qualitative und quantitative untersuchungen an nervus suralis ...

MATSUMOTO, S., KUSAKA, H., ITO, H., SHIBATA, N., ASAYAMA, T., IMAI, T. (1996)
Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-
positive Lewy body-like inclusions.
Clinical Neuropathology, VOL. 15, NO.1, 41-46
MOSS, T.H. and CAMPELL, M.J. (1987)
Atypical motor neuron disease with features of a multisystem degeneration: a non-familial
case with prominent sensory involvement.
Clinical Neuropathology, VOL, 6, NO. 2, 55-60
MULDER, D.W., BUSHEK, W., SPRING, E., KARNES, J., DYCK, P.J. (1983)
Motor neuron disease (ALS): Evaluation of detection thresolds of cutaneous sensation.
Neurology, 33, 1625-1627
MULDER, D.W., KURLAND, L.T., OFFORD, M.S., BEARD, C.M. (1986)
Familial adult motor neuron disease: amyotrophic lateral sclerosis.
Neurology, 36, 511-517
OCHOA, J., MAIR, W.G.P. (1969)
The normal sural nerve in man. II. Changes in the axons and schwann cells due to ageing.
Acta neuropathologica, 13, 217-230
OHNISHI, A., O´BRIEN, P.C., DYCK, P.J. (1974)
Studies to improve fixation of human nerves. Part 2. Effect of time elapsed between death and
glutaraldehyde fixation on relationship of axonal area to number of myelin lamellae.
Journal of the neurological sciences, 23: 387-390
PÉRÉON, M.D., JARDEL, J., GUILLON, B., GUIHÉNEUC, P. (1994)
Central nervous system involvement in multifocal demyelinating neuropathy with persistent
conduction block.
Muscle & Nerve, 17, 1278-1285
PESTRONK, A., CORNBLATH, D.R., ILYAS, A.A., BABA, H., QUARLES, R.H.,
GRIFFIN, J.W., ALDERSON, K., ADAMS, R.N. (1988)
A treatable multifocal motor neuropathy with antibodies to GM1 ganglioside.
Annals Neurology, 24, 73-78
124