Gait analysis of sporadic and hereditary spastic paraplegia

Journal of Neurology

Volumn 251, Issue 5, 2004, Pages 571-578

  Klebe, S ^a   Stolze, H ^a   Kopper, F ^a   Lorenz, D ^a   Wenzelburger, R ^a   Volkmann, J ^a   Porschke, H ^a   Deuschl, G ^a  

^a UNIVERSITY OF KIEL   (Germany)

Author keywords

Gait analysis; Hereditary spastic paraplegia; Spasticity

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE COURSE; DISEASE SEVERITY; FEMALE; GAIT; GENETIC HETEROGENEITY; HUMAN; MALE; MEDICAL ASSESSMENT; MOTOR NERVE CONDUCTION; PRIORITY JOURNAL; SPASTIC PARAPLEGIA; SPASTIC PARESIS; VELOCITY;

ADULT; CASE-CONTROL STUDIES; ELECTRIC STIMULATION; EXERCISE TEST; FEMALE; GAIT; HUMANS; INFRARED RAYS; LOCOMOTION; LOWER EXTREMITY; MAGNETICS; MALE; MIDDLE AGED; MUSCLE, SKELETAL; NEUROLOGIC EXAMINATION; PARAPARESIS, SPASTIC; REACTION TIME; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 2542497085     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-004-0366-7     Document Type: Article

References (27)

1. Barker AT, Jalinous R, Freeston II (1985) Non-invasive magnetic stimulation of human motor cortex. Lancet 11:1106-1107
2. Behan WM, Maia M (1974) Strumpell's familial spastic paraplegia: genetics and neuropathology. J Neurol Neurosurg Psychiatry 37:8-20
3. Bickerstaff E (1950) Hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 13:134-145
4. Bohannon RW, Smith MB (1987) Interrater reliability of a modified Ashworth scale of muscle spasticity. Phys Ther 67:206-207
5. Chen R, Tam A, Butefisch C, Corwell B, Ziemann U, Rothwell JC, Cohen LG (1998) Intracortical inhibition and facilitation in different representations of the human motor cortex. J Neurophysiol 80:2870-2881
6. Council MR (1976) Aids to the examination of the peripheral nervous system. Her Majesty's Stationery Office. Vol. 45. London
7. Durr A, Brice A, Serdaru M, Rancurel G, Derouesne C, Lyon-Caen O, et al. (1994) The phenotype of "pure" autosomal dominant spastic paraplegia. Neurology 44:1274-1277
8. Finsterer J (2003) Heriditäre spastische Paraplegien. Nervenarzt 74:497-504
9. Harding AE (1981) Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families. J Neurol Neurosurg Psychiatry 44:871-883
10. Hazan J, Fonknechten N, Mavel D, Paternotte C, Samson D, Artiguenave F, et al. (1999) Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet 23:296-303
11. Kahlstorf A (1937) Klinischer und histopathologischer Beitrag zur hereditären spastischen Spinalparalyse. Zeitschrift für die gesamte Neurologie und Psychiatrie 159:774-780
12. Lance J (1984) Pyramidal and extrapyramidal disorders. In: DT S, editor. Electromyography in CNS Disorders: Central EMG. Boston, pp. 1-19
13. Magistris MR, Rosler KM, Truffert A, Landis T, Hess CW (1999) A clinical study of motor evoked potentials using a triple stimulation technique. Brain 122:265-279
14. McDermott C, White K, Bushby K, Shaw P (2000) Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry 69:150-160
15. Noth J (1991) Trends in the pathophysiology and pharmacotherapy of spasticity. J Neurol 28:131-139
16. Priebe MM, Sherwood AM, Thornby JI, Kharas NF, Markowski J (1996) Clinical assessment of spasticity in spinal cord injury, a multidimensional problem. Arch Phys Med Rehabil 77: 713-716
17. Polo JM, Calleja J, Combarros O, Berciano J (1991) Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study. Brain 114:855-866
18. Reid E (1999) The hereditary spastic paraplegias. J Neurol 246:995-1003
19. Reid E, Grayson C, Rogers MT (1999) Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia: a clinical and molecular genetic study of 28 United Kingdom families. Brain 122:1741-1755
20. Rossini PM, Caramia M, Roma V, Zarola F (1985) Nervous propagation along "central" motor pathways in intact man: characteristics of motor responses to "bifocal" and "unifocal" spine and scalp non-invasive stimulation. Electroencephalogr Clin Neurophysiol 61:272-286
21. Sack GH, Huether CA, Garg N (1978) Familial spastic paraplegia: clinical and pathological studies in a large kindred. Johns Hopkins Med J 143:117-121
22. Schady W, Dick JP, Sheard A, Crampton S (1991) Central motor conduction studies in hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 54:775-779
23. Silva MC, Coutinho P, Pinheiro CD, Neves JM, Serrano P (1997) Hereditary ataxias and spastic paraplegias: methodological aspects of a prevalence study in Portugal. J Clin Epidemiol 50:1377-1384
24. Stolze H, Kuhtz-Buschbeck JP, Mondwurf C, Boczek-Funcke A, Johnk K, Deuschl G, et al. (1997) Gait analysis during treadmill and overground locomotion in children and adults. Electroencephalogr Clin Neurophysiol 105:490-497
25. Strümpell (1880) Beiträge zur Pathologie des Rückenmarkes. Arch Psychiatr Nervenerkr 10:676-717
26. Sutherland J (1975) Familial spastic paraplegia. In: Vinken PJ, Bruyn GW (eds) Handbook of clinical neurology. Amsterdam: North-Holland, pp 421-431
27. White KD, Ince PG, Lusher M, Lindsey J, Cookson M, Bashir R, Shaw PJ, Bushby KMD (2000) Clinical and pathological findings in hereditary spastic paraparesis with spastin mutation. Neurology 55:89-94