Detalles de la búsqueda
1.
Genetic analysis of non-severe hemophilia A phenotype with A discrepancy between one-stage and chromogenic factor VIII activity assays.
Transfus Apher Sci
; 60(5): 103194, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-34275734
2.
The activity of labile coagulation factors and fibrinogen in thawed plasma during a 5 day storage period in the hospital blood bank refrigerator.
Transfus Med
; 31(6): 494-498, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34605106
3.
Correlation of bleeding score with frequency and severity of bleeding symptoms in FXIII deficiency assessing by the ISTH Bleeding Assessment Tool.
Transfus Apher Sci
; 58(4): 495-497, 2019 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-31303509
4.
Procoagulant Activity of Red Blood Cell-Derived Microvesicles during Red Cell Storage.
Transfus Med Hemother
; 46(4): 224-230, 2019 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-31700504
5.
Utility of the international society on thrombosis and hemostasis-bleeding assessment tool in the diagnosis of patients who suspected of platelet function disorders.
Blood Coagul Fibrinolysis
; 35(1): 8-13, 2024 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37994630
6.
Frequency, clinical, and laboratory findings of platelet secretion disorders in patients referred to the specialized coagulation laboratory of the Iranian Blood Transfusion Organization.
Blood Coagul Fibrinolysis
; 35(3): 115-123, 2024 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38477834
7.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-36792472
8.
Isolation of the Anticoagulant and Procoagulant Fractions of the Venom of Iranian Endemic Echis carinatus.
Iran J Pharm Res
; 21(1): e127240, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36942067
9.
Homozygous SOD1 Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian Family.
Neurol Genet
; 8(1): e645, 2022 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-34926808
10.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-35092343
11.
Heparin-Induced Thrombocytopenia in Iranian Cardiac Surgery Patients Using the 4Ts Clinical Scoring System and Laboratory Methods.
Int J Hematol Oncol Stem Cell Res
; 15(4): 230-238, 2021 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35291665
12.
Severe Prekallikrein Deficiency Associated with Low Level of Factor XII: A Case Report.
Iran J Pathol
; 16(3): 332-336, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34306130
13.
Von Willebrand disease combined with coagulation defects in Iran.
Blood Transfus
; 19(5): 428-434, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34059196
14.
Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.
Blood Adv
; 5(15): 2987-3001, 2021 08 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34351388
15.
Effects of L-Carnitine supplement on plasma coagulation and anticoagulation factors in hemodialysis patients.
Ren Fail
; 32(9): 1109-14, 2010.
Artículo
en Inglés
| MEDLINE | ID: mdl-20863217
16.
Are Iranian patients with von Willebrand disease type 2N properly differentiated from hemophilia A and do they receive appropriate treatment?
Blood Coagul Fibrinolysis
; 31(6): 382-386, 2020 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-32815913
17.
Discrepancy between the results of one-stage and chromogenic factor VIII: C assays in patients with mild/moderate hemophilia A.
Blood Coagul Fibrinolysis
; 31(8): 530-535, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-33141777
18.
Comparative evaluation of the safety and efficacy of recombinant FVIII in severe hemophilia A patients.
J Pharmacopuncture
; 21(2): 76-81, 2018 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-30151307
19.
Long-term prophylaxis in patients with severe congenital factor XIII deficiency is not complicated by inhibitor formation.
Blood Coagul Fibrinolysis
; 28(4): 276-278, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-27306330
20.
The caspase-3 inhibitor (peptide Z-DEVD-FMK) affects the survival and function of platelets in platelet concentrate during storage.
Blood Res
; 49(1): 49-53, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24724067