949 results on '"Reynier, Pascal"'
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2. An immuno-lipidomic signature revealed by metabolomic and machine-learning approaches in labial salivary gland to diagnose primary Sjögrens syndrome.
3. Oral vitamin B12 supplementation in pernicious anemia: a prospective cohort study
4. A Tear Metabolomic Profile Showing Increased Ornithine Decarboxylase Activity and Spermine Synthesis in Thyroid-Associated Orbitopathy
5. Discordant Predictions of Extraglandular Involvement in Primary Sjögren’s Syndrome According to the Anti-SSA/Ro60 Antibodies Detection Assay in a Cohort Study
6. Correction: Autophagy protein 5 controls flow-dependent endothelial functions
7. Autophagy protein 5 controls flow-dependent endothelial functions
8. Genetic susceptibility to optic neuropathy in patients with alcohol use disorder
9. Long‐term persistence of mitochondrial dysfunctions after viral infections and antiviral therapies: A review of mechanisms involved.
10. Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders
11. Dominant optic atrophy: Culprit mitochondria in the optic nerve
12. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
13. Methodology and Best-Practice Guidelines for Thermally Optimized Driver Design
14. Validation of Simulation Results on Coupled Problems
15. Measurements for RF Amplifiers, Bond Wire Fusing and MOS Power Cells
16. Test Cases for Power-MOS Devices and RF-Circuitry
17. The cytokine profile of follicular fluid changes during ovarian ageing
18. Dominant Optic Atrophy: How to Determine the Pathogenicity of Novel Variants?
19. Plasma 25-Hydroxyvitamin D and 1,25-Dihydroxyvitamin D Levels in Breast Cancer Risk in Mali: A Case–Control Study
20. Case report: Diagnosis of ADCY5-related dyskinesia explaining the entire phenotype in a patient with atypical citrullinemia type I
21. Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming
22. ACO2 clinicobiological dataset with extensive phenotype ontology annotation
23. Ocular growth and metabolomics are dependent upon the spectral content of ambient white light
24. Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy
25. Dominant Optic Atrophy: How to Determine the Pathogenicity of Novel Variants?
26. Apparent resistance to thyroid hormones: From biological interference to genetics
27. Mutations in aARS genes revealed by targeted next-generation sequencing in patients with mitochondrial diseases
28. Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis
29. Warburg-like effect is a hallmark of complex I assembly defects
30. Mitochondrial Dysfunction in Mitochondrial Medicine: Current Limitations, Pitfalls, and Tomorrow
31. Effects of sildenafil on maximum walking time in patients with arterial claudication: The ARTERIOFIL study
32. Microcapteurs électrochimiques pour des mesures durables en Environnement-Santé et Agroalimentaire
33. CARENCE EN VITAMINE D ET RISQUE DE CANCER DU SEIN AVANCE AU MALI.
34. Rapid haemoglobin A and S quantification using Tosoh HLC‐723G8 in variant mode for patients with sickle cell disease.
35. Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria
36. Kynurenic Acid: A Novel Player in Cardioprotection against Myocardial Ischemia/Reperfusion Injuries
37. Serum ferritin/C-reactive protein ratio is a simple and effective biomarker for diagnosing iron deficiency in the context of systemic inflammation
38. Pathologies liées à des mutations de l’ADN mitochondrial
39. Metabo-lipidomics of Fibroblasts and Mitochondrial-Endoplasmic Reticulum Extracts from ALS Patients Shows Alterations in Purine, Pyrimidine, Energetic, and Phospholipid Metabolisms
40. eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data
41. A serum metabolomics signature of hypothermia fatalities involving arginase activity, tryptophan content, and phosphatidylcholine saturation
42. Combined Metabolipidomic and Machine Learning Approach in a Rat Model of Stroke Reveals a Deleterious Impact of Brain Injury on Heart Metabolism
43. An immuno-lipidomic signature revealed by metabolomic and machine-learning approaches in labial salivary gland to diagnose primary Sjögren’s syndrome
44. Laboratory medicine unveiling an unusual cause of D-lactic acidosis as the trigger of decompensation of a rare inborn error of metabolism
45. Sexual Dimorphism of Metabolomic Profile in Arterial Hypertension
46. Tryptophane–kynurenine pathway in the remote ischemic conditioning mechanism
47. Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria.
48. A Metabolomic Signature of Ischemic Stroke Showing Acute Oxidative and Energetic Stress.
49. Retinal Neuronal Loss in Visually Asymptomatic Patients With Myoclonic Epilepsy With Ragged-Red Fibers
50. OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database
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