These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

242 related items for PubMed ID: 26459092

  • 1. Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.
    Klein KM, Pendziwiat M, Cohen R, Appenzeller S, de Kovel CG, Rosenow F, Koeleman BP, Kuhlenbäumer G, Sheintuch L, Veksler R, Friedman A, Afawi Z, Helbig I.
    J Neurol; 2016 Jan; 263(1):11-6. PubMed ID: 26459092
    [Abstract] [Full Text] [Related]

  • 2. 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. PubMed ID: 25616465
    [Abstract] [Full Text] [Related]

  • 3. Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation.
    Michelucci R, Dazzo E, Volpi L, Pasini E, Riguzzi P, Minardi R, Marliani AF, Tappatà M, Bisulli F, Tassinari CA, Nobile C.
    Epileptic Disord; 2020 Aug 01; 22(4):443-448. PubMed ID: 32723706
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations.
    Michelucci R, Pulitano P, Di Bonaventura C, Binelli S, Luisi C, Pasini E, Striano S, Striano P, Coppola G, La Neve A, Giallonardo AT, Mecarelli O, Serioli E, Dazzo E, Fanciulli M, Nobile C.
    Epilepsy Behav; 2017 Mar 01; 68():103-107. PubMed ID: 28142128
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. A novel LGI1 missense mutation causes dysfunction in cortical neuronal migration and seizures.
    Liu F, Du C, Tian X, Ma Y, Zhao B, Yan Y, Lin Z, Lin P, Zhou R, Wang X.
    Brain Res; 2019 Oct 15; 1721():146332. PubMed ID: 31301272
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. A new locus for familial temporal lobe epilepsy on chromosome 3q.
    Chahine L, Abou-Khalil B, Siren A, Andermann F, Hedera P, Ge Q, Andermann E, Pandolfo M.
    Epilepsy Res; 2013 Oct 15; 106(3):338-44. PubMed ID: 24021842
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Clinical characteristics and LGI1 gene mutation analysis on an autosomal dominant lateral temporal lobe epilepsy].
    Xi ZQ, Wang XF, Lü Y, Wang L, Xiao F, Guan LF.
    Zhonghua Yi Xue Za Zhi; 2009 Jan 20; 89(3):195-7. PubMed ID: 19537038
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.