Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Aminasnafi A"'
Autor:
Ali Aminasnafi, Sadegh Khodavaisy, Maryam Moslem, Marziye Esmaeilpour Jouneghani, Fatemeh Sarbandi, Mahsa Falahatinejad, Bahareh Bashardoust, Hamid Badali, Neda kiasat
Publikováno v:
Current Medical Mycology, Vol 9, Iss 1, Pp 32-35 (2023)
Background and Purpose: Wickerhamomyces myanmarensis is a new opportunistic yeast previously named Pichai myanmarensis, which belongs to the order Saccharomycetales. Since its discovery, one environmental isolate of W. myanmarensis has been reported
Externí odkaz:
https://doaj.org/article/dd1f696810af456491a026905b9e7d46
Publikováno v:
Journal of Advanced Biomedical Sciences, Vol 11, Iss 1, Pp 3715-3724 (2021)
Background & Objective: Beta-thalassemia are among the most common autosomal recessive genetic disorders in Iran, especially in Khuzestan province. Beta-thalassemia exhibits significant phenotype heterogeneity and there are currently more than 200 kn
Externí odkaz:
https://doaj.org/article/72e886b6529a472aafb86ef2133c2e9a
Autor:
Aminasnafi, Ali1, Khodavaisy, Sadegh2,3, Moslem, Maryam4, Jouneghani, Marziye Esmaeilpour5, Sarbandi, Fatemeh6, Falahatinejad, Mahsa7, Bashardoust, Bahareh2, Badali, Hamid8, Kiasat, Neda4,5 nedakiasat1402@gmail.com
Publikováno v:
Current Medical Mycology. Mar2023, Vol. 9 Issue 1, p32-35. 4p.
Autor:
Farshad Abbasi, Gholam Abbas Kaydani, Zari Tahannejad, Mohsen Nakhaie, Ali Aminasnafi, Maryam Moradi
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 15, Iss 3 (2021)
Background: Immune thrombocytopenic purpura (ITP) is defined as a bleeding disorder in which the number and production of platelets are reduced by the immune system; however, the destruction of peripheral blood platelets also occurs. Although its exa
Externí odkaz:
https://doaj.org/article/72bee1733918466d9ac6480d114ce05b
Autor:
Ali Aminasnafi, Solmaz Heidari, Mohsen Alisamir, Mohammadreza Mirkarimi, Najmeh Namehgoshayfard, Seyed Pezeshki
Publikováno v:
Clinical laboratory. 68(4)
In this study, we investigated the predictive value of routine coagulation parameters including D-dimer, Prothrombin Time (PT), International Normalized Ratio (INR), activated Partial Thromboplastin Time (aPTT) and Complete Blood Count (CBC) test par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::428de5e05c7101782f573fc23372019d
https://pubmed.ncbi.nlm.nih.gov/35443600
https://pubmed.ncbi.nlm.nih.gov/35443600
Publikováno v:
Journal of Advanced Biomedical Sciences.
Background & Objective: Beta-thalassemia are among the most common autosomal recessive genetic disorders in Iran, especially in Khuzestan province. Beta-thalassemia exhibits significant phenotype heterogeneity and there are currently more than 200 kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::453b111a6f4d8784cf7ca2dbc837764a
https://doi.org/10.18502/jabs.v11i1.8756
https://doi.org/10.18502/jabs.v11i1.8756
Akademický článek
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Publikováno v:
Case Reports in Oncological Medicine, Vol 2012 (2012)
Opsoclonus myoclonus ataxia syndrome (OMS) is a rare neurologic syndrome. In a high proportion of children, it is associated with neuroblastoma. The etiology of this condition is thought to be immune mediated. In children, immunotherapy with conventi
Externí odkaz:
https://doaj.org/article/de8be25455dc437f9201b840410958d6
Publikováno v:
Annals of Hematology. 97:679-684
The impaired biosynthesis of the β-globin chain in β-thalassemia leads to the accumulation of unpaired alpha globin chains, failure in hemoglobin formation, and iron overload due to frequent blood transfusion. Iron excess causes oxidative stress an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f2c90e2ee42db60e61b456ab8abce28
https://doi.org/10.1007/s00277-017-3223-3
https://doi.org/10.1007/s00277-017-3223-3
Autor:
Aminasnafi, Ali, Heidari, Solmaz, Alisamir, Mohsen, Mirkarimi, Mohammadreza, Namehgoshayfard, Najmeh, Pezeshki, Seyed M. S.
Publikováno v:
Clinical Laboratory; 2022, Vol. 68 Issue 4, p784-790, 7p