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Research Article

Cerebellar diseases

Pages 261-267 | Published online: 11 Jul 2009

References

  • ANDERSON, B. (1988). Para-neoplastic cerebellar degeneration: clinical immunological correlations. Annals of Neurology, 24, 559-567.
  • BOTEZ, M.I., BOTEZ-MARQUARD, T., ELIE, R., PEDRAZA, O.L., GOYETTE, K. & LALONDE, R. (1996). Amantadine hydrochloride treatment in heredodegenerative ataxias: a double blind study. Journal of Neurology, Neurosurgery and Psychiatry, 61, 259-264.
  • BRADLEY, J.L., BLAKE, J.C., CHAMBERLAIN, S., THOMAS, P.K., COOPER, J.M. & SHAPIRA, A.H. (2000). Clinical, biochemical and molecular genetic correlations in Friedreich’s ataxia. Human Molecular Genetics, 9, 275-282.
  • BUSHARA, K.O., GOEBEL, S.U., SHILL, H., GOLDFARB L.G. & HALLETT, M. (2001). Gluten sensitivity in sporadic and hereditary cerebellar ataxia. Annals of Neurology, 49, 540-543.
  • DEVOS, D., SCHAREN-MASCHEKE, S., VUILLAUME, I., DULARDIN, K., NAZE, P., WILLOTEAUX, C. DESTEE, A. & SABLONNIERE, B. (2001). Clinical features and genetic analysis of a new form of spinocerebellar ataxia. Neurology, 56, 234-238.
  • DEUSCHL, G., TORO, C., ZEFFIRO, T., MASSAQUOI, S. & HALLETT, M. (1996). Adaptation motor learning of arm movements in patients with cerebellar disease. Journal of Neurology, Neurosurgery and Psychiatry, 60, 515-519.
  • FISHER, C.M. (1982). Lacunar infarcts: a review. Neurology, 32, 871-876.
  • FISHER, C.M., KARNES, W. & KUBIK, C. (1961). Lateral medullary infarction: the pattern of vascular occlusion. Journal of Neuropathology and Experimental Neurology, 20, 323-333.
  • GENY, C., NGUYEN, J.P., POLLIN, B., FEVE, A., RICOLFI, F., CESARO, P. & DEGOS, J.D. (1996). Improvement of severe postural cerebellar tremor in multiple sclerosis by chronic thalamic stimulation. Movement Disorders, 11, 489-494.
  • GILMAN, S., BLOEDEL, J.R. & LECHTENBERG, R. (1981). Disorders of the cerebellum. Philadelphia, PA: F.A. Davis.
  • GILMAN, S., LITTLE, R., JOHANNS, J., HEUMANN, M., KLUIN, K.J., JUNCK, L., KOEPPE, R.A. & AN, H. (2000). Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy. Neurology, 55, 527-532.
  • GORDON, N. (1998). Episodic ataxia and channelopathies. Brain and Development, 20, 9-13.
  • HALLETT, M., BERARDELLI, A., MATHESON, J., ROTHWELL, J. & MARSDEN, C.D. (1991). Physiological analysis of simple rapid movements in patients with cerebellar deficits. Journal of Neurology, Neurosurgery and Psychiatr y, 53, 124-133.
  • HARDING, A.E. (1983). Classification of the hereditary ataxia and paraplegias. Lancet, 1, 1151-1155.
  • HELVESTON, W., CIBULA, J.E., HURD, R., UTHMAN, B.M. & WILDER, B.J. (1996a). Abnormalities of antioxidant metabolism in a case of Friedreich’s disease. Clinical Neuropharmacology, 19, 271-275.
  • HELVESTON, W., CIBULA, J.E., HURD, R., UTHMAN, B.M. & WILDER, B.J. (1996b). Abnormalities of glutathione peroxidase and glutathione reductase in four patients with Friedreich’s ataxia. Movement Disorders, 11, 106-107.
  • HOLMES, G. (1907). An attempt to classify cerebellar disease, with a note on Marie’s hereditary ataxia. Brain, 30, 545-567.
