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  • Haleh Akhavan-Niaki, P Derakhshandeh-Peykar, +6 authors Maryam Mitra Elmi
  • Biology, Medicine
  • Blood cells, molecules & diseases
  • 2011 (First Publication: 1 June 2011)
  • In Iran, the prevalence of beta-thalassemia trait is approximately 4-8% in most areas, and in Mazandaran province 10% of the population are carriers. Twenty four beta-globin gene mutations wereContinue Reading
  • Hajar Eftekhari, Ahmad Tamaddoni, +6 authors Haleh Akhavan-Niaki
  • Medicine, Biology
  • Hemoglobin
  • 2017 (First Publication: 2 January 2017)
  • Abstract α-Thalassemia (α-thal) is the most common monogenic disease that is caused by the absence or reduced expression of α-globin genes. The aim of this study was to investigate common α-globinContinue Reading
  • Haleh Akhavan-Niaki, Ali Banihashemi, +4 authors Maryam Mitra Elmi
  • Biology, Medicine
  • Hemoglobin
  • 2012 (First Publication: 1 April 2012)
  • Hb Constant Spring (Hb CS, codon 142, TAA>CAA, α2) (HBA2:c.427T>C) and α2 IVS-I donor site (GAGGTGAGG>GAGG – – – – –) (HBA2:c.95+2_95+6delTGAGG) are nondeletional α-thalassemia (α-thal) mutationsContinue Reading
  • Hajar Eftekhari, Maryam Pilehchian Langroudi, Ali Banihashemi, Mandana Azizi, Reza Youssefi Kamangar, Haleh Akhavan-Niaki
  • Medicine
  • Indian Journal of Clinical Biochemistry
  • 2017 (First Publication: 1 April 2018)
  • Abstractα-Thalassemia (α-thal) is considered as the most common inherited hemoglobin disorder worldwide. The present study describes the first observation of a combination of rare α-chain variants,Continue Reading