Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Soudabeh, Hosseini"'
Autor:
Azita Tavasoli, Khadije Arjmandi Rafsanjani, Saba Hemmati, Marziyeh Mojbafan, Elham Zarei, Soudabeh Hosseini
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Manganese is a critical trace element that not only has antioxidant properties, but also is essential for various metabolic pathways and neurotransmitters production. However, it can be toxic at high levels, particularly in the ce
Externí odkaz:
https://doaj.org/article/27010929c87b44c9b3dcb3e2e2081938
Autor:
Mahsa Ahmadi, Ali Dehghanifard, Alireza Isazadeh, Saba Hajazimian, Mahshad Mehdizadeh, Shiva Rahaei, Soudabeh Hosseini, Ebrahim Kalantari
Publikováno v:
Acta Medica Iranica, Vol 56, Iss 5 (2018)
MYO7A is an unconventional myosin that is essential for ordinary hearing and vision; mutations in the MYO7A gene result in Usher syndrome type 1B and other disorders. In this manuscript, we reported a mutation (c.4705delA) in exon 35, causing the alt
Externí odkaz:
https://doaj.org/article/f0c677c6b87c408e92069cc2cec96e90
Autor:
Majid Naderi, Shadi Tabibian, Maryam Sadat Hosseini, Shaban Alizadeh, Soudabeh Hosseini, Hossein Karami, Hassan Mahmoodi Nesheli, Akbar Dorgalaleh
Publikováno v:
Journal of Pediatrics Review, Vol 2, Iss 2, Pp 31-46 (2014)
Rare bleeding disorders (RBDs) are a heterogeneous group of disorders including different types of coagulation factor deficiencies. The disorders are inherited in an autosomal recessive manner with different frequencies varying from 1:500000 to 1:200
Externí odkaz:
https://doaj.org/article/ffd2f18c9ee2440fb0f7a83bb5b09da3
Autor:
Soudabeh Hosseini, Shahla Ansari, Parvaneh Vosough, Gholamreza Bahoush, Morteza Shamsizadeh, Mitra Mehrazma, Akbar Dorgalaleh
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 10, Iss 2 (2016)
Isolated extramedullary relapse of chronic myelogenous leukemia (CML) after allogeneic stem cell transplant is rare. There is a case report of a child who developed a granulocytic sarcoma of the maxillary and sphenoid sinuses and lumbosacral spinal c
Externí odkaz:
https://doaj.org/article/b55ed61d77d84561b695f25f54811ec9
Autor:
Nakysa, Hooman, Mahmoud, Khodadost, Mahnaz, Sadeghian, Fariba, Jahangiri, Soudabeh, Hosseini, Fatemeh, Sarvi
Publikováno v:
Iranian journal of kidney diseases. 14(3)
HUS is a leading cause of AKI in infants. Though new classification of HUS is based on underlying disease, it traditionally defines as diarrhea positive (typical) and negative (atypical). We have no figure of the incidence and prevalence of HUS, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49010b5553210c66e3004b05699ab372
https://pubmed.ncbi.nlm.nih.gov/32361693
https://pubmed.ncbi.nlm.nih.gov/32361693
Autor:
Marziyeh Mojbafan, Soudabeh Hosseini, Elham Zarei, Saba Hemmati, Azita Tavasoli, Khadije Arjmandi Rafsanjani
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
Background Manganese is a critical trace element that not only has antioxidant properties, but also is essential for various metabolic pathways and neurotransmitters production. However, it can be toxic at high levels, particularly in the central ner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f6a439f9869eede21950e2e72682ffb
http://europepmc.org/articles/PMC6615235
http://europepmc.org/articles/PMC6615235
Autor:
Soudabeh Hosseini, Shadi Tabibian, Morteza Shamsizadeh, Saeed Dorgalele, Farhad Zaker, Akbar Dorgalaleh, Shaban Alizadeh
Publikováno v:
Blood Coagulation & Fibrinolysis. 27:324-327
Congenital factor X deficiency is one of the most severe forms of rare bleeding disorders transmitted in autosomal recessive manner. According to the World Federation of Hemophilia survey, 153 patients with factor X deficiency (FXD) live in Iran, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f86676f355e4a2a85c14669bf2e1bf36
https://doi.org/10.1097/mbc.0000000000000435
https://doi.org/10.1097/mbc.0000000000000435
Publikováno v:
Medical Journal of the Islamic Republic of Iran
Background: At early ages, recurrent or persistent infections are associated with increased serum C-reactive protein (CRP). Inflammatory mediators release inhibitory cells named myeloid-derived suppressor cell (MDSC) into circulating and tumor tissue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c2aa99cd1a013723a84d798536b4986
http://europepmc.org/articles/PMC7722956
http://europepmc.org/articles/PMC7722956
Autor:
Mahdi Pakjoo, Soudabeh Hosseini, Nader Safarian, Saba Seifpour, Ali Dabbagh, Shadi Tabibian, Sanaz Khaseb, Peyman Beigi, Pegah Kiyamehr, Akbar Dorgalaleh, Majid Naderi, Masoud Eslami
Publikováno v:
Annals of Blood. 4:26-26
Thromboembolic disorders are among the leading causes of morbidity and mortality in Iran. Anticoagulation therapy of affected patients is achieved using a variety of agents, including vitamin K antagonists (VKAs), heparin, and direct oral anticoagula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::248652801c1c10b4b7ca99615b64ba87
https://doi.org/10.21037/aob.2019.11.01
https://doi.org/10.21037/aob.2019.11.01
Autor:
Majid Naderi, Shaban Alizadeh, Maryam Hosseini, Shadi Tabibian, Peyman Eshghi, Akbar Dorgalaleh, Soudabeh Hosseini
Publikováno v:
Seminars in Thrombosis and Hemostasis. 41:323-329
Factor XIII deficiency (FXIIID) is a rare bleeding disorder with an estimated prevalence of 1 in 2-million population worldwide. In Iran, a Middle Eastern country with a high rate of consanguineous marriages, there are approximately 473 patients affl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03d425b70c93d9dccaad475b61c20e3a
https://doi.org/10.1055/s-0034-1395350
https://doi.org/10.1055/s-0034-1395350