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1. Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions

2. Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

4. Titin copy number variations associated with dominant inherited phenotypes

5. Titin copy number variations associated with dominant inherited phenotypes

6. Titin copy number variations associated with dominant inherited phenotypes

9. Delayed-Onset Friedreichʼs Ataxia Revisited

10. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

11. An Atypical Case of Head Tremor and Extensive White Matter in an Adult Female Caused by 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency

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

14. Adult-onset genetic leukoencephalopathies: A MRI pattern-based approach in a comprehensive study of 154 patients

20. Quantitative Assessment of the Evolution of Cerebellar Signs in Spinocerebellar Ataxias

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

23. CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

24. Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment

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

26. Phenotype associated with APP duplication in five families

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

29. Novel VCP mutations expand the mutational spectrum of frontotemporal dementia

31. New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay

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

33. Delayed-onset Friedreich's ataxia revisited

34. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

35. HeterozygousHTRA1mutations are associated with autosomal dominant cerebral small vessel disease

36. Adult-onset genetic leukoencephalopathies: A MRI pattern-based approach in a comprehensive study of 154 patients

38. PRRT2 mutations cause hemiplegic migraine

39. Intermediate repeat expansions of TBPand STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

42. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

43. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.

44. FXTAS.

45. Factors Influencing Disease Progression in Autosomal Dominant Cerebellar Ataxia and Spastic Paraplegia.

47. Mutation of the PDGFRBgene as a cause of idiopathic basal ganglia calcification

49. PRRT2mutations cause hemiplegic migraine

50. Novel VCP mutations expand the mutational spectrum of frontotemporal dementia

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