Marie Vidailhet

Summary

Country: France

Publications

  1. ncbi request reprint Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up study
    Marie Vidailhet
    INSERM U679, Neurology and Experimental Therapeutics, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Lancet Neurol 6:223-9. 2007
  2. doi request reprint Interruption of deep brain stimulation of the globus pallidus in primary generalized dystonia
    David Grabli
    Neurology Department and Centre de Référence des Maladies Neurogénétiques, Hopital de la Salpetriere, Paris, France
    Mov Disord 24:2363-9. 2009
  3. doi request reprint EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
    Suzanne Lesage
    Universite Pierre et Marie Curie PARIS6, Centre de Recherche de l Institut du Cerveau et de la Moelle Epiniere, UMR S975, INSERM, U975, CNRS, UMR 7225, Hopital de la Pitie Salpetriere, Paris, France
    Neurobiol Aging 33:2233.e1-2233.e5. 2012
  4. pmc REM sleep behavior disorder in patients with guadeloupean parkinsonism, a tauopathy
    Valerie Cochen De Cock
    Service de Neurologie, Hopital Saint Antoine, Paris, France
    Sleep 30:1026-32. 2007
  5. doi request reprint Bilateral pallidal deep brain stimulation for the treatment of patients with dystonia-choreoathetosis cerebral palsy: a prospective pilot study
    Marie Vidailhet
    AP HP, Groupe Hospitalier Pitie Salpetriere, Federation de Neurologie, Paris, F 75013, France
    Lancet Neurol 8:709-17. 2009
  6. doi request reprint Bilateral deep brain stimulation of the pallidum for myoclonus-dystonia due to ε-sarcoglycan mutations: a pilot study
    Julie Azoulay-Zyss
    Service de Neurologie, Groupe Hospitalier Paris Saint Joseph, Universite Paris 5, Paris, France
    Arch Neurol 68:94-8. 2011
  7. pmc The coeruleus/subcoeruleus complex in rapid eye movement sleep behaviour disorders in Parkinson's disease
    Daniel García-Lorenzo
    Institut du Cerveau et de Moelle épinière, Centre de NeuroImagerie de Recherche, Paris, France
    Brain 136:2120-9. 2013
  8. doi request reprint A motor signature of REM sleep behavior disorder
    Delphine Oudiette
    Sleep Disorders Unit, Pitie Salpetriere Hospital, APHP, Paris, France
    Mov Disord 27:428-31. 2012
  9. doi request reprint Risk factors for spinal cord lesions in dystonic cerebral palsy and generalised dystonia
    Emilie Guettard
    AP HP, Department of Neurology, Groupe Hospitalier Pitie Salpetriere, Paris, France
    J Neurol Neurosurg Psychiatry 83:159-63. 2012
  10. doi request reprint Dystonic tremor caused by mutation of the glucose transporter gene GLUT1
    Anne Roubergue
    AP HP, Service de Neuropediatrie, Hopital Trousseau, Paris, France
    J Inherit Metab Dis 34:483-8. 2011

Detail Information

Publications81

  1. ncbi request reprint Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up study
    Marie Vidailhet
    INSERM U679, Neurology and Experimental Therapeutics, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Lancet Neurol 6:223-9. 2007
    ....
  2. doi request reprint Interruption of deep brain stimulation of the globus pallidus in primary generalized dystonia
    David Grabli
    Neurology Department and Centre de Référence des Maladies Neurogénétiques, Hopital de la Salpetriere, Paris, France
    Mov Disord 24:2363-9. 2009
    ..The interruption of GP DBS in dystonia results in a progressive worsening which is rapidly reversible once the neurostimulator is turned ON...
  3. doi request reprint EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
    Suzanne Lesage
    Universite Pierre et Marie Curie PARIS6, Centre de Recherche de l Institut du Cerveau et de la Moelle Epiniere, UMR S975, INSERM, U975, CNRS, UMR 7225, Hopital de la Pitie Salpetriere, Paris, France
    Neurobiol Aging 33:2233.e1-2233.e5. 2012
    ..G686C) and in a control subject (p.R1197W). These data do not support the pathogenicity of several EIF4G1 variants in PD, at least in the French population...
  4. pmc REM sleep behavior disorder in patients with guadeloupean parkinsonism, a tauopathy
    Valerie Cochen De Cock
    Service de Neurologie, Hopital Saint Antoine, Paris, France
    Sleep 30:1026-32. 2007
    ..It is possibly caused by the ingestion of sour sop (corossol), a tropical fruit containing acetogenins, which are mitochondrial poisons...
