Articles
- Familial agenesis of the cerebellar vermisA syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardationMarie Joubert, Jean-Jacques Eisenring, J. Preston, Frederick Andermann
- Para‐albumins in cerebrospinal fluidOldrich J. Kolar, Alexander T. Ross, Jean T. Herman
- Ultrastnicture of rectal biopsies in juvenile amaurotic idiocyBoris Eisner, Arthur L. Prensky
- Enzyme‐inhibiting factor in subacute necrotizing encephalomyelopathyJ. H. Pincus, Y. Itokawa, J. R. Cooper
- Calcium activation of electrically inexcitable muscle fibers in primary hypokalemic periodic paralysisAndrew G. Engel, Edward H. Lambert
- Evidence against pyridoxine deficiency as the mechanism of penicillin seizuresGranger G. Sutton, Michael B. A. Oldstone
- A new genetic variant of spinal muscular atrophyHans Zellweger, Hans Schneider, Dennis R. Schuldt
- Auditory perceptual deficit correlated with EEG dysrhythmiasResponse to diphenylhydantoin sodiumJ. Cordon Millichap, Rosemary W. Egan, Zwi H. Hart, Loretta H. Sturgis
- Intracranial meningiomasA retrospective analysis of the diagnostic value of plain skull filmsLawrence H. A. Cold, Stephen A. Kieffer, Harold O. Peterson
- Cornelia de Lange syndrome in an adult maleMichael Cherington, John E. Ott, Arthur Robinson
- Remitting demyelinating disease associated with a myeloproliferative syndrome and histiocytosis of the spleenRichard A. Thompson, Margaret Jones
- Familial “myotubular” myopathyGeorge K. van Wijngaarden, Paul Fleury, Jaap Bethlem, A. E. F. Hugo Meijer
- Paramyotonia and progressive neurogenic atrophyRobert M. Woolsey, James S. Nelson, Aldo A. Rossini
- Paraplegia secondary to hypotension and cardiac arrest in a patient who has had previous thoracic surgeryMartin L. Albert, William E. R. Greer, Warren Kantrowitz
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