ردیف

عنوان مقاله

نویسندگان

عنوان مجله

سال

۱

Beta Thalassemia: Epidemiology and Diagnostic and Treatment Approaches in Iran.

Najmaldin Saki, Ali dehghani Fard, Saeid Kaviani, Mohammad Ali Jalali Far, Seyed Hadi Mousavi, Kheirollah Al –Ali, Fakher Rahim.*

IJHOSCR

۲۰۱۲

۲

Lymphoid Genes Expression in Mouse Embryonic Stem Cells with Differentiation on feeder free condition

Najmaldin Saki3.

IJHOSCR

۲۰۱۲

۳

Hypermethylation Status of Promoter is an Epigenetic Change in Lymphoid Malignancies

Najmaldin Saki2.

(IJHOSCR

۲۰۱۲

۴

Molecular Aspects of Glucose-6-Phosphate Dehydrogenase  Deficiency in Iran.

Najmaldin Saki3.

Zahedan journal of Research in Medical Sciences.

۲۰۱۲

۵

Chronic myeloid leukemia as a stem cell-derived malignancy.

Sadegh Babashah1, Mostafa Rezaei-Tavirani2,*, Mona Zamanian-Azodi2, Najmaldin Saki3. 

Journal of Paramedical Sciences (JPS)

۲۰۱۲

۶

Synergistic Effect of Sodium Butyrate and Thalidomide in the Induction of Fetal Hemoglobin Expression in Erythroid Progenitors Derived from Cord Blood CD133 + Cells.

Ali Dehghanifard,1 Saeid Kaviani,*1 Mehrdad Noruzinia,2Masoud Soleimani,1 Saeid Abroun,1 Abbas Hajifathali,3 Ali Akbar Pourfathollah,4Yousef Mortazavi,5Mohammad Ahmadvand,6 Maryam Mahmoodinia-Meymand,7 Zeinab Kaviani,8 Majid Farshdousti-Hagh9, Najmaldin Saki10.

Zahedan Journal of Research in Medical Sciences.

۲۰۱۲

۷

Impact of N-myc Amplification on Median Survival in Children With Neuroblastoma.

Mohammad Pedram 1*, Morteza Heidari 2, Bijan Keikhaei 1, Reza Azizi Malamiri 3, Behzad Poopak 4, Kiavash Fekri 5.

journal of comprehensive  Pediatrics.vol3,N5,summer۲۰۱۲

۲۰۱۲

۸

Co-existing triple different α-thalassemia mutations and sickle cell disease in a pregnant woman

Najmaldin Saki .

Lab Medicine

۲۰۱۲

۹

Evaluation of plasma activity level of anticoagulant proteins in patients with acute lymphoblastic leukemia in shafa hospital ahwaz 2010.

Bijan Keikhaei3, latifi M 5.

Eur Rey Med Pharmacol

۲۰۱۲

۱۰

biology and bioinformatics of myeloma cell.. Myeloma and Bone Lesion

Najmaldin Saki2 .

(Laboratory Hematology)

۲۰۱۲

۱۱

Beta-Globin Gene Cluster Haplotypes in Iranian Sickle Cell Patients: Relation to Some Hematologic Parameters.

Keikhaei B, Galehdari H, Pedram M,jaseb K, Bashirpour SH,Zandian KH,samadi B.

Iranian Journal of Blood & Cancer (IJBC).

۲۰۱۲

۱۲

Heterozygote Hemoglobin J Iran in Combination with Hemoglobin H Disease.

Keikhaei B1*, Galehdari H2, Mohammadpour M3, Hamed M4.

Iranian Journal of Blood & Cancer (IJBC).

۲۰۱۲

۱۳

the emerging role of immunomodulatoryagents in fetal hemoglobin induction.

saki 2 .

IJHOSCR

۲۰۱۲

۱۴

The first Molecular genetics analysis of individuals suffering from nephropatic cystinosis in the Southwestern Iran.

Sepideh Shahkarami1, Hamid Galehdari2, Ali Ahmadzadeh1, Mahnaz Babaahmadi3,Mohammad Pedram1

Nefrologia

۲۰۱۳

۱۵

Evaluation of diagnostic efficacy of serum sTfR assay in iron-deficiency anemia and Beta-thalassemia trait in Shafa Hospital, Ahvaz, Iran 2010.

M.T. JALALI, A. MOHSENI, B. KEIKHAEI, M. LATIFI.

European Review for Medical and Pharmacological Sciences.

۲۰۱۲

۱۶

Feasibility of cell therapy in Multiple Sclerosis: A systematic review of 83 studies.

Abdolreza Ardeshirylajimi1, Majid Farshdousti Hagh2, Najmaldin Saki3, Esmaeil Mortaz4, Masoud Soleimani5, Fakher Rahim.

IJHOSCR 7(1) - ijhoscr.

۲۰۱۳

۱۷

molecular mechanisms of hemoglobin F induction

Najmaldin Saki3.

IJHOSCR

2011

۱۸

The role of exon 45 and 16 in the pathogenesis of Von Willebrand disease in Iranian Patients.

Nasiri M1 PhD, Galehdari H PhD2, Darbouy M PhD1, Yavarian M MD3, Keikhaee B MD2.

Iranian Journal of Pediatric Hematology Oncology

۲۰۱۳

۱۹

Three Different Co-existing α-Thalassemia Mutations and Sickle Cell Disease in a Pregnant Woman

Fakher Rahim, PhD,1 Fateme Hamid, MSc,2 Hamid Galedari, PhD,3 Gholamreza Khamisipour, PhD,4 Bijan Keikhaei, MD,2 Kaveh Jaseb, MD,2 Najmaldin Saki, PhD2.

Lab Medicine

۲۰۱۳

۲۰

Signs and symptoms of Neuroblastoma.

Keikhaei B, Pedram M, Popak B, Heidari M, Hadadi N, Samadi B.

Journal of Medicine and Medical Science

۲۰۱۲

۲۱

Selective mutation searching of exon 28 in the gene type 3 Von Willebrand disease patients from Southwest Iran.

Nasiri Mahboobeh1, Galehdari Hamid2, Darbouy Mojtaba1, Yavarian Majid3, Keikhaie Bijan2.

HealthMED

۲۰۱۲

۲۲

Results of Transcranial Doppler in Children withSickle Cell Disease: Correlation between the Time-Averaged Mean of Maximum Velocity and Some Hematological Characteristics.

Keikhaei B 1*, Mousakhani H 1, Oghbaee M 2.

IJBC

۲۰۱۳

۲۳

Numerical Chromosomal Abnormalities in Patients with Acute Lymphoblastic and Myeloid Leukemia in Iran.

Ali mohamad malekas gar1,*, Mohamad Pe dram2, Sayye d kamal Es hagh hous aini3.

Clinical Medicine and Diagnostics

۲۰۱۲