The impact of child-specific characteristics on warfarin dosing requirements.

Autor: Alakeel YS; Department Pharmaceutical Care Services, King Abdulaziz Medical City, Ministry of the National Guard - Health Affairs, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia., Jijeh AMZ; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; Department of Cardiac Sciences, Division of Pediatric Cardiac Intensive Care, Ministry of the National Guard - Health Affairs, Riyadh, Saudi Arabia., BinSabbar NS; Department Pharmaceutical Care Services, King Abdulaziz Medical City, Ministry of the National Guard - Health Affairs, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia., Almeshary MF; Department Pharmaceutical Care Services, King Abdulaziz Medical City, Ministry of the National Guard - Health Affairs, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia., Alabdan NA; Department Pharmaceutical Care Services, King Abdulaziz Medical City, Ministry of the National Guard - Health Affairs, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia., Gramish JA; Department Pharmaceutical Care Services, King Abdulaziz Medical City, Ministry of the National Guard - Health Affairs, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia., Al Essa MA; Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

Publikováno v: Research and practice in thrombosis and haemostasis [Res Pract Thromb Haemost] 2024 Jan 22; Vol. 8 (1), pp. 102321. Date of Electronic Publication: 2024 Jan 22 (Print Publication: 2024).

Reconstruction of facial dermatofibrosarcoma protuberans using an anterolateral thigh flap: a case report and literature review.

Autor: Besharah BO; Department of Head and Neck, Center of Head and Neck, and Skull Base Health Center, King Abdullah Medical City Hospital, Mecca 21955, KSA., Ghazzawi RA; Umm Al-Qura University, Mecca 21955, KSA., Al-Kaff HH; Department of Head and Neck, Center of Head and Neck, and Skull Base Health Center, King Abdullah Medical City Hospital, Mecca 21955, KSA., Abdelmonim SK; Department of Head and Neck, Center of Head and Neck, and Skull Base Health Center, King Abdullah Medical City Hospital, Mecca 21955, KSA., Al-Essa MA; Department of Head and Neck, Center of Head and Neck, and Skull Base Health Center, King Abdullah Medical City Hospital, Mecca 21955, KSA.

Publikováno v: Journal of surgical case reports [J Surg Case Rep] 2020 Sep 21; Vol. 2020 (9), pp. rjaa340. Date of Electronic Publication: 2020 Sep 21 (Print Publication: 2020).

Classic homocystinuria: clinical, biochemical and radiological observations, and therapeutic outcome of 24 Saudi patients

Autor: al-Essa Ma, Pinar Ozand, Rashed Ms

Publikováno v: Eastern Mediterranean Health Journal. 5:1196-1203

We considered the clinical, biochemical and radiological findings, and response to pyridoxine [vitamin B6]of 24 classic homocystinuric patients [15 females, 9 males]diagnosed at King Faisal Specialist Hospital and Research Centre. Common clinical fin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8d5becf376fce63d749b89edcb0933fe
https://doi.org/10.26719/1999.5.6.1196

Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency

Autor: Marios Kambouris, Brian F. Meyer, M H Al-Hamed, Nadia Sakati, Sami A. Sanjad, M S Rashed, al-Essa Ma, E Al-Jishi, Pinar Ozand

Publikováno v: Clinical Genetics. 55:444-449

Pyroglutamic aciduria (5-oxoprolinuria) is a rare autosomal recessive disorder caused by either glutathione synthetase deficiency (GSSD) or 5-oxoprolinase deficiency. GSSD results in low glutathione levels in erythrocytes and may present with hemolyt

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0cff31912437c710b401fe0743982dc2
https://doi.org/10.1034/j.1399-0004.1999.550608.x

Knowledge and barriers to screening for colorectal cancer among individuals aged 40 years or older visiting primary healthcare clinics in Al-Khobar, Eastern Province.

Autor: Alabdulkader, Assim M.¹, Mustafa, Tajammal¹, Almutailiq, Danah A.² dana.alialmutlaq@gmail.com, Al-Maghrabi, Razan A.², Alzanadi, Rabab H.², Almohsen, Danyah S.², Alkaltham, Nourah K.¹

Publikováno v: Journal of Family & Community Medicine. Jan-Mar2024, Vol. 31 Issue 1, p25-35. 11p.