therapy have been reported in a limited number of clinical trial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e004bf6d82af60808cf83e864312a58b
https://doi.org/10.1111/j.1365-2516.2009.02042.x
https://doi.org/10.1111/j.1365-2516.2009.02042.x