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Pediatric Neurology
Volume 24, Issue 5
, Pages 371-372
, May 2001
Acute onset of infantile spinal muscular atrophy
References
- . Spinal muscular atrophy. Semin Neurol. 1998;18:19–26
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Neuromusc Disord. 1992;2:423–428
- . Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy (Further delineation on the basis of SMN gene deletion findings). Neuropediatrics. 1996;27:8–15
- Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region. Ann Neurol. 1997;42:364–368
- . Acute respiratory insufficiency as the initial clinical manifestation of spinal muscular atrophy. Monatsschr Kinderheilkd. 1990;138:157–159
- Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy. J Child Neurol. 1998;13:327–331
- . Assessment of current diagnostic criteria for Guillain-Barre syndrome. Ann Neurol. 1990;27(Suppl.):S21–S24
- . Neonatal Guillain-Barré syndrome. Pediatr Neurol. 1988;4:255–256
- . First report of Guillain-Barré syndrome after rotavirus-induced gastroenteritis in a very young infant. [letter] Eur J Pediatr. 2000;159:224
- . Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werding-Hofman disease. Brain. 1969;92:9–24
- . Acute onset spinal muscular atrophy in siblings. Neuropediatrics. 1991;22:45–46
PII: S0887-8994(01)00271-5
© 2001 Elsevier Science Inc. All rights reserved.
« Previous
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Pediatric Neurology
Volume 24, Issue 5
, Pages 371-372
, May 2001
