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32 results on '"Ribaï, Pascale"'

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1. A clinical scoring system for congenital contractural arachnodactyly

2. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

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

4. Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease

5. The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease

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

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

13. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

14. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

15. Depression comorbidity in spinocerebellar ataxia.

16. Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings.

17. Self-rated health status in spinocerebellar ataxia--results from a European multicenter study.

18. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

19. Composite cerebellar functional severity score: Validation of a quantitative score of cerebellar impairment

20. Usefulness of prolonged video-EEG monitoring and provocative procedure with saline injection for the diagnosis of non epileptic seizures of psychogenic origin

21. Acute Balint’s syndrome is not always a stroke

22. Brachial plexus neuritis: is prognosis worse in children?

23. Acute Balint’s syndrome is not always a stroke

25. Sialic acid residues in the labial salivary glands from Sjögren's syndrome patients.

26. D-mannose and N-acetylglucosamine moieties and their respective binding sites in salivary glands of Sjögren's syndrome.

27. The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease

28. Mental deficiency in three families with SPG4 spastic paraplegia.

29. Identification of genetic variants associated with Huntington's disease progression

30. Clinical manifestations of intermediate allele carriers in Huntington disease

31. Usefulness of prolonged video-EEG monitoring and provocative procedure with saline injection for the diagnosis of non epileptic seizures of psychogenic origin.

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