FAMILIAL MOTOR NEURON DISEASE, NON-CHAMORRO TYPE: REPORT OF KINSHIP-Reference-Cited by-同舟云学术

FAMILIAL MOTOR NEURON DISEASE, NON-CHAMORRO TYPE: REPORT OF KINSHIP

Published:1971-07 Issue:3 Volume:47 Page:341-349
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:

Author:

Amick L. D.,Nelson J. W.,Zellweger H.

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1971.tb07488.x/fullpdf

Reference32 articles.

1. Electromyographic studies in peroneal muscular atrophy;Amick;Arch. Neurol.,1963

2. An unusual spectrum of progressive spinal muscular atrophy;Amick;Acta neurol. scand.,1966

3. Recherches sur une maladie non encore décrite du système musculaire (atrophie musculaire progressive);Aran;Arch. gén. Méd.,1850

4. Becker, P. E. (1966): Krankheiten mit hauptsaechlicher Beteiligung von Pyramidenbahn, Vorderhorn und bulbaeren motorischen Kernen (Spastik, spinale Muskel-atrophie, und Bulbaerparalyse) in P. E. Becker. Humangenetik V/1, 314-410.

5. Ueber Poliomyelitis chronica mit Hinterstrangsklerose;Biemond;Confin. neurol.,1940

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