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July 01, 1994; 44 (7) Articles

The phenotype of “pure” autosomal dominant spastic paraplegia

A. Dürr, A. Brice, M. Serdaru, G. Rancurel, C. Derouesné, O. Lyon-Caen, Y. Agid, B. Fontaine
First published July 1, 1994, DOI: https://doi.org/10.1212/WNL.44.7.1274
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Article Information

vol. 44 no. 7 1274
DOI: 
https://doi.org/10.1212/WNL.44.7.1274
PubMed: 
8035929
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 July 1, 1994.
Copyright & Usage: 
© 1994 by the American Academy of Neurology

Author Disclosures

    1. A. Dürr, MD,
    2. A. Brice, MD,
    3. M. Serdaru, MD,
    4. G. Rancurel, MD,
    5. C. Derouesné, MD,
    6. O. Lyon-Caen, MD,
    7. Y. Agid, MD, PhD and
    8. B. Fontaine, MD, PhD
  1. A. Dürr, MD,
  2. A. Brice, MD,
  3. M. Serdaru, MD,
  4. G. Rancurel, MD,
  5. C. Derouesné, MD,
  6. O. Lyon-Caen, MD,
  7. Y. Agid, MD, PhD and
  8. B. Fontaine, MD, PhD
  1. INSERM U289 (Drs. Dürr, Brice, and Agid), the Federation de Neurologie (Drs. Dürr, Brice, Serdaru, Lyon-Caen, Agid, and Fontaine), Service d'Urgences Cérébrovasculaires (Dr. Rancurel), Service de Neurologie (Dr. Derouesné), INSERM U360 (Dr. Lyon-Caen), and INSERM U134 (Dr. Fontaine), Hôpital de la Salpêtrière, Paris, France.

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