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46. Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome. Bertini E, Sabatelli M, Di Capua M, Cilio MR, Mignogna T, Federico A, Tonali P. Eur J Paediatr Neurol; 1998; 2(5):245-54. PubMed ID: 10726827 [Abstract] [Full Text] [Related]
48. Severe cranial nerve involvement in longstanding demyelinating polyneuropathy: a clinicopathologic correlation. McCann EL, Smith TW, Chad DA, Sargent J. Acta Neuropathol; 1996; 91(3):309-12. PubMed ID: 8834544 [Abstract] [Full Text] [Related]
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50. [Interstitial hypertrophic neuritis. Study of 3 cases]. Werneck LC, Mendonça E. Arq Neuropsiquiatr; 1978 Sep; 36(3):250-8. PubMed ID: 687159 [Abstract] [Full Text] [Related]
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52. A case of progressive hypertrophic neuropathy in childhood with facial diplegia (Dejerine-Sottas disease). Sunwoo IN, Kim JS, Chi JG, Suh YL. Yonsei Med J; 1988 Jan; 29(3):278-85. PubMed ID: 3195160 [No Abstract] [Full Text] [Related]
53. A prospective clinical and electrophysiologic survey of acute flaccid paralysis in Chinese children. Wu HS, Liu TC, Lü ZL, Zou LP, Zhang WC, Zhaori G, Zhang J. Neurology; 1997 Dec; 49(6):1723-5. PubMed ID: 9409379 [Abstract] [Full Text] [Related]
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56. Orthopaedic management of childhood neuromuscular disease. Part I: Spinal muscular atrophy. Shapiro F, Bresnan MJ. J Bone Joint Surg Am; 1982 Jun; 64(5):785-9. PubMed ID: 7085707 [No Abstract] [Full Text] [Related]
57. Onion bulb neuropathy in the trembler mouse: a model of hypertrophic interstitial neuropathy (Dejerine-Sottas) in man. Ayers MM, Anderson RM. Acta Neuropathol; 1973 Jun 26; 25(1):54-70. PubMed ID: 4727733 [No Abstract] [Full Text] [Related]
58. Infantile polyneuropathy with defective myelination: an autopsy study. Karch SB, Urich H. Dev Med Child Neurol; 1975 Aug 26; 17(4):504-11. PubMed ID: 169177 [Abstract] [Full Text] [Related]
59. Chronic inflammatory demyelinating polyneuropathy in childhood: ultrastructural features of peripheral nerve biopsies in four cases. Vital A, Vital C, Brechenmacher C, Fontan D, Castaing Y. Eur J Pediatr; 1990 Jun 26; 149(9):654-8. PubMed ID: 2373121 [Abstract] [Full Text] [Related]
60. Hereditary hypertrophic neuropathy with facial and trigeminal involvement. Report of a case and comments on its possible identity with Hellsing syndrome. Kalyanaraman K, Smith BH, Schlagenhauff RE. Arch Neurol; 1974 Jul 26; 31(1):15-7. PubMed ID: 4834537 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]