Corticomotoneuronal connections in primary lateral sclerosis (PLS)

References

• Fisher CM. Pure spastic paralysis of corticospinal origin. Can I Neurol Sci 1977; 4(4): 251–258.
   Web of Science ®Google Scholar
• Konagaya M, Sakai M, Iida M, Hashizume Y. [An autopsied case of dominantly affecting upper motor neuron with atrophy of the frontal and temporal lobes-with special ref-erence to primary lateral sclerosis]. Rinsho Shinkeigaku 1995; 35(4): 384–390.
   PubMedGoogle Scholar
• Pringle CE, Hudson AJ, Munoz DG, Kiernan JA, Brown WF, Ebers GC. Primary lateral sclerosis. Clinical features, neu-ropathology and diagnostic criteria. Brain 1992; 115 (Pt 2): 495–520.
   Google Scholar
• Forsyth PA, Dalmau J, Graus F, Cwik V, Rosenblum MK, Posner JB. Motor neuron syndromes in cancer patients]see comments]. Ann Neurol 1997; 41(6): 722–730.
   PubMed Web of Science ®Google Scholar
• Rowland LP. Primary lateral sclerosis: disease, syndrome, both or neither? [editorial; comment]. J Neurol Sci 1999; 170(1): 1–4.
   PubMed Web of Science ®Google Scholar
• Swash M, Desai J, Misra VP. What is primary lateral sclerosis? [see comments]. J Neurol Sci 1999; 170(1): 5–10.
   PubMed Web of Science ®Google Scholar
• Bruyn RP, Koelman JH, Troost D, de Jong JM. Motor neuron disease (amyotrophic lateral sclerosis) arising from long-standing primary lateral sclerosis. J Neurol Neurosurg Psy-chiatry 1995; 58(6): 742–744.
   PubMed Web of Science ®Google Scholar
• Le Forestier N, Maisonobe T, Piquard A, Rivaud S, Crevier-Buchman L, Salachas F et al. Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature. Brain 2001; 124(Pt 10): 1989–1999.
   Google Scholar
• Le Forestier N, Maisonobe T, Spelle L, Lesort A, Salachas F, Lacomblez L et al. Primary lateral sclerosis: further clarifica-tion. J Neurol Sci 2001; 185(2): 95–100.
   Google Scholar
• Brown WF, Ebers GC, Hudson AJ, Pringle CE, Veitch J. Motor-evoked responses in primary lateral sclerosis. Muscle Nerve 1992; 15(5): 626–629.
   PubMed Web of Science ®Google Scholar
• Caramia MD, Cicinelli P, Paradiso C, Mariorenzi R, Zarola F, Bernardi G et al. Excitability changes of muscular responses to magnetic brain stimulation in patients with central motor disorders. Electroencephalogr Clin Neurophysiol 1991; 81(4): 243–250.
   Google Scholar
• Salerno A, Carlander B, Camu W, Georgesco M. Motor evoked potentials (MEPs): evaluation of the different types of responses in amyotrophic lateral sclerosis and primary lateral sclerosis. Electromyogr Clin Neurophysiol 1996; 36(6): 361–368.
   PubMedGoogle Scholar
• Eisen A, Shytbel W, Murphy K, Hoirch M. Cortical magnetic stimulation in amyotrophic lateral sclerosis. Muscle Nerve 1990; 13(2): 146–151.
   PubMed Web of Science ®Google Scholar
• Ingram DA, Swash M. Central motor conduction is abnor-mal in motor neuron disease.) Neurol Neurosurg Psychiatry 1987; 50(2): 159–166.
   PubMed Web of Science ®Google Scholar
• Pouget J, Trefouret S, Attarian S. Transcranial magnetic stim-ulation (TMS): compared sensitivity of different motor response parameters in ALS. Amyotrophic lateral sclerosis and other motor neuron disorders 2000; 1 (Supplement 2): S45–S50.
   Google Scholar
• Eisen A, Pant B, Stewart H. Cortical excitability in amy-otrophic lateral sclerosis: a clue to pathogenesis. Can] Neurol Sci 1993; 20(1): 11–16.
   PubMed Web of Science ®Google Scholar
• Mills KR, Nithi KA. Corticomotor threshold is reduced in early sporadic amyotrophic lateral sclerosis [see comments]. Muscle Nerve 1997; 20(9): 1137–1141.
   PubMed Web of Science ®Google Scholar
• Awiszus F, Feistner H. Comparison of single motor unit responses to transcranial magnetic and peroneal nerve stim-ulation in the tibialis anterior muscle of patients with amy-otrophic lateral sclerosis. Electroencephalogr Clin Neurophysiol 1995; 97(2): 90–95.
   PubMedGoogle Scholar
• Day BL, Dressier D, Maertens dN, Marsden CD, Nakashima K, Rothwell JC et al. Electric and magnetic stimulation of human motor cortex: surface EMG and single motor unit responses [published erratum appears in 1 Physiol (Lond) 1990 Nov;430:617]. I Physiol (Lond) 1989; 412: 449–473.
