A. Banihashemi

发表

High-resolution melting analysis for noninvasive prenatal diagnosis of IVS-II-I (G-A) fetal DNA in minor beta-thalassemia mothers

P. Gill, A. Alipour, M. Zafari, 2015, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Non invasive prenatal diagnosis of β- Thalassemia, A narrative review study

P. Gill, M. Zafari, Mehrnoush Kowsaryan, 2017 .

Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis

P. Gill, A. Alipour, M. Zafari, 2016, Annals of Hematology.

Identification of a Rare Synonymous Beta Globin Mutation, HBB:c.180G>A codon 59 (G>A) in an Iranian Patient

H. Akhavan-Niaki, A. Banihashemi, R. Y. Kamangari, 2015 .

Simultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran

H. Akhavan-Niaki, M. M. Elmi, A. Mostafazadeh, 2012, Hemoglobin.

IVSII-666 of human beta-globin gene: a polymorphic marker linked to codon 8(-AA) mutation.

H. Akhavan-Niaki, A. Banihashemi, Siamak Shafiezadeh Seresti, 2011, Genetic testing and molecular biomarkers.

Calcium carbonate nanoparticles fabricated by a facile method based on the colloidal gas aphrons for removal of fluoride ions from aqueous solutions

Vahid Javanbakht, Hossein Mohammadifard, A. Banihashemi, 2021 .

A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran

H. Akhavan-Niaki, A. Banihashemi, A. Tamaddoni, 2017, Hemoglobin.

Designing Strategic Competencies Model of Directors of Lorestan Province Education Department

A. Banihashemi, Hossein Mehrdad, Amin Rahimikia, 2020, Iranian Journal of Educational Sociology.

Numerical estimation and practical validation of Hooputra’s ductile damage parameters

F. Haji Aboutalebi, A. Banihashemi, A. Banihashemi, 2014 .

Effect of postweld heat treatment on interface microstructure and metallurgical properties of explosively welded bronze—carbon steel

G. Khalaj, H. Bakhtiari, A. Khoshakhlagh, 2018, Journal of Central South University.

Hematologic Features of Alpha Thalassemia Carriers

H. Akhavan-Niaki, A. Banihashemi, Vahid Kholghi Oskooei, 2012, International journal of molecular and cellular medicine.

A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population.

Mohammad Ahmadifard, H. Akhavan-Niaki, M. M. Elmi, 2011, Blood cells, molecules & diseases.

PREVALENCE OF COMMON POINT MUTATIONS OF ALPHA GLOBIN GENE IN BABOL, IRAN (2005-09)

H. A. Niaki, A. Banihashemi, A. Firouzjahi, 2012 .

Identification of a Rare β0-Thalassemia Mutation, Codon 54 (–T) (HBB: c.165delT) in an Iranian Family

H. Akhavan-Niaki, A. Banihashemi, M. Azizi, 2015, Hemoglobin.

Beta Globin Frameworks in Thalassemia Major Patients from North Iran

H. Akhavan-Niaki, A. Banihashemi, M. Azizi, 2012, Iranian journal of pediatrics.

A bimetallic nanocomposite modified genosensor for recognition and determination of thalassemia gene.

J. Raoof, R. Ojani, Ezat Hamidi-Asl, 2016, International journal of biological macromolecules.

Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia

H. Akhavan-Niaki, A. Banihashemi, Reza Youssefi Kamangar, 2014, Indian Journal of Hematology and Blood Transfusion.

IBBJ Autumn 2015 , Vol 1 , No 4 Identification of a Rare Synonymous Beta Globin Mutation , HBB : c . 180 G > A codon 59 ( G > A ) in an Iranian Patient

H. Akhavan-Niaki, A. Banihashemi, R. Y. Kamangari, 2018 .

Coinheritance of Sicilian (δβ)0-Thalassemia and Two Rare Hemoglobin Variants: A Complex Case of Hemoglobinopathy

Maryam Pilehchian Langroudi, A. Banihashemi, H. Eftekhari, 2017, Indian Journal of Clinical Biochemistry.