PubMed (OMIM) for id: 1643229

Year	Number of Results
1975	1
1994	1
1995	1
1996	1
1999	1
2000	2
2002	3
2004	2
2024	0

1

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. Ottman R, et al. Neurology. 2004 Apr 13;62(7):1120-6. doi: 10.1212/01.wnl.0000120098.39231.6e. Neurology. 2004. PMID: 15079011 Free PMC article.

2

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. Berkovic SF, et al. Neurology. 2004 Apr 13;62(7):1115-9. doi: 10.1212/01.wnl.0000118213.94650.81. Neurology. 2004. PMID: 15079010

3

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures.

Gu W, Brodtkorb E, Steinlein OK. Gu W, et al. Ann Neurol. 2002 Sep;52(3):364-7. doi: 10.1002/ana.10280. Ann Neurol. 2002. PMID: 12205652

4

Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.

Brodtkorb E, Gu W, Nakken KO, Fischer C, Steinlein OK. Brodtkorb E, et al. Epilepsia. 2002 Mar;43(3):228-35. doi: 10.1046/j.1528-1157.2002.32001.x. Epilepsia. 2002. PMID: 11906506 Free article.

5

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. Kalachikov S, et al. Nat Genet. 2002 Mar;30(3):335-41. doi: 10.1038/ng832. Epub 2002 Jan 28. Nat Genet. 2002. PMID: 11810107 Free PMC article.

6

Supporting evidence of a gene for partial epilepsy on 10q.

Mautner VF, Lindenau M, Gottesleben A, Goetze G, Kluwe L. Mautner VF, et al. Neurogenetics. 2000 Sep;3(1):31-4. doi: 10.1007/s100480000091. Neurogenetics. 2000. PMID: 11085594

7

Autosomal dominant partial epilepsy with auditory features: defining the phenotype.

Winawer MR, Ottman R, Hauser WA, Pedley TA. Winawer MR, et al. Neurology. 2000 Jun 13;54(11):2173-6. doi: 10.1212/wnl.54.11.2173. Neurology. 2000. PMID: 10851389 Free PMC article.

8

Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q.

Poza JJ, Sáenz A, Martínez-Gil A, Cheron N, Cobo AM, Urtasun M, Martí-Massó JF, Grid D, Beckmann JS, Prud'homme JF, López de Munain A. Poza JJ, et al. Ann Neurol. 1999 Feb;45(2):182-8. doi: 10.1002/1531-8249(199902)45:2<182::aid-ana8>3.0.co;2-g. Ann Neurol. 1999. PMID: 9989620

9

Familial temporal lobe epilepsy: a common disorder identified in twins.

Berkovic SF, McIntosh A, Howell RA, Mitchell A, Sheffield LJ, Hopper JL. Berkovic SF, et al. Ann Neurol. 1996 Aug;40(2):227-35. doi: 10.1002/ana.410400214. Ann Neurol. 1996. PMID: 8773604

10

Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder.

Scheffer IE, Bhatia KP, Lopes-Cendes I, Fish DR, Marsden CD, Andermann F, Andermann E, Desbiens R, Cendes F, Manson JI, et al. Scheffer IE, et al. Lancet. 1994 Feb 26;343(8896):515-7. doi: 10.1016/s0140-6736(94)91463-x. Lancet. 1994. PMID: 7906762 Review.

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