  5. doi request reprint Bilateral pallidal deep brain stimulation for the treatment of patients with dystonia-choreoathetosis cerebral palsy: a prospective pilot study
    Marie Vidailhet
    AP HP, Groupe Hospitalier Pitie Salpetriere, Federation de Neurologie, Paris, F 75013, France
    Lancet Neurol 8:709-17. 2009
    ..Our aim was to test the effectiveness of BP-DBS in adults with dystonia-choreoathetosis CP...
  6. doi request reprint Bilateral deep brain stimulation of the pallidum for myoclonus-dystonia due to ε-sarcoglycan mutations: a pilot study
    Julie Azoulay-Zyss
    Service de Neurologie, Groupe Hospitalier Paris Saint Joseph, Universite Paris 5, Paris, France
    Arch Neurol 68:94-8. 2011
    ..To assess the efficacy of bilateral deep brain stimulation of the internal pallidum in patients with myoclonus-dystonia due to genetically proved ε-sarcoglycan (SGCE-M-D) deficiency...
  7. pmc The coeruleus/subcoeruleus complex in rapid eye movement sleep behaviour disorders in Parkinson's disease
    Daniel García-Lorenzo
    Institut du Cerveau et de Moelle épinière, Centre de NeuroImagerie de Recherche, Paris, France
    Brain 136:2120-9. 2013
    ..In longitudinal studies, the technique may also provide early markers of non-dopaminergic Parkinson's disease pathology to predict the occurrence of Parkinson's disease. ..
  8. doi request reprint A motor signature of REM sleep behavior disorder
    Delphine Oudiette
    Sleep Disorders Unit, Pitie Salpetriere Hospital, APHP, Paris, France
    Mov Disord 27:428-31. 2012
    ..The purpose of this study was to determine if there was a common pattern in movements during REM sleep behavior disorder (RBD)...
  9. doi request reprint Risk factors for spinal cord lesions in dystonic cerebral palsy and generalised dystonia
    Emilie Guettard
    AP HP, Department of Neurology, Groupe Hospitalier Pitie Salpetriere, Paris, France
    J Neurol Neurosurg Psychiatry 83:159-63. 2012
    ..The aim of this study is to identify the risk factors and clinical characteristics of CM in patients with generalised dystonia, including dystonic CP...
  10. doi request reprint Dystonic tremor caused by mutation of the glucose transporter gene GLUT1
    Anne Roubergue
    AP HP, Service de Neuropediatrie, Hopital Trousseau, Paris, France
    J Inherit Metab Dis 34:483-8. 2011
    ..Patients who present with dystonic tremor, with or without mental retardation, seizures, movement disorders and/or a family history, should therefore be screened for GLUT1-DS...
  11. doi request reprint Reinforcement learning and Gilles de la Tourette syndrome: dissociation of clinical phenotypes and pharmacological treatments
    Yulia Worbe
    Centre de Recherche de l Institut du Cerveau et de la Moelle Epiniere, Hopital Pitie Salpetriere, Paris, France
    Arch Gen Psychiatry 68:1257-66. 2011
    ..The heterogeneity of clinical phenotypes may relate to the dysfunction of distinct frontal cortex-basal ganglia circuits...
  12. doi request reprint PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population
    Aurélie Méneret
    INSERM, UMRS 975, Hopital Pitie Salpetriere, Paris, France
    Neurology 79:170-4. 2012
    ..Mutations in the PRRT2 gene were recently identified in patients with PKD and ICCA. We studied the prevalence of PRRT2 mutations and characteristics of the patients in a European population of patients with PKD and ICCA...
  13. doi request reprint Dopaminergic deficit is not the rule in orthostatic tremor
    Jean Marc Trocello
    Department of Neurology, Lariboisiere Hospital, AP HP, Paris, France
    Mov Disord 23:1733-8. 2008
    ..c) 2008 Movement Disorder Society...
  14. pmc Defective cerebellar control of cortical plasticity in writer's cramp
    Cécile Hubsch
    Department of Neurology, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Brain 136:2050-62. 2013
    ..The loss of cerebellar control over sensorimotor plasticity might also lead to building up an incorrect motor program to specific adaptation tasks such as writing. ..
  15. doi request reprint Functional immaturity of cortico-basal ganglia networks in Gilles de la Tourette syndrome
    Yulia Worbe
    INSERM, Groupe Hospitalier Pitie Salpetriere, Assistance Publique Hopitaux de Paris, Centre d Investigation Clinique CIC 9503, Pôle des maladies du système nerveux, Paris, France
    Brain 135:1937-46. 2012
    ..They also support the hypothesis that distinct regions of cortico-basal ganglia networks contribute to the clinical heterogeneity of this syndrome...
