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Journal Abstract Search
69 related items for PubMed ID: 897927
1. An obscure inherited neuropathy characterized by pain and weakness. Isaacs H, Badenhorst M. S Afr Med J; 1977 Aug 06; 52(7):285-8. PubMed ID: 897927 [Abstract] [Full Text] [Related]
2. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies]. Jedrzejowska H, Drac H, Sawicka E. Neuropatol Pol; 1975 Aug 06; 13(1):93-106. PubMed ID: 1118064 [No Abstract] [Full Text] [Related]
3. [Tomaculous neuropathy. A histopathological study and electroclinical correlates in 10 cases]. Pellissier JF, Pouget J, de Victor B, Serratrice G, Toga M. Rev Neurol (Paris); 1987 Aug 06; 143(4):263-78. PubMed ID: 3476973 [Abstract] [Full Text] [Related]
4. [Polyneuropathy and necrotizing myopathy following desensitization therapy]. Möbius HJ, Schlote W, Pfeifer H. Nervenarzt; 1987 Mar 06; 58(3):190-7. PubMed ID: 3035390 [No Abstract] [Full Text] [Related]
5. [Four cases of hereditary motor and sensory neuropathy in childhood--light and electron microscopic studies of sural nerve biopsies]. Sugie Y, Sugama M, Sugama S, Kosaka S, Shibuya T, Sugie H, Fukuyama Y. No To Hattatsu; 1985 Nov 06; 17(6):500-6. PubMed ID: 4084416 [No Abstract] [Full Text] [Related]
6. Severe hypomyelination and marked abnormality of conduction in Dejerine-Sottas hypertrophic neuropathy: myelin thickness and compound action potential of sural nerve in vitro. Dyck PJ, Lambert EH, Sanders K, O'Brien PC. Mayo Clin Proc; 1971 Jun 06; 46(6):432-6. PubMed ID: 5088981 [No Abstract] [Full Text] [Related]
7. Orthopaedic management of childhood neuromuscular disease. Part I: Spinal muscular atrophy. Shapiro F, Bresnan MJ. J Bone Joint Surg Am; 1982 Jun 06; 64(5):785-9. PubMed ID: 7085707 [No Abstract] [Full Text] [Related]
8. Atrophy and degeneration in sciatic nerve of presymptomatic mice carrying the Huntington's disease mutation. Wade A, Jacobs P, Morton AJ. Brain Res; 2008 Jan 10; 1188():61-8. PubMed ID: 18062944 [Abstract] [Full Text] [Related]
10. Chronic polyradiculoneuropathy of infancy. A report of three cases with familial incidence. Kasman M, Bernstein L, Schulman S. Neurology; 1976 Jun 10; 26(6 PT 1):565-73. PubMed ID: 945500 [Abstract] [Full Text] [Related]
11. Minimal pathologic expression of a mutant gene for hereditary motor and sensory neuropathy. Dyck PJ, Karnes JL, Windebank AJ, Sparks M, Stevens JC, O'Brien PC. Mayo Clin Proc; 1983 Jul 10; 58(7):419-25. PubMed ID: 6865475 [Abstract] [Full Text] [Related]
12. Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy). Thomas PK, Calne DB, Stewart G. Ann Hum Genet; 1974 Oct 10; 38(2):111-53. PubMed ID: 4467779 [No Abstract] [Full Text] [Related]
14. [Hereditary motor and sensory neuropathy type III. Case report and review of the literature]. Haverkamp F, Behring B. Klin Padiatr; 1995 Oct 10; 207(1):24-7. PubMed ID: 7885014 [Abstract] [Full Text] [Related]
15. Alcoholic neuropathy is clinicopathologically distinct from thiamine-deficiency neuropathy. Koike H, Iijima M, Sugiura M, Mori K, Hattori N, Ito H, Hirayama M, Sobue G. Ann Neurol; 2003 Jul 10; 54(1):19-29. PubMed ID: 12838517 [Abstract] [Full Text] [Related]
16. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification. Davis CJ, Bradley WG, Madrid R. J Genet Hum; 1978 Dec 10; 26(4):311-49. PubMed ID: 752065 [Abstract] [Full Text] [Related]
17. Thin axons relative to myelin spiral length in hereditary motor and sensory neuropathy, type I. Nukada H, Dyck PJ, Karnes JL. Ann Neurol; 1983 Dec 10; 14(6):648-55. PubMed ID: 6316837 [Abstract] [Full Text] [Related]
18. Chronic neuropathy presenting as a floppy infant with respiratory distress. Moss RB, Sriram S, Kelts KA, Forno LS, Lewiston NJ. Pediatrics; 1979 Oct 10; 64(4):459-64. PubMed ID: 492811 [Abstract] [Full Text] [Related]
19. The nature of myelinated nerve fiber degeneration in dominantly inherited hypertrophic neuropathy. Dyck PJ, Lais AC, Offord KP. Mayo Clin Proc; 1974 Jan 10; 49(1):34-9. PubMed ID: 4358565 [No Abstract] [Full Text] [Related]
20. Tomaculous neuropathy: hereditary predisposition to pressure palsies. Fewings JD, Blumbergs PC, Mukherjee TM, Hallpike JF. Aust N Z J Med; 1985 Oct 10; 15(5):598-603. PubMed ID: 3004403 [Abstract] [Full Text] [Related] Page: [Next] [New Search]