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Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia – lessons learned for prophylaxis

Journal of international medical research, 2021-12, Vol.49 (12), p.3000605211055385-3000605211055385

2021

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Multi-center study on mortality in children, and adults with sickle cell anemia-risk factors and causes of death

Scientific reports, 2024-04, Vol.14 (1), p.8584-8584, Article 8584

2024

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Predictors of impending acute chest syndrome in patients with sickle cell anaemia

Scientific reports, 2020-02, Vol.10 (1), p.2470-2470, Article 2470

2020

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Prevalence of methicillin resistant Staphylococcus aureus [MRSA] colonization or carriage among health-care workers

Journal of infection and public health, 2016-09, Vol.9 (5), p.571-576

2016

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Influence of Voxelotor-hemoglobin complexes in the estimation of hemoglobin S levels by the current standard of care laboratory evaluation techniques

Frontiers in medicine, 2023-04, Vol.10, p.1149281-1149281

2023

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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®)

Frontiers in medicine, 2021-10, Vol.8, p.731102-731102

2021

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Comparison of Methicillin Resistant Staphylococcus Aureus in Healthy Community Hospital Visitors [CA-MRSA] and Hospital Staff [HA-MRSA]

Mediterranean journal of hematology and infectious diseases, 2015-10, Vol.7 (1), p.e2015053-e2015053

2015

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Prevalence of Hepatitis B, Hepatitis C, and HIV in Multiply Transfused Sickle Cell Disease Patients from Oman

Mediterranean journal of hematology and infectious diseases, 2019, Vol.11 (1), p.e2019058-e2019058

2019

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CORRELATION OF TRANSIENT ELASTOGRAPHY WITH LIVER IRON CONCENTRATION, AND SERUM FERRITIN LEVELS IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS FROM OMAN

Mediterranean journal of hematology and infectious diseases, 2023-08, Vol.15 (1), p.e2023048

2023

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Clinical, laboratory and ultrastructural findings in patients with storage pool disease: A case series

Pediatric hematology oncology journal, 2023-12, Vol.8 (4), p.207-212

2023

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Respiratory Viral Infections in Sickle Cell Anemia: Special Emphasis on H1N1 Co-Infection

Oman medical journal, 2020-11, Vol.35 (6), p.1-7

2020

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INCREASED VASOOCCLUSIVE CRISIS IN “O” BLOOD GROUP SICKLE CELL DISEASE PATIENTS: ASSOCIATION WITH UNDERLYING THROMBOSPONDIN LEVELS

Mediterranean journal of hematology and infectious diseases, 2017-04, Vol.9 (1), p.e2017028-e2017028

2017

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ALLOIMMUNIZATION IN PATIENTS WITH SICKLE CELL DISEASE AND THALASSAEMIA: EXPERIENCE OF SINGLE CENTRE FROM OMAN

Mediterranean journal of hematology and infectious diseases, 2017-02, Vol.9 (1), p.e2017013-e2017013

2017

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Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients

Journal of human genetics, 2012-10, Vol.57 (10), p.665-669

2012

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Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred—PK deficiency masquerading as congenital dyserythropoietic anemia

Clinical case reports, 2022-02, Vol.10 (2), p.e05315-n/a

2022

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Red Cell Alloimmunization to Rhesus Antigen among Pregnant Women Attending a Tertiary Care Hospital in Oman

Oman medical journal, 2016, Vol.31 (1), p.77-80

2016

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The Use of HPLC as a Tool for Neonatal Cord Blood Screening of haemoglobinopathy: A Validation Study

Mediterranean journal of hematology and infectious diseases, 2019, Vol.11 (1), p.e2019005-e2019005

2019

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A stepwise α-thalassemia screening strategy in high-prevalence areas

European journal of haematology, 2013-08, Vol.91 (2), p.164-169

2013

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Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors

Oman medical journal, 2018-01, Vol.33 (1), p.43-47

2018

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Regulatory B Cells Are Functionally Impaired in Patients Having Hemophilia A With Inhibitors

