Search

Your search keyword '"Pariente, Jérémie"' showing total 15 results

Search Constraints

Start Over You searched for: Author "Pariente, Jérémie" Remove constraint Author: "Pariente, Jérémie" Topic male Remove constraint Topic: male
15 results on '"Pariente, Jérémie"'

Search Results

1. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.

2. Analysis of Psychological Symptoms Following Disclosure of Amyloid-Positron Emission Tomography Imaging Results to Adults With Subjective Cognitive Decline

3. Clinical and genetic characteristics of late-onset Huntington's disease

4. Thrombocytopenia is independently associated with poor outcome in patients hospitalized for COVID‐19

5. Déjà-rêvé: Prior dreams induced by direct electrical brain stimulation

6. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

7. Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype

8. Cognitive decline in Huntington's disease expansion gene carriers

9. Cerebral microbleeds and CSF Alzheimer biomarkers in primary progressive aphasias

10. App, psen1, and psen2 mutations in early-onset alzheimer disease:a genetic screening study of familial and sporadic cases

11. A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease

12. The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkers

13. Clinical Effect of Early vs Late Amyloid Positron Emission Tomography in Memory Clinic Patients: The AMYPAD-DPMS Randomized Clinical Trial

14. The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire

15. Clinical manifestations of intermediate allele carriers in Huntington disease

Catalog

Books, media, physical & digital resources