Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.

Author:

Boysen G,Galassi G,Kamieniecka Z,Schlaeger J,Trojaborg W

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference15 articles.

1. Luis, M. L. S. (1978). Electroneurophysiological

2. A peculiar form of peripheral neuropathy. Familial atypical generalised amystudies in familial amyloid polyneuropathyPoriuguese type;Andrade, C.;Journal of Neurology, Neurosurgery, and Psychiatry,1952

3. The genetic amyloidosis, with parconduction in the nerves of the leg in man. Journal ticular reference to hereditary neuropathic, of;Hartmann, W.H.; Lambird, R.A.; McKusick, Behse; F.; Buchthal, F.;Neurology, Neurosurgery, and Psychiatry,1971

4. Familial systemic paramyloidosis atrophy and related disorders. Histological findings witlh lattice dystrophia of the cornea, progressive in sural nerves;Behse, F.; Buchthal, F.;Brain,1977

5. ternal symptoms;Behse, F.; Buchthal, F.; Carlsen, F.; Knappeis;Annals of C.linical Research; Hereditary neuropathy with liability 314-324,1972

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