Emmanuelle Campana-Salort

Summary

Country: France

Publications

  1. ncbi request reprint [Muscular disorders: unusual or focal presentations]
    Emmanuelle Campana-Salort
    Centre de référence des maladies neuromusculaires et de la SLA, Hopital La Timone, 13385 Marseille Cedex 5, France
    Rev Prat 58:2245-52. 2008
  2. pmc Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study
    Emmanuelle Salort-Campana
    AP HM, Reference Center of Neuromuscular Disorders and ALS, Timone University Hospital, Aix Marseille University, 264 rue Saint Pierre, Marseille, Cedex 05, 13385, France
    Orphanet J Rare Dis 10:2. 2015
  3. doi request reprint [Necrotizing myopathies: From genetic to acquired forms]
    E Salort-Campana
    Centre de référence des maladies neuromusculaires et de la SLA, Universite d Aix Marseille, CHU La Timone, avenue Jean Moulin, 13005 Marseille, France Electronic address
    Rev Med Interne 35:430-6. 2014
  4. doi request reprint [Clinical and molecular diagnosis of facioscapulohumeral dystrophy type 1 (FSHD1) in 2012]
    E Salort-Campana
    Centre de référence des maladies neuromusculaires et de la SLA, Hopital La Timone, avenue Jean Moulin, 13005 Marseille, France Inserm UMR_S 910 de génétique médicale et de génomique fonctionnelle, Faculté de Médecine secteur Timone, Universite Aix Marseille, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 5, France Electronic address
    Rev Neurol (Paris) 169:573-82. 2013

Collaborators

  • Andoni Echaniz-Laguna
  • Christine Tranchant
  • Sabrina Sacconi
  • Karine Nguyen
  • S Attarian
  • E Salort-Campana
  • Emmanuelle Salort-Campana
  • J Pouget
  • Marie Christine Arne-Bes
  • Julien Niederhauser
  • Thierry Kuntzer
  • Xavier Ferrer
  • Francoise Bouhour
  • Elisabeth Jouve
  • Marc Bartoli
  • Jean Pouget
  • Aleksandra Nadaj-Pakleza
  • Frédérique Magdinier
  • Guilhem Solé
  • Claude Desnuelle
  • Estelle Charles
  • Elisabeth Ollagnon
  • Rafaelle Bernard
  • Nicolas Levy
  • Christophe Vial
  • D Figarella-Branger
  • A M de Paula
  • N Levy

Detail Information

Publications4

  1. ncbi request reprint [Muscular disorders: unusual or focal presentations]
    Emmanuelle Campana-Salort
    Centre de référence des maladies neuromusculaires et de la SLA, Hopital La Timone, 13385 Marseille Cedex 5, France
    Rev Prat 58:2245-52. 2008
    ..This paper reviews the main atypical clinical features of myopathies and their causes...
  2. pmc Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study
    Emmanuelle Salort-Campana
    AP HM, Reference Center of Neuromuscular Disorders and ALS, Timone University Hospital, Aix Marseille University, 264 rue Saint Pierre, Marseille, Cedex 05, 13385, France
    Orphanet J Rare Dis 10:2. 2015
    ..Our objective was to study the penetrance of FSHD1 in patients carrying alleles ranging between 6 to10 RUs and to evaluate the influence of sex, age, and several environmental factors on clinical expression of the disease...
  3. doi request reprint [Necrotizing myopathies: From genetic to acquired forms]
    E Salort-Campana
    Centre de référence des maladies neuromusculaires et de la SLA, Universite d Aix Marseille, CHU La Timone, avenue Jean Moulin, 13005 Marseille, France Electronic address
    Rev Med Interne 35:430-6. 2014
    ..Both clinicoserologic and pathologic data must be taken into account to improve this diagnosis. We propose guidelines for diagnosis of NAM according to clinical course, to be used in clinical practice...
  4. doi request reprint [Clinical and molecular diagnosis of facioscapulohumeral dystrophy type 1 (FSHD1) in 2012]
    E Salort-Campana
    Centre de référence des maladies neuromusculaires et de la SLA, Hopital La Timone, avenue Jean Moulin, 13005 Marseille, France Inserm UMR_S 910 de génétique médicale et de génomique fonctionnelle, Faculté de Médecine secteur Timone, Universite Aix Marseille, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 5, France Electronic address
    Rev Neurol (Paris) 169:573-82. 2013
    ..Diagnosis of facioscapulohumeral dystrophy type 1 (FSHD1) is supported by a suggestive clinical presentation and associated with a heterozygous contraction of the D4Z4 repeat array on chromosome 4q35...