  • HOLT, I.J., HARDING, A.E., PETTY, R.K. & MORGAN-HUGHES, J.A. (1990). American Journal of Human Genetics, 46, 428-433.
  • HSIAO, K., BAKER, H.F., CROW, T.J., POULTER, M., OWEN, F., TERWILLIGER, J.D., WESTAWAY, D., OTT, J. & PRUISNER, S.B. (1989). Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome. Nature, 338, 342-345.
  • KREIGER, M.D., MCCOMB, J.G. & LEVY, M.L. (1999). Toward a simpler surgical management of Chiari I malformation in a pediatric population. Pediatric Neurosurgery, 30, 113-121.
  • LOPEZ-ARLANDIS, J.M., VILCHEZ, J.J., PALAU, F. & SEVILLA, T. (1995). Friedreich’s ataxia: an epidemiological study in Valencia, Spain, based on a consanguinity analysis. Neuroepidemiology, 14, 14-19.
  • LOUIS-BAR, D. (1941). Sur un syndrome progressif comprenant des télagiectasies capillaries cutanées et conjonctivales symétriques, á disposition naevode et de troubles cérébelleux. Confinia Neurologica, 4, 32-42.
  • MOSELEY, M.L., BENZOW, W.J., SCHUT, L.J., BIRD, T.D., GOMEZ, C.M., BARKAUS, P.E., BLINDAUER, K.A., LABUDA, M., PANDOLFO, M., KOOB, M.D. & RANUM, L.P. (1998). Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology, 51, 1666-1671.
  • MULLER, D.P.R., LLOYD, J.K. & WOLFF, O.H. (1983). Vitamin E and neurological function. Lancet, 1, 225-227.
  • PAPP, M.L. & LANTOS, P.L. (1994). The distribution of oligodendroglial inclusions in multiple system atrophy Cerebellar diseases 267 and its relevance to clinical symptomatology. Brain, 117, 235-243.
  • POSNER, J.B. & CHERNIK, N.L. (1978) Intracranial metastasis from systemic cancer. Advances in Neurology, 19, 575-587.
  • REKATE, H.L., GRUBB, R.L., ARAM, D.M., HAHN J.F. & RATCHESON R.A. (1985). Muteness of cerebellar origin. Archives of Neurology, 42, 697-698.
  • ROJAS, I., GRAUS, F., KEIME-GUIBERT, F., RENE, R., DELATTRE, J.Y., RAMON, J.M., DALMAU, J. & POSNER, J.B. (2000). Long-term clinical outcome of paraneoplastic cerebellar degenration and anti-Yo antibodies. Neurology, 55, 713-715.
  • RUSTIN, P., VON KLEIST-RETZOW, J.C., CHANTREL-GROUSSARD, K., SIDI, D., MUNNICH, A. & ROTIG, A. (1999). Effect of idebenone on cardiomyopathy in Friedreich’s ataxia: a preliminary study. Lancet, 354, 477-479.
  • SCHMAHMANN, J.D. & SHERMAN, J.C. (1998). The cerebellar cognitive affective syndrome. Brain, 121, 561-579.
  • SCHOLS, L., SZYMANSKI, S., PETERS, S., PRZUNTEK, H., EPPLEN, J.T., HARDT, C. & REISS, O. (2000). Genetic background of apparently idiopathic sporadic cerebellar ataxia. Human Genetics, 107, 132-137.
  • SYPER, A.W. & ALVORD, E.C. (1975). Cerebellar infarction: a clinicopathological study. Archives of Neurology, 32, 357-359.
  • TROUILLAS, P., XIE, J., ADELEINE, P., MICHEL, D., VIGHETTO, A., HONNORAT, J., DUMAS, R., NIGHOGHOSSIAN, N. & LAURENT, B. (1997). Buspirone, a 5-hydroxytryptamine1A agonist, is active in cerebellar ataxia. Results of a double-blind drug placebo study in patients with cerebellar cortical atrophy. Archives of Neurology, 54, 749-752.
  • WENNING, G.K., SCHLOMO, Y., MAGALHAES, M., DANIEL, S.E. & QUINN, N.P. (1994). Clinical features and natural history of multiple system atrophy: an analysis of 100 cases. Brain, 117, 835-845.

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