Maryam Neishabury

Years Active: 2021-2024
Publications (10 Years): 4

This page only lists publications with an associated author ORCID identifier.

Publications

Razieh Zarifian Yeganeh, Masoumeh Akbari Kelishomi, Atiyeh Ahmadpour Jenaghard, Banafsheh Salmani, Zohreh Vahidi, Mina Makvand, Maryam Azad, Mahdieh Kooshki, Yassin Bouraqi, Azita Azarkeivan, Hossein Najmabadi, Maryam Neishabury
HFE and Non- HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience. Genetic testing and molecular biomarkers (2024)
Razieh Zarifian Yeganeh, Masoumeh Akbari Kelishomi, Atiyeh Ahmadpour Jenaghard, Banafsheh Salmani, Zohreh Vahidi, Mina Makvand, Maryam Azad, Mahdieh Kooshki, Yassin Bouraqi, Azita Azarkeivan, Hossein Najmabadi, Maryam Neishabury
HFE and Non- HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience. Genetic testing and molecular biomarkers 28 (7) (2024)
Jafar Mehrabi Sisakht, Maghsood Mehri, Hossein Najmabadi, Azita Azarkeivan, Maryam Neishabury
Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing. Archives of Iranian medicine 25 (10) (2022)
Maryam Neishabury, Azita Azarkeivan, Maghsood Mehri, Hossein Najmabadi, Taher Cheraghi
The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran. Journal of clinical immunology 41 (4) (2021)

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