  16. ncbi request reprint Myoclonus or tremor in orthostatism: an under-recognized cause of unsteadiness in Parkinson's disease
    Smaranda Leu-Semenescu
    Department of Neurology, Saint Antoine Hospital, AP HP, Paris, France
    Mov Disord 22:2063-9. 2007
    ..These observations show the usefulness of neurophysiological investigations for diagnosing and treating unexplained unsteadiness in Parkinson's disease...
  17. ncbi request reprint Restoration of normal motor control in Parkinson's disease during REM sleep
    Valerie Cochen De Cock
    Service de Neurologie, Hopital Saint Antoine, Paris, France
    Brain 130:450-6. 2007
    ..These movements would eventually be transmitted to lower motor neurons because of brainstem lesions interrupting the pontomedullary pathways which mediate the REM sleep atonia...
  18. doi request reprint Somatosensory cortical remodelling after rehabilitation and clinical benefit of in writer's cramp
    Jean Pierre Bleton
    Université Paris Descartes EA 4055 ISERM U894, Paris, France
    J Neurol Neurosurg Psychiatry 82:574-7. 2011
    ..The authors hypothesise that prolonged tailored rehabilitation in WC may induce long-term plasticity phenomena, lateralised to the cortex controlling the dystonic hand...
  19. doi request reprint Dopamine-dependent reinforcement of motor skill learning: evidence from Gilles de la Tourette syndrome
    Stefano Palminteri
    institut du cerveau et de la moelle épinière, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Brain 134:2287-301. 2011
    ..These results support the hypothesis that overactive dopamine transmission leads to excessive reinforcement of motor sequences, which might explain the formation of tics in Gilles de la Tourette syndrome...
  20. ncbi request reprint Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia
    Marie Vidailhet
    Department of Neurology, Saint Antoine Hospital, Paris, France
    N Engl J Med 352:459-67. 2005
    ..Severe forms of dystonia respond poorly to medical treatment. Deep-brain stimulation is a reversible neurosurgical procedure that has been used for the treatment of dystonia, but assessment of its efficacy has been limited to open studies...
  21. doi request reprint Predominant cortical dysfunction in Guadeloupean parkinsonism
    Emmanuelle Apartis
    Department of Physiology, Saint Antoine Hospital, AP HP, Paris VI University, Paris, France
    Brain 131:2701-9. 2008
    ..This electrophysiological study, added to previous clinical, neuropsychological and neuroradiological studies, has enriched the characterization of Guadeloupean atypical parkinsonism, which thus appears to be a new clinical entity...
  22. doi request reprint Myoclonus and dystonia in cerebrotendinous xanthomatosis
    Julien Lagarde
    AP HP Département de Neurologie, Hopital de la Salpetriere, Paris, France
    Mov Disord 27:1805-10. 2012
    ..Myoclonic dystonia has been reported on in the setting of various neurometabolic diseases. Anecdotal reports describe movement disorders associated with CTX, but no dystonia with myoclonic events...
  23. doi request reprint Normal and pathological gait: what we learn from Parkinson's disease
    David Grabli
    Universite Pierre et Marie Curie Paris 6, CR Icm, UMR S975, Paris, France
    J Neurol Neurosurg Psychiatry 83:979-85. 2012
    ..In addition, we review recent evidence regarding functional neurosurgery for gait disorders in PD and propose new directions for future therapeutic research...
  24. doi request reprint Is obstructive sleep apnea a problem in Parkinson's disease?
    Valerie Cochen De Cock
    Sleep Disorders Unit, Pitie Salpetriere Hospital, APHP, Paris, France
    Sleep Med 11:247-52. 2010
    ..Upper airway dysfunction in PD may promote obstructive sleep apnea. However, the frequency and clinical relevance of sleep-disordered breathing in PD remains unclear...
  25. doi request reprint Myoclonus-dystonia: an update
    Kiyoka Kinugawa
    INSERM U679, Pitie Salpetriere Hospital, Paris, France
    Mov Disord 24:479-89. 2009
    ..On the basis of a comprehensive literature search, this review summarizes current knowledge on M-D, with a focus on recent findings. We also propose modified diagnostic criteria and recommendations for clinical management...
  26. doi request reprint Impaired saccadic adaptation in DYT11 dystonia
    Cécile Hubsch
    Assistance Publique Hopitaux de Paris, Pitie Salpetriere Hospital, Department of Neurology, Paris, France
    J Neurol Neurosurg Psychiatry 82:1103-6. 2011
    ..The authors investigated the association between sensorimotor adaptation, cerebellar dysfunction and the myoclonus-dystonia phenotype...
