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A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease

The New England journal of medicine, 2019-08, Vol.381 (6), p.509-519

2019

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Use of thrombopoietin receptor agonists for immune thrombocytopenia in pregnancy: results from a multicenter study

Blood, 2020-12, Vol.136 (26), p.3056-3061

2020

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Treatment of sickle cell crises

Hematology, Transfusion and Cell Therapy, 2020-10, Vol.42, p.8-8

Alkindi, Salam

2020

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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.30006052110553-3000605211055385

2021

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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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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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TREATMENT OF SICKLE CELL ANEMIA

Hematology, Transfusion and Cell Therapy, 2022-10, Vol.44, p.S10

Alkindi, Dr. Salam

2022

Volltextzugriff (PDF)

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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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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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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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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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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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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Treatment of sickle cell in 2021

Hematology, Transfusion and Cell Therapy, 2021-11, Vol.43, p.S71-S71

Alkindi, Salam

2021

Volltextzugriff (PDF)

Physical therapy pathway and protocol for patients undergoing hematopoietic stem cell transplantation: Recommendations from The Eastern Mediterranean Blood and Marrow Transplantation (EMBMT) Group

Hematology/oncology and stem cell therapy, 2019-09, Vol.12 (3), p.127-132

2019

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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

Volltextzugriff (PDF)

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

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

2013

Volltextzugriff (PDF)

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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Nutritional and hematological status of Sudanese women of childbearing age with steady-state sickle cell anemia

Oman medical journal, 2021-05, Vol.36 (3), p.1-6

2021

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Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors: A quality initiative

Sultan Qaboos University medical journal, 2017-08, Vol.17 (3), p.e309-313

2017

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Impact of Aberrant Myeloid Antigen Expression on Outcomes of Patients with T-Cell Acute Lymphoblastic Leukemia

Oman medical journal, 2017-05, Vol.32 (3), p.189-193

2017

Volltextzugriff (PDF)

SP-052 WHEN TO CONSIDER BONE MARROW TRANSPLANT IN SCD?

Leukemia research, 2014-10, Vol.38, p.S21-S22

Alkindi, Salam

2014

Volltextzugriff (PDF)

Umbilical Cord Blood Banking and Transplantation: A short review

Sultan Qaboos University medical journal, 2011-11, Vol.11 (4), p.455-461

2011

Volltextzugriff (PDF)

Complications of PORT-A-CATH® in patients with sickle cell disease

Journal of infection and public health, 2012-03, Vol.5 (1), p.57-62

2012

Volltextzugriff (PDF)

dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state

European journal of haematology, 2012-04, Vol.88 (4), p.350-355

2012

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1 – 25 von 106

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A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease

Use of thrombopoietin receptor agonists for immune thrombocytopenia in pregnancy: results from a multicenter study

Treatment of sickle cell crises

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

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

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

TREATMENT OF SICKLE CELL ANEMIA

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

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

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

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

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®)

Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients

Treatment of sickle cell in 2021

Physical therapy pathway and protocol for patients undergoing hematopoietic stem cell transplantation: Recommendations from The Eastern Mediterranean Blood and Marrow Transplantation (EMBMT) Group

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

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

Nutritional and hematological status of Sudanese women of childbearing age with steady-state sickle cell anemia

Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors: A quality initiative

Impact of Aberrant Myeloid Antigen Expression on Outcomes of Patients with T-Cell Acute Lymphoblastic Leukemia

SP-052 WHEN TO CONSIDER BONE MARROW TRANSPLANT IN SCD?

Umbilical Cord Blood Banking and Transplantation: A short review

Complications of PORT-A-CATH® in patients with sickle cell disease

dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state

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