Muneer Albagshi

Patient preference for deferasirox film-coated versus dispersible tablet formulation: a sequential-design phase 2 study in patients with thalassemia

Vip Viprakasit, Mona Hamdy, Hoda Hassab, Laila M. Sherief et autres

th, Égypte, sa, Maroc, vn, tr, in, ch, lb (code pays fourni par la source)

Sickle Cell Disease (SCD) Burden on Patients Treated With Hydroxyurea (HU): Results from the Real-World Assessment Survey for SCD in Saudi (ROARS)

Hatoon Ezzat, Abdullah Hasan Al Zayed, Hussain H. Al Saeed, Mohamed Al Darwish et autres

The prevalence of SCD in the Kingdom of Saudi Arabia (KSA) is one of the highest in the world with up to 2.6% of the population affected. The Real-World Assessment Survey for Sickle Cell Disease in Saudi (ROARS) was conducted to evaluate …

sa (code pays fourni par la source)

Evidence Gaps in the Management of Patients with Sickle Cell Disease (SCD) by Non-specialist Healthcare Professionals (HCPs): Results from the Real-World Assessment Survey for SCD in Saudi (ROARS)

Wasil Jastaniah, Abdullah Hasan Al Zayed, Hussain H. Al Saeed, Mohamed Al Darwish et autres

The Kingdom of Saudi Arabia (KSA) exhibits an extremely high prevalence of SCD and is regarded as one of the worst-affected countries in the world. Up to 2.6% of the population diagnosed with SCD in parts of KSA, and the Real-World Assessment …

sa (code pays fourni par la source)

Blood Demand and Challenges for Patients With Beta-Thalassemia Major in Eastern Saudi Arabia

Muneer Albagshi, Mona M. G. Saad, Abdulmohsin M. Aljassem, Abdulaziz Abdullah Bushehab et autres

Background β-thalassemia major is a hereditary disorder of hemoglobin (Hb) that results in defective Hb synthesis, leading to severe chronic anemia. The mainstay of its treatment is lifelong regular packed red cell transfusions associated with iron-chelating therapy. Globally, there is a gap …

us, sa (code pays fourni par la source)

SARS-CoV-2 infection in beta thalassemia: Is it real threat?

Muneer Albagshi, Khaled Salem

Topical Silver Sulfadiazine Trigger Hemolysis in a Child with Burn and Glucose 6 Phosphate Dehydrogenase Deficiency

Muneer Albagshi, Jaber Alhabeeb, Randa Hussein, Hakeema Alkamis et autres

Glucose 6 phosphate dehydrogenase deficiency (G6PD deficiency) is the commonest red blood cell enzyme disorder that affects hundreds of millions around the globe. The red cells deficient in the enzyme become vulnerable to oxidative stress after exposure to certain drugs, chemicals, or …

Prevalence of Glucose-6-Phosphate Dehydrogenase Deficiency Among Children in Eastern Saudi Arabia

Muneer Albagshi, Suad Alomran, Somaya Sloma, Abdullah Alsuweel et autres

Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common red blood cell enzyme deficiency worldwide. The disease is widely distributed in regions where malaria is prevalent, affecting mostly males because the enzyme is inherited as an X-link recessive pattern. In Saudi Arabia, …

us, sa (code pays fourni par la source)

Management of Glanzmann's Thrombasthenia – Guidelines based on an expert panel consensus from gulf cooperation council countries

Ahmad Tarawah, Tarek Owaidah, Naima Al-Mulla, MuhammadFaisal Khanani et autres

Glanzmann thrombasthenia is a rare disorder, due to quantitative and/or qualitative abnormalities of the platelet integrin αIIbβ3 and/or αIIbβ3. Although it is considered a rare disorder with a global incidence of 1/1,000,000 population, the case is different at the Gulf Cooperation Council …

sa, qa, ae, om, kw (code pays fourni par la source)

Sickle cell disease awareness among school children in Saudi Arabia

Muneer Albagshi, Hassan Altaweel, Mohammed Khalid Al-Alwan, Hussain Yaseen Alhashem et autres

Background: Sickle cell disease (SCD) affects millions of people throughout the world. Previous studies suggested the need for more public education. This study aimed to assess and compare the knowledge about SCD among intermediate and high school students. Methodology: An analytic cross-sectional …

Congenital sideroblastic anemia of a Saudi child.

Muneer Albagshi, Somaya H Saloma, Hassan M Albagshi

Sideroblastic anemia is a heterogeneous group of disorders characterized by the presence of ring sideroblasts in the bone marrow, and has congenital and acquired forms. Congenital sideroblastic anemia is a rare condition, which is mostly X-linked, caused by mutations of delta-aminolevulinic acid …

sa (code pays fourni par la source)

Infantile cortical hyperostosis - a report of Saudi family.

Muneer Albagshi, Heji I ALZoayed

A 2-weeks-old Saudi neonate was apparently well till the 10th day of life when a swelling of the right groin was noted accompanied by irritability and fever, without history of trauma. On examination: the girl was irritable and febrile, the mass was …

sa (code pays fourni par la source)

Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area

Mohamad Qari, Yasser Wali, Muneer Albagshi, Mohammad Alshahrani et autres

Thalassemia syndrome has diverse clinical presentations and a global spread that has far exceeded the classical Mediterranean basin where the mutations arose. The mutations that give rise to either alpha or beta thalassemia are numerous, resulting in a wide spectrum of clinical …

us, sa, qa, ae, fr (code pays fourni par la source)