E Fournier

Summary

Country: France

Publications

  1. ncbi request reprint [Electrophysiological signs of muscle channelopathies by causal mutation]
    E Fournier
    Fédération de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, Paris
    Rev Neurol (Paris) 161:1251-9. 2005
  2. doi request reprint [Conduction block: a notion to let through]
    E Fournier
    Departement de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, 47 Boulevard de l Hopital, Paris, France
    Rev Neurol (Paris) 168:952-9. 2012
  3. ncbi request reprint Cold extends electromyography distinction between ion channel mutations causing myotonia
    Emmanuel Fournier
    Fédération de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, Assistance Publique Hopitaux de Paris, Universite Pierre et Marie Curie, Paris
    Ann Neurol 60:356-65. 2006
  4. doi request reprint [Simplified exploration of brachial plexopathies by reduction to well-known mononeuropathies and radiculopathies]
    E Fournier
    Departement de Physiologie, Faculté de Médecine Pitié Salpêtrière, Universite Pierre et Marie Curie Paris 6, 91, Boulevard de l Hopital, 75013 Paris, France
    Rev Neurol (Paris) 165:1127-33. 2009
  5. ncbi request reprint New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
    S Vicart
    Fédération de Neurologie and INSERM U546, Groupe Hospitalier Pitie Salpetriere, Assistance Publique Hopitaux de Paris, and Universite Pierre et Marie Curie, Paris, France
    Neurology 63:2120-7. 2004
  6. ncbi request reprint [The hypolossal-facial anastomosis in man. A model for studying peripheral and central nervous system plasticity]
    F Tankere
    Equipe Mixte INSERM 0349 et Fédération de Neurophysiologie Clinique, Hopital de la Pitie Salpetriere, 47 Boulevard de l Hopital, 75013 Paris
    Rev Med Liege 59:91-103. 2004
  7. doi request reprint [Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]
    B Eymard
    Centre de référence des affections neuromusculaires Paris Est, Service de neurologie 2, Institut de Myologie, Hopital de la Pitie Salpetriere, 47 bd de l Hopital, 75013 Paris, France
    Rev Neurol (Paris) 169:S45-55. 2013
  8. doi request reprint Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases
    S LaRue
    Centre de Référence Maladies Neuromusculaires Rares, Hôpital Pitié Salpêtrière and Université Paris VI, Paris, France
    Eur J Neurol 18:899-905. 2011
  9. doi request reprint Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
    I Wargon
    AP HP, Groupe Hospitalier Pitie Salpetriere, Bâtiment Lhermitte, Centre de Recherche de l Institut du Cerveau et de la Moelle Epiniere, UMR S975, Paris, France
    Neuromuscul Disord 22:318-24. 2012
  10. doi request reprint [Multifocal motor neuropathy: a retrospective study of sensory nerve conduction velocities in long-term follow-up of 21 patients]
    I Lievens
    Centre national de référence maladies neuromusculaires rares, Batiment Babinski, Hopital Pitie Salpetriere, AP HP, 47, Boulevard de l Hopital, 75651 Paris Cedex 13, France
    Rev Neurol (Paris) 165:243-8. 2009

