Browsing by Author "Motwakil, Imam Awadelkareim Imam"

Browsing by Author "Motwakil, Imam Awadelkareim Imam"

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  • Motwakil, Imam Awadelkareim Imam; Osheik, Abu Asha Seidi (European Journal of Biomedical and European Journal of Biomedical AND Pharmaceutical sciences, 2019-06-24)
    Background: The cerebral venous sinus thrombosis (CVST) is a rare origin of stroke worldwide. However, the mode of presentation and aetiology are various. The prognosis is better than arterial thrombosis. The age of the ...
  • Motwakil, Imam Awadelkareim Imam; Faiza, Ahmed Saeed Mousa; Mohammed, Ibrahim Osman Ahmed; Amna, Omer Abdalrahman Alrayah (European Journal of Biomedical AND Pharmaceutical sciences, 2019-09-29)
    Background: Cardiac catheterization is widely used for diagnostic evaluation and therapeutic intervention in the management of patients with cardiac disease. The nurse's role in pre catheterization teaching and intra ...
  • Motwakil, Imam Awadelkareim Imam (European Journal of Biomedical AND Pharmaceutical sciences, 2019-11-01)
    Introduction: Benign recurrent intrahepatic cholestasis (BRIC) is characterized by episodes of liver dysfunction called cholestasis. Episodes of cholestasis can last from weeks to months, and the time between episodes, ...
  • Motwakil, Imam Awadelkareim Imam; Wamda, Hamed Ahmed Mohammed (European Journal of Biomedical and European Journal of Biomedical AND Pharmaceutical sciences, 2019-07-01)
    Introduction: Marfan syndrome is rare autosomal disorder of the connective tissue affect both male and female equally, manifested with skeletal, ligamentous, orooculofacial, ophthalmic, pulmonary, neurological and most fatal ...
  • Motwakil, Imam Awadelkareim Imam; Moawia, Abdelrahim Osman Mohamed (European Journal of Biomedical and European Journal of Biomedical AND Pharmaceutical sciences, 2019-06-17)
    Introduction: Deficiency of vitamin B12 produces protean effects on the nervous system, most commonlyneuropathy, myelopathy, cognitive and behavioral symptoms, and optic atrophy. Involuntary movements comprise a relatively ...
  • Motwakil, Imam Awadelkareim Imam (European Journal of Biomedical and European Journal of Biomedical AND Pharmaceutical sciences, 2019-06-07)
    Tuberous Sclerosis exhibits an autosomal dominant inheritance pattern, with a high spontaneous mutation rate. The TSC2 gene was named tuberin. The highest levels of tuberin are found in adult human brain, heart, and kidney; ...
  • Motwakil, Imam Awadelkareim Imam; Sara, Azhary (European Journal of Biomedical and European Journal of Biomedical AND Pharmaceutical sciences, 2019-06-30)
    RARE CASE OF QUADRIPARESIS WITH RT HORNER’S SYNDROME DUETO CERVICAL SPINE DURAL ARTERIO-VENOUS FISTULA cervical spine dural arterio-venous fistula account for approximately 70% of all vascular spinal malformations, 5– ...
  • Motwakil, Imam Awadelkareim Imam; Safaa, Sir alkhatim Mohammed Awad Allah (European Journal of Biomedical and European Journal of Biomedical AND Pharmaceutical sciences, 2019-05-27)
    Megaloblastic anemia is condition in which the bone marrow produces unusually large, structurally abnormal, immature red blood cell, megaloblast from asynchronous maturation of the nucleus and cytoplasm of the erythroblast. ...