   Google Scholar
• Day BL, Rothwell)C, Thompson PD, Dick JP, Cowan)M, Berardelli A et al. Motor cortex stimulation in intact man. 2. Multiple descending volleys. Brain 1987; 110 (Pt 5): 1191–1209.
   Google Scholar
• Eisen A, Entezari-Taher M, Stewart H. Cortical projections to spinal motoneurons: changes with aging and amyotrophic lateral sclerosis. Neurology 1996; 46(5): 1396–1404.
   PubMed Web of Science ®Google Scholar
• Fetz EE, Gustafsson B. Relation between shapes of post-synaptic potentials and changes in firing probability of cat motoneurones.) Physiol (Lond) 1983; 341: 387–410.
   Google Scholar
• Kohara N, Kaji R, Kojima Y, Mills KR, Fujii H, Hamano T et al. Abnormal excitability of the corticospinal pathway in patients with amyotrophic lateral sclerosis: a single motor unit study using transcranial magnetic stimulation. Elec-troencephalogr Clin Neurophysiol 1996; 101(1): 32–41.
   Google Scholar
• Mills KR. Corticomotoneuronal PSTH studies [editorial; comment]. Muscle Nerve 1999; 22(3): 297–298.
   PubMedGoogle Scholar
• Nakajima M, Eisen A, Stewart H. Diverse abnormalities of corticomotoneuronal projections in individual patients with amyotrophic lateral sclerosis. Electroencephalogr Clin Neu-rophysiol 1997; 105(6): 451–457.
   PubMedGoogle Scholar
• Weber M, Eisen A. Assessment of upper and lower motor neurons in Kennedy’s disease: implications for corticomo-toneuronal PSTH studies [see comments]. Muscle Nerve 1999; 22(3): 299–306.
   PubMed Web of Science ®Google Scholar
• Rossini PM. The anatomical and physiological bases of motor-evoked potentials. Neurol Clin 1988; 6(4): 751–769.
   PubMed Web of Science ®Google Scholar
• Brooks BR. El Escorial World Federation of Neurology crite-ria for the diagnosis of amyotrophic lateral sclerosis. Sub-committee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial “Clin-ical limits of amyotrophic lateral sclerosis” workshop con-tributors]see comments]. J Neurol Sci 1994; 124 Suppl: 96–107.
   Google Scholar
• Weber M, Eisen A, Nakajima M. Corticomotoneuronal activ-ity in ALS: changes in the peristimulus time histogram over time. Clin Neurophysiol 2000; 111(1): 169–177.
   PubMed Web of Science ®Google Scholar
• Rothwell)C, Hallet M, Berardelli A, Eisen A, Rossini P, Paulus W. Magnetic stimulation: motor evoked potentials. In: Deuschl G, Eisen A, editors. Recommendations for the practice of clinical neurophysiology: guidelines of the Inter-national Federation of Clinical Neurophysiology. 1999: 99.
   Google Scholar
• Weber M, Eisen A. Peristimulus time histograms (PSTHs)-a marker for upper motor neuron involvement in ALS? Amy-otrophic lateral sclerosis and other motor neuron disorders 2000; 1, suppl 2: S51–S56.
   Google Scholar
• Beal MF, Richardson EP, Jr. Primary lateral sclerosis: a case report. Arch Neurol 1981; 38(10):630–633.
   PubMedGoogle Scholar
• Hudson AJ, Kiernan JA, Munoz DG, Pringle CE, Brown WF, Ebers GC. Clinicopathological features of primary lateral sclerosis are different from amyotrophic lateral sclerosis. Brain Res Bull 1993; 30(3-4): 359–364.
   PubMed Web of Science ®Google Scholar
• lnce PG, Shaw PJ, Slade JY, Jones C, Hudgson P. Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changes. Acta Neuropathol (Bed) 1996; 92(4): 395–403.
   PubMed Web of Science ®Google Scholar
• Troost D, Sillevis Smitt PA, de Jong JM, Swaab DF. Neurofila-ment and glial alterations in the cerebral cortex in amy-otrophic lateral sclerosis. Acta Neuropathol (Berl) 1992; 84(6): 664–673.
   PubMed Web of Science ®Google Scholar
• Gredal O, Pakkenberg H, Karlsborg M, Pakkenberg B. Unchanged total number of neurons in motor cortex and neocortex in amyotrophic lateral sclerosis: a stereological study. J Neurosci Methods 2000; 95(2): 171–176.
   PubMed Web of Science ®Google Scholar
• Cruz MA, Trejo JM. Transcranial magnetic stimulation in amyotrophic and primary lateral sclerosis. Electromyogr Clin Neurophysiol 1999; 39(5): 285–288.
