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Items: 1 to 20 of 111

1.

Evaluation of depression risk in LGI1 mutation carriers.

Heiman GA, Kamberakis K, Gill R, Kalachikov S, Pedley TA, Hauser WA, Ottman R.

Epilepsia. 2010 Sep;51(9):1685-90. doi: 10.1111/j.1528-1167.2010.02677.x. Epub 2010 Jul 26.

2.

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

Michelucci R, Pasini E, Malacrida S, Striano P, Bonaventura CD, Pulitano P, Bisulli F, Egeo G, Santulli L, Sofia V, Gambardella A, Elia M, de Falco A, Neve Al, Banfi P, Coppola G, Avoni P, Binelli S, Boniver C, Pisano T, Marchini M, Dazzo E, Fanciulli M, Bartolini Y, Riguzzi P, Volpi L, de Falco FA, Giallonardo AT, Mecarelli O, Striano S, Tinuper P, Nobile C.

Epilepsia. 2013 Jul;54(7):1288-97. doi: 10.1111/epi.12194. Epub 2013 Apr 26.

3.

LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA.

Neurology. 2004 Apr 13;62(7):1120-6.

4.

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.

5.

Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.

Hedera P, Abou-Khalil B, Crunk AE, Taylor KA, Haines JL, Sutcliffe JS.

Epilepsia. 2004 Mar;45(3):218-22.

6.

A rat model for LGI1-related epilepsies.

Baulac S, Ishida S, Mashimo T, Boillot M, Fumoto N, Kuwamura M, Ohno Y, Takizawa A, Aoto T, Ueda M, Ikeda A, LeGuern E, Takahashi R, Serikawa T.

Hum Mol Genet. 2012 Aug 15;21(16):3546-57. doi: 10.1093/hmg/dds184. Epub 2012 May 15.

7.

Two novel epilepsy-linked mutations leading to a loss of function of LGI1.

Chabrol E, Popescu C, Gourfinkel-An I, Trouillard O, Depienne C, Senechal K, Baulac M, LeGuern E, Baulac S.

Arch Neurol. 2007 Feb;64(2):217-22.

PMID:
17296837
8.

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.

Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, Hauser WA, Ottman R, Gilliam TC.

Nat Genet. 2002 Mar;30(3):335-41. Epub 2002 Jan 28.

9.

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
10.

Altered language processing in autosomal dominant partial epilepsy with auditory features.

Ottman R, Rosenberger L, Bagic A, Kamberakis K, Ritzl EK, Wohlschlager AM, Shamim S, Sato S, Liew C, Gaillard WD, Wiggs E, Berl MM, Reeves-Tyer P, Baker EH, Butman JA, Theodore WH.

Neurology. 2008 Dec 9;71(24):1973-80. doi: 10.1212/01.wnl.0000336923.29538.5b.

11.

LGI1 mutations in temporal lobe epilepsies.

Berkovic SF, Izzillo P, McMahon JM, Harkin LA, McIntosh AM, Phillips HA, Briellmann RS, Wallace RH, Mazarib A, Neufeld MY, Korczyn AD, Scheffer IE, Mulley JC.

Neurology. 2004 Apr 13;62(7):1115-9.

PMID:
15079010
12.

Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1/epitempin gene.

Berghuis B, Brilstra EH, Lindhout D, Baulac S, de Haan GJ, van Kempen M.

Epilepsy Behav. 2013 Jul;28(1):41-6. doi: 10.1016/j.yebeh.2013.03.032. Epub 2013 May 5.

PMID:
23651915
13.

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

Fanciulli M, Santulli L, Errichiello L, Barozzi C, Tomasi L, Rigon L, Cubeddu T, de Falco A, Rampazzo A, Michelucci R, Uzzau S, Striano S, de Falco FA, Striano P, Nobile C.

Neurology. 2012 Apr 24;78(17):1299-303. doi: 10.1212/WNL.0b013e3182518328. Epub 2012 Apr 11.

14.

Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism.

Pizzuti A, Flex E, Di Bonaventura C, Dottorini T, Egeo G, Manfredi M, Dallapiccola B, Giallonardo AT.

Ann Neurol. 2003 Mar;53(3):396-9. Erratum in: Ann Neurol. 2003 Jul;54(1):137.

PMID:
12601709
15.

A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.

Striano P, de Falco A, Diani E, Bovo G, Furlan S, Vitiello L, Pinardi F, Striano S, Michelucci R, de Falco FA, Nobile C.

Arch Neurol. 2008 Jul;65(7):939-42. doi: 10.1001/archneur.65.7.939.

PMID:
18625862
16.

A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy.

Lee MK, Kim SW, Lee JH, Cho YJ, Kim DE, Lee BI, Kim HM, Lee MG, Heo K.

Seizure. 2014 Jan;23(1):69-73. doi: 10.1016/j.seizure.2013.10.001. Epub 2013 Oct 12.

17.

Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families.

Kawamata J, Ikeda A, Fujita Y, Usui K, Shimohama S, Takahashi R.

Epilepsia. 2010 Apr;51(4):690-3. doi: 10.1111/j.1528-1167.2009.02309.x. Epub 2009 Sep 22.

18.

Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2.

Limviphuvadh V, Chua LL, Rahim RA, Eisenhaber F, Maurer-Stroh S, Adhikari S.

BMC Biochem. 2010 Sep 24;11:39. doi: 10.1186/1471-2091-11-39.

19.

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.

20.

Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras.

Dazzo E, Santulli L, Posar A, Fattouch J, Conti S, Lodén-van Straaten M, Mijalkovic J, De Bortoli M, Rosa M, Millino C, Pacchioni B, Di Bonaventura C, Giallonardo AT, Striano S, Striano P, Parmeggiani A, Nobile C.

Epilepsy Res. 2015 Feb;110:132-8. doi: 10.1016/j.eplepsyres.2014.12.004. Epub 2014 Dec 16.

PMID:
25616465
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