Search

Your search keyword '"M. Chaouch"' showing total 43 results

Search Constraints

Start Over You searched for: Author "M. Chaouch" Remove constraint Author: "M. Chaouch" Search Limiters Full Text Remove constraint Search Limiters: Full Text
43 results on '"M. Chaouch"'

Search Results

2. Wood thermodegradation: experimental analysis and modeling of mass loss kinetics

3. Preparation and Characterisation A Catalytic System Cu-Clay for Catalytic Oxidation of Methyl Orange with H2O2

4. New Varieties of Zinc–Chromium–Sulfate Lamellar Double Hydroxides

5. Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C

6. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

8. Genome Tunisia Project: paving the way for precision medicine in North Africa.

9. Emergence of Plasmid-Mediated Quinolone Resistance (PMQR) Genes in Campylobacter coli in Tunisia and Detection of New Sequence Type ST13450.

10. Thermo-Hydric Study of Wood-Based Materials under Thermal Comfort Conditions.

11. Retrospective Phylodynamic and Phylogeographic Analysis of the Bluetongue Virus in Tunisia.

12. PHINDaccess Hackathons for COVID-19 and Host-Pathogen Interaction: Lessons Learned and Recommendations for Low- and Middle-Income Countries.

13. Developing Clinical Phenotype Data Collection Standards for Research in Africa.

14. The unrestricted global effort to complete the COOL trial.

15. Historical Westward Migration Phases of Ovis aries Inferred from the Population Structure and the Phylogeography of Occidental Mediterranean Native Sheep Breeds.

16. First Report of Two Jaculus Rodents as Potential Reservoir Hosts of Leishmania Parasites in Tunisia.

17. Evaluation of the Taxonomic Status of Lesser Egyptian Jerboa, Jaculus jaculus : First Description of New Phylogroups in Tunisia.

18. African Genomic Medicine Portal: A Web Portal for Biomedical Applications.

19. Ten simple rules for developing bioinformatics capacity at an academic institution.

20. Data Management Plans in the genomics research revolution of Africa: Challenges and recommendations.

21. H3ABioNet genomic medicine and microbiome data portals hackathon proceedings.

22. Investigation of natural infection of Phlebotomine (Diptera: Psychodidae) by Leishmania in Tunisian endemic regions.

23. Human OMICs and Computational Biology Research in Africa: Current Challenges and Prospects.

24. A review of clinical pharmacogenetics Studies in African populations.

25. Proposed minimum information guideline for kidney disease-research and clinical data reporting: a cross-sectional study.

26. Development and Assessment of Leishmania major and Leishmania tropica Specific Loop-Mediated Isothermal Amplification Assays for the Diagnosis of Cutaneous Leishmaniasis in Tunisia.

27. Extraction of Essential Oils of Rosmarinus officinalis L. by Two Different Methods: Hydrodistillation and Microwave Assisted Hydrodistillation.

28. Development and Evaluation of a Loop-mediated Isothermal Amplification Assay for Rapid Detection of Theileria annulata Targeting the Cytochrome B Gene.

29. Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

30. Familial epilepsy in Algeria: Clinical features and inheritance profiles.

31. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

32. Sequence Polymorphism of Cytochrome b Gene in Theileria annulata Tunisian Isolates and Its Association with Buparvaquone Treatment Failure.

33. Galanin pathogenic mutations in temporal lobe epilepsy.

34. Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders.

35. Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family.

36. Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western Africa.

37. Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H.

38. Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11.

39. Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.

40. Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations.

41. Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.

42. Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.

43. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.

Catalog

Books, media, physical & digital resources