Detalhe da pesquisa
1.
Late side effects of cancer treatment in childhood cancer survivors.
J Oncol Pharm Pract
; 29(4): 885-892, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35289220
2.
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
3.
Prevalence of occult hepatitis C virus infection in beta-thalassemia major patients in Ahvaz, Iran.
Arch Virol
; 166(10): 2703-2710, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34275067
4.
Association between HLA-DRB1*01 and HLA-DRB1*15 with alloimmunisation in transfusion-dependent patients with thalassaemia.
Transfus Med
; 30(4): 275-280, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32227529
5.
Two Novel and Five Rare Mutations in the Non Coding Regions of the ß-Globin Gene in the Iranian Population.
Hemoglobin
; 44(4): 225-230, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32672086
6.
Retrospective study of the incidence of portal vein thrombosis after splenectomy in hematological disorders: Risk factors and clinical presentation.
Blood Cells Mol Dis
; 74: 1-4, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30293687
7.
Iranian patients with hemoglobin H disease: genotype-phenotype correlation.
Mol Biol Rep
; 46(5): 5041-5048, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31273613
8.
A review of molecular mechanisms involved in anticancer and antiangiogenic effects of natural polyphenolic compounds.
Phytother Res
; 33(8): 2002-2014, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31373113
9.
Genetics of Iranian Alpha-Thalassemia Patients: A Comprehensive Original Study.
Biochem Genet
; 56(5): 506-521, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29627922
10.
Thiamine-responsive megaloblastic anemia syndrome with Ebstein anomaly: a case report.
Eur J Pediatr
; 173(12): 1663-5, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24357267
11.
von Willebrand factor neutralizing and non-neutralizing alloantibodies in 213 subjects with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.
J Thromb Haemost
; 21(4): 787-799, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36792472
12.
Genotype-phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran.
Sci Rep
; 12(1): 4856, 2022 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35319015
13.
Long non-coding RNA signatures and related signaling pathway in T-cell acute lymphoblastic leukemia.
Clin Transl Oncol
; 24(11): 2081-2089, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35852681
14.
Hb Narges Lab, a Novel Hemoglobin Variant of the ß-Globin Gene.
Arch Iran Med
; 25(5): 339-342, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35943011
15.
Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study.
J Thromb Haemost
; 20(5): 1106-1114, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35092343
16.
Occult Hepatitis B Virus Infection among ß-Thalassemia Major Patients in Ahvaz City, Iran.
Am J Trop Med Hyg
; 106(1): 174-181, 2021 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34607305
17.
Chloroquine/hydroxychloroquine: an inflammasome inhibitor in severe COVID-19?
Naunyn Schmiedebergs Arch Pharmacol
; 394(5): 997-1001, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33416933
18.
A maternal death due to the intracerebral hemorrhage caused by antiphospholipid syndrome: a case report.
Clin Rheumatol
; 40(8): 3329-3333, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33392889
19.
Radiographic Features of the Maxillofacial Anomalies in Beta-Thalassemia Major: With New View.
World J Plast Surg
; 10(3): 78-83, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34912670
20.
Alpha-globin gene triplication and its effect in beta-thalassemia carrier, sickle cell trait, and healthy individual.
EJHaem
; 2(3): 366-374, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35844714