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October 24, 2006; 67 (8) Brief Communications

Diagnostic challenges in facioscapulohumeral muscular dystrophy

S. Sacconi, L. Salviati, I. Bourget, D. Figarella, Y. Péréon, R. Lemmers, S. van der Maarel, C. Desnuelle
First published October 23, 2006, DOI: https://doi.org/10.1212/01.wnl.0000240071.62540.6f
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Article Information

vol. 67 no. 8 1464-1466
DOI: 
https://doi.org/10.1212/01.wnl.0000240071.62540.6f
PubMed: 
17060574
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published October 23, 2006.
Copyright & Usage: 
© 2006

Author Disclosures

    1. S. Sacconi, MD,
    2. L. Salviati, MD, PhD,
    3. I. Bourget, BS,
    4. D. Figarella, MD,
    5. Y. Péréon, MD,
    6. R. Lemmers, PhD,
    7. S. van der Maarel, PhD and
    8. C. Desnuelle, MD, PhD
  1. S. Sacconi, MD,
  2. L. Salviati, MD, PhD,
  3. I. Bourget, BS,
  4. D. Figarella, MD,
  5. Y. Péréon, MD,
  6. R. Lemmers, PhD,
  7. S. van der Maarel, PhD and
  8. C. Desnuelle, MD, PhD
  1. From Fédération des Maladies Neuromusculaires (S.S., I.B., C.D.), CHU de Nice and INSERM U638, Nice, France; Servizio di Genetica Clinica (L.S.), Department of Pediatrics, Università di Padova, Italy; Laboratoire de Neuropathologie (D.F.), CHU Timone-Marseille, France; Laboratoire d'Explorations Fonctionnelles à la place de Clinique Neurologique (Y.P.), Hôtel-Dieu, Nantes, France; Leiden University Medical Center (R.L., S. vd M.), Center for Human and Clinical Genetics, Leiden, The Netherlands.
  1. Address correspondence and reprint requests to Dr. Sabrina Sacconi, Féderation des maladies neuromusculaires, Archet 1, Route Saint Antoine de Ginestière, B.P. 3079, 06202 Nice, France; e-mail: sacconi{at}unice.fr
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