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42 results on '"CHU Fattouma Bourguiba [Monastir] (HFB)"'

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1. Impact of 3-week citrulline supplementation on postprandial protein metabolism in malnourished older patients: The Ciproage randomized controlled trial

2. Epidemiology of heart failure and long-term follow-up outcomes in a north-African population: Results from the NAtional TUnisian REgistry of Heart Failure (NATURE-HF)

3. Promising proteins detected by Western blot from Echinococcus granulosus protoscoleces for predicting early post-surgical outcomes in CE-affected Tunisian children

4. Soluble programmed death‐1 (sPD‐1) as predictor of early surgical outcomes of paediatric cystic echinococcosis

5. First isolation and molecular characterization of Toxoplasma gondii strains from human congenital toxoplasmosis cases in Monastir, tunisia

6. Seroprevalence of Toxoplasma gondii among healthy blood donors in two locations in Tunisia and associated risk factors

7. Identification of a functional FADS1 3′UTR variant associated with erythrocyte n-6 polyunsaturated fatty acids levels

8. Efficacy and safety of low-dose colchicine after myocardial infarction

9. A four-year survey (2011–2014) of West Nile virus infection in humans, mosquitoes and birds, including the 2012 meningoencephalitis outbreak in Tunisia

10. Physical activity and sedentary levels in children with juvenile idiopathic arthritis and inflammatory bowel disease. A systematic review and meta-analysis

11. High-intensity interval training in overweight and obese children and adolescents: systematic review and meta-analysis

12. Correlation of trans fatty acids with the severity of coronary artery disease lesions

13. A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

14. Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

15. High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry

16. Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

17. Chronic myeloid leukemia patients in Tunisia: epidemiology and outcome in the imatinib era (a multicentric experience)

18. Short-term effect of outdoor mould spore exposure on prescribed allergy medication sales in Central France

19. Increased factor VIII plays a significant role in plasma hypercoagulability phenotype of patients with cirrhosis

20. Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)

21. Risk factors for positive paracetamol drug provocation testing and procedure optimization

22. Cosavirus, Salivirus and Bufavirus in Diarrheal Tunisian Infants

23. Pro- and anti-angiogenic VEGF mRNAs in autoimmune thyroid diseases

24. Comorbidity in the Tunisian population

25. Plasma VEGF-related polymorphisms are implied in autoimmune thyroid diseases

26. Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency

27. Combined analysis of interferon-γ and interleukin-10 gene polymorphisms and chronic hepatitis C severity

28. Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

29. A Cluster Study of Predictors of Severe West Nile Virus Infection

30. Mortality and acute exacerbation of COPD: a pilot study on the influence of myocardial injury

31. CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia

32. Nou tout an dlo-la: a swimming-based physical activity promotion program

33. Search for a gene expression signature of breast cancer local recurrence in young women

34. Effects of discontinuing or continuing ongoing statin therapy in severe sepsis and septic shock: a retrospective cohort study

35. Evaluation of the Contribution of Renin Angiotensin System Polymorphisms to the Risk of Coronary Artery Disease Among Tunisians

36. Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family

37. Genetic analysis of hereditary multiple exostoses in Tunisian families: a novel frame-shift mutation in the EXT1 gene

38. Prevalence and factors of intensive care unit conflicts: the conflicus study

39. Association of interleukin-18 polymorphisms and plasma level with the outcome of chronic HCV infection

40. Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients

41. Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations

42. Development of an ELISA for the detection of scorpion venoms in sera of humans envenomed by Androctonus australis garzonii (Aag) and Buthus occitanus tunetanus (Bot): correlation with clinical severity of envenoming in Tunisia

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