Articles

• Familial agenesis of the cerebellar vermisA syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation

  Marie Joubert, Jean-Jacques Eisenring, J. Preston, Frederick Andermann

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• Para‐albumins in cerebrospinal fluid

  Oldrich J. Kolar, Alexander T. Ross, Jean T. Herman

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• Ultrastnicture of rectal biopsies in juvenile amaurotic idiocy

  Boris Eisner, Arthur L. Prensky

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• Enzyme‐inhibiting factor in subacute necrotizing encephalomyelopathy

  J. H. Pincus, Y. Itokawa, J. R. Cooper

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• Successful treatment in action myoclonus

  Ira Sherwin, William Redmon

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• Calcium activation of electrically inexcitable muscle fibers in primary hypokalemic periodic paralysis

  Andrew G. Engel, Edward H. Lambert

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• Evidence against pyridoxine deficiency as the mechanism of penicillin seizures

  Granger G. Sutton, Michael B. A. Oldstone

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• A new genetic variant of spinal muscular atrophy

  Hans Zellweger, Hans Schneider, Dennis R. Schuldt

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• Auditory perceptual deficit correlated with EEG dysrhythmiasResponse to diphenylhydantoin sodium

  J. Cordon Millichap, Rosemary W. Egan, Zwi H. Hart, Loretta H. Sturgis

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• Intracranial meningiomasA retrospective analysis of the diagnostic value of plain skull films

  Lawrence H. A. Cold, Stephen A. Kieffer, Harold O. Peterson

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• Cornelia de Lange syndrome in an adult male

  Michael Cherington, John E. Ott, Arthur Robinson

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• Remitting demyelinating disease associated with a myeloproliferative syndrome and histiocytosis of the spleen

  Richard A. Thompson, Margaret Jones

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• Pompe's disease

  Gwendolyn R. Hogan, Ludwig Gutmann, Roland Schmidt, Enid Gilbert

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• Familial “myotubular” myopathy

  George K. van Wijngaarden, Paul Fleury, Jaap Bethlem, A. E. F. Hugo Meijer

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• Paramyotonia and progressive neurogenic atrophy

  Robert M. Woolsey, James S. Nelson, Aldo A. Rossini

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• Paraplegia secondary to hypotension and cardiac arrest in a patient who has had previous thoracic surgery

  Martin L. Albert, William E. R. Greer, Warren Kantrowitz

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