Transcranial magnetic stimulation study in hereditary spastic paraparesis

European Neurology

Volumn 49, Issue 4, 2003, Pages 234-237

  Nardone, Raffaele ^a,b   Tezzon, F ^a  

^a 'F Tappeiner' Hospital   (Italy)

^b 'F Tappeiner' Hospital   (Italy)

Author keywords

Hereditary spastic paraparesis; Intracortical inhibition; Paraplegin; Spastin; Transcranial magnetic stimulation

Indexed keywords

SPASTIN;

ADULT; ARTICLE; BRAIN CORTEX; BRAIN DYSFUNCTION; BRAIN ELECTROPHYSIOLOGY; CHROMOSOME 16Q; CHROMOSOME 2P; CLINICAL ARTICLE; CLINICAL FEATURE; EVOKED MUSCLE RESPONSE; EXCITABILITY; FAMILY STUDY; FEMALE; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOTOR CORTEX; MOTOR NERVE CONDUCTION; PRIORITY JOURNAL; TRANSCRANIAL MAGNETIC STIMULATION;

ADULT; AGED; ELECTROPHYSIOLOGY; EVOKED POTENTIALS, MOTOR; FEMALE; HUMANS; MALE; MIDDLE AGED; MOTOR CORTEX; PARAPARESIS, SPASTIC; PEDIGREE; PHYSICAL STIMULATION; REFRACTORY PERIOD, ELECTROPHYSIOLOGICAL; TRANSCRANIAL MAGNETIC STIMULATION;

EID: 0037963056     PISSN: 00143022     EISSN: None     Source Type: Journal    
DOI: 10.1159/000070193     Document Type: Article

References (20)

1. Harding AE: Classification of the hereditary ataxias and paraplegias. Lancet 1983;i:1151-1155.
2. Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dube MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T: Hereditary spastic paraplegia: Advances in genetic research. Hereditary Spastic Paraplegia Working group. Neurology 1996;46:1507-1514.
3. Casari G, De Fusco M, Ciarmatori S, Zeviani M, Mora M, Fernandez P, De Michele G, Filla A, Cocozza S, Marconi R, Durr A, Fontaine B, Ballabio A: Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metallopro-tease. Cell 1998;93:973-983.
4. Hazan J, Fonknechten N, Mavel D, Paternotte C, Samson D, Artiguenave F, Davoine CS, Cruaud C, Durr A, Wincker P, Brottier P, Cattolico L, Barbe V, Burgunder JM, Proud'homme JF, Brice A, Fontaine B, Heilig B, Weissenbach J: Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet 1999;23:296-303.
5. Heinzlef O, Paternotte C, Mahiex F, Proud'homme JF, Dien J, Madigand M, Pouget J, Weissenbach J, Roullet E, Hazan J: Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. J Med Genet 1998;35:89-93.
6. Webb S, Coleman D, Byrne P, Parfrey N, Burke T, Hutchinson J, Hutchinson M: Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p. Brain 1998;121:601-609.
7. Byrne PC, McMonagle P, Webb S, Fitzgerald B, Parfrey N, Hutchinson M: Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p. Neurology 2000;54: 1510-1517.
8. Patel S, Latterich M: The AAA team: Related ATPases with diverse functions. Trends Cell Biol 1998;8:65-71.
9. Rossini PM, Barker T, Berardelli A, Caramia MD, Caruso G, Cracco RQ, Dimitrijevic MR, Hallett M, Katayama Y, Lucking CH, Maert-ens de Noordhout AL, Marsden CD, Murray NMF, Rothwell JC, Swash M, Tomberg C: Non-invasive electrical and magnetic stimulation of the brain, spinal cord and roots: Basic principles and procedures for routine clinical application. Report of an IFCN committee. Electroencephalogr Clin Neurophysiol 1994; 91:79-92.
10. Kujirai T, Caramia MD, Rothwell JC, Day BL, Thompson PD, Ferbert A, Wroe S, Asselman P, Marsden CD: Corticocortical inhibition in human motor cortex. J Physiol 1993;471:501-519.
11. Nakamura H, Kitagawa H, Kawaguchi Y, Tsu-ji H: Intracortical facilitation and inhibition after transcranial magnetic stimulation in conscious humans. J Physiol 1997;498:817-823.
12. Ziemann U: Intracortical inhibition and facilitation in the conventional paired TMS paradigm. Electroencephalogr Clin Neurophysiol Suppl 1999;51:127-136.
13. Nataraj AJ, Olivos-Glander I, Kusukawa N, Highsmith WE: Single-strand conformation polymorphism and heteroduplex analysis for gel-based mutation detection. Electrophoresis 1999;20:1177-1185.
14. Pelosi L, Lanzillo B, Perretti A, Santoro L, Blumhardt L, Caruso G: Motor and somatosensory evoked potentials in hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 1991;54:1099-1102.
15. Shady W, Dick JP, Sheard A, Crampton S: Central motor conduction studies in hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 1991;54:775-779.
16. White KD, Ince PG, Lusher M, Lindsey J, Cookson M, Bashir R, Shaw PJ, Bushby KM: Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation. Neurology 2000;55:89-94.
17. De Carvalho M, de Mendonca A, Miranda PC, García C, Luis ML: Magnetic stimulation in Alzheimer's disease. J Neurol 1997;244:304-307.
18. Alagona G, Bella R, Ferri R, Carnemolla A, Pappalardo A, Costanzo E, Pennisi G: Transcranial magnetic stimulation in Alzheimer disease: Motor cortex excitability and cognitive severity. Neurosci Lett 2001;13:57-60.
19. Liepert J, Bär KJ, Meske U, Weiller C: Motor cortex dishinibition in Alzheimer's disease. Clin Neurophysiol 2001;112:1436-1441.
20. Liepert J, Wessel K, Schwenkreis P, Trillenberg P, Otto V, Vorgerd M, Malin JP, Tegenthoff M: Reduced intracortical facilitation in the motor cortex of patients with cerebellar degeneration. Acta Neurol Scand 1998;98:318-323.