Causes of hospitalization in sickle cell diseased children in western region of Saudi Arabia. A single center study von Abd Elmoneim, Abeer A, Al Hawsawi, Zakaria M, Mahmoud, Badr Z, Bukhari, Abdullah A, Almulla, Abdulmalik A, Sonbol, Abdullah M, Makhdoum, Anas M

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High prevalence of iron deficiency anemia in infants attending a well-baby clinic in northwestern Saudi Arabia von Hawsawi, Zakaria M. Al, Rehali, Sami A. Al, Mahros, Amani M, Sisi, Ali M. Al, Harbi, Khalid D. Al, Yousef, Ahmed M

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Age-related changes in biochemical bone profile in thalassemic children von Abd El-Moneim, Ehab S., Zolaly, Mohammed A., Al-Hawsawi, Zakaria M., Abdelmoneim, Abeer A., Abosdera, Mostafa M.

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Fanconi anemia associated with moyamoya disease in Saudi Arabia von Al-Hawsawi, Zakaria M, Al-Zaid, Mohamed A, Barnawi, Ashwaq I, Yassine, Saadeddine M

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Comprehensive patient care improves quality of life in transfusion dependent patients with β-thalassemia von Ali, Salah S, Tarawah, Ahmad M, Al-Hawsawi, Zakaria M, Zolaly, Mohammed A, Turkustani, Waheed

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Assessment of Cardiac Functions in Children with Sickle Cell Anemia: Doppler Tissue Imaging Study von AboHadeed, Hany M.A, Zolaly, Mohamed A, Khoshhal, Saad Q, El-Harbi, Khaled M, Tarawah, Ahmed M, Al-Hawsawi, Zakaria M, Al-Mozainy, Ibrahim

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Endocrinopathies in beta-thalassemia major. Prevalence, risk factors, and age at diagnosis in Northwest Saudi Arabia von Habeb, Abdelhadi M, Al-Hawsawi, Zakaria M, Morsy, Mohamed M, Al-Harbi, Abdallah M, Osilan, Adnan S, Al-Magamsi, Mohamed S, Zolaly, Mohamed A

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Ceftriaxone induced acute multi-organ failure syndrome in a Saudi boy with sickle cell disease von AL-HAWSAWI, Zakaria M, TURKISTANI, WaheedA, AL-AIDAROS, Mohamed A, AL-HARBI, Dalal L

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Acute chest syndrome in sickle cell disease von Al-Hawsawi, Zakaria M

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Unusual location of eosinophilic granuloma von HAOUIMI, Ammar S, AL-HAWSAWI, Zakaria M, JAMEEL, Ahmed N

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Comprehensive patient care improves quality of life in transfusion dependent patients with [beta]-thalassemia von Ali, Salah S, Tarawah, Ahmad M, Hawsawi, Zakaria M. Al, Zolaly, Mohammed A, Turkustani, Waheed

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Hereditary protein C deficiency in a Saudi neonate with bilateral adrenal gland haemorrhages: A rare case report von Al Hawsawi, Zakaria M., Alhejaili, Amal A., Mohy Uddin, Moeen, Abdelkarim, Mohamed E.

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Screening for congenital hypothyroidism in North-West region of Saudi Arabia von AL-MAGHAMSI, Mohammad S, AL-HAWSAWI, Zakaria M, GHULAM, Ghulam N, OKASHA, Ahmad M

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Unusual location of eosinophilic granuloma von HAOUIMI, Ammar S, AL-HAWSAWI, Zakaria M, JAMEEL, Ahmed N

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Portal vein thrombosis after splenectomy for beta-thalassemia major von AL-HAWSAWI, Zakaria M, HAOUIMI, Ammar S, HASSAN, Ruhul Amin A, TARAWAH, Ahmnd M

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Hypoxic ischemic encephalopathy. Incidence and risk factors in North Western Saudi Arabia von Itoo, Bashir A, Al-Hawsawi, Zakaria M, Khan, Anwar H

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Sickle cell hemoglobin C disease in Saudi Arabia von AL-HAWSAWI, Zakaria M, ISLAM, Mohammed S, SHEHATA, Nabil S

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Hypoxic ischemic encephalopathy: Incidence and risk factors in North Western Saudi Arabia von ITOO, Bashir A, AL-HAWSAWI, Zakaria M, KHAN, Anwar H

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Acute splenic sequestration crisis in children with Sickle Cell Disease von AL-HAWSAWI, Zakaria M, ISMAIL, Ghousia A

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Splenic abscess in childhood B-Thalassemia Major von AL-HAWSAWI, Zakaria M, HUMMAIDA, Tarig I

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