  27. doi request reprint Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene
    Domitille Gras
    AP HP, Service de Neuropediatrie, Hopital Trousseau, Paris, France
    J Neurol Neurosurg Psychiatry 83:956-62. 2012
    ..The aim of the study was to refine the movement disorders phenotype. We also studied disease course and response to therapy in a large series of genetically proven patients...
  28. doi request reprint Hallucinations in narcolepsy with and without cataplexy: contrasts with Parkinson's disease
    Smaranda Leu-Semenescu
    Sleep Disorders Unit, Pitie Salpetriere Hospital, AP HP, Paris 6 University, Paris, France
    Sleep Med 12:497-504. 2011
    ..partial (PD, narcolepsy without cataplexy) hypocretin-1 deficiency...
  29. doi request reprint The COMT Val158Met polymorphism affects the response to entacapone in Parkinson's disease: a randomized crossover clinical trial
    Jean Christophe Corvol
    INSERM French National Institute of Medical Research and Health, Clinical Investigation Center CIC 9503, Pitie Salpetriere Hospital, Paris, France
    Ann Neurol 69:111-8. 2011
    ..The objective of this study was to determine the response to entacapone in COMT(HH) and COMT(LL) PD patients...
  30. ncbi request reprint Clinical analysis in familial cortical myoclonic tremor allows differential diagnosis with essential tremor
    Frederic Bourdain
    Department of Neurology, Hopital Saint Antoine, Paris, France
    Mov Disord 21:599-608. 2006
    ..We emphasize that a precise clinical analysis can lead to a correct diagnosis before electrophysiological confirmation. This is also the first-ever report of efficacy of levetiracetam in FCMT...
  31. doi request reprint Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease
    Suzanne Lesage
    Universite Pierre et Marie Curie Paris 6, Centre de Recherche de l Institut du Cerveau et de la Moelle Epiniere, UMR S975, and Department of Genetics and Cytogenetics, Pitie Salpetriere Hospital, Paris, France
    Hum Mol Genet 20:202-10. 2011
    ..These genotype and clinical analyses on the largest homogeneous sample of European patients studied to date confirmed that GBA mutations are the most common genetic risk factor for PD, particularly in familial forms...
  32. ncbi request reprint Deep brain stimulation of the globus pallidus for generalized dystonia in GM1 Type 3 gangliosidosis: technical case report
    Emmanuel Roze
    Department of Neurology, Saint Antoine Hospital, Paris, France
    Neurosurgery 59:E1340; discussion E1340. 2006
    ..We performed bilateral pallidal stimulation in a patient with GM1 gangliosidosis and report the 12-month postoperative course...
  33. doi request reprint Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms
    Pablo Ibanez
    Institut National de la Sante et de la Recherche Medicale INSERM, Unité Mixte de Recherche en Santé UMR _S679 Neurologie and Thérapeutique Expérimentale, F 75013, Paris, France
    Arch Neurol 66:102-8. 2009
    ..The aim of this study was to assess the frequency and phenotype of SNCA rearrangements in a large series of families with typical or atypical AD parkinsonism...
  34. pmc Repetitive behaviours in patients with Gilles de la Tourette syndrome: tics, compulsions, or both?
    Yulia Worbe
    Centre d Investigation Clinique INSERM CIC 9503, Pôle des maladies du système nerveux, Assistance Publique Hopitaux de Paris, Groupe Hospitalier Pitie Salpetriere, Universite Pierre et Marie Curie Paris 6, Paris, France
    PLoS ONE 5:e12959. 2010
    ..Repetitive behaviours (RB) in patients with Gilles de la Tourette syndrome (GTS) are frequent. However, a controversy persists whether they are manifestations of obsessive-compulsive disorder (OCD) or correspond to complex tics...
  35. doi request reprint Deep brain stimulation for hyperkinetics disorders: dystonia, tardive dyskinesia, and tics
    Marie Laure Welter
    AP HP, Fédération des Maladies du Système Nerveux, Université Pierre et Marie Curie Paris, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Curr Opin Neurol 23:420-5. 2010
    ..This review focuses on new insights in deep brain stimulation (DBS) for patients with hyperkinetic movement disorders: dystonia, tardive dyskinesia and Gille de la Tourette's syndrome, during the last 18 months...
  36. pmc Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study
    Gilbert Bensimon
    Departement de Pharmacologie Clinique, Hopital de la Pitie Salpetriere, Assistance Publique Hôpitaux de Paris and UPMC University Paris 06, UMR 7087, Paris, France
    Brain 132:156-71. 2009
    ..The NNIPPS diagnostic criteria were consistent and valid. They can be used to distinguish between PSP and MSA with high accuracy, and should facilitate research into these conditions relatively early in their evolution...
