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2. Diagnostic and prognostic biomarkers in immune checkpoint inhibitor-related encephalitis: a retrospective cohort study

6. Functional and Molecular Characterization of New SPTLC1 Missense Variants in Patients with Hereditary Sensory and Autonomic Neuropathy Type 1 (HSAN1)

13. A previously unreported NARS1 variant causes dominant distal hereditary motor neuropathy in a French family.

14. Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms

21. Neurofilaments contribution in clinic: state of the art

23. CSF biomarker variability in the Alzheimer's Association quality control program

24. Modeling Neurodegenerative Diseases Using In Vitro Compartmentalized Microfluidic Devices

30. Clinical reporting following the quantification of cerebrospinal fluid biomarkers in Alzheimer's disease: An international overview

34. Oral transmission of L-type bovine spongiform encephalopathy in primate model

36. Core cerebrospinal fluid biomarker profile in anti-LGI1 encephalitis

38. Les neurofilaments : un nouveau biomarqueur clé pour les cliniciens. Partie 1 : Intérêt des neurofilaments dans la prise en charge des maladies neurodégénératives.

39. Prion potentiation after life-long dormancy in mice devoid of PrP

40. International initiative for harmonization of cerebrospinal fluid diagnostic comments in Alzheimer's disease

47. Impact of harmonization of collection tubes on Alzheimer's disease diagnosis

49. International initiative for harmonization of cerebrospinal fluid diagnostic comments in Alzheimer's disease

50. Severe Malaria with Neurological Manifestations: What Contribution of Neurofilament Light Chain?

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