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64 results on '"Tranchant C"'

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1. French validation of the Quality of life in Essential Tremor Questionnaire (QUEST) and the Essential Tremor Embarrassment Assessment (ETEA)

2. Early hyperdopaminergic state following sub-thalamic nucleus deep brain stimulation in Parkinson disease

3. Analyses génétiques et affections spino-cérébelleuses : splendeurs et misères

4. Gestione chirurgica della miastenia autoimmune (o miastenia grave)

5. Formes neurologiques de la maladie de Lyme

7. Enrayage cinétique (ou freezing of gait) sévère persistant en ON : essayez de diminuer la lévodopa !

9. Movement disorders in mitochondrial diseases

11. Syndromes parkinsoniens rares de causes héréditaires

12. Borreliosi di Lyme e neuroborreliosi

17. Étude rétrospective multicentrique de 15 cas adultes de xanthomatose cérébrotendineuse : aspects cliniques et paracliniques typiques et atypiques

18. High insulinlike growth factor I is associated with cognitive decline in Huntington disease

19. Intérêt de la tomoscintigraphie cardiaque à la 123I-mIBG couplée à la perfusion myocardique dans le diagnostic de l’atrophie multisystématisée

20. Dehydroepiandrosterone for myotonic dystrophy type 1SYMBOL

21. Myoclonus–dystonia

22. Relevance of the antibody index to diagnose Lyme neuroborreliosis among seropositive patients

24. The Role of Calcium and Magnesium Ions in Uptake of β-Amyloid Peptides by Microglial Cells

25. Introduction and classical environmental risk factors for Parkinson

29. MRI in multiple sclerosis of the spinal cord: evaluation of fast short-tan inversion-recovery and spin-echo sequences

30. Basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

31. A new peroxisomal disease with impaired phytanic and pipecolic acid oxidation

32. Immunochemical molecular genetic and transmission studies on a case of GerstmannStrausslerScheinker syndrome

33. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

34. Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation

36. Impact de la stimulation cérébrale profonde sur les troubles du contrôle des impulsions dans la maladie de Parkinson

37. A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy

38. Kennedy's Disease Initially Manifesting as an Endocrine Disorder

39. Phenotypic variability of aprataxingene mutations

40. MR findings in mannosidosis

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