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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 23415449)

  • 1. Copy number variants in adult patients with Lennox-Gastaut syndrome features.
    Lund C; