M. Ashki

发表

Point mutations which should not be overlooked in Hb H disease

S. Farashi, H. Najmabadi, A. Azarkeivan, 2016, Expert review of hematology.

Homozygosity for the AATAAA > AATA– – Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report

S. Farashi, H. Najmabadi, F. Zeinali, 2015, Hemoglobin.

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

S. Farashi, H. Najmabadi, A. Azarkeivan, 2015, Hemoglobin.

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

S. Farashi, H. Najmabadi, F. Zeinali, 2015, Hemoglobin.

Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population

S. Farashi, H. Najmabadi, A. Azarkeivan, 2016, Hemoglobin.

Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes

S. Farashi, H. Najmabadi, A. Azarkeivan, 2015, Expert review of hematology.

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia

S. Farashi, H. Najmabadi, S. Zeinali, 2015, Hemoglobin.

STUDYING THE EFFECT ECHINOPHORA PLATYLOBA EXTRACT ON BACTIRA (STAPHILOCOCUS AUREUS AND PSEUDOMONAS AEROGINOSA) AND FUNGI (CANDIDIA ALBICANS, ASPERGILUS FLAVUS AND ASPERGILUS NIGER) IN VITRO

M. Bayat, M. Entezari, M. Hashemi, 2009 .

Novel Mutations Responsible for α-Thalassemia in Iranian Families

N. Hafezi-Nejad, S. Farashi, H. Najmabadi, 2013, Hemoglobin.

Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia

S. Farashi, H. Najmabadi, A. Azarkeivan, 2015, Hemoglobin.

Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene

S. Farashi, H. Najmabadi, F. Zeinali, 2016, Hemoglobin.