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10. Heterogeneous system degeneration of the central nervous system associated with peripheral neuropathy. Weinmann RL. Neurology; 1967 Jun; 17(6):597-603. PubMed ID: 4165195 [No Abstract] [Full Text] [Related]
12. [Hereditary neuropathy with a tendency to compression paralysis. Electrophysiological, morphometric and ultrastructural study of 2 familial cases]. Cavallari V, Di Pasquale MR, Scuderi D. Acta Neurol Quad (Napoli); 1981 Mar; 42():187-96. PubMed ID: 6267867 [No Abstract] [Full Text] [Related]
13. Peripheral neuropathy with myokymia, sustained muscular contraction, and continuous motor unit activity. Welch LK, Appenzeller O, Bicknell JM. Neurology; 1972 Feb; 22(2):161-9. PubMed ID: 4333031 [No Abstract] [Full Text] [Related]
14. [Peripheral neurogenic amyotrophy in the Marinesco-Sjögren syndrome]. Serratrice G, Gastaut JL, Dubois-Gambarelli D. Rev Neurol (Paris); 1973 Jun; 128(6):432-41. PubMed ID: 4368207 [No Abstract] [Full Text] [Related]
15. Evidence for neuropathy in myotonic muscular dystrophy. Kalyanaraman K, Smith BH, Chadha AL. Bull Los Angeles Neurol Soc; 1973 Oct; 38(4):188-96. PubMed ID: 4355568 [No Abstract] [Full Text] [Related]
16. Abnormalities of nerve conduction studies in myotonic dystrophy type 1: primary involvement of nerves or incidental coexistence? Bae JS, Kim OK, Kim SJ, Kim BJ. J Clin Neurosci; 2008 Oct; 15(10):1120-4. PubMed ID: 18657426 [Abstract] [Full Text] [Related]
17. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Dyck PJ, Lambert EH. Arch Neurol; 1968 Jun; 18(6):603-18. PubMed ID: 4297451 [No Abstract] [Full Text] [Related]
18. [Toxic neurologic manifestations during angina pectoris treatment (perhexiline maleate and amiotadone hydrochloride)]. Bady B, Bourrat C, Trillet M, Girard PF, Carrier H. Int J Neurol; 1978 Jun; 11(4):371-82. PubMed ID: 232499 [No Abstract] [Full Text] [Related]
19. Hereditary hypertrophic neuropathy. Report of two cases of an autosomal recessive variant. Kalyanaraman K, Cancilla PA, Munsat T, Pearson CM. Bull Los Angeles Neurol Soc; 1970 Apr; 35(2):58-68. PubMed ID: 4314732 [No Abstract] [Full Text] [Related]
20. A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder. Manganelli F, Dubbioso R, Esposito M, Marinò C, Pisciotta C, Pignatelli S, Santoro L. Mov Disord; 2013 Apr; 28(4):559-60. PubMed ID: 23408394 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]