Table of contents

August 1956 - Volume 19 - 3


B

  1. Björk, Å.

    1. RETINAL DEGENERATION IN HEREDITARY ATAXIA (1 August, 1956)
      Å. Björk, U. Lindblom, L. Wadensten
  2. Brierley, James B.

C

  1. Crawford, T.

G

  1. Geschwind, Norman

    1. BENIGN CONGENITAL MYOPATHY WITH MYASTHENIC FEATURES (1 August, 1956)
      John N. Walton, Norman Geschwind, J. A. Simpson

H

  1. Hécaen, H.

    1. PAROXYSMAL DYSPHASIA AND THE PROBLEM OF CEREBRAL DOMINANCE (1 August, 1956)
      H. Hécaen, Malcolm Piercy

K

  1. Kramer, W.

    1. MULTILOCULAR ENCEPHALOMALACIA (1 August, 1956)
      W. Kramer

L

  1. Lindblom, U.

    1. RETINAL DEGENERATION IN HEREDITARY ATAXIA (1 August, 1956)
      Å. Björk, U. Lindblom, L. Wadensten

P

  1. Piercy, Malcolm

    1. PAROXYSMAL DYSPHASIA AND THE PROBLEM OF CEREBRAL DOMINANCE (1 August, 1956)
      H. Hécaen, Malcolm Piercy
  2. Press, Elizabeth M.

S

  1. Shepherd, Michael

  2. Simpson, J. A.

    1. BENIGN CONGENITAL MYOPATHY WITH MYASTHENIC FEATURES (1 August, 1956)
      John N. Walton, Norman Geschwind, J. A. Simpson
  3. Strich, Sabina J.

W

  1. Wadensten, L.

    1. RETINAL DEGENERATION IN HEREDITARY ATAXIA (1 August, 1956)
      Å. Björk, U. Lindblom, L. Wadensten
  2. Walton, John N.

    1. BENIGN CONGENITAL MYOPATHY WITH MYASTHENIC FEATURES (1 August, 1956)
      John N. Walton, Norman Geschwind, J. A. Simpson
  3. Watt, David C.