References
Logemann JA (1983) Evaluation and treatment of swallowing disorders 1st ed. San Diego, CA
Kagel MC, Leopold NA (1992) Dysphagia in Huntington’s disease: a 16–year retrospective. Dysphagia 7:106–114
Leopold NA, Kagel MC (1996) Prepharyngeal dysphagia in Parkinson’s disease. Dysphagia 11:14–22
Leopold NA, Kagel MC (1997) Pharyngo–esophageal dysphagia in Parkinson’s disease. Dysphagia 12: 11–18
Litvan I, Sastry N, Sonies BC (1997) Characterizing swallowing abnormalities in progressive supranuclear palsy. Neurology 48:1654–1662
Nilsson H, Ekberg O, Olsson R, Hindfelt B (1996) Swallowing in hereditary sensory ataxia. Dysphagia 11:140–143
Nagaya M, Kachi T, Yamada T, Igata A (1998) Videofluorographic study of swallowing in Parkinson’s disease. Dysphagia 13:95–100
Harding AE (1984) The hereditary ataxias and related disorders. Churchill Livingstone. Edinburgh
Pou–Serradell A, Russi A, Ferrer I, Galofre E, Escudero D (1987) Machado–Joseph disease in a family of Spanish origin. Rev Neurol (Paris) 143:520–525
Orozco G, Estrada R, Perry TL, Arana J, Fernandez R, Gonzalez–Quevedo A, Galarraga J, Hansen S (1989) Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings. J Neurol Sci 93:37–50
Durr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, Brice A (1993) Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity. Brain 116(Pt 6):1497–1508
Sequeiros J, Coutinho P (1993) Epidemiology and clinical aspects of Machado–Joseph disease. In: Harding AE, Deufel T (eds) The hereditary ataxias. 61 ed. New York
Ranum LP, Schut LJ, Lundgren JK, Orr HT, Livingston DM (1994) Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. Nat Genet 8:280–284
Durr A, Smadja D, Cancel G, Lezin A, Stevanin G, Mikol J, Bellance R, Buisson GG, Chneiweiss H, Dellanave J (1995) Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families. Brain 118(Pt 6):1573–1581
Gennis D, Matilla T, Volpini V, Rosell J, Davalos A, Ferrer I, Molins A, Estivill X (1995) Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred: (CAG)n expansion and early premonitory signs and symptoms. Neurology 45:24–30
Burk K, Abele M, Fetter M, Dichgans J, Skalej M, Laccone F, Didierjean O, Brice A, Klockgether T (1996) Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3. Brain 119(Pt 5):1497–1505
Durr A, Stevanin G, Cancel G, Duyckaerts C, Abbas N, Didierjean O, Chneiweiss H, Benomar A, Lyon–Caen O, Julien J, Serdaru M, Penet C, Agid Y, Brice A (1996) Spinocerebellar ataxia 3 and Machado–Joseph disease: clinical, molecular, and neuropathological features. Ann Neurol 39:490–499
Klockgether T, Ludtke R, Kramer B, Abele M, Burk K, Schols L, Riess O, Laccone F, Boesch S, Lopes–Cendes I, Brice A, Inzelberg R, Zilber N, Dichgans J (1998) The natural history of degenerative ataxia: a retrospective study in 466 patients. Brain 121(Pt 4):589–600
Pujana MA, Corral J, Gratacos M, Combarros O, Berciano J, Genis D, Banchs I, Estivill X, Volpini V (1999) Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group. Hum Genet 104:516–522
Harding AE (1981) “Idiopathic” late onset cerebellar ataxia. J Neurol Sci 51:259–271
Gilman S, Low PA, Quinn N, Albanese A, Ben Shlomo Y, Fowler CJ, Kaufman H, Klockgether T, Lang AE, Lantos Pl, Litvan I, Mathias CJ, Oliver E, Robertson D, Wenning GK (1999) Consensus statement on the diagnosis of multiple system atrophy. J Neurol Sci 163:94–98
Kurtzke JF (1983) Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology 33:1444–1452
Litvan I, Sastry N, Sonies BC (1997) Characterizing swallowing abnormalities in progressive supranuclear palsy. Neurology 48:1654–1662
Logemann JA (1993) Manual for the videofluorographic study of swallowing. Austin, TX
Ferrer I, Genis D, Davalos A, Bernado L, Sant F, Serrano T (1994) The Purkinje cell in olivopontocerebellar atrophy. A Golgi and immunocytochemical study. Neuropathol Appl Neurobiol 20:38–46
Robitaille Y, Schut L, Kish SJ (1995) Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA–1) mutation define a unique phenotype. Acta Neuropathol (Berl) 90:572–581
Rub U, Brunt ER, Del Turco D, de Vos RA, Gierga K, Paulson H, Braak H (2003) Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient. Neuropathol Appl Neurobiol 29:1–13
Zald DH, Pardo JV (1999) The functional neuroanatomy of voluntary swallowing. Ann Neurol 46:281–286
Suzuki M, Asada Y, Ito J, Hayashi K, Inoue H, Kitano H (2003) Activation of cerebellum and basal ganglia on volitional swallowing detected by functional magnetic resonance imaging. Dysphagia 18:71–77
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Ramio-Torrentia, L., Gomez, E. & Genis, D. Swallowing in degenerative ataxias. J Neurol 253, 875–881 (2006). https://doi.org/10.1007/s00415-006-0122-2
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DOI: https://doi.org/10.1007/s00415-006-0122-2