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مقالات الدوريات
3
0
Clinical and laboratory parameters, risk factors predisposing to the development of priapism in sickle cell patients.
Al-Kindi, Salam.
SAGE Publications Inc.
2020-01-01
Clinical and laboratory parameters, risk factors predisposing to the development of priapism in sickle cell patients.
مقالات الدوريات
3
0
Effectiveness of nurse led intervention on health related quality of life among children with sickle cell disease in Oman : a pilot study.
Pandarakutty, Suthan.
Hindawi Limited.
2019-01-01
Effectiveness of nurse led intervention on health related quality of life among children with sickle cell disease in Oman : a pilot study.
مقالات الدوريات
0
0
Non-S sickling hemoglobin variants : historical, genetic, diagnostic, and clinical perspectives.
Ahmed, Sagir G.
Oman Medical Specialty Board.
2021-05
Non-S sickling hemoglobin variants : historical, genetic, diagnostic, and clinical perspectives.
مقالات الدوريات
0
0
Adult sickle cell disease : a five-year experience of intensive care management in a university hospital in Oman.
Tawfic, Qutaiba Amir.
College of Medicine, Sultan Qaboos University.
2012-05
Adult sickle cell disease : a five-year experience of intensive care management in a university hospital in Oman.
مقالات الدوريات
3
0
Cytokine profile of sickle cell disease in Oman.
Pathare, Anil.
Wiley-Liss, Inc.
2004-12-01
Cytokine profile of sickle cell disease in Oman.
مقالات الدوريات
3
0
Distribution of sickle cell disease and assessment of risk factors based on transcranial doppler values in the Gulf region.
Wali, Yasser.
Taylor and Francis Ltd.
2020-01-01
Distribution of sickle cell disease and assessment of risk factors based on transcranial doppler values in the Gulf region.
مقالات الدوريات
0
0
Impact of mannose-binding protein gene polymorphisms in omani sickle cell disease patients.
Zachariah, Mathew.
Universita Cattolica del Sacro Cuore.
2016-02
Impact of mannose-binding protein gene polymorphisms in omani sickle cell disease patients.
مقالات الدوريات
0
0
Genotypic and phenotypic composition of sickle cell disease in the Arab population : a systematic review.
Saleem, Irfan.
Dove Press.
2023-02
Genotypic and phenotypic composition of sickle cell disease in the Arab population : a systematic review.
مقالات الدوريات
4
0
Preoperative transfusion versus no transfusion policy in sickle cell disease patients : a randomized trial.
Elshinawy, Mohamed.
Blackwell Publishing Inc.
2020-02-01
Preoperative transfusion versus no transfusion policy in sickle cell disease patients : a randomized trial.
الرسائل والأطروحات الجامعية
0
0
Adverse pregnancy, fetal and neonatal outcomes in women with sickle cell disease : a retrospective case control study.
Al-Harthiyah, Salwa.
Sultan Qaboos University.
2022
Adverse pregnancy, fetal and neonatal outcomes in women with sickle cell disease : a retrospective case control study.
مقالات الدوريات
0
0
Serum total bilirubin, not cholelithiasis, is influenced by UGT1A1 polymorphism, alpha thalassemia and β<sup>s</sup> haplotype: First report on comparison between Arab-Indian and African β<sup>s</sup> genes.
Al-Kindi, Said Y.
Universita Cattolica del Sacro Cuore.
2015-11
Serum total bilirubin, not cholelithiasis, is influenced by UGT1A1 polymorphism, alpha thalassemia and β
s
haplotype: First report on comparison between Arab-Indian and African β
s
genes.
مقالات الدوريات
0
0
Autosplenectomy of sickle cell disease in Zaria, Nigeria : an ultrasonographic assessment.
Babadoko, A. A.
Oman Medical Specialty Board.
2012-03
Autosplenectomy of sickle cell disease in Zaria, Nigeria : an ultrasonographic assessment.
مقالات الدوريات
3
0
The use of HPLC as a tool for neonatal cord blood screening of haemoglobinopathy : a validation study.
Al-Madhani, A.
Universita Cattolica del Sacro Cuore.
2019-01-01
The use of HPLC as a tool for neonatal cord blood screening of haemoglobinopathy : a validation study.
مقالات الدوريات
0
0
Deaths from sickle cell disease in Intensive Care Units : Can we do better?.
Al-Lamki, Lamk.
College of Medicine, Sultan Qaboos University.
2012-05
Deaths from sickle cell disease in Intensive Care Units : Can we do better?.
الرسائل والأطروحات الجامعية
0
0
Exploring alterations of B regulatory cells in patients with sickle cell disease and systemic lupus erythematous
Al-Naamaniyah, Amal Abdullah.
Sultan Qaboos University
2016
Exploring alterations of B regulatory cells in patients with sickle cell disease and systemic lupus erythematous
مقالات الدوريات
0
0
Compound heterozygosity for Hb S and Hb S-Oman : case report.
Venugopal, Suresh.
College of Medicine, Sultan Qaboos University.
2008-11
Compound heterozygosity for Hb S and Hb S-Oman : case report.
مقالات الدوريات
0
0
Avascular necrosis of the hip in sickle cell disease in Oman : is it serious enough to warrant bone marrow transplantation?.
Wali, Yasser.
College of Medicine, Sultan Qaboos University.
2011-02
Avascular necrosis of the hip in sickle cell disease in Oman : is it serious enough to warrant bone marrow transplantation?.
مقالات الدوريات
0
0
Alloimmunization in patients with sickle cell disease and thalassemia : experience of a single centre in oman.
Al-Kindi, Salam.
Universita Cattolica del Sacro Cuore.
2017-02
Alloimmunization in patients with sickle cell disease and thalassemia : experience of a single centre in oman.
مقالات الدوريات
0
0
Human parvovirus B19 in children with sickle cell disease : poking the spleen.
Saad, Ashraf Abdullah.
Oman Medical Specialty Board.
2017-09
Human parvovirus B19 in children with sickle cell disease : poking the spleen.
مقالات الدوريات
0
0
Hydroxyurea : pattern of use, patient adherence, and safety profile in patients with sickle cell disease in Oman.
Jose, Jimmy.
Oman Medical Specialty Board.
2019-07
Hydroxyurea : pattern of use, patient adherence, and safety profile in patients with sickle cell disease in Oman.
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