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1. Large-scale analysis of structural brain asymmetries during neurodevelopment : Associations with age and sex in 4265 children and adolescents.

2. Large‐scale analysis of structural brain asymmetries during neurodevelopment: Associations with age and sex in 4265 children and adolescents.

4. Multiple-Object Tracking in Children: The 'Catch the Spies' Task

10. Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders

11. Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders

12. A sweep-based algorithm for the fleet size and mix vehicle routing problem

13. PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides. An in vitro study

14. Mutation in candidate genes account for a small minority of hypobetalipoproteinemias and NGS analysis support polygenicity in mutation-negative patients

15. Molecular characterization of patients with and without coronary artery disease with “extreme LDL-C phenotypes”

16. Subcortical brain volume, regional cortical thickness, and cortical surface area across disorders: Findings from the ENIGMA ADHD, ASD, and OCD Working Groups

17. Mapping Cortical and Subcortical Asymmetry in Obsessive-Compulsive Disorder: Findings From the ENIGMA Consortium

18. Subcortical Brain Volume, Regional Cortical Thickness, and Cortical Surface Area Across Disorders: Findings From the ENIGMA ADHD, ASD, and OCD Working Groups

19. Structural neuroimaging biomarkers for obsessive-compulsive disorder in the ENIGMA-OCD consortium: medication matters

20. Rectal mucosa inflammation in non-celiac wheat sensitivity: comparison with duodenal histology

21. Identification Of P.Leu167Del Apoe Gene Mutation By Next Generation Sequencing In A Large Hypercholesterolemic Family

22. P.06.7 RECTAL MUCOSA INFLAMMATION AND EOSINOPHILS INFILTRATION IN NON-CELIAC WHEAT SENSITIVITY PATIENTS AS POSSIBLE BIOMARKERS FOR DIAGNOSIS

23. Coronary artery calcium is independently associated to pulse wave velocity and LDL cholesterol burden in patients with familial hypercholesterolemia

24. Cluster analysis of patterns generated from a web repository of HEPG2 transcriptomes. Genes of unknown functions coregulated in concert with cholesterol synthesis pathway

25. Detection of copy number variations (CNVS) in LDLR gene by next generation sequencing in patients with familial hypercholesterolemia

26. Familial hypobetalipoproteinemia: Analysis by next generation sequencing and identification of novel mutations in the APOB gene

28. Familial hypobetalipoproteinemia: Analysis by next generation sequencing and identification of a novel frameshift mutation in the apoB gene

29. A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia

30. The PCSK9 gene: a new gene controlling cholesterolemia

31. Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia identified in the lipigen centre of Palermo

33. Familial hypobetalipoproteinemia: Analysis by next generation sequencing and identification of a novel frameshift mutation in the apoB gene

34. Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing

35. Genetic epidemiology of ARH in Sicily

37. I livelli di cistatina C sono ridotti nell’infarto miocardico acuto. Effetto del polimorfismo G273A sui livelli plasmatici

39. Some efficient multi-heuristic procedures for resource-constrained project scheduling

40. Fire alarm signal recognition

49. PO3-78 FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION

50. Multivisceral transplantation in pigs: technical aspects

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