91 results on '"Oussalah, Abderrahim"'
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2. Multiparametric renal function assessment in cirrhotic patients shows high prevalence of medically actionable changes in multiple modules
3. Correction: A transgenic mice model of retinopathy of cblG‑type inherited disorder of one‑carbon metabolism highlights epigenome‑wide alterations related to cone photoreceptor cells development and retinal metabolism
4. A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism
5. MicroRNAs miR-16 and miR-519 control meningioma cell proliferation via overlapping transcriptomic programs shared with the RNA-binding protein HuR
6. Epigenome alterations in food allergy: A systematic review of candidate gene and epigenome‐wide association studies
7. Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive cases
8. Usefulness of procalcitonin at admission as a risk-stratifying biomarker for 50-day in-hospital mortality among patients with community-acquired bloodstream infection: an observational cohort study
9. MUC13 Cell Surface Mucin Limits Salmonella Typhimurium Infection by Protecting the Mucosal Epithelial Barrier
10. The Smoothing Method for DNA Methylome Analysis Identifies Highly Accurate Epigenomic Signatures in Epigenome-Wide Association Studies
11. Stemness of Normal and Cancer Cells: The Influence of Methionine Needs and SIRT1/PGC-1α/PPAR-α Players
12. The Smoothing Method for DNA Methylome Analysis Identifies Highly Accurate Epigenomic Signatures in Epigenome-Wide Association Studies
13. Usefulness of Procalcitonin at Admission as a Risk-Stratifying Biomarker for 50-Day In- Hospital Mortality Among Patients with Community-Acquired Bloodstream Infection: An Observational Cohort Study
14. Hyperhomocysteinemia in Cardiovascular Diseases: Revisiting Observational Studies and Clinical Trials
15. Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis
16. Ascitic fluid mid-regional-pro-adrenomedullin (MR-pro-ADM): a novel rapid-assay sepsis biomarker to diagnose spontaneous bacterial peritonitis in cirrhotic patients
17. Multistage epigenome-wide association study identifies highly accurate epigenomic signatures in association with hepatocellular carcinoma: The HCC epigenome score
18. Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B12
19. Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genes
20. Un long ARN non codant régule l’activité de la phénylalanine hydroxylase, l’enzyme responsable de la phénylcétonurie
21. Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study
22. Ionizing radiations induce shared epigenomic signatures unraveling adaptive mechanisms of cancerous cell lines with or without methionine dependency
23. Next‐generation sequencing and genotype association studies reveal the association of HLA‐DRB3*02:02 with delayed hypersensitivity to penicillins
24. Low-frequency Coding Variants Associated With Body Mass Index Affect the Success of Bariatric Surgery
25. Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review
26. Integrative genomics analysis of nasal intestinal-type adenocarcinomas demonstrates the major role of CACNA1C and paves the way for a simple diagnostic tool in male woodworkers
27. Accuracy of procalcitonin for diagnosing peripheral blood culture contamination among patients with positive blood culture for potential contaminants
28. Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study
29. Next-Generation Sequencing and Genotype Association Studies Reveal the Association of HLA-DRB3*02:02 With Delayed Hypersensitivity to Penicillins
30. PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations
31. Cardiovascular manifestations of intermediate and major hyperhomocysteinemia due to vitamin B12 and folate deficiency and/or inherited disorders of one-carbon metabolism: a 3.5-year retrospective cross-sectional study of consecutive patients
32. Le dépistage de la phénylcétonurie en France
33. Next-Generation Sequencing and Genotype Association Studies Reveal the Association of HLA-DRB3*02:02 With Delayed Hypersensitivity to Penicillins
34. Elastase and exacerbation of neutrophil innate immunity are involved in multi‐visceral manifestations of COVID‐19
35. Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia
36. Health outcomes associated with vegetarian diets: An umbrella review of systematic reviews and meta-analyses
37. Elastase and Exacerbation of Neutrophil Innate Immunity are Involved in Multi-Visceral Manifestations of COVID-19
38. The spectrum of biochemical alterations associated with organ dysfunction and inflammatory status and their association with disease outcomes in severe COVID-19: A longitudinal cohort and time-series design study
39. La phénylcétonurie
40. Long-term ACE Inhibitor/ARB Use Is Associated With Severe Renal Dysfunction and Acute Kidney Injury in Patients With Severe COVID-19: Results From a Referral Center Cohort in the Northeast of France
41. Coronavirus disease 2019: acute Fanconi syndrome precedes acute kidney injury
42. Folinic acid improves the score of Autism in the EFFET placebo-controlled randomized trial
43. Genetic, epigenetic and genomic mechanisms of methionine dependency of cancer and tumor-initiating cells: What could we learn from folate and methionine cycles
44. Prolonged 25-OH Vitamin D Deficiency Does Not Impair Bone Mineral Density in Adult Patients With Vitamin D 25-Hydroxylase Deficiency (CYP2R1)
45. E‐health education interventions on HbA1cin patients with type 1 diabetes on intensive insulin therapy: A systematic review and meta‐analysis of randomized controlled trials
46. Analysis of fibroblasts from patients with cblC and cblG genetic defects of cobalamin metabolism reveals global dysregulation of alternative splicing
47. Follow-Up of Multi-Organ Dysfunction and Inflammation Using Biomarker Kinetics in Patients with Severe COVID-19 Disease and Association with Disease Outcomes: Results from a Referral Center Cohort in the North East of France
48. Kinetics of Biomarkers Associated with Organ Dysfunction and Inflammatory Status and Their Association with Disease Outcomes in Severe COVID-19: A Longitudinal Cohort Study
49. Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study
50. GNAI2 variants predict nonsteroidal anti‐inflammatory drug hypersensitivity in a genome‐wide study
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