   PubMedGoogle Scholar
• Wu CW, Bichot NP, Kass JH. Converging evidence from microstimulation, architecture, and connections for multiple motor areas in the frontal and cingulate cortex of prosimian primates. J Comp Neurol 2000; 423: 140–177.
   PubMed Web of Science ®Google Scholar
• Ashby P, Zilm D. Relationship between EPSP shape and cross-correlation profile explored by computer simulation for studies on human motoneurons. Exp Brain Res 1982; 47(1): 33–40.
   PubMed Web of Science ®Google Scholar
• Kernell D, Chien-Ping W. Post-synaptic effects of cortical stimulation on forelimb motoneurones in the baboon. J Physiol (Lond) 1967; 191(3): 673–690.
   Google Scholar
• Awiszus F, Feistner H. Abnormal EPSPs evoked by magnetic brain stimulation in hand muscle motoneurons of patients with amyotrophic lateral sclerosis. Electroencephalogr Clin Neurophysiol 1993; 89(6): 408–414.
   PubMedGoogle Scholar
• Kohara N, Kaji R, Kojima Y, Kimura J. An electrophysiological study of the corticospinal projections in amyotrophic lateral sclerosis. Clin Neurophysiol 1999; 110(6): 1123–1132.
   PubMed Web of Science ®Google Scholar
• Mills KR. Motor neuron disease. Studies of the corticospinal excitation of single motor neurons by magnetic brain stimu-lation. Brain 1995; 118 (Pt 4): 971–982.
   Google Scholar
• Weber M, Eisen A, Stewart HG, Andersen PM. Preserved slow conducting corticomotoneuronal projections in amy-otrophic lateral sclerosis with autosomal recessive D90A CuZn-superoxide dismutase mutation [In Process Citation], Brain 2000; 123 Pt 7: 1505–1515.
   Google Scholar
• Andersen PM, Forsgren L, Binzer M, Nilsson P, Ala-Hurula V, Keranen ML et al. Autosomal recessive adult-onset amy-otrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients [published erratum appears in Brain 1998 Jan;121(Pt 1):187). Brain 1996; 119 (Pt4): 1153–1172.
   Google Scholar
• Ugawa Y, Kanazawa I. Motor-evoked potentials: unusual findings. Clin Neurophysiol 1999; 110(9): 1641–1645.
   PubMed Web of Science ®Google Scholar
• Mazevet D, Pierrot-Deseilligny E, Rothwell JC. A pro-priospinal-like contribution to electromyographic responses evoked in wrist extensor muscles by transcranial stimulation of the motor cortex in man. Exp Brain Res 1996; 109(3): 495–499.
   PubMed Web of Science ®Google Scholar
• Eisen A, Nakajima M, Weber M. Corticomotorneuronal hyper-excitability in amyotrophic lateral sclerosis. J Neurol Sci 1998; 160 Suppl 1: S64–S68.
   PubMedGoogle Scholar
• Weber M, Stewart H, Hirota N, Eisen A. Test/retest reliability of peristimulus time histograms. Muscle Nerve 1999; 9: 1323.
   Google Scholar
• Eisen A. Corticospinal motor neurons: pathophysiology. In: Brown RH, Meininger V, Swash M, editors. Amyotrophic lateral sclerosis. London, U.K.: Martin Dunitz Ltd., 2000: 161–177.
   Google Scholar
• Lin CL, Bristol LA, Jin L, Dykes-Hoberg M, Crawford T, Clawson L et al. Aberrant RNA processing in a neurodegen-erative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis. Neuron 1998; 20(3): 589–602.
   Google Scholar
• Pioro EP, Majors AW, Mitsumoto H, Nelson DR, NgTC. 1 PI-MRS evidence of neurodegeneration and excess glutamate + glutamine in ALS medulla. Neurology 1999; 53(1): 71–79.
   PubMed Web of Science ®Google Scholar
• Shaw PJ. Calcium, glutamate, and amyotrophic lateral scler-osis: more evidence but no certainties [editorial; comment). Ann Neurol 1999; 46(6): 803–805.
   PubMed Web of Science ®Google Scholar
• Bristol LA, Rothstein JD. Glutamate transporter gene expres-sion in amyotrophic lateral sclerosis motor cortex. Ann Neurol 1996; 39(5): 676–679.
   PubMed Web of Science ®Google Scholar
• Urushitani M, Shimohama S, Kihara T, Sawada H, Akaike A, Ibi M et al. Mechanism of selective motor neuronal death after exposure of spinal cord to glutamate: involvement of glutamate-induced nitric oxide in motor neuron toxicity and nonmotor neuron protection. Ann Neurol 1998; 44(5): 796–807.
   Google Scholar
• Howland DS, Liu J, She Y, Goad B, Maragakis NJ, Kim B et al. Focal loss of the glutamate transporter EAAT2 in a trans-genic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS). Proc Natl Acad Sci U S A 2002; 99(3): 1604–1609.
   Google Scholar