Diagnostic workup for neuromuscular diseases

Handbook of Clinical Neurology

Volumn 113, Issue , 2013, Pages 1291-1297

  Fardeau, Michel ^a   Desguerre, Isabelle ^b  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84876880928     PISSN: 00729752     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-444-59565-2.00001-0     Document Type: Chapter

References (9)

1. Brooke M.H. A Clinician's views of Neuromuscular Diseases 1986, William and Wilkins, Baltimore. 2nd edn.
2. Dubowitz V. Muscle Disorders in Childhood 1995, WB Saunders, London. 2nd edn.
3. Kinali M., Beeson D., Pitt M.C., et al. Congenital myasthenic syndromes in childhood: diagnostic and management challenges. J Neuroimmunol 2008, 201-202:6-12.
4. Mercuri E., Pichiecchio A., Allsop J., et al. Muscle MRI in inherited neuromuscular disorders: past, present, and future. J Magn Reson Imaging 2007, 25:433-440.
5. Muntoni F., Guicheney P., Voit T. 158th ENMC international workshop on congenital muscular dystrophy (Xth international CMD workshop), 8th-10th February 2008, Naarden. Neuromuscul Disord 2009, 19:229-234.
6. Natalie Randles K., Morris G.E. Workshop on the nuclear envelope and Emery-Dreifuss muscular dystrophy, 29th March 2006, Oswestry, UK. Neuromuscul Disord 2006, 16:608-612.
7. Udd B., Meola G., Krahe R., et al. 140th ENMC international workshop: myotonic dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management. Neuromuscul Disord 2006, 16:403-413.
8. Van Laere J. Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems. Rev Neurol (Paris) 1966, 115:289-295.
9. Zerres K., Rudnik-Schöneborn S. 93rd ENMC international workshop: non-5q-spinal muscular atrophies (SMA) - clinical picture, 6-8 April 2001, Naarden, The Netherlands. Neuromuscul Disord 2003, 13:179-183.