Detalhe da pesquisa
1.
Effectiveness of ß-thalassemia prenatal diagnosis in Southern Iran: a cohort study.
Prenat Diagn
; 35(12): 1238-42, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26296249
2.
ß-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.
Hemoglobin
; 35(4): 331-7, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21797700
3.
Epidemiologic study of patients with thrombotic events referred to a tertiary hospital in Southern Iran.
Heliyon
; 7(8): e07734, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34409192
4.
The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura.
Haematologica
; 94(2): 289-93, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19116307
5.
Factor XI deficiency in Southern Iran: identification of a novel missense mutation.
Ann Hematol
; 88(4): 359-63, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18758779
6.
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency.
Haematologica
; 93(6): 934-8, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18403394
7.
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.
Haematologica
; 93(10): 1505-13, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18728029
8.
Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews.
Arch Med Res
; 39(2): 212-4, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18164966
9.
Premarital screening for beta-thalassaemia in Southern Iran: options for improving the programme.
J Med Screen
; 14(2): 62-6, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17626703
10.
Evaluation of Thrombin Generation Assay in Patients With Hemophilia.
Clin Appl Thromb Hemost
; 22(4): 322-6, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25354749
11.
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency.
Thromb Haemost
; 113(3): 567-76, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25427968
12.
Prevalence of diabetes mellitus and impaired glucose tolerance in beta-thalassemia patients with and without hepatitis C virus infection.
Pediatr Endocrinol Rev
; 2 Suppl 2: 282-4, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16462712
13.
Negative predictive value of the chorionic villous sampling (CVS) in diagnosis of thalassemia in genetic laboratory of Dastgheib Hospital, Shiraz, Iran, 2012.
Arch Iran Med
; 17(7): 483-5, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24979560
14.
Comparison of thrombin generation assay with conventional coagulation tests in evaluation of bleeding risk in patients with rare bleeding disorders.
Clin Appl Thromb Hemost
; 20(6): 637-44, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23393288
15.
Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran.
Blood Coagul Fibrinolysis
; 25(4): 360-3, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24389588
16.
Inherited thrombophilia and recurrent pregnancy loss.
Iran Red Crescent Med J
; 15(12): e13708, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24693393
17.
Genotype-phenotype correlation related to lipid profile in beta-thalassemia major and intermedia in southern Iran.
J Clin Lipidol
; 6(2): 108-13, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22385543
18.
Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease in southern Iran.
Blood Coagul Fibrinolysis
; 22(4): 325-30, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21415708
19.
Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern Iran.
Blood Coagul Fibrinolysis
; 22(5): 396-401, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21451397
20.
Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory.
Blood Coagul Fibrinolysis
; 20(8): 642-5, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19710607