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14 results on '"Pariente, Jérémie"'

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

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

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

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

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

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

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

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

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

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

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

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

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

14. Clinical manifestations of intermediate allele carriers in Huntington disease

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