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Results: 1 to 20 of 39

References for PMC Articles for PubMed (Select 19064878)

1.

Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

Rosanoff MJ, Ottman R.

Neurology. 2008 Aug 19;71(8):567-71. doi: 10.1212/01.wnl.0000323926.77565.ee.

2.

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.

Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R.

J Neurol. 2008 Jan;255(1):16-23. Epub 2007 Nov 21.

PMID:
18004642
3.

Atypical language in lesional and nonlesional complex partial epilepsy.

Gaillard WD, Berl MM, Moore EN, Ritzl EK, Rosenberger LR, Weinstein SL, Conry JA, Pearl PL, Ritter FF, Sato S, Vezina LG, Vaidya CJ, Wiggs E, Fratalli C, Risse G, Ratner NB, Gioia G, Theodore WH.

Neurology. 2007 Oct 30;69(18):1761-71.

PMID:
17967992
4.

Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1.

Tessa C, Michelucci R, Nobile C, Giannelli M, Della Nave R, Testoni S, Bianucci D, Tinuper P, Bisulli F, Sofia V, De Feo MR, Giallonardo AT, Tassinari CA, Mascalchi M.

Neurology. 2007 Sep 18;69(12):1298-300. No abstract available.

PMID:
17875918
5.

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.

Michelucci R, Mecarelli O, Bovo G, Bisulli F, Testoni S, Striano P, Striano S, Tinuper P, Nobile C.

Neurology. 2007 Jun 12;68(24):2150-1. No abstract available.

PMID:
17562837
6.

Reversible nonfluent aphasia and left frontal hypoperfusion during topiramate treatment.

Cappa SF, Ortelli P, Garibotto V, Zamboni M.

Epilepsy Behav. 2007 Feb;10(1):192-4. Epub 2006 Dec 12.

PMID:
17166774
7.

The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface.

Sirerol-Piquer MS, Ayerdi-Izquierdo A, Morante-Redolat JM, Herranz-Pérez V, Favell K, Barker PA, Pérez-Tur J.

Hum Mol Genet. 2006 Dec 1;15(23):3436-45. Epub 2006 Oct 26.

8.

Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission.

Fukata Y, Adesnik H, Iwanaga T, Bredt DS, Nicoll RA, Fukata M.

Science. 2006 Sep 22;313(5794):1792-5.

9.

Neuroscience. Adam finds an exciting mate.

Snyder SH.

Science. 2006 Sep 22;313(5794):1744-5. No abstract available.

PMID:
16990538
10.

Functional MRI reveals declined prefrontal cortex activation in patients with epilepsy on topiramate therapy.

Jansen JF, Aldenkamp AP, Marian Majoie HJ, Reijs RP, de Krom MC, Hofman PA, Eline Kooi M, Nicolay K, Backes WH.

Epilepsy Behav. 2006 Aug;9(1):181-5. Epub 2006 Jun 21.

PMID:
16793345
11.

The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1.

Schulte U, Thumfart JO, Klöcker N, Sailer CA, Bildl W, Biniossek M, Dehn D, Deller T, Eble S, Abbass K, Wangler T, Knaus HG, Fakler B.

Neuron. 2006 Mar 2;49(5):697-706.

12.
13.

Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation.

Brodtkorb E, Michler RP, Gu W, Steinlein OK.

Epilepsia. 2005 Jun;46(6):963-6.

PMID:
15946341
14.

ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy.

Senechal KR, Thaller C, Noebels JL.

Hum Mol Genet. 2005 Jun 15;14(12):1613-20. Epub 2005 Apr 27.

15.

Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation.

Pisano T, Marini C, Brovedani P, Brizzolara D, Pruna D, Mei D, Moro F, Cianchetti C, Guerrini R.

Epilepsia. 2005 Jan;46(1):118-23.

PMID:
15660777
16.

LGI1 gene mutation screening in sporadic partial epilepsy with auditory features.

Flex E, Pizzuti A, Di Bonaventura C, Douzgou S, Egeo G, Fattouch J, Manfredi M, Dallapiccola B, Giallonardo AT.

J Neurol. 2005 Jan;252(1):62-6.

PMID:
15654555
18.

A de novo LGI1 mutation in sporadic partial epilepsy with auditory features.

Bisulli F, Tinuper P, Scudellaro E, Naldi I, Bagattin A, Avoni P, Michelucci R, Nobile C.

Ann Neurol. 2004 Sep;56(3):455-6. No abstract available.

PMID:
15349881
19.

Rapid change of tonotopic maps in the human auditory cortex during pitch discrimination.

Ozaki I, Jin CY, Suzuki Y, Baba M, Matsunaga M, Hashimoto I.

Clin Neurophysiol. 2004 Jul;115(7):1592-604.

PMID:
15203060
20.

Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.

Bisulli F, Tinuper P, Avoni P, Striano P, Striano S, d'Orsi G, Vignatelli L, Bagattin A, Scudellaro E, Florindo I, Nobile C, Tassinari CA, Baruzzi A, Michelucci R.

Brain. 2004 Jun;127(Pt 6):1343-52. Epub 2004 Apr 16. Review.

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