Detalhe da pesquisa
1.
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficiencies.
Haemophilia
; 29(3): 827-835, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36897560
2.
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran.
Hemoglobin
; 47(4): 147-151, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37548174
3.
Clinical and genetic characteristics of hemoglobin H disease in Iran.
Pediatr Hematol Oncol
; 39(6): 489-499, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34951342
4.
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
Transfus Apher Sci
; 60(6): 103203, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34275736
5.
Prognostic Value Evaluation of HLA-DRB1*07:01, *10, *12, *13:01 Alleles for Alloimmunization in Transfusion-Dependent Thalassemia.
Transfus Apher Sci
; 60(6): 103271, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34535395
6.
Developing a databank for multiple transfusion patients: Rh antigen and phenotype distribution among 3000 regular blood donors in Iran.
Transfus Apher Sci
; 60(3): 103124, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33839013
7.
Hepcidin gene polymorphisms and iron overload in ß-thalassemia major patients refractory to iron chelating therapy.
BMC Med Genet
; 21(1): 75, 2020 04 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32268883
8.
Resistance-associated substitutions (RASs) to HCV direct-acting antivirals (DAAs) at baseline of treatment in thalassemia patients: a referral center study.
Arch Virol
; 165(10): 2193-2203, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32638116
9.
miR-30a regulates γ-globin expression in erythoid precursors of intermedia thalassemia through targeting BCL11A.
Mol Biol Rep
; 47(5): 3909-3918, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32406020
10.
Evaluation of Efficacy, Safety, and Satisfaction Taking Deferasirox Twice Daily Versus Once Daily in Patients With Transfusion-Dependent Thalassemia.
J Pediatr Hematol Oncol
; 42(1): 23-26, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31568183
11.
Fertility and pregnancy in Iranian thalassemia patients: An update on transfusion complications.
Transfus Med
; 30(5): 352-360, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820581
12.
Distribution of Red Blood Cell Alloantibodies Among Transfusion-Dependent ß-Thalassemia Patients in Different Population of Iran: Effect of Ethnicity.
Hemoglobin
; 44(1): 31-36, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32400249
13.
Hb S (HBB: c.20A>T) and α- and ß-Thalassemia Coinheritance in Iranian Patients.
Hemoglobin
; 44(2): 109-112, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32370567
14.
The Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in ß-Thalassemia Major.
Hemoglobin
; 43(1): 34-37, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31084365
15.
Effect of quercetin on oxidative stress and liver function in beta-thalassemia major patients receiving desferrioxamine: A double-blind randomized clinical trial.
J Res Med Sci
; 24: 91, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31741663
16.
Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing.
Blood Cells Mol Dis
; 71: 39-44, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29499877
17.
The correlation between cardiac magnetic resonance T2* and left ventricular global longitudinal strain in people with ß-thalassemia.
Echocardiography
; 35(4): 438-444, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29399871
18.
Frequency of α-Globin Gene Triplications and Coinheritance with ß-Globin Gene Mutations in the Iranian Population.
Hemoglobin
; 42(4): 252-256, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30451045
19.
T2* Magnetic Resonance Imaging Study of Pancreatic Iron Overload and its Relation With the Diabetic State in Thalassemic Patients.
J Pediatr Hematol Oncol
; 39(5): 337-340, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28085743
20.
Comparison of MicroRNAs Mediated in Reactivation of the γ-Globin in ß-Thalassemia Patients, Responders and Non-Responders to Hydroxyurea.
Hemoglobin
; 41(2): 110-115, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28696844