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British Journal of Haematology|December 3, 1999
The erythrocyte effects of haemoglobin O(ARAB)R L Nagel, R Krishnamoorthy, S Fattoum, et al.Hematology and Cell Therapy|August 11, 1998
Antiphospholipid antibodies: lupus anticoagulants, anticardiolipin and antiphospholipid isotypes in patients with sickle cell diseaseB Nsiri, E Ghazouani, N Gritli, et al.Revue De Pneumologie Clinique|January 1, 1986
[Intrathoracic extra-bone marrow hematopoiesis. Apropos of a case with thalassemia intermedia]S Ghezel, S Ladjimi, F Guemira, et al.Thyroidology|August 1, 1994
Puzzling biochemical thyroid profile in patients with multinodular goitre originating from a mild iodine deficient area in TunisiaM V el May, A Kraiem, T Messaoud, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutationsT Messaoud, C Verlingue, E Denamur, et al.Hemoglobin|January 1, 1992
Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from TunisiaT P Molchanova, J B Wilson, L H Gu, et al.Hemoglobin|January 1, 1991
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among TunisiansS Fattoum, F Guemira, C Oner, et al.The Journal of Sports Medicine and Physical Fitness|June 21, 2014
Impaired oxygen uptake kinetics in the first high-level athlete with Hb Hope: a case studyI Touhami, D Le Gallais, S Perrey, et al.Pediatric Radiology|January 1, 1987
Radiological abnormalities of the skeleton in patients with sickle-cell anemia. A study of 222 cases in TunisiaM F Ben Dridi, A Oumaya, H Gastli, et al.Annales De Biologie Clinique|December 13, 2006
[Difference albumin-transferrin interest in the iron deficiency detection in a cohort of 1288 schoolchildren in the district of Tunis]A Bibi, S Benmoussa, A Torjman, et al.Pageof 4