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Results: 1 to 20 of 101

1.

Clinical reasoning: a middle-aged man with episodes of gait imbalance and a newly found genetic mutation.

Yugrakh MS, Levy OA.

Neurology. 2012 Oct 16;79(16):e135-9. doi: 10.1212/WNL.0b013e31826e9b40. No abstract available.

PMID:
23071170
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

4-Aminopyridine improves gait variability in cerebellar ataxia due to CACNA 1A mutation.

Schniepp R, Wuehr M, Ackl N, Danek A, Brandt T, Strupp M, Jahn K.

J Neurol. 2011 Sep;258(9):1708-11. doi: 10.1007/s00415-011-5987-z. Epub 2011 Mar 23. No abstract available.

PMID:
21431381
[PubMed - indexed for MEDLINE]
3.

Causes of imbalance and abnormal gait that may be misdiagnosed.

Shill HA, Fife TD.

Semin Neurol. 2013 Jul;33(3):270-5. doi: 10.1055/s-0033-1354601. Epub 2013 Sep 21. Review.

PMID:
24057830
[PubMed - indexed for MEDLINE]
4.

A 75-year-old man with cognitive impairment and gait changes.

Lippa CF, Boeve BF, Parisi JE, Keegan BM.

Neurology. 2007 Sep 11;69(11):1183-9. No abstract available.

PMID:
17846418
[PubMed - indexed for MEDLINE]
5.

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.

Jouvenceau A, Eunson LH, Spauschus A, Ramesh V, Zuberi SM, Kullmann DM, Hanna MG.

Lancet. 2001 Sep 8;358(9284):801-7.

PMID:
11564488
[PubMed - indexed for MEDLINE]
6.

CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.

Türkmen S, Guo G, Garshasbi M, Hoffmann K, Alshalah AJ, Mischung C, Kuss A, Humphrey N, Mundlos S, Robinson PN.

PLoS Genet. 2009 May;5(5):e1000487. doi: 10.1371/journal.pgen.1000487. Epub 2009 May 22.

PMID:
19461874
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

A case of fragile X premutation tremor/ataxia syndrome with evidence of mitochondrial dysfunction.

Rizzo G, Pizza F, Scaglione C, Tonon C, Lodi R, Barbiroli B, Ambrosetto P, Martinelli P.

Mov Disord. 2006 Sep;21(9):1541-2. No abstract available.

PMID:
16830323
[PubMed - indexed for MEDLINE]
8.

Late onset hereditary episodic ataxia.

Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K.

J Neurol Neurosurg Psychiatry. 2009 May;80(5):566-8. doi: 10.1136/jnnp.2008.150615.

PMID:
19372292
[PubMed - indexed for MEDLINE]
9.

Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.

Amador C, Mathews AM, Del Carmen Montoya M, Laughridge ME, Everman DB, Holden KR.

J Child Neurol. 2008 Aug;23(8):901-5. doi: 10.1177/0883073808317730.

PMID:
18660473
[PubMed - indexed for MEDLINE]
10.

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.

Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C.

J Neurol Sci. 2007 Mar 15;254(1-2):69-71. Epub 2007 Feb 12.

PMID:
17292920
[PubMed - indexed for MEDLINE]
11.

Variable manifestations of familial hemiplegic migraine associated with reversible cerebral edema in children.

Asghar SJ, Milesi-Hallé A, Kaushik C, Glasier C, Sharp GB.

Pediatr Neurol. 2012 Sep;47(3):201-4. doi: 10.1016/j.pediatrneurol.2012.05.006.

PMID:
22883286
[PubMed - indexed for MEDLINE]
12.

Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.

Blumkin L, Michelson M, Leshinsky-Silver E, Kivity S, Lev D, Lerman-Sagie T.

J Child Neurol. 2010 Jul;25(7):892-7. doi: 10.1177/0883073809351316. Epub 2010 Jan 21.

PMID:
20097664
[PubMed - indexed for MEDLINE]
13.

[A case of spinocerebellar ataxia 6 accompanied with schizophrenia].

Nakanishi I, Miwa H, Hayata T, Kawada A, Kondo T.

No To Shinkei. 2004 Jan;56(1):49-52. Japanese.

PMID:
15024829
[PubMed - indexed for MEDLINE]
14.

Adult-onset Alexander disease : report on a family.

Balbi P, Seri M, Ceccherini I, Uggetti C, Casale R, Fundarò C, Caroli F, Santoro L.

J Neurol. 2008 Jan;255(1):24-30. Epub 2007 Nov 21.

PMID:
18004641
[PubMed - indexed for MEDLINE]
15.

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.

Takahashi T, Igarashi S, Kimura T, Hozumi I, Kawachi I, Onodera O, Takano H, Saito M, Tsuji S.

J Neurol Neurosurg Psychiatry. 2002 May;72(5):676-7. No abstract available.

PMID:
11971066
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A novel de novo pathogenic mutation in the CACNA1A gene.

Fujioka S, Rayaprolu S, Sundal C, Broderick DF, Langley WA, Shoffner J, Hyams LC, Rademakers R, Graff-Radford NR, Tatum W, Ross OA, Wszolek ZK.

Mov Disord. 2012 Oct;27(12):1578-9. doi: 10.1002/mds.25198. Epub 2012 Oct 4. No abstract available.

PMID:
23038654
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Posterior pusher syndrome: A report of two cases.

Cardoen S, Santens P.

Clin Neurol Neurosurg. 2010 May;112(4):347-9. doi: 10.1016/j.clineuro.2009.12.007. Epub 2010 Jan 6.

PMID:
20056311
[PubMed - indexed for MEDLINE]
18.

[Mild form of the middle interhemispheric variant of holoprosencephaly].

Lettau M, Laible M.

Rofo. 2012 Nov;184(11):1059-60. doi: 10.1055/s-0032-1313046. Epub 2012 Jul 31. German. No abstract available.

PMID:
22851296
[PubMed - indexed for MEDLINE]
19.

Gait and balance disorders.

Ondo W.

Med Clin North Am. 2003 Jul;87(4):793-801, viii.

PMID:
12834149
[PubMed - indexed for MEDLINE]
20.

Gait and bilateral limb ataxia as isolated feature of a lower midbrain tegmental infarction. A clinical-MRI study.

Cerrato P, Lentini A, Colonna R, Bosco G, Destefanis E, Caprioli M, Bergui M.

J Neurol. 2008 Feb;255(2):290-1. doi: 10.1007/s00415-006-0506-3. Epub 2008 Feb 14. No abstract available.

PMID:
18274811
[PubMed - indexed for MEDLINE]

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