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Vestibulocerebellar syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Vestibulocerebellar syndrome" in English language version.

refsWebsite
Global rank English rank
10nih.gov
4th place
4th place
9doi.org
2nd place
2nd place
5semanticscholar.org
11th place
8th place

doi.org

  • Theunissen EJ, Huygen PL, Verhagen WI (February 1989). "Familial vestibulocerebellar dysfunction: a new syndrome?". Journal of the Neurological Sciences. 89 (2–3): 149–55. doi:10.1016/0022-510x(89)90016-6. PMID 2926446. S2CID 31498395.
  • Damji KF, Allingham RR, Pollock SC, et al. (April 1996). "Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias". Archives of Neurology. 53 (4): 338–44. doi:10.1001/archneur.1996.00550040074016. PMID 8929156.
  • Small KW, Pollock SC, Vance JM, Stajich JM, Pericak-Vance M (June 1996). "Ocular motility in North Carolina autosomal dominant ataxia". J Neuroophthalmol. 16 (2): 91–5. doi:10.1097/00041327-199606000-00002. PMID 8797163. S2CID 39897382.
  • Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM (January 2003). "Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus". J. Med. Genet. 40 (1): 37–41. doi:10.1136/jmg.40.1.37. PMC 1735258. PMID 12525540.
  • Harris CM, Walker J, Shawkat F, Wilson J, Russell-Eggitt I (June 1993). "Eye movements in a familial vestibulocerebellar disorder". Neuropediatrics. 24 (3): 117–22. doi:10.1055/s-2008-1071526. PMID 8355816. S2CID 19694620.
  • FARMER TW, MUSTIAN VM (May 1963). "Vestibulocerebellar ataxia. A newly defined hereditary syndrome with periodic manifestations". Arch. Neurol. 8: 471–80. doi:10.1001/archneur.1963.00460050021002. PMID 13944410.
  • Farris BK, Smith JL, Ayyar DR (October 1986). "Neuro-ophthalmologic findings in vestibulocerebellar ataxia". Archives of Neurology. 43 (10): 1050–3. doi:10.1001/archneur.1986.00520100056015. PMID 3489454.
  • Jen J, Kim GW, Baloh RW (January 2004). "Clinical spectrum of episodic ataxia type 2". Neurology. 62 (1): 17–22. doi:10.1212/01.wnl.0000101675.61074.50. PMID 14718690. S2CID 28147381.
  • Baloh RW, Winder A (March 1991). "Acetazolamide-responsive vestibulocerebellar syndrome: clinical and oculographic features". Neurology. 41 (3): 429–33. doi:10.1212/wnl.41.3.429. PMID 2006014. S2CID 45489324.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Theunissen EJ, Huygen PL, Verhagen WI (February 1989). "Familial vestibulocerebellar dysfunction: a new syndrome?". Journal of the Neurological Sciences. 89 (2–3): 149–55. doi:10.1016/0022-510x(89)90016-6. PMID 2926446. S2CID 31498395.
  • Damji KF, Allingham RR, Pollock SC, et al. (April 1996). "Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias". Archives of Neurology. 53 (4): 338–44. doi:10.1001/archneur.1996.00550040074016. PMID 8929156.
  • Small KW, Pollock SC, Vance JM, Stajich JM, Pericak-Vance M (June 1996). "Ocular motility in North Carolina autosomal dominant ataxia". J Neuroophthalmol. 16 (2): 91–5. doi:10.1097/00041327-199606000-00002. PMID 8797163. S2CID 39897382.
  • Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM (January 2003). "Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus". J. Med. Genet. 40 (1): 37–41. doi:10.1136/jmg.40.1.37. PMC 1735258. PMID 12525540.
  • Harris CM, Walker J, Shawkat F, Wilson J, Russell-Eggitt I (June 1993). "Eye movements in a familial vestibulocerebellar disorder". Neuropediatrics. 24 (3): 117–22. doi:10.1055/s-2008-1071526. PMID 8355816. S2CID 19694620.
  • FARMER TW, MUSTIAN VM (May 1963). "Vestibulocerebellar ataxia. A newly defined hereditary syndrome with periodic manifestations". Arch. Neurol. 8: 471–80. doi:10.1001/archneur.1963.00460050021002. PMID 13944410.
  • Farris BK, Smith JL, Ayyar DR (October 1986). "Neuro-ophthalmologic findings in vestibulocerebellar ataxia". Archives of Neurology. 43 (10): 1050–3. doi:10.1001/archneur.1986.00520100056015. PMID 3489454.
  • Jen J, Kim GW, Baloh RW (January 2004). "Clinical spectrum of episodic ataxia type 2". Neurology. 62 (1): 17–22. doi:10.1212/01.wnl.0000101675.61074.50. PMID 14718690. S2CID 28147381.
  • Baloh RW, Winder A (March 1991). "Acetazolamide-responsive vestibulocerebellar syndrome: clinical and oculographic features". Neurology. 41 (3): 429–33. doi:10.1212/wnl.41.3.429. PMID 2006014. S2CID 45489324.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

  • Theunissen EJ, Huygen PL, Verhagen WI (February 1989). "Familial vestibulocerebellar dysfunction: a new syndrome?". Journal of the Neurological Sciences. 89 (2–3): 149–55. doi:10.1016/0022-510x(89)90016-6. PMID 2926446. S2CID 31498395.
  • Small KW, Pollock SC, Vance JM, Stajich JM, Pericak-Vance M (June 1996). "Ocular motility in North Carolina autosomal dominant ataxia". J Neuroophthalmol. 16 (2): 91–5. doi:10.1097/00041327-199606000-00002. PMID 8797163. S2CID 39897382.
  • Harris CM, Walker J, Shawkat F, Wilson J, Russell-Eggitt I (June 1993). "Eye movements in a familial vestibulocerebellar disorder". Neuropediatrics. 24 (3): 117–22. doi:10.1055/s-2008-1071526. PMID 8355816. S2CID 19694620.
  • Jen J, Kim GW, Baloh RW (January 2004). "Clinical spectrum of episodic ataxia type 2". Neurology. 62 (1): 17–22. doi:10.1212/01.wnl.0000101675.61074.50. PMID 14718690. S2CID 28147381.
  • Baloh RW, Winder A (March 1991). "Acetazolamide-responsive vestibulocerebellar syndrome: clinical and oculographic features". Neurology. 41 (3): 429–33. doi:10.1212/wnl.41.3.429. PMID 2006014. S2CID 45489324.