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S Koussa

Showing results (21-30 of 40) with videos related to

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Thrombosis and Haemostasis|April 2, 2003
Incidence of thromboembolic events in Lebanese thalassemia intermedia patientsP A Zalloua, H Shbaklo, Y Abou Mourad, et al.
European Journal of Haematology|September 13, 2001
Comparison between deferoxamine and deferiprone (L1) in iron-loaded thalassemia patientsA Taher, M Sheikh-Taha, S Koussa, et al.
Haematologia|June 1, 2002
Effect of oral iron chelation therapy with deferiprone (L1) on the psychosocial status of thalassaemia patientsL Zahed, F H Mourad, R Alameddine, et al.
Revue Neurologique|February 24, 2004
[Neurobrucellosis: clinical features and therapeutic responses in 15 patients]S Koussa, A Tohmé, E Ghayad, et al.
Acta Haematologica|November 13, 2008
Survival and complications of beta-thalassemia in Lebanon: a decade's experience of centralized careK Charafeddine, H Isma'eel, M Charafeddine, et al.
Annals of Tropical Medicine and Parasitology|June 26, 2002
Hepatitis-C-virus genotypes and hepatitis-G-virus infection in Lebanese thalassaemicsS Ramia, S Koussa, A Taher, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 28, 2002
Acute paraplegia revealing an intraspinal neurenteric cyst in a childT Rizk, G A Lahoud, J Maarrawi, et al.
Multiple Sclerosis and Related Disorders|March 1, 2020
Restless legs syndrome among multiple sclerosis patients in LebanonJ Makhoul, N Ghaoui, G Sleilaty, et al.
European Journal of Haematology|February 13, 2003
Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in LebanonA Inati, A Taher, W Bou Alawi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 16, 2013
Leg ulcers in patients with β-thalassaemia intermedia: a single centre's experienceB N Matta, O Abbas, J E Maakaron, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Thrombosis and Haemostasis|April 2, 2003
Incidence of thromboembolic events in Lebanese thalassemia intermedia patientsP A Zalloua, H Shbaklo, Y Abou Mourad, et al.
European Journal of Haematology|September 13, 2001
Comparison between deferoxamine and deferiprone (L1) in iron-loaded thalassemia patientsA Taher, M Sheikh-Taha, S Koussa, et al.
Haematologia|June 1, 2002
Effect of oral iron chelation therapy with deferiprone (L1) on the psychosocial status of thalassaemia patientsL Zahed, F H Mourad, R Alameddine, et al.
Revue Neurologique|February 24, 2004
[Neurobrucellosis: clinical features and therapeutic responses in 15 patients]S Koussa, A Tohmé, E Ghayad, et al.
Acta Haematologica|November 13, 2008
Survival and complications of beta-thalassemia in Lebanon: a decade's experience of centralized careK Charafeddine, H Isma'eel, M Charafeddine, et al.
Annals of Tropical Medicine and Parasitology|June 26, 2002
Hepatitis-C-virus genotypes and hepatitis-G-virus infection in Lebanese thalassaemicsS Ramia, S Koussa, A Taher, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 28, 2002
Acute paraplegia revealing an intraspinal neurenteric cyst in a childT Rizk, G A Lahoud, J Maarrawi, et al.
Multiple Sclerosis and Related Disorders|March 1, 2020
Restless legs syndrome among multiple sclerosis patients in LebanonJ Makhoul, N Ghaoui, G Sleilaty, et al.
European Journal of Haematology|February 13, 2003
Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in LebanonA Inati, A Taher, W Bou Alawi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 16, 2013
Leg ulcers in patients with β-thalassaemia intermedia: a single centre's experienceB N Matta, O Abbas, J E Maakaron, et al.
Pageof 4