Clinical and applied thrombosis/hemostasis, 2018-05, Vol.24 (4), p.618-624

2018

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Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients

Mediterranean journal of hematology and infectious diseases, 2016, Vol.8 (1), p.e2016013-e2016013

2016

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Portal Vein Thrombosis in Adult Omani Patients: A Retrospective Cohort Study

Oman medical journal, 2017-11, Vol.32 (6), p.522-527

2017

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Cytokine profile of sickle cell disease in Oman

American journal of hematology, 2004-12, Vol.77 (4), p.323-328

2004

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Portal Vein Thrombosis in Adult Omani Patients: A Retrospective Cohort Study

Oman medical journal, 2017-11, Vol.32 (6), p.522-527

2017

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SERUM TOTAL BILIRUBIN, NOT CHOLELITHIASIS, IS INFLUENCED BY UGT1A1 POLYMORPHISM, ALPHA THALASSEMIA AND S GENOTYPE: FIRST REPORT ON COMPARISON BETWEEN ARAB-INDIAN AND AFRICAN S GENES

Mediterranean journal of hematology and infectious diseases, 2015-10, Vol.7 (1), p.e2015060-e2015060

2015

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Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia – lessons learned for prophylaxis

Multi-center study on mortality in children, and adults with sickle cell anemia-risk factors and causes of death

Predictors of impending acute chest syndrome in patients with sickle cell anaemia

Prevalence of methicillin resistant Staphylococcus aureus [MRSA] colonization or carriage among health-care workers

Influence of Voxelotor-hemoglobin complexes in the estimation of hemoglobin S levels by the current standard of care laboratory evaluation techniques

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®)

Comparison of Methicillin Resistant Staphylococcus Aureus in Healthy Community Hospital Visitors [CA-MRSA] and Hospital Staff [HA-MRSA]

Prevalence of Hepatitis B, Hepatitis C, and HIV in Multiply Transfused Sickle Cell Disease Patients from Oman

CORRELATION OF TRANSIENT ELASTOGRAPHY WITH LIVER IRON CONCENTRATION, AND SERUM FERRITIN LEVELS IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS FROM OMAN

Clinical, laboratory and ultrastructural findings in patients with storage pool disease: A case series

Respiratory Viral Infections in Sickle Cell Anemia: Special Emphasis on H1N1 Co-Infection

INCREASED VASOOCCLUSIVE CRISIS IN “O” BLOOD GROUP SICKLE CELL DISEASE PATIENTS: ASSOCIATION WITH UNDERLYING THROMBOSPONDIN LEVELS

ALLOIMMUNIZATION IN PATIENTS WITH SICKLE CELL DISEASE AND THALASSAEMIA: EXPERIENCE OF SINGLE CENTRE FROM OMAN

Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients

Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred—PK deficiency masquerading as congenital dyserythropoietic anemia

Red Cell Alloimmunization to Rhesus Antigen among Pregnant Women Attending a Tertiary Care Hospital in Oman

The Use of HPLC as a Tool for Neonatal Cord Blood Screening of haemoglobinopathy: A Validation Study

A stepwise α-thalassemia screening strategy in high-prevalence areas

Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors

Regulatory B Cells Are Functionally Impaired in Patients Having Hemophilia A With Inhibitors

Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients

Portal Vein Thrombosis in Adult Omani Patients: A Retrospective Cohort Study

Cytokine profile of sickle cell disease in Oman

Portal Vein Thrombosis in Adult Omani Patients: A Retrospective Cohort Study

SERUM TOTAL BILIRUBIN, NOT CHOLELITHIASIS, IS INFLUENCED BY UGT1A1 POLYMORPHISM, ALPHA THALASSEMIA AND S GENOTYPE: FIRST REPORT ON COMPARISON BETWEEN ARAB-INDIAN AND AFRICAN S GENES

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