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