Detalhe da pesquisa
1.
Spectrum, clinical characteristics and outcome of von Willebrand disease in Oman.
Haemophilia
; 2024 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38738970
2.
Multi-center study on mortality in children, and adults with sickle cell anemia-risk factors and causes of death.
Sci Rep
; 14(1): 8584, 2024 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38615021
3.
Impact of splenectomy on circulating microparticles in patients with sickle cell anemia.
Int J Lab Hematol
; 46(1): 141-147, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37661331
4.
A stepwise α-thalassemia screening strategy in high-prevalence areas.
Eur J Haematol
; 91(2): 164-9, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23668236
5.
Transcranial Doppler ultrasonography in sickle cell disease: a study in Omani patients.
J Pediatr Hematol Oncol
; 35(1): 18-23, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23249960
6.
Comparative assessment of deferiprone and deferasirox in thalassemia major patients in the first two decades-single centre experience.
Pediatr Hematol Oncol
; 30(2): 104-12, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23363369
7.
Influence of Voxelotor-hemoglobin complexes in the estimation of hemoglobin S levels by the current standard of care laboratory evaluation techniques.
Front Med (Lausanne)
; 10: 1149281, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37153104
8.
Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients.
J Hum Genet
; 57(10): 665-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22854539
9.
dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state.
Eur J Haematol
; 88(4): 350-5, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22126643
10.
Warfarin pharmacogenetics: polymorphisms of the CYP2C9, CYP4F2, and VKORC1 loci in a genetically admixed Omani population.
Hum Biol
; 84(1): 67-77, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22452429
11.
Clinical and laboratory characteristics of patients with sickle-cell and autoimmune/connective tissue diseases.
Rheumatol Int
; 32(2): 373-8, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21113811
12.
Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred-PK deficiency masquerading as congenital dyserythropoietic anemia.
Clin Case Rep
; 10(2): e05315, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35154711
13.
Measurement of hematopoietic progenitor cells using XN2000 hematology analyzer.
Int J Lab Hematol
; 44(1): 82-87, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34409726
14.
Protein Z levels in pregnant Omani women: correlation with pregnancy outcome.
J Thromb Thrombolysis
; 32(4): 453-8, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21837382
15.
Pattern and outcome of vascular involvement of Omani patients with Behcet's disease.
Rheumatol Int
; 31(6): 731-5, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20130881
16.
Iron Overload in Patients With Heavily Transfused Sickle Cell Disease-Correlation of Serum Ferritin With Cardiac T2* MRI (CMRTools), Liver T2* MRI, and R2-MRI (Ferriscan®).
Front Med (Lausanne)
; 8: 731102, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34760898
17.
Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia - lessons learned for prophylaxis.
J Int Med Res
; 49(12): 3000605211055385, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34855536
18.
Deferasirox (Exjade) significantly improves cardiac T2* in heavily iron-overloaded patients with beta-thalassemia major.
Ann Hematol
; 89(4): 405-9, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19798501
19.
Cytogenetic, clinical, and hematological features of pediatric myelodysplastic syndrome in Oman.
Pediatr Blood Cancer
; 62(2): 367-368, 2015 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25382798
20.
Coexistence of immune thrombocytopenic purpura and idiopathic membranous glomerulonephritis successfully treated with rituximab.
Platelets
; 21(7): 575-7, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20624006