SEARCH

SEARCH BY CITATION

References

  • Bisulli F, Tinuper P, Scudellaro E, Naldi I, Bagattin A, Avoni P, Michelucci R, Nobile C. (2004) A de novo LGI1 mutation in sporadic partial epilepsy with auditory features. Ann Neurol 56:455456.
  • Buchanan SG, Gay NJ. (1996) Structural and functional diversity in the leucine-rich repeat family of proteins. Prog Biophys Mol Biol 65:144.
  • Furlan S, Roncaroli F, Forner F, Vitiello L, Calabria E, Piquer-Sirerol S, Valle G, Perez-Tur J, Michelucci R, Nobile C. (2006) The LGI1/Epitempin gene encodes two protein isoforms differentially expressed in human brain. J Neurochem 98:985991.
  • Grantham R. (1974) Amino acid difference formula to help explain protein evolution. Science 185:862864.
  • Heiman GA, Kamberakis K, Gill R, Kalachikov S, Pedley TA, Hauser WA, Ottman R. (2010) Evaluation of depression risk in LGI1 mutation carriers. Epilepsia 51:16851690.
  • 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. (2002) Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 30:335341.
  • Kawamata J, Ikeda A, Fujita Y, Usui K, Shimohama S, Takahashi R. (2010) Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal epilepsy: the first report from Asian families. Epilepsia 51:690693.
  • Michelucci R, Poza JJ, Sofia V, de Feo MR, Binelli S, Bisulli F, Scudellaro E, Simionati B, Zimbello R, D’Orsi G, Passarelli D, Avoni P, Avanzini G, Tinuper P, Biondi R, Valle G, Mautner VF, Stephani U, Tassinari CA, Moschonas NK, Siebert R, Lopez de Munain A, Perez-Tur J, Nobile C. (2003) Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families. Epilepsia 44:12891297.
  • Michelucci R, Gardella E, de Haan G-J, Bisulli F, Zaniboni A, Cantalupo G, Tassinari CA, Tinuper P, Nobile C, Nichelli P, Kasteleijn-Nolst Trenitè DGA. (2004) Telephone-induced seizures: a new type of reflex epilepsy. Epilepsia 45:280283.
  • Michelucci R, Mecarelli O, Bovo G, Bisulli F, Testoni S, Striano P, Striano S, Tinuper P, Nobile C. (2007) A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures. Neurology 68:21502151.
  • Morante-Redolat JM, Gorostidi-Pagola A, Piquer-Sirerol S, Saenz A, Poza JJ, Galan J, Gesk S, Sarafidou T, Mautner VF, Binelli S, Staub E, Hinzmann B, French L, Prud’homme JF, Passarelli D, Scannapieco P, Tassinari CA, Avanzini G, Marti-Masso JF, Kluwe L, Deloukas P, Moschonas NK, Michelucci R, Siebert R, Nobile C, Perez-Tur J, Lopez de Munain A. (2002) Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 11:11191128.
  • Nobile C, Michelucci R, Andreazza S, Pasini E, Tosatto SCE, Striano P. (2009) LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. Hum Mutat 30:530536.
  • Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH, Barker-Cummings C, Lustenberger A, Nagle KJ, Lee KS, Scheuer ML, Neystat M, Susser M, Wilhelmsen KC. (1995) Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet 10:5660.
  • Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA. (2004) LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 62:11201126.
  • Rosanoff MJ, Ottman R. (2008) Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 71:567571.
  • Senechal KR, Thaller C, Noebels JL. (2005) ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy. Hum Mol Genet 14:16131620.
  • Sirerol-Piquer MS, Ayerdi-Izquierdo A, Morante-Redolat JM, Herranz-Perez V, Favell K, Barker PA, Perez-Tur J. (2006) The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface. Hum Mol Genet 15:34363445.
  • Staub E, Perez-Tur J, Siebert R, Nobile C, Moschonas NK, Deloukas P, Hinzmann B. (2002) The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders. Trends Biochem Sci 27:441444.
  • Striano P, Busolin G, Santulli L, Leonardi E, Coppola A, Vitiello L, Rigon L, Michelucci R, Tosatto SC, Striano S, Nobile C. (2011) Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation. Neurology 76:11731176.