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1.
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficiencies.
Haemophilia
; 29(3): 827-835, 2023 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-36897560
2.
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
Transfus Apher Sci
; 60(6): 103203, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34275736
3.
Tailored prophylaxis in children with severe hemophilia: A four-year Iranian study.
Transfus Apher Sci
; 60(6): 103212, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34257016
4.
Effects of short-term aerobic, resistance and combined exercises on the lipid profiles and quality of life in overweight individuals with moderate hemophilia A: A randomized controlled trial.
Med J Islam Repub Iran
; 35: 70, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34277507
5.
Inflammatory and immune response genes: A genetic analysis of inhibitor development in Iranian hemophilia A patients.
Pediatr Hematol Oncol
; 36(1): 28-39, 2019 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-30888230
6.
Inhibitor development in patients with type 3 Von Willebrand disease, a comprehensive study on 99 Iranian patients.
Haemophilia
; 27(4): 520-e524, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-33550685
7.
Patients with Congenital Bleeding Disorders Appear to be Less Severely Affected by SARS-CoV-2: Is Inherited Hypocoagulability Overcoming Acquired Hypercoagulability of Coronavirus Disease 2019 (COVID-19)?
Semin Thromb Hemost
; 46(7): 853-855, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32557449
8.
Genotypes and phenotypes characterization of 17 Iranian patients with inherited factor X deficiency: identification of a novel mutation: Leu487Phe.
Blood Coagul Fibrinolysis
; 33(2): 75-82, 2022 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35140190
9.
Congenital Combined Bleeding Disorders, a Comprehensive Study of a Large Number of Iranian Patients.
Clin Appl Thromb Hemost
; 27: 1076029621996813, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33764796
10.
Challenges and concerns of patients with congenital bleeding disorders affected by coronavirus disease 2019.
Blood Coagul Fibrinolysis
; 32(3): 200-203, 2021 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33560003
11.
Association of FXII 5'UTR 46C>T polymorphism with FXII activity and risk of thrombotic disease.
Turk J Haematol
; 27(1): 15-9, 2010 Mar 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-27265792
12.
Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience.
Int J Hematol
; 111(4): 535-543, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-31939074
13.
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
Int J Lab Hematol
; 42(5): 619-627, 2020 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-32639687
14.
Prevalence of factor VIII inhibitors among Afghan patients with hemophilia A: a first report.
Blood Coagul Fibrinolysis
; 29(8): 697-700, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-30439768
15.
Polymorphisms in the TGF-ß1 (rs1982037) and IL-2 (rs2069762, rs4833248) genes are not associated with inhibitor development in Iranian patients with hemophilia A.
Hematology
; 23(10): 839-843, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29993342
16.
Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19-A common clinical feature between a rare disorder and a new, common infection.
Int J Lab Hematol
; 42(6): e277-e279, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32845081
17.
A large deletion, spanning exons 1 to 25 of F8 gene, and a high-titer factor VIII inhibitor, in severe hemophilia A.
Int J Lab Hematol
; 42(3): e138-e140, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32125779
18.
Factor XIII mutation spectrum in Iranian patients with hereditary factor XIII deficiency: Detection of 3 novel mutations.
Int J Lab Hematol
; 41(3): e61-e65, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30578706
19.
A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease.
Thromb Haemost
; 108(5): 946-54, 2012 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-23014764
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