  37. ncbi request reprint Impaired modulation of motor cortex excitability by homonymous and heteronymous muscle afferents in focal hand dystonia
    George Lourenco
    INSERM U731, Paris, France
    Mov Disord 22:523-7. 2007
    ..These findings support the view that a global abnormal somatosensory coupling in focal hand dystonia may contribute to an inadequate motor command to wrist muscles...
  38. doi request reprint Myoclonus-dystonia due to maternal uniparental disomy
    Emilie Guettard
    Service de Neurologie, Hopital Saint Antoine, AP HP, Paris, France
    Arch Neurol 65:1380-5. 2008
    ..Silver-Russell syndrome is a heterogeneous disorder characterized by prenatal and postnatal growth restriction and a characteristic facies, caused in some cases by maternal uniparental disomy of chromosome 7...
  39. ncbi request reprint Propriospinal myoclonus: utility of magnetic resonance diffusion tensor imaging and fiber tracking
    Emmanuel Roze
    Department of Neurology, Saint Antoine Hospital, AP HP, Paris, France
    Mov Disord 22:1506-9. 2007
    ..Tract-specific analysis may provide new insights into the pathophysiology of propriospinal myoclonus...
  40. pmc RAD51 haploinsufficiency causes congenital mirror movements in humans
    Christel Depienne
    INSERM, U CRICM, Hopital Pitie Salpetriere, Paris, France
    Am J Hum Genet 90:301-7. 2012
    ..These findings open a new field of investigation for researchers attempting to unravel the molecular pathways underlying bimanual motor control in humans...
  41. doi request reprint The clinical and anatomical heterogeneity of environmental dependency phenomena
    Julien Lagarde
    AP HP, Department of Neurology, Groupe Hospitalier Pitie Salpetriere, Paris, France
    J Neurol 260:2262-70. 2013
    ..Within this large network, grasping and imitation behaviors can be dissociated from both neuropsychological and anatomical standpoints, underlining the clinical and anatomical heterogeneity of environmental dependency phenomena. ..
  42. doi request reprint Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients
    Cyril Gitiaux
    Universite Paris Descartes, Service de Neurologie Pediatrique et Maladies Metaboliques, Hopital Necker Enfants Malades, AP HP, Paris, France
    Mov Disord 23:2392-7. 2008
    ..The types and outcome of movement disorders in this setting should be taken into consideration during rehabilitation and for patient selection and evaluation in therapeutic trials...
  43. doi request reprint Urodynamic analysis in multiple system atrophy: characterisation of detrusor-sphincter dyssynergia
    Frederic Bloch
    AP HP, centre d investigation clinique, Universite Pierre et Marie Curie Paris 6, Groupe Hospitalier Pitie Salpetriere, 75013, Paris, France
    J Neurol 257:1986-91. 2010
    ..This new approach may prove useful for differential diagnosis of parkinsonian syndromes, and especially MSA...
  44. ncbi request reprint Head tremor in Parkinson's disease
    Emmanuel Roze
    Department of Neurology, Saint Antoine Hospital, Assistance Publique Hopitaux de Paris AP HP, Paris, France
    Mov Disord 21:1245-8. 2006
    ..We describe five patients with Parkinson's disease and head tremor in whom clinical and neurophysiological findings suggested that head tremor was a manifestation of Parkinson's disease...
  45. ncbi request reprint Dystonia and parkinsonism in GM1 type 3 gangliosidosis
    Emmanuel Roze
    Department of Neurology, Saint Antoine Hospital AP HP Paris, France
    Mov Disord 20:1366-9. 2005
    ..GM1 gangliosidosis must be considered as a cause of early-onset generalized dystonia, particularly in patients with short stature and skeletal dysplasia...
  46. ncbi request reprint How much phenotypic variation can be attributed to parkin genotype?
    Ebba Lohmann
    INSERM U289, Hopital de la Salpetriere, Paris, France
    Ann Neurol 54:176-85. 2003
    ..Patients with a single heterozygous mutation had significantly later and more asymmetrical onset and more frequent levodopa-induced fluctuations and dystonia than patients with two mutations...
  47. doi request reprint Speech disturbances in patients with dystonia or chorea due to neurometabolic disorders
    Constance Flamand-Rouvière
    Service de Neurologie, CHU de Bicetre, AP HP, Le Kremlin Bicetre, France
    Mov Disord 25:1605-11. 2010
    ..These findings have important implications for speech rehabilitation, and may provide new insights into the pathophysiology of dystonia due to neurometabolic disorders...
