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F Ala

Explore the profile of F Ala including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 46
Citations 101
Followers 0
Related Specialties
Hematology
Allergy & Immunology
General Medicine
Top 10 Co-Authors
C Harbour
B Nikbin
M Jazebi
M K Sharma
N Foroozanfar
A Massoud
S Ravanbod
F Anaraki
M S Enayat
H Farzadegan
Published In
Haemophilia
Vox Sang
J Immunol Methods
Rev Fr Transfus Immunohematol
Biochim Biophys Acta
Affiliations
Soon will be listed here.
Recent Articles
1.
Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient
Enayat M, Ravanbod S, Rassoulzadegan M, Jazebi M, Ala F, Budde U, et al.
Haemophilia . 2013 May; 19(4):e261-4. PMID: 23647747
No abstract available.
2.
Isolation of fungi from housefly (Musca domestica L.) at Slaughter House and Hospital in Sanandaj, Iran
Davari B, Khodavaisy S, Ala F
J Prev Med Hyg . 2013 Feb; 53(3):172-4. PMID: 23362625
Objective: Houseflies have long been regarded as potential carriers of microorganisms especially fungi. Since pathogenic microorganisms are widespread in the hospital environment, there is abundant opportunity for flies to become...
3.
Identification of 123 previously unreported mutations in the F8 gene of Iranian patients with haemophilia A
Ravanbod S, Rassoulzadegan M, Rastegar-Lari G, Jazebi M, Enayat S, Ala F
Haemophilia . 2011 Nov; 18(3):e340-6. PMID: 22117735
In Haemophilia A (HA), the deficiency in coagulation factor VIII is caused by mutations in the F8 gene. In the past, HA carrier detection in Iran used to be carried...
4.
How to deal with medical and social aspects of bleeding disorders--preparing women and the family in developing countries
Karimi M, Ravanbod S, Cohan N, Ala F
Haemophilia . 2011 Jun; 17 Suppl 1:42-4. PMID: 21692929
There is a considerable number of women with inherited bleeding disorders in Iran. von Willebrand disease, Glanzman thrombasthenia and factor XIII deficiency are the most common coagulation disorders. The main...
5.
Classification of Iranian patients with Glanzmann's Thrombasthenia using a flow cytometric method
Farsinejad A, Abolghasemi H, Kazemi A, Aghaiipour M, Hadjati E, Faranoush M, et al.
Platelets . 2011 Apr; 22(5):321-7. PMID: 21526886
Glanzmann's Thrombasthenia (GT) is a rare inherited autosomal recessive platelet disorder caused by a deficiency or dysfunction of the GPIIb-IIIa receptor on platelets, which is characterized by a lack of...
6.
A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation
Enayat M, Guilliatt A, Short P, Rastegar-Lari G, Jazebi M, Ravonbod S, et al.
Haemophilia . 2010 May; 16(6):966-9. PMID: 20491956
No abstract available.
7.
Clinical outcome of interferon and ribavirin combination treatment in hepatitis C virus infected patients with congenital bleeding disorders in Iran
Rahmani M, Toosi M, Ghannadi K, Lari G, Jazebi M, Rasoulzadegan M, et al.
Haemophilia . 2009 Jun; 15(5):1097-103. PMID: 19500170
Hepatitis C virus (HCV) infection is a major cause of morbidity and mortality in patients with inherited bleeding disorders. The results of interferon and ribavirin combination therapy have been reported...
8.
Seven novel point mutations in the F11 gene in Iranian FXI-deficient patients
Fard-Esfahani P, Lari G, Ravanbod S, Mirkhani F, Allahyari M, Rassoulzadegan M, et al.
Haemophilia . 2007 Nov; 14(1):91-5. PMID: 18005151
Factor XI (FXI) deficiency disorder is caused by defects in the F11 gene. The affected patients may suffer unexpected and major bleeding after trauma. Hence, the aim of this study...
9.
Identification of intron 1 and 22 inversion mutations in the factor VIII gene of 124 Iranian families with severe haemophilia A
Rastegar Lari G, Enayat M, Arjang Z, Lavergne J, Ala F
Haemophilia . 2004 Jul; 10(4):410-1. PMID: 15230960
No abstract available.
10.
Transfusion-associated graft-versus-host disease: current concepts and future trends
Seghatchian M, Ala F
Transfus Sci . 1995 May; 16(2):99-105. PMID: 10155741
Since the initial reports, in the early 1960s, of Transfusion-Associated Graft-versus-Host Disease (TA-GVHD) in infants with congenital immunodeficiency and individuals with various haematological malignancies, our knowledge of this rare but...