Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Abdulkarim Al-Momen"'
Autor:
Fahad Al-Hameed, Hasan M Al-Dorzi, Abdulkarim Al Momen, Farjah Algahtani, Hazzaa Al Zahrani, Khalid Al Saleh, Mohammed Al Sheef, Tarek Owaidah, Waleed Alhazzani, Ignacio Neumann, Wojtek Wiercioch, Jan Brozek, Holger Schünemann, Elie A. Akl
Publikováno v:
Annals of Saudi Medicine, Vol 35, Iss 2, Pp 95-106 (2015)
BACKGROUND AND OBJECTIVES: Venous thromboembolism (VTE) is commonly encountered in the daily clinical practice. Cancer is an important VTE risk factor. Proper thromboprophylaxis is key to prevent VTE in patients with cancer, and proper treatment is e
Externí odkaz:
https://doaj.org/article/a57a2828f701475ca9ecd2d70e12e6db
Autor:
Waleed Alhazzani, Elie A. Akl, Holger J. Schünemann, Khalid Alsaleh, Tarek Owaidah, Hazzaa Alzahrani, Abdulkarim Al-Momen, Ignacio Neumann, Wojtek Wiercioch, Hasan M. Al-Dorzi, Farjah H. Algahtani, Fahad Al-Hameed, Jan Brozek, Mohammed AlSheef
Publikováno v:
Saudi Medical Journal
Venous thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE) is commonly encountered in daily clinical practice. After diagnosis, its management frequently carries significant challenges to the clinical practitioner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14c33a8948ed32f9c4b6660ae7d3051
https://doi.org/10.15537/smj.2015.8.12024
https://doi.org/10.15537/smj.2015.8.12024
Autor:
Khalid Alsaleh, Elie A. Akl, Holger J. Schünemann, Jan Brozek, Ignacio Neumann, Wojtek Wiercioch, Farjah H. Algahtani, Hazzaa Alzahrani, Tarek Owaidah, Mohammed AlSheef, Hasan M. Al-Dorzi, Abdulkarim Al-Momen, Waleed Alhazzani, Fahad Al-Hameed
Publikováno v:
Annals of Saudi Medicine, Vol 35, Iss 2, Pp 95-106 (2015)
BACKGROUND AND OBJECTIVES: Venous thromboembolism (VTE) is commonly encountered in the daily clinical practice. Cancer is an important VTE risk factor. Proper thromboprophylaxis is key to prevent VTE in patients with cancer, and proper treatment is e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1361e901c1cce84e49c73b6e56a147f3
https://doi.org/10.5144/0256-4947.2015.95
https://doi.org/10.5144/0256-4947.2015.95
Autor:
Mohsen A. F. El-Hazmi, Sivaling Kandaswamy, Mohamed Harakati, Arjumand S. Warsy, Fahd Al-Mohareb, Abdulkarim Al-Momen, Sameer Huraib
Publikováno v:
Acta Haematologica. 94:128-134
Seven sickle cell disease (SCD) patients [sickle cell anaemia = 4 (males 2, females 2, age range 18-40 years), and sickle cell beta (0)-thalassaemia = 3 (all females, age range 20-47 years)], suffering from a severe form of the disease were enrolled
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc02827eaaf4aeaf3a18ab4e84729c4b
https://doi.org/10.1159/000203994
https://doi.org/10.1159/000203994
Autor:
Arjumand S. Warsy, Mohammad Harakati, Mohsen A. F. El-Hazmi, Ibrahim Al-Fawwaz, Abdulkarim Al-Momen, Sameer Huraib, Abdullah Al-Wazzan, Hassan M. Bahakim
Publikováno v:
Molecular and Cellular Biochemistry. 124:17-22
Sickle cell anaemia (SCA) exhibits significant variations in clinical presentation in different populations for which several genetic factors including SCA-associated α-and β-thalassaemias, G-6-PD deficiency and elevated Hb F level have been implic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc96694d472a498c2337ba00909b0b08
