qualitative und quantitative untersuchungen an nervus suralis ...

JAMAL, G.A., WEIR, A.I., HANSEN, S., BALLANTYNE, J.P. (1985)
Sensory involvement in motor neuron disease: further evidence from automated thermal
threshold determination.
Journal of Neurology, Neurosurgery, and Psychiatry, 48, 906-910
JERUSALEM, F. (1994)
Klassifikation, Terminologie und Epidemiologie
in: Amyotrophe Lateralsklerose, Hrsg.: R. Dengler, St. Zierz, F. Jerusalem,
Georg Thieme Verlag Stuttgart, New York, 1-6
JOKELAINEN, M. (1977)
Amyotrophic lateral sclerosis in Finland. II. Clinical characteristics.
Acta Neurologica Scandinavica, 56, 194-204
KAISER, W.,A. (1994)
Bildgebende Diagnostik
in: Amyotrophe Lateralsklerose, Hrsg.: R. Dengler, St. Zierz, F. Jerusalem,
Georg Thieme Verlag Stuttgart, New York, 62-66
KATO, T., HIRANO, A., KURLAND, L.T. (1987)
Asymmetric involvement of the spinal cord involving both large and small anterior horn cells
in a case of familial amyotrophic lateral sclerosis.
Clinical Neuropathology, Vol. 6, No.2-(67-70)
KAWAMURA, Y., DYCK, P.J., SHIMONO, M., OKAZAKI, H., TATEISHI, J.,
DOI; H. (1981)
Morphometric comparison of the vulnerability of peripheral motor and sensory neurons in
amyotrophic lateral sclerosis.
Journal Neuropathology Exp Neurol, Vol 40, 667-674
KENNEDY, W., ALTER, M., SUNG, K. (1968)
Progressive proximal spinal and bulbar muscular atrophy of late onset: a sex-linked recessive
trait.
Neurology, 18, 671-680
KINSELLA, L.J., LANGE, D.J., TROJABORG, W., SADIQ, S.A., YOUNGER, D.S.,
LATOV, N. (1994)
Clinical and electrophysiologic correlates of elevated anti-GM1 antibody titers.
Neurology, 44, 1278-1282
122