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5. [Familial recurrent amyotrophic neuralgia in children]. Kaláb Z; Fajt M; Steinerová H Cesk Pediatr; 1965 Oct; 20(10):883-6. PubMed ID: 5850717 [No Abstract] [Full Text] [Related]
6. [Hreditary myopathies]. Kuhn E Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097 [No Abstract] [Full Text] [Related]
7. [Current views on the diagnosis, etiology and genetics of the most frequent non-metabolic congenital myopathies]. Herrmann V Padiatr Grenzgeb; 1983; 22(1):27-45. PubMed ID: 6866527 [No Abstract] [Full Text] [Related]
9. [Myogenic muscular atrophy, neurogenic muscular atrophy and congenital generalized arthrogryposis. The distinctiveness of each of these genetic diseases and the significance of their relative definitions based on the system in which the disease is most noticeable]. Salvioli G Clin Pediatr (Bologna); 1968 Oct; 50(10):605-24. PubMed ID: 5743023 [No Abstract] [Full Text] [Related]
10. Classification of the neuromuscular disorders. Appendix A to the Minutes of the Meeting of the Research Group on Neuromuscular Diseases, held in Montreal, Canada, on 21 September, 1967. J Neurol Sci; 1968; 6(1):165-77. PubMed ID: 4296280 [No Abstract] [Full Text] [Related]
11. [Clinical study of muscular atrophy]. Shinoda M Hokkaido Igaku Zasshi; 1974 Jan; 49(1):23-31. PubMed ID: 4376121 [No Abstract] [Full Text] [Related]
12. [Nosography of infantile and juvenile neurogenic amyotrophias in the light of histoenzymological studies]. Scarlato G; Cornelio F; Bollati A Acta Neurol (Napoli); 1970; 25(2):225-8. PubMed ID: 4246411 [No Abstract] [Full Text] [Related]
13. Intrafamilial variability in spinal muscular atrophy. Prot J; Sawicka E Pol Med J; 1969; 8(5):1165-9. PubMed ID: 5383931 [No Abstract] [Full Text] [Related]
14. [On the position of hereditary areflectory dysstasia (Roussy and Lévy) in the group of heredodegenerative and systemic diseases of the central nervous system. With particular consideration of one family observation]. Heinroth H Dtsch Z Nervenheilkd; 1967; 191(1):10-21. PubMed ID: 6051944 [No Abstract] [Full Text] [Related]