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Items: 1 to 20 of 85

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.

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
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
4.

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
5.

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
6.

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
7.

Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

Ohmori H, Hara A, Ishikawa K, Mizusawa H, Ando Y.

J Neurogenet. 2015;29(2-3):80-4. doi: 10.3109/01677063.2015.1054992. Epub 2015 Jul 13.

PMID:
26004545
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
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
10.

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
11.

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
12.

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
13.

Clinical Reasoning: A 28-year-old man with progressive gait disturbance and encephalopathy.

Massaro AM, Pruitt A.

Neurology. 2014 Dec 9;83(24):e204-8. doi: 10.1212/WNL.0000000000001064. No abstract available.

PMID:
25488997
14.

[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
15.

[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
16.

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
17.

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.

18.

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
19.

May a suspicious psychiatric disorder hide sporadic hemiplegic migraine? Genetic test as prompting factor for diagnosis.

Liguori C, Albanese M, Sancesario G, Stefani A, Marciani MG, Pierantozzi M.

Neurol Sci. 2013 Oct;34(10):1845-6. doi: 10.1007/s10072-013-1325-9. Epub 2013 Feb 10. No abstract available.

PMID:
23397224
20.

Delayed leukoencephalopathy after hypoxic-ischemic injury.

Chen-Plotkin AS, Pau KT, Schmahmann JD.

Arch Neurol. 2008 Jan;65(1):144-5. doi: 10.1001/archneurol.2007.7. No abstract available.

PMID:
18195154

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