42 results on '"Noreau, Anne"'
Search Results
2. Autosomal Recessive Cerebellar Ataxias
3. Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
4. Autosomal Recessive Cerebellar Ataxias
5. Autosomal Recessive Cerebellar Ataxias
6. Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family
7. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
8. Therapies for Ataxias
9. Dopamine transporter SLC6A3 genotype affects cortico-striatal activity of set-shifts in Parkinson’s disease
10. Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
11. Molecular aspects of hereditary spastic paraplegia
12. Expanding the Clinical Phenotype Associated With ELOVL4 Mutation: Study of a Large French-Canadian Family With Autosomal Dominant Spinocerebellar Ataxia and Erythrokeratodermia
13. Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation
14. SYNE1 Mutations in Autosomal Recessive Cerebellar Ataxia
15. Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis
16. Exome sequencing reveals SPG11 mutations causing juvenile ALS
17. SYNE1 mutations cause adult onset autosomal recessive ataxia with retained reflexes in Brazilian patients (P3.004)
18. Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the BDNF gene through the expression of antisense: A pilot prospective control study
19. Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals
20. Études génétiques de familles récessives d’ataxies et de paraplégies spastiques
21. Pure hereditary spastic paraplegia due to a de-novo mutation in the NIPA1 gene
22. SYNE1 mutations cause autosomal-recessive ataxia with retained reflexes in Brazilian patients
23. Two Novel Ataxia Phenotypes in the French-Canadian Population (P2.116)
24. Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
25. Early influence of the rs4675690 on the neural substrates of sadness
26. Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia
27. SYNE1Mutations in Autosomal Recessive Cerebellar Ataxia
28. Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia
29. Investigation of C9orf72 repeat expansions in Parkinson's disease
30. Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor (P05.031)
31. Exome Sequencing Reveals PMM2-CDG Gene Mutations in French-Canadian Siblings with Recessive Cerebellar Ataxia, Hand Tremor and Cognitive Impairment (P05.041)
32. Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor
33. CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects
34. Glucocerebrosidase Mutations in a French-Canadian Parkinson's Disease Cohort
35. Increased exonic de novo mutation rate in individuals with schizophrenia
36. Early impact of 5-HTTLPR polymorphism on the neural correlates of sadness
37. De novoSTXBP1mutations in mental retardation and nonsyndromic epilepsy
38. Mutations inSYNGAP1in Autosomal Nonsyndromic Mental Retardation
39. De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
40. Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the BDNF gene through the expression of antisense: A pilot prospective control study
41. Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the BDNF gene through the expression of antisense: A pilot prospective control study
42. Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum.
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