Search Results - "Gheidishahran, Maryam"

A large dataset of white blood cells containing cell locations and types, along with segmented nuclei and cytoplasm by Kouzehkanan, Zahra Mousavi, Saghari, Sepehr, Tavakoli, Sajad, Rostami, Peyman, Abaszadeh, Mohammadjavad, Mirzadeh, Farzaneh, Satlsar, Esmaeil Shahabi, Gheidishahran, Maryam, Gorgi, Fatemeh, Mohammadi, Saeed, Hosseini, Reshad

“…Accurate and early detection of anomalies in peripheral white blood cells plays a crucial role in the evaluation of well-being in individuals and the diagnosis…”
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Molecular epidemiology and phylogenetic analysis of human T-lymphotropic virus type 1 in the tax gene and it association with adult t-cell leukemia/lymphoma disorders by Pourrezaei, Samira, Shadabi, Shahrzad, Gheidishahran, Maryam, Rahimiforoushani, Abbas, Akhbari, Masoume, Tavakoli, Mahnaz, Safavi, Mahshid, Madihi, Mobina, Norouzi, Mehdi

“…Human T-lymphotropic virus type-1 (HTLV-1) belongs to retrovirus family that causes the neurological disorder HTLV-1 adult T-cell leukemia/lymphoma (ATLL)…”
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Laboratory Diagnosis of Factor XIII Deficiency in Developing Countries: An Iranian Experience by Dorgalaleh, Akbar, Tabibian, Shadi, Shams, Mahmood, Tavasoli, Behnaz, Gheidishahran, Maryam, Shamsizadeh, Morteza

“…Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with an approximately 12-times higher than the rest of the world. The International…”
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Thalassemia an update: molecular basis, clinical features and treatment by Tari, Kaveh, Valizadeh Ardalan, Pooya, Abbaszadehdibavar, Mahnoosh, Atashi, Amir, Jalili, Ali, Gheidishahran, Maryam

“…Thalassemia are a group of inherited blood disorders caused by the decrease or absence of beta-globin chain synthesis will be determined with decrease in…”
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Molecular diagnosis of factor XIII deficiency, data from comprehensive coagulation laboratory in Iran by Gheidishahran, Maryam, Dorgalaleh, Akbar, Tabibian, Shadi, Shams, Mahmood, Sanei Moghaddam, Esmaeil, Khosravi, Sohaila, Naderi, Majid, Kahraze, Sara, Lotfi, Fereshte, Kazeme, Ahmad, Safa, Majid

“…Diagnosis of factor XIII (FXIII) deficiency (FXIIID) as a rare bleeding disorder is a challenge worldwide. Thus, in the present study, we used different…”
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