Chronic hereditary ataxic polyneuropathy;Polineuropatia ataxica hereditaria cronica

Medicina

Volumn 60, Issue 3, 2000, Pages 316-320

  Nogues, Martin ^a,b   Leiguarda, Ramon ^a   Sevlever, Gustavo ^a   Garcia, Horacio ^a  

^a Instituto de Investigaciones Neurologicas Raul Carrera   (Argentina)

^b FLENI   (Argentina)

Author keywords

Ataxic; Hereditary; Neuropathy; Sensory; Spinocerebellar

Indexed keywords

AGED; ARTICLE; ATAXIA; CASE REPORT; CHRONIC DISEASE; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; FEMALE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MIDDLE AGED; NUCLEAR FAMILY;

AGED; AGED, 80 AND OVER; CHRONIC DISEASE; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; FEMALE; GAIT ATAXIA; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; NUCLEAR FAMILY;

EID: 0033648373     PISSN: 00257680     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Dalakas MC. Chronic idiopatic ataxic neuropathy. Ann Neurol 1986; 19: 545-54.
2. Denny-Brown D. Primary sensory neuropathy with muscular changes associated with carcinoma. J Neurol Neurosurg Psych 1948; 11: 73-87.
3. Graus F, Bonaventura I, Uchuya M, et al. Indolent anti-Hu-associated paraneoplastic sensory neuropathy. Neurology 1994; 44: 2258-61.
4. Mellgren SI; Conn DL, Stevens JC, Dyck PJ. Peripheral neuropathy in primary Sjogren's syndrome. Neurology 1989; 39: 390-4.
5. Griffin JW, Cornblath DR, Alexander E, et al. Ataxic sensory neuropathy and dorsal root ganglionitis associated with Sjogren's syndrome. Ann Neurol 1990; 27: 304-15.
6. Thompson SW, Davis LE, Kornfeld M, Hilgers RD, Standefer JC. Cisplatin neuropathy: clinical, electrophysiologic, morphologic, and toxicologic studies. Cancer 1984; 54: 1269-75.
7. Schaumburg H, Kaplan J, Windebank A, et al. Sensory neuropathy from pyridoxine abuse. A new megavitamin syndrome. N Engl J Med 1983; 309: 445-8.
8. Feit H, Glasberg M, Ireton C, Rosenberg RN, Thal E. Peripheral neuropathy and starvation after gastric partitioning for morbid obesity. Ann Intern Med 1982; 96: 453-5.
9. Sobue G, Senda Y, Matsuoka Y, Sobue I. Sensory ataxia: a residual disability of Guillain-Barré syndrome. Arch Neurol 1983; 40: 86-9.
10. van Dijk GW, Wokke JHJ, Oey PL, et al. A new variant of sensory ataxic neuropathy with autosomal dominant inheritance. Brain 1995; 118: 1557-63.
11. Biemond A. La forme radiculo-cordonale postériure de dégénerescences spino-cerebelleuses. Rev Neurol 1954; 95: 3-21.
12. Poch GF, Martín AJ, Mariyos M, Rivero C. Degeneración espino-cerebelosa con predominio proprioceptivo de aparición tardía en una fratria. Pren Med Argent 1969; 56: 1299-301.
13. Harding AE. Clinical features and classification of inherited ataxias. Adv Neurol 1993; 61: 1-14.
14. rd. ed. Philadelphia: W.B. Saunders, 1993, p 1094-136.
15. Manyam BV. Friederich's disease. In: Vinken PJ, Bruyn GW, Klawans HL, de Jong JMBV (eds.). Handbook of Clinical Neurology, vol. 60. Amsterdam: Elsevier, 1991, p 299-333.