https://doi.org/10.1007/bf01096377
https://doi.org/10.1007/bf01096377
Autor:
Arjum S. Warsy, J.H. Alexandre, Filiz Hincal, P.P. Kearney, Yohko Minamoto, Şinasi Özsoylu, Masatsugu Ueda, F. Bauduer, G. Cesarman, S. Hussain, Hitoshi Hasegawa, Kengo Gohchi, Masaki Yasukawa, Takaaki Hato, Emanuel Sikuler, Yasunori Enoki, Nir Hilzenrat, Yukari Miyajima, R.S. Verma, R.A. Stark, Akemi Yano, A. Delmer, Mo-Ping Chow, Hidehisa Kohno, Abdulkarim Al-Momen, Yuzuru Kobayashi, Juzo Matsuda, Le Tourneau, Mohsen A. F. El-Hazmi, M. Coleman, Miyo Tsukamoto, Tai-Fai Fok, Toshifumi Kondo, Susumu Sakata, Noriko Saitoh, Tai-Kwan Lam, Mutsuyoshi Kazama, J.C. Biggs, Mohamed Harakati, C. Guettier, Chi-Shun Feng, R. Zittoun, A. Bernadou, Chi-Kong Li, A.M.A. Gader, E.H. Rao, I.M. Al-Fawaz, Shigeru Fujita, Kohsuke Yanagisawa, Gönenc Ciliv, Vivian Chanh, Nurşen Baçaran, L. Wright, S. Acaron, Down Zilberman, A.A. Al-Saleh, Sevgi Yetgin
Publikováno v:
Acta Haematologica. 88:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0948281e96858b367a3eb9932515884
https://doi.org/10.1159/000204679
https://doi.org/10.1159/000204679
Autor:
Hatem F, Alameri, Aamer, Aleem, Walid, Kardas, Ahmed, Jehangir, Mohammad, Owais, Abdulkarim, Al-Momen
Publikováno v:
Saudi medical journal. 29(5)
To examine pulmonary function, dyspnea and exercise capacity in adult Saudi sickle cell disease (SCD) patients.The patients were recruited from the hematology clinic at King Khalid University Hospital in Riyadh from January to December 2005. The stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e091072e369aba890b60f4c3abfc0ea4
https://pubmed.ncbi.nlm.nih.gov/18454219
https://pubmed.ncbi.nlm.nih.gov/18454219
Autor:
Aamer, Aleem, Ahmed, Jehangir, Mohammad, Owais, Abdulkarim, Al-Momen, Abdulrahman, Al-Diab, Huda, Abdulkarim, Hatem, Alameri
Publikováno v:
Saudi medical journal. 28(7)
Cardiovascular complications in sickle cell disease (SCD) have been well documented but cardiac involvement in Saudi patients with SCD is not known. We sought to identify cardiac abnormalities by echocardiography in adolescent and adult Saudi patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b826804a7a8e593fe1bf663f7dc57630
https://pubmed.ncbi.nlm.nih.gov/17603714
https://pubmed.ncbi.nlm.nih.gov/17603714
Autor:
Abdulkarim Al-Momen, Abdulkarim Al-Bakry, Zain Alabedeen B. Jamjoom, Abdul-Rahman Tahan, Tajuddin Malabary, Basim Yacub
Publikováno v:
Surgery today. 23(6)
An unusual case of bilateral femoral nerve compression caused by iliacus hematomas in a patient on anti-coagulant therapy is herein reported with special reference to the comparative diagnostic value of ultrasonography, computerized tomorgraphy, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3401d584598e7c9dc004fa96b7fbf2b0
https://pubmed.ncbi.nlm.nih.gov/8358198
https://pubmed.ncbi.nlm.nih.gov/8358198
Publikováno v:
Acta haematologica. 88(4)
In this study 21 adults with severe form of sickle cell disease (SCD; sickle cell anaemia, n = 15; Hb S/beta degree-thal, n = 6) were treated with hydroxyurea (HU) to assess the effectiveness of the drug in managing SCD. The individual dose was selec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cea75492fbae5d39f16d88e3677b9e6
https://pubmed.ncbi.nlm.nih.gov/1292305
https://pubmed.ncbi.nlm.nih.gov/1292305