Articles

• Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2‐13.3 (SMA 5q)

  T. L. Munsat, L. Skerry, B. Korf, B. Pober, Y. Schapira, G. G. Gascon, S. M. Al-Rajeh, V. Dubowitz, K. Davies, L. M. Brzustowicz, G. K. Penchaszadeh, T. C. Gilliam

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• Routine and quantitative EEG analysis in Gilles de la Tourette's syndrome

  M. Y. Neufeld, Y. Berger, J. Chapman, A. D. Korczyn

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• Conjugal temporal arteritis

  S. L. Galetta, E. C. Raps, A. E. Wulc, M. G. Farber, G. L. Plock, C. W. Nichols, H. M. Friedman

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• The significance of myoclonic status epilepticus in postanoxic coma

  G. Bryan Young, Joseph J. Gilbert, Douglas W. Zochodne

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• SPECT in patients with epilepsia partialis continua

  Amiram Katz, Arani Bose, Sharon J. Lind, Susan S. Spencer

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• Internuclear ophthalmoplegia in the Chiari type II malformation

  Anthony C. Arnold, Robert W. Baloh, Robert D. Yee, Robert S. Hepler

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• Defective dystrophin in Duchenne and Becker dystrophy myotubes in cell culture

  R. M. Sklar, A. H. Beggs, A. A. Lev, L. Specht, F. Shapiro, R. H. Brown

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• Sensory visual testing in idiopathic intracranial hypertensionMeasures sensitive to change

  Michael Wall

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• Deteriorating ischemic strokeRisk factors and prognosis

  A. Dávalos, E. Cendra, J. Teruel, M. Martinez, D. Genís

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• Hippocampal sclerosis can be reliably detected by magnetic resonance imaging

  G. D. Jackson, S. F. Berkovic, B. M. Tress, R. M. Kalnins, G. C. A. Fabinyi, P. F. Bladin

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• Infantile CNS spongy degeneration‐14 casesClinical update

  G. G. Gascon, P. T. Ozand, A. Mahdi, A. Jamil, A. Haider, J. Brismar, M. Al-Nasser

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• Dominantly inherited apathy, central hypoventilation, and Parkinson's syndromeClinical, biochemical, and neuropathologic studies of 2 new cases

  T. L. Perry, J. M. Wright, K. Berry, S. Hansen, T. L. Perry

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• Constant relationships between force, phosphate concentration, and pH in muscles with differential fatigability

  M. W. Weiner, R. S. Moussavi, A. J. Baker, M. D. Boska, R. G. Miller

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