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1
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84910792002
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Hereditary spastic ataxia
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de Jong, JMBV, editor. Hereditary neuropathies and spinocerebellar atrophies. Amsterdam: Elsevier
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[1] Eadie JM. Hereditary spastic ataxia. In: de Jong, JMBV, editor. Hereditary neuropathies and spinocerebellar atrophies. Handbook of clinical neurology, Vol. 16. Amsterdam: Elsevier, 1991:461-466.
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Eadie, J.M.1
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2
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0010351573
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On hereditary ataxia and spastic paraplegia
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Fisher RA, editor. Nervous diseases and muscular dystrophies. London: Cambridge
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Bell, J.1
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3
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0008414335
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Complicated forms of hereditary spastic paraplegia
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New York: Churchill Livingstone
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Harding, A.E.1
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4
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0014085911
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The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting
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0023629668
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New type of spinocerebellar degeneration syndrome in a northern Swedish population
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Gustavson, K.-H.1
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6
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0022474187
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Autosomally inherited recessive spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs. Report of a Bedouin family - A new syndrome
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[6] Mousa AM, Al-Din ASN, Al-Nassar KE, et al. Autosomally inherited recessive spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs. Report of a Bedouin family - a new syndrome. J Neurol Sci 1986;76:105-121.
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8
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0027417491
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Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix-Saguenay in Northeastern Quebec
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[8] De Braekeleer M, Giasson F, Mathieu J, Roy M, Bouchard J-P, Morgan K. Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix-Saguenay in Northeastern Quebec. Genet Epidemiol 1993;10:17-25.
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De Braekeleer, M.1
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Morgan, K.6
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9
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0000195198
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Recessive spastic ataxia of Charlevoix-Saguenay
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de Jong J.M.B.V., editor. Hereditary neuropathies and spinocerebellar atrophies Amsterdam: Elsevier
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[9] Bouchard J-P. Recessive spastic ataxia of Charlevoix-Saguenay. In: de Jong J.M.B.V., editor. Hereditary neuropathies and spinocerebellar atrophies. Handbook of clinical neurology, Vol. 16. Amsterdam: Elsevier, 1991:451-459.
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Bouchard, J.-P.1
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10
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0001775483
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Recessive spastic ataxia of Charlevoix-Saguenay (RSACS): Clinical, morphological and genetic studies
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Lechtenberg R, editor New York: Marcel Dekker
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[10] Bouchard J-P, Bouchard RW, Gagné F, Richter A, Melançon S. Recessive spastic ataxia of Charlevoix-Saguenay (RSACS): clinical, morphological and genetic studies. In: Lechtenberg R, editor. Handbook of cerebellar disease. New York: Marcel Dekker, 1993:491-494.
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Bouchard, J.-P.1
Bouchard, R.W.2
Gagné, F.3
Richter, A.4
Melançon, S.5
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11
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0018776321
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Electroencephalographic findings in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay
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[11] Bouchard RW, Barbeau A, Bouchard R, Bouchard J-P. Electroencephalographic findings in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay. Can J Neurol Sci 1979;6:191-194.
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Bouchard, R.W.1
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Bouchard, J.-P.4
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12
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0018766158
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Electromyography and nerve conduction studies in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay
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[12] Bouchard J-P, Barbeau A, Bouchard R, Bouchard RW. Electromyography and nerve conduction studies in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay. Can J Neurol Sci 1979;6:185-189.
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Bouchard, J.-P.1
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Bouchard, R.3
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13
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0018751255
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The neuropathy of Charlevoix-Saguenay ataxia: An electrophysiological and pathological study
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[13] Peyronnard JM, Charron L, Barbeau A. The neuropathy of Charlevoix-Saguenay ataxia: an electrophysiological and pathological study. Can J Neurol Sci 1979;6:199-203.
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Peyronnard, J.M.1
Charron, L.2
Barbeau, A.3
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14
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0010356016
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Central pathway conduction in recessive spastic ataxia of Charlevoix-Saguenay
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abstract
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[14] DeLéan J, Mathieu J, Bouchard J-P. Central pathway conduction in recessive spastic ataxia of Charlevoix-Saguenay (abstract). Can J Neurol Sci 1989;16:272.