Collaborators

Detail Information

Publications16

  1. ncbi request reprint [Electrophysiological signs of muscle channelopathies by causal mutation]
    E Fournier
    Fédération de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, Paris
    Rev Neurol (Paris) 161:1251-9. 2005
    ..This classification may guide molecular diagnosis in clinical practice...
  2. doi request reprint [Conduction block: a notion to let through]
    E Fournier
    Departement de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, 47 Boulevard de l Hopital, Paris, France
    Rev Neurol (Paris) 168:952-9. 2012
    ..Several pitfalls have to be avoided if a conduction block is to be afforded real diagnostic value. Similar precautions and discussions are also needed to establish an opposing sign, the "excitability block" or "inverse block"...
  3. ncbi request reprint Cold extends electromyography distinction between ion channel mutations causing myotonia
    Emmanuel Fournier
    Fédération de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, Assistance Publique Hopitaux de Paris, Universite Pierre et Marie Curie, Paris
    Ann Neurol 60:356-65. 2006
    ..We designed an easy electromyography (EMG) protocol combining repeated short exercise and cold as provocative tests to discriminate groups of mutations...
  4. doi request reprint [Simplified exploration of brachial plexopathies by reduction to well-known mononeuropathies and radiculopathies]
    E Fournier
    Departement de Physiologie, Faculté de Médecine Pitié Salpêtrière, Universite Pierre et Marie Curie Paris 6, 91, Boulevard de l Hopital, 75013 Paris, France
    Rev Neurol (Paris) 165:1127-33. 2009
    ..This method of simplification allows to demystify the brachial plexopathies and to facilitate their comprehension and exploration...
  5. ncbi request reprint New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
    S Vicart
    Fédération de Neurologie and INSERM U546, Groupe Hospitalier Pitie Salpetriere, Assistance Publique Hopitaux de Paris, and Universite Pierre et Marie Curie, Paris, France
    Neurology 63:2120-7. 2004
    ..Periodic paralysis is classified into hypokalemic (hypoPP) and hyperkalemic (hyperPP) periodic paralysis according to variations of blood potassium levels during attacks...
  6. ncbi request reprint [The hypolossal-facial anastomosis in man. A model for studying peripheral and central nervous system plasticity]
    F Tankere
    Equipe Mixte INSERM 0349 et Fédération de Neurophysiologie Clinique, Hopital de la Pitie Salpetriere, 47 Boulevard de l Hopital, 75013 Paris
    Rev Med Liege 59:91-103. 2004
    ....
  7. doi request reprint [Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]
    B Eymard
    Centre de référence des affections neuromusculaires Paris Est, Service de neurologie 2, Institut de Myologie, Hopital de la Pitie Salpetriere, 47 bd de l Hopital, 75013 Paris, France
    Rev Neurol (Paris) 169:S45-55. 2013
    ..Tolerability was good. Therapeutic responses were encouraging even in the most severely affected patients, particularly with DOK7 and COLQ. Salbutamol was a good alternative in one patient who was allergic to ephedrine...
  8. doi request reprint Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases
    S LaRue
    Centre de Référence Maladies Neuromusculaires Rares, Hôpital Pitié Salpêtrière and Université Paris VI, Paris, France
    Eur J Neurol 18:899-905. 2011
    ..The aim of this retrospective study was to investigate patients with DADS neuropathy without anti-MAG antibodies, and study their response to immunotherapy...
  9. doi request reprint Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
    I Wargon
    AP HP, Groupe Hospitalier Pitie Salpetriere, Bâtiment Lhermitte, Centre de Recherche de l Institut du Cerveau et de la Moelle Epiniere, UMR S975, Paris, France
    Neuromuscul Disord 22:318-24. 2012
    ..There was no genotype-phenotype correlation. At the end of the follow-up, 80% of patients were ambulant and 87% of patients had no respiratory trouble in spite of severe relapses...
  10. doi request reprint [Multifocal motor neuropathy: a retrospective study of sensory nerve conduction velocities in long-term follow-up of 21 patients]
    I Lievens
    Centre national de référence maladies neuromusculaires rares, Batiment Babinski, Hopital Pitie Salpetriere, AP HP, 47, Boulevard de l Hopital, 75651 Paris Cedex 13, France
    Rev Neurol (Paris) 165:243-8. 2009
    ....
  11. doi request reprint Pregnancy in congenital myasthenic syndrome
    L Servais
    Service of therapeutic trials and databases, Institut de Myologie, Groupe Hospitalier Pitie Salpetriere, Paris, France
    J Neurol 260:815-9. 2013
    ..However, the overall clinical prognosis is good since the vast majority of patients recovered their pre-pregnancy clinical status six months after the delivery...
  12. ncbi request reprint Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis
    D Sternberg
    Federations of Biochemistry, Centre Hospitalier Universitaire Pitie Salpetriere, Assistance Publique Hôpitaux de Paris et Université Paris VI, Paris, France
    Neurology 61:857-9. 2003
    ..Furthermore, there was no segregation of this gene variant with the disease. These observations weaken the proposal that MiRP2-R83H causes periodic paralysis...
  13. ncbi request reprint Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSK
    F Chevessier
    INSERM U582, Institut de Myologie, Hopital de la Salpetriere, Paris, France
    Acta Myol 24:55-9. 2005
    ..There are hundreds of molecules known to be present at the NMJ and mutations in the genes coding for these synaptic molecules are likely to be responsible for a neuromuscular block...
  14. ncbi request reprint Hypoglossal-facial nerve anastomosis: dynamic insight into the cross-innervation phenomenon
    F Tankere
    ENT Department, Pitie Salpetriere Hospital, Paris, France
    Neurology 61:693-5. 2003
    ..Ipsilateral reinnervation was observed by the fourth month, progressed to the 12th to 18th month, and remained stable for the remainder of the follow-up period...
  15. doi request reprint A European multicentre reappraisal of distal compound muscle action potential duration in chronic inflammatory demyelinating polyneuropathy
    Y A Rajabally
    Department of Neurology and Neurophysiology, Neuromuscular Clinic, University Hospitals of Leicester, Leicester, UK
    Eur J Neurol 19:638-42. 2012
    ..Cut-offs proposed have not been widely evaluated. The influence of low-cut EMG filter settings ≤ 10 Hz as used in Europe is uncertain...
  16. ncbi request reprint [Electrodiagnosis, EMG, ENMG...: what do the future and the past tell us about the present?]
    E Fournier
    Fédération de Neurophysiologie Clinique, Groupe Hospitalier Pitie Salpetriere, 47 Boulevard de l Hopital, 75013 Paris, France
    Rev Med Liege 59:3-14. 2004
    ....