C Tranchant

Summary

Country: France

Publications

  1. ncbi Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?
    C Tranchant
    Service des Maladies du Système Nerveux et du Muscle, Hopitaux Universitaires, 1 Place de l Hopital, 67091 Strasbourg, France christine
    J Neurol 247:853-6. 2000
  2. ncbi A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy
    A Echaniz-Laguna
    Departement de Neurologie, Hopital Civil de Strasbourg, 1 Place de l Hopital, BP426, 67091 Strasbourg, France
    Neurology 64:1458-60. 2005
  3. ncbi [What is the role of other complementary examination in amyotrophic lateral sclerosis?]
    C Tranchant
    Departement de Neurologie, Hopitaux Universitaires, Strasbourg
    Rev Neurol (Paris) 162:4S50-4S56. 2006
  4. pmc Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes
    S Tezenas du Montcel
    Service de Biostatistique et Information Medicale, Hopital Pitie Salpetriere, AP HP, Paris, France
    J Med Genet 43:394-400. 2006
  5. ncbi [Acute myelitis and Lyme disease]
    F Blanc
    Departement de Neurologie, Hopitaux Universitaires de Strasbourg, Strasbourg
    Rev Neurol (Paris) 163:1039-47. 2007
  6. ncbi Phenotypic variability of aprataxin gene mutations
    C Tranchant
    Clinique Neurologique, Hopitaux Universitaires, CNRS, INSERM, Strasbourg France
    Neurology 60:868-70. 2003
  7. doi Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations
    E Roze
    Service de Neurologie, Hopital Saint Antoine, 184 rue du Faubourg Saint Antoine, 75571 Paris Cedex 12, France
    Neurology 70:1010-6. 2008
  8. ncbi [Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature]
    M Anheim
    Clinique Neurologique, Hopital Civil, Centre Hospitalier Universitaire de Strasbourg, B P 426, 1, Place de l Hopital, 67091 Strasbourg Cedex, France
    Rev Neurol (Paris) 164:363-8. 2008
  9. ncbi Relevance of the antibody index to diagnose Lyme neuroborreliosis among seropositive patients
    F Blanc
    Department of Neurology, University Hospital of Strasbourg, Louis Pasteur University, Strasbourg, France
    Neurology 69:953-8. 2007
  10. ncbi [Precoce survey: a new self-assessment patient card for early detection and management of Parkinson disease fluctuations]
    J P Azulay
    Service de Neurologie, Hopital La Timone, 13005 Marseille, France
    Rev Neurol (Paris) 164:354-62. 2008