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Deléan, J.1
Mathieu, J.2
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15
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0018761915
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Oculomotor and vestibular findings in autosomal recessive spastic ataxia of Charlevoix-Saguenay
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[15] Dionne J, Wright G, Barber H, Bouchard R, Bouchard J-P. Oculomotor and vestibular findings in autosomal recessive spastic ataxia of Charlevoix-Saguenay. Can J Neurol Sci 1979;6:177-184.
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Dionne, J.1
Wright, G.2
Barber, H.3
Bouchard, R.4
Bouchard, J.-P.5
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16
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0018751539
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Computed tomography of posterior fossa in hereditary ataxias
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[16] Langelier R, Bouchard J-P, Bouchard R. Computed tomography of posterior fossa in hereditary ataxias. Can J Neurol Sci 1979;6:195-198.
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Langelier, R.1
Bouchard, J.-P.2
Bouchard, R.3
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17
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4243982282
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ARSACS: Possibly a lysosomal storage disease?
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abstract
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[17] Richter A, Morgan K, Bouchard J-P, Mathieu J, Lamarche J, Rioux J, Hudson T, Melançon SB. ARSACS: possibly a lysosomal storage disease? (abstract). Am J Hum Genet 1996;59:A379.
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Richter, A.1
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Bouchard, J.-P.3
Mathieu, J.4
Lamarche, J.5
Rioux, J.6
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Melançon, S.B.8
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18
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84990746711
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Progress on the mapping of autosomal recessive spastic ataxia of Charlevoix-Saguenay
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abstract
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[18] Richter A, Melançon SB, Poirier J, Mercier J, Rozen R, Morgan K, Gosselin F, Bouchard J-P. Progress on the mapping of autosomal recessive spastic ataxia of Charlevoix-Saguenay (abstract). Am J Hum Genet 1989;45:A214.
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Richter, A.1
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Bouchard, J.-P.8
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19
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0010309772
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): Exclusion of the ARSACS gene from linkage to human chromosome 9
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abstract
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[19] Richter A, Morgan K, Bouchard J-P, Poirier J, Mercier J, Melançon SB. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): exclusion of the ARSACS gene from linkage to human chromosome 9 (abstract). Am J Hum Genet 1991;49:357.
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Richter, A.1
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Poirier, J.4
Mercier, J.5
Melançon, S.B.6
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20
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0027355956
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Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay
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Harding A, Deufel T, editors. New York: Raven Press
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[20] Richter A, Morgan K, Bouchard J-P, Poirier J, Mercier J, Gosselin F, Melançon SB. Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay. In: Harding A, Deufel T, editors. Hereditary ataxias. Advances in neurology, Vol. 61. New York: Raven Press, 1993:97-103.
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Richter, A.1
Morgan, K.2
Bouchard, J.-P.3
Poirier, J.4
Mercier, J.5
Gosselin, F.6
Melançon, S.B.7
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21
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0028231090
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The 1993-94 Genethon human genetic linkage map
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[21] Gyapay G, Morissette J, Vignal A, et al. The 1993-94 Genethon human genetic linkage map. Nature Genet 1994;7:246-339.
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Gyapay, G.1
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Vignal, A.3
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22
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0000926583
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A non-radioactive multiplex procedure for genotyping of microsatellite markers
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Vignal, A.1
Gyapay, G.2
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24
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0021850103
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Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
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0028931597
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Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome
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Dubovsky, J.1
Sheffield, V.C.2
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Weber, J.4
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26
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0010310010
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): Linkage and linkage desiquilibrium mapping to chromosome region 13q12
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in press
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[26] Richter A, Rioux J, Bouchard J-P, et al. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): linkage and linkage desiquilibrium mapping to chromosome region 13q12. Am J Hum Genet 1998; in press.
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27
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0000098668
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L'ataxie spastique autosomique récessive: Étude clinique, neurophysiologique, ophtalmologique et IRM de deux cas familiaux
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abstract
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[27] Chaigne D, Brauer E, Ruh D, Jouart D, Juif JG. L'ataxie spastique autosomique récessive: étude clinique, neurophysiologique, ophtalmologique et IRM de deux cas familiaux (abstract). Rev Neurol (Paris) 1993;149:585.
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Chaigne, D.1
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Juif, J.G.5
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28
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0010357701
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Un nouveau regard sur les hérédodégénérescences spino-cérébelleuses
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