  48. ncbi request reprint Interictal myoclonus with paroxysmal kinesigenic dyskinesia
    Valerie Cochen De Cock
    Service de Neurologie, Hopital Saint Antoine, Assistance Publique Hopitaux de Paris, France
    Mov Disord 21:1533-5. 2006
    ..By definition, PKD is transient, but the overexcitability of the neuronal system that induces these attacks may be permanent. Interictal myoclonus could be a manifestation of permanent overexcitability...
  49. doi request reprint Risk factors of multiple system atrophy: a case-control study in French patients
    Jean Sébastien Vidal
    INSERM U708, Neuroepidemiology, Paris, France
    Mov Disord 23:797-803. 2008
    ..004). This case-control study provided new findings about risk factors of MSA. On another hand, it did not confirm the previously reported association between MSA and exposure to pesticides...
  50. doi request reprint Deep brain stimulation for dystonia
    Marie Vidailhet
    AP HP, Department of Neurology, Groupe Hospitalier Pitie Salpetriere, Paris, France
    J Neurol Neurosurg Psychiatry 84:1029-42. 2013
    ..From this overview, the main results and limits for each subgroup of patients that may help in the selection of dystonic patients who will benefit from DBS are discussed. ..
  51. doi request reprint Parkinson's disease patients show reduced cortical-subcortical sensorimotor connectivity
    Michael Sharman
    UMR S975, CRICM INSERM UPMC Paris 6, Paris, Ile de France, France
    Mov Disord 28:447-54. 2013
    ..Increases in functional connectivity in other cortico-basal ganglia thalamocortical circuits may be indicative of compensatory effects in response to system deficits elsewhere...
  52. doi request reprint FXTAS: new insights and the need for revised diagnostic criteria
    Emmanuelle Apartis
    AP HP, Paris, France
    Neurology 79:1898-907. 2012
    ..We delineate the clinical, neurophysiologic, and morphologic characteristics of FXTAS...
  53. doi request reprint Distinct structural changes underpin clinical phenotypes in patients with Gilles de la Tourette syndrome
    Yulia Worbe
    Centre d Investigation Clinique INSERM CIC 9503, Fédération des Maladies du Système Nerveux, Groupe Hospitalier Pitie Salpetriere, AssistancePublique Hôpitaux de Paris, Paris, France
    Brain 133:3649-60. 2010
    ....
  54. ncbi request reprint REM sleep behavior disorder and REM sleep without atonia in patients with progressive supranuclear palsy
    Isabelle Arnulf
    Fédération des Pathologies du Sommeil and Upres EA 2397, Paris, France
    Sleep 28:349-54. 2005
    ....
  55. doi request reprint Pathophysiology of dystonia
    Marie Vidailhet
    Federation de Neurologie, Groupe Hospitalier Pitie Salpetriere, AP HP, Universite Pierre et Marie Curie PARIS6, INSERM, UMRS 975, CNRS UMR 7225, Paris, France
    Curr Opin Neurol 22:406-13. 2009
    ..Moreover, new advances in genetics have broadened the spectrum of dystonia. Here, we discuss these findings and their implication in the pathophysiology of dystonia...
  56. ncbi request reprint Time-frequency analysis reveals decreased high-frequency oscillations in writer's cramp
    Zoé Cimatti
    Pierre and Marie Curie University, Paris, France
    Brain 130:198-205. 2007
    ..This supports the assumption that abnormal HFOs reflect pathophysiological mechanisms occurring in focal dystonia, possibly resulting from a dysfunction of somatosensory processing...
  57. doi request reprint Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia
    Fabienne Clot
    AP HP, Département de génétique et cytogénétique, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Brain 132:1753-63. 2009
    ..Although the yield of mutations exceeds 80% in pure Dopa-responsive dystonia and Dopa-responsive dystonia-plus syndromes groups, the genes involved are clearly different: GCH1 in the former and TH and SPR in the later...
  58. doi request reprint Transcranial magnetic stimulation as an efficient treatment for psychogenic movement disorders
    Beatrice Garcin
    Departement de Neurologie, Hopital Pitie Salpetriere, Centre de Référence Maladie de Parkinson, APHP, Paris, France
    J Neurol Neurosurg Psychiatry 84:1043-6. 2013
    ..Recent studies suggested a possible therapeutic effect of repeated transcranial magnetic stimulation (TMS) in psychogenic paralysis and tremor...
  59. doi request reprint The anatomical basis of dystonia: Current view using neuroimaging
    Stephane Lehericy
    Institut du Cerveau et de la Moelle ICM epiniere, Centre de NeuroImagerie de Recherche CENIR, Paris, France Université Pierre et Marie Curie Paris 6, Centre de Recherche de l ICM epiniere, UMR S975, INSERM, U975, CNRS, UMR 7225, Paris, France Service de neuroradiologie, Groupe Hospitalier Pitie Salpetriere, Paris, France
    Mov Disord 28:944-57. 2013
    ..The application of imaging as a tool to monitor therapy and its use as an outcome measure will be discussed. © 2013 Movement Disorder Society. ..
  60. pmc Nonmotor symptoms in Parkinson's disease in 2012: relevant clinical aspects
    Anne Marie Bonnet
    APHP, Department of Neurology, Hospital Pitié Salpêtrière, Paris, France
    Parkinsons Dis 2012:198316. 2012
    ..NMSs play a large role in degradation of quality of life. More relevant NMSs are described in this review, mood disorders, impulse control disorders, cognitive deficits, hallucinations, pain, sleep disorders, and dysautonomia...
  61. doi request reprint Long-term outcome of 32 patients with chorea and systemic lupus erythematosus or antiphospholipid antibodies
    Peggy Reiner
    Service de Neurologie, AP HP, Hopital Lariboisiere, Paris, France
    Mov Disord 26:2422-7. 2011
    ..The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome...
  62. pmc Evidence for the re-enactment of a recently learned behavior during sleepwalking
    Delphine Oudiette
    Sleep Disorders Unit, Pitie Salpetriere Hospital, APHP, Paris, France
    PLoS ONE 6:e18056. 2011
    ..Our observation also suggests that the study of such sleep disorders may provide unique and critical information about cognitive functions operating during sleep...
  63. ncbi request reprint Psychogenic parkinsonism: a combination of clinical, electrophysiological, and [(123)I]-FP-CIT SPECT scan explorations improves diagnostic accuracy
    Sandrine Benaderette
    Department of Neurology, Saint Antoine Hospital, Paris, France
    Mov Disord 21:310-7. 2006
    ..A combination of clinical, electrophysiological, and [(123)I]-FP-CIT SPECT scan explorations improves diagnostic accuracy in order to distinguish PP from PP + PD...
  64. ncbi request reprint Parkin mutations are frequent in patients with isolated early-onset parkinsonism
    Magali Periquet
    INSERM U289, Hopital de la Salpetriere, Paris, France
    Brain 126:1271-8. 2003
    ..However, a single case presenting with cerebellar ataxia several years before typical parkinsonism extends the spectrum of parkin related-disease...
  65. ncbi request reprint Long-term follow-up and adult outcome of 6-pyruvoyl-tetrahydropterin synthase deficiency
    Emmanuel Roze
    Department of Neurology, Saint Antoine Hospital, Paris, France, and Division of Clinical Chemistry and Biochemistry, University Children s Hospital, Zurich, Switzerland
    Mov Disord 21:263-6. 2006
    ..This report illustrates the role of dopamine modulation in motor, psychiatric, and endocrine functions...
  66. ncbi request reprint Effects of internal clock and memory disorders on duration reproductions and duration productions in patients with Parkinson's disease
    Severine Perbal
    Unité de Neurosciences Cognitives et Imagerie Cérébrale, CNRS UPR 640, Hopital de la Salpetriere, Paris, France
    Brain Cogn 58:35-48. 2005
    ..The whole results indicate that dopamine administration in patients might have overshadowed the slowing rate of the internal clock usually reported in non medicated PD patients, without entirely restoring all of the memory functions...
  67. ncbi request reprint LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans
    Suzanne Lesage
    Institut National de la Santé et de la Recherche Médicale Unité 679, Neurology and Experimental Therapeutics, and Faculté de Médecine, Universite Pierre et Marie Curie, 75651 Paris Cedex 13, France
    Arch Neurol 64:425-30. 2007
    ..Mutations in leucine-rich repeat kinase 2 gene (LRRK2), particularly the G2019S mutation in exon 41, have been detected in familial and sporadic Parkinson disease (PD) cases...
  68. ncbi request reprint Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation
    Anne Roubergue
    Department of Neurology, Hopital Saint Antoine, AP HP, Paris, France
    Mov Disord 19:344-6. 2004
    ..These features, not previously described, illustrate an extension of the cerebral and digestive neurological involvement in this syndrome...
  69. ncbi request reprint Micrographia secondary to lenticular lesions
    Pascal Derkinderen
    Department of Neurology, Hopital Saint Antoine, Paris, France
    Mov Disord 17:835-7. 2002
    ..We conclude that infarct of the left lenticular nucleus could either mimic pure micrographia similar to that of Parkinson's disease or micrographia associated with dystonia...
  70. ncbi request reprint Dystonia: lessons from brain mapping
    Sabine Meunier
    Clinical Neurophysiology, Hopital de la Salpetriere, Paris, France
    Neuroscientist 9:76-81. 2003
    ..Techniques using specific markers have recently focused on the type of receptors that may be dysactivated and on the kind of neurotransmitter that may be dysregulated in dystonia...
  71. ncbi request reprint Deep brain stimulation for dystonia: make the lame walk
    Marie Vidailhet
    Ann Neurol 57:613-4. 2005
  72. ncbi request reprint Effects of pulse width variations in pallidal stimulation for primary generalized dystonia
    Laurent Vercueil
    Neurology and Neurosurgery, CHU Grenoble, 38043 Grenoble, France
    J Neurol 254:1533-7. 2007
    ..Various pulse widths (from 60-450 mus) have been used for bilateral pallidal stimulation in generalized dystonia but, to date, no comparison of this parameter's effects is available...
  73. ncbi request reprint Reliability of the Burke-Fahn-Marsden scale in a multicenter trial for dystonia
    Pierre Krystkowiak
    Department of Neurology and Movement Disorders, Lille University Medical Center, Lille, France
    Mov Disord 22:685-9. 2007
    ..However, the reliability of this tool has rarely been evaluated and its use in a multicenter study has never been assessed prospectively...
  74. ncbi request reprint Acute deep-brain stimulation of the internal and external globus pallidus in primary dystonia: functional mapping of the pallidum
    Jean Luc Houeto
    Service de Neurologie, Centre Hospitalier Universitaire La Miletrie, BP 577, 86021 Poitiers Cedex, France
    Arch Neurol 64:1281-6. 2007
    ..Patients with the severe and generalized forms can benefit from bilateral high-frequency pallidal stimulation...
  75. ncbi request reprint Motor execution and imagination networks in post-stroke dystonia
    Stephane Lehericy
    Service Hospitalier Frederic Joliot, CEA, Orsay, France
    Neuroreport 15:1887-90. 2004
    ..Mental representation of movements with each hand resulted in overactivity in bilateral parietal, premotor and prefrontal areas. These results suggest that execution and mental representation of movement are altered in these patients...
  76. ncbi request reprint Globus pallidus internus stimulation in primary generalized dystonia: a H215O PET study
    Olivier Detante
    Department of Biological and Clinical Neurosciences, Grenoble University Hospital, Grenoble, France
    Brain 127:1899-908. 2004
    ..According to the present study, generalized dystonia is associated with prefrontal overactivation which can be reversed by effective GPi DBS...
  77. doi request reprint Sleep disturbances in patients with parkinsonism
    Valerie Cochen De Cock
    National Center for MSA, Sleep Department, Purpan Hospital, Toulouse, France
    Nat Clin Pract Neurol 4:254-66. 2008
    ..The use of dopamine agonists increases the risk of sleep attacks, especially when driving, suggesting a drug-disease interaction...
  78. ncbi request reprint Myoclonus in spinal dysraphism
    Jane E Warren
    Department of Neurology, Royal Adelaide Hospital, Adelaide, Australia
    Mov Disord 18:961-4. 2003
    ..In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences...
  79. ncbi request reprint Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype
    Friedrich Asmus
    Neurologische Klinik Grosshadern, Ludwig Maximilians Universitat, Munich, Germany
    Ann Neurol 52:489-92. 2002
    ..Six novel and one previously known heterozygous SGCE mutations were identified. SGCE deficiency seems to be the common pathogenetic mechanism in myoclonus-dystonia syndrome...
  80. ncbi request reprint Dopaminergic function and dopamine transporter binding assessed with positron emission tomography in Parkinson disease
    Maria Joao Ribeiro
    URA CEA CNRS 2210, Service Hospitalier Frederic Joliot, 4, place du General Leclerc, 91401 Orsay, Cedex, France
    Arch Neurol 59:580-6. 2002
    ..The latter might be assessed using newly developed ligands of the membrane dopamine transporter...
  81. ncbi request reprint [Heterogeneity of Parkinson's disease]
    Marie Vidailhet
    Service de Neurologie, Hopital Saint Antoine, 184, rue du Faubourg Saint Antoine 75012 Paris
    Bull Acad Natl Med 187:259-75; discussion 275-6. 2003
    ..It is likely that clarification of the combined genetic and environmental factors undelying these various disorders will lead to novel diagnostic and therapeutic strategies...