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Infantile osteopetrosis and neuronal storage disease.

Ambler, M ; Trice, J ; Grauerholz, J ; O'Shea, P Ambler, M (correspondence author)

Neurology, 1983, Vol.33(4), pp.437-441 [Peer Reviewed Journal]

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Cytomegalovirus polyradiculoneuropathy in acquired immune deficiency syndrome.

Behar, R ; Wiley, C ; Mccutchan, Ja Behar, R (correspondence author)

Neurology, 1987, Vol.37(4), pp.557-561 [Peer Reviewed Journal]

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Acute trimethyltin limbic-cerebellar syndrome.

Besser, R ; Kraemer, G ; Thuemler, R ; Bohl, J ; Gutmann, L ; Hopf, H Besser, R (correspondence author)

Neurology, 1987, Vol.37(6), pp.945-950 [Peer Reviewed Journal]

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A hereditary moyamoya syndrome with multisystemic manifestations

Herve, D ; Touraine, P ; Verloes, A ; Miskinyte, S ; Krivosic, V ; Logeart, D ; Alili, N ; Laredo, J ; Gaudric, A ; Houdart, E ; Metzger, J ; Tournier-Lasserve, E ; Woimant, F Herve, D (correspondence author)

Neurology, Jul 20, 2010, Vol.75(3), pp.259-264 [Peer Reviewed Journal]

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A dominantly inherited myopathy with excessive tubular aggregates.

Rohkamm, R ; Boxler, K ; Ricker, K ; Jerusalem, F Rohkamm, R (correspondence author)

Neurology, 1983, Vol.33(3), pp.331-336 [Peer Reviewed Journal]

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A new mutation in the prion protein gene: A patient with dementia and white matter changes

Van Harten, B. ; Van Gool, W.A. ; Van Langen, I.M. ; Deekman, J.M. ; Meijerink, P.H.S. ; Weinstein, H.C. Department of Genetics ; Reproductive Origins of Adult Health and Disease ; Health Psychology Research

Neurology, 2000, Vol.55(7), pp.1055-1057 [Peer Reviewed Journal]

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by this author/creator:

  1. Rohkamm, R
  2. Gaudric, A.
  3. Verloes, A
  4. Tournier-Lasserve, E.
  5. Krivosic, V

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