Collaborators

Detail Information

Publications23

  1. ncbi Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?
    C Tranchant
    Service des Maladies du Système Nerveux et du Muscle, Hopitaux Universitaires, 1 Place de l Hopital, 67091 Strasbourg, France christine
    J Neurol 247:853-6. 2000
    ..However, this response cannot be used as a diagnostic test because of its poor specificity...
  2. ncbi A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy
    A Echaniz-Laguna
    Departement de Neurologie, Hopital Civil de Strasbourg, 1 Place de l Hopital, BP426, 67091 Strasbourg, France
    Neurology 64:1458-60. 2005
    ....
  3. ncbi [What is the role of other complementary examination in amyotrophic lateral sclerosis?]
    C Tranchant
    Departement de Neurologie, Hopitaux Universitaires, Strasbourg
    Rev Neurol (Paris) 162:4S50-4S56. 2006
    ....
  4. pmc Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes
    S Tezenas du Montcel
    Service de Biostatistique et Information Medicale, Hopital Pitie Salpetriere, AP HP, Paris, France
    J Med Genet 43:394-400. 2006
    ..Myoclonus dystonia syndrome (MDS) is an autosomal dominant movement disorder caused by mutations in the epsilon-sarcoglycan gene (SGCE) on chromosome 7q21...
  5. ncbi [Acute myelitis and Lyme disease]
    F Blanc
    Departement de Neurologie, Hopitaux Universitaires de Strasbourg, Strasbourg
    Rev Neurol (Paris) 163:1039-47. 2007
    ..In the literature, simultaneous spinal MRI and cerebrospinal fluid (CSF) investigations are presented for only 8 cases. We describe here 3 cases of acute Lyme myelitis...
  6. ncbi Phenotypic variability of aprataxin gene mutations
    C Tranchant
    Clinique Neurologique, Hopitaux Universitaires, CNRS, INSERM, Strasbourg France
    Neurology 60:868-70. 2003
    ..Patients 2 and 3 were French siblings and did not present with either OMA or hypoalbuminemia. They were compound heterozygous for the nonsense W279X mutation and a missense K197Q mutation...
  7. doi Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations
    E Roze
    Service de Neurologie, Hopital Saint Antoine, 184 rue du Faubourg Saint Antoine, 75571 Paris Cedex 12, France
    Neurology 70:1010-6. 2008
    ..To clarify the clinical and neurophysiologic spectrum of myoclonus-dystonia patients with mutations of the SGCE gene...
  8. ncbi [Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature]
    M Anheim
    Clinique Neurologique, Hopital Civil, Centre Hospitalier Universitaire de Strasbourg, B P 426, 1, Place de l Hopital, 67091 Strasbourg Cedex, France
    Rev Neurol (Paris) 164:363-8. 2008
    ..We present a review of the literature on this rare disease mostly described in Quebec...
  9. ncbi Relevance of the antibody index to diagnose Lyme neuroborreliosis among seropositive patients
    F Blanc
    Department of Neurology, University Hospital of Strasbourg, Louis Pasteur University, Strasbourg, France
    Neurology 69:953-8. 2007
    ..However, these studies included only typical clinical cases of meningitis or meningoradiculitis, and none had a control group with CSF anti-Borrelia antibodies...
  10. ncbi [Precoce survey: a new self-assessment patient card for early detection and management of Parkinson disease fluctuations]
    J P Azulay
    Service de Neurologie, Hopital La Timone, 13005 Marseille, France
    Rev Neurol (Paris) 164:354-62. 2008
    ..The investigators have recognized the usefulness of this self-assessment in order to detect fluctuations in 81% of fluctuating patients, which lead them to modify the treatment in 76% of them...
  11. ncbi [Subthalamic stimulation in a patient with multiple system atrophy: a clinicopathological report]
    V Talmant
    Departement de Neurologie, Hopital Civil, CHU, Strasbourg
    Rev Neurol (Paris) 162:363-70. 2006
    ..We report a patient with a clinical misdiagnosed MSA-P, later confirmed by neuropathological study, who was improved by DBS for one year...
  12. ncbi [Ataxia associated with gluten sensitivity, myth or reality?]
    M Anheim
    Service des Maladies du Système Nerveux et du Muscle, Clinique Neurologique, Hopital Civil de Strasbourg, Strasbourg
    Rev Neurol (Paris) 162:214-21. 2006
    ..Gluten ataxia refers to the association of idiopathic ataxia despite exhaustive investigations with gluten sensitivity defined by anti-gliadin antibodies (AGA) presence in blood. This is a controversial concept...
  13. pmc Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation
    M Anheim
    J Neurol Neurosurg Psychiatry 78:1414-5. 2007
  14. ncbi [Report from the 57th Annual Meeting of the American Academy of Neurology]
    I Bonnaud
    Rev Neurol (Paris) 161:610-23. 2005
  15. ncbi [Hemicontracture and facial myokimia as the first manifestation of multiple sclerosis]
    A Dupeyron
    , , Strasbourg, Cedex, France
    Rev Neurol (Paris) 157:315-7. 2001
    ..We report two cases of CMF as first manifestation of multiple sclerosis. Multiple sclerosis is the first diagnosis to suspect in young people with CFM...
  16. ncbi Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodies
    M Giraud
    INSERM U25, , Paris, France
    Neurology 57:1555-60. 2001
    ..Moreover, DR3 and DR7, or closely linked genes, have opposing effects on MG phenotypes. Nonthymomatous patients with ATA may be a pathogenetically distinct subset of MG patients...
  17. ncbi [Digestive tract disorders revealing mitochondrial cytopathy: MNGIE syndrome]
    F Chaury
    Service de Neurologie, Hopitaux Universitaires, 67091 Strasbourg Cedex, France
    Rev Neurol (Paris) 158:111-3. 2002
  18. ncbi Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
    P Ibanez
    INSERM U289, Neurologie et Thérapeutique Expérimentale, Hopital de la Salpetriere, Paris, France
    Neurology 62:2133-4. 2004
  19. ncbi [Report from the 56th annual meeting of the American Academy of Neurology]
    C Adam
    Rev Neurol (Paris) 160:606-22. 2004
  20. ncbi [Acute relapse in Charcot-Marie-Tooth 1B neuropathy: can protein P0 behave like an autoantigen?]
    M Fleury
    Departement de Neurologie, Hopitaux Universitaires, Strasbourg
    Rev Neurol (Paris) 160:839-42. 2004
    ..The natural history of Charcot-Marie-Tooth neuropathy is marked by accentuated motor and sensitive deficits suggestive of acute polyradiculoneuritis or, more generally, chronic inflammatory demyelinizing polyneuropathy...
  21. ncbi [Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]
    B Degos
    Departement de Neurologie, Hopital Civil de Strasbourg, Strasbourg, France
    Rev Neurol (Paris) 160:1203-6. 2004
    ..It is usually caused by a 1.5 Mb deletion of the PMP22 gene (17p11.2)...
  22. ncbi [A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy]
    A Echaniz-Laguna
    Departement de Neurologie, Hopital Civil de Strasbourg
    Rev Neurol (Paris) 161:437-44. 2005
    ..Material and method. We report the detailed phenotypic study in a series of 12 SBMA patients evaluated in four kindreds...
  23. doi [American Academy of Neurology, Chicago, 12-18 April 2008]
    I Bonnaud
    Service de Neurologie 1, Hopital de la Salpetriere, 47, Boulevard de l Hopital, 75651 Paris Cedex 13, France
    Rev Neurol (Paris) 164:486-99. 2008