Search Results - "Al Saeed, Hussain H."

Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease by Alshabeeb, Mohammad A, Alwadaani, Deemah, Al Qahtani, Farjah H, Abohelaika, Salah, Alzahrani, Mohsen, Al Zayed, Abdullah, Al Saeed, Hussain H, Al Ajmi, Hala, Alsomaie, Barrak, Rashid, Mamoon, Daly, Ann K

“…Background: Sickle cell disease (SCD) is a Mendelian disease characterized by multigenic phenotypes. Previous reports indicated a higher rate of thromboembolic…”
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Pure red cell aplasia, a disease of a great diversity by Mona M Alfaraj, Hussain H Al Saeed

“…Pure red cell aplasia (PRCA) is a type of normocytic or sometimes macrocytic anemia characterized by reticulocytopenia. The cause of hypo erythropoiesis is…”
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Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area by Qari, Mohamad H, Wali, Yasser, Albagshi, Muneer H, Alshahrani, Mohammad, Alzahrani, Azzah, Alhijji, Ibrahim A, Almomen, Abdulkareem, Aljefri, Abdullah, Al Saeed, Hussain H, Abdullah, Shaker, Al Rustumani, Ahmad, Mahour, Khoutir, Mousa, Shaker A

“…Thalassemia syndrome has diverse clinical presentations and a global spread that has far exceeded the classical Mediterranean basin where the mutations arose…”
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Management of adult immune thrombocytopenia: Recommendations by an expert Saudi panel by Hazzaa Al-Zahrani, Aamer Aleem, Fahad Al Mohareb, Said Yousuf Ahmed, Ahmed M Al-Suliman, Hussain H Al Saeed, Mubarak S Al-Ghamdi, Hani Al-Hashmi

“…Immune thrombocytopenia (ITP) is a disorder characterized by an isolated thrombocytopenia in the absence of an identifiable cause. Management of ITP patients…”
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Endocrinopathies in patients with thalassemias by Al-Elq, Abdulmohsen H, Al-Saeed, Hussain H

“…Thalassemia major is a hereditary disorder of hemoglobin synthesis resulting in severe anemia. Treatment consists of multiple blood transfusions, a…”
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Prevalence of Gaucher Disease in Patients of Unknown Cause of Splenomegaly and/or Thrombocytopenia in Saudi Arabia by Elbagoury, Marwan, Qadi, Abdulelah Ismail, Hejazi, Ayman, Alabbas, Fahad, El Yamany, Ghaleb, Al Saeed, Hussain H., Kashari, Ohoud F.

“…Rationale: Gaucher disease (GD) is the most common amongst the lysosomal storage disorders. Prevalence of GD in Saudi Arabia is not available in published…”
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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) by Jastaniah, Wasil, Al Zayed, Abdullah Hasan, Al Saeed, Hussain H., Al Darwish, Mohamed, Albagshi, Muneer, Malhan, Hafiz, Tarawah, Ahmad, Al Manea, Aljawhara, Alhazmi, Iman, Qari, Mohamed, Alzahrani, Azzah, Alzahrani, Mohsen, Soliman, Wesam, Askar, Farid, Almustafa, Sukina, Ezzat, Hatoon M.

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Sickle Cell Disease (SCD) Burden on Patients Treated With Hydroxyurea (HU): Results from the Real-World Assessment Survey for SCD in Saudi (ROARS) by Ezzat, Hatoon M., Al Zayed, Abdullah Hasan, Al Saeed, Hussain H., Al Darwish, Mohamed, Albagshi, Muneer, Malhan, Hafiz, Tarawah, Ahmad, Al Manea, Aljawhara, Alhazmi, Iman, Qari, Mohamed, Alzahrani, Azzah, Alzahrani, Mohsen, Soliman, Wesam, Askar, Farid, Yassin, Al Shaimaa, Jastaniah, Wasil

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Management Algorithms for Gaucher Disease Type 1 in Saudi Arabia: A Consensus Result from a National Meeting by Alhejazi, Ayman, Almomen, Abdul Kareem, Tarawah, Ahmad M, AlSuliman, Ahmed M, Al Saeed, Hussain H., AlSaleh, Mahsen, Kashari, Ohoud F, Elbagoury, Marwan, Hussein, Omar

“…Background and Objectives Management and treatment of Gaucher disease are quite challenging because of its progressive nature and multisystem involvement…”
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Principles of blood transfusion in sickle cell anemia by Al-Saeed, Hussain H, Al-Salem, Ahmed H

“…Sickle cell anemia (SCA) is one of the commonly inherited hemoglobinopathies in the Kingdom of Saudi Arabia. It is characterized by periods of remissions and…”
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Management algorithms for gaucher disease by Ayman Alhejazi, Abdulkareem AlMomen, Ahmad M Tarawah, Ahmed M AlSuliman, Hussain H Al Saeed, Mahasen Saleh, Marwan ElBagoury, Ohoud F Kashari, Omar M Hussein

“…INTRODUCTION: Gaucher disease is a challenging disease because of the progressive nature and multiple systems that are involved. Gaucher disease is…”
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Acute appendicitis in patients with sickle cell disease by Al-Nazer, Mona A, Al-Saeed, Hussain H, Al-Salem, Ahmed H

“…Patients with sickle cell disease (SCD) often present with abdominal pain, usually attributed to vaso-occlusive crisis, but not rarely, it may be caused by…”
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Kikuchi[corrected]-Fujimoto [corrected] disease by Al-Nazer, Mona A, Al-Hadad, Ali M, Al-Aithan, Soror A, Al-Salem, Ahmed H, Al-Faraj, Ahmed A, Al-Saeed, Hussain H

“…Kukuchi-Fujimito disease is a rare, benign and self limiting condition, which usually presents with lymphadenopathy or fever of an unknown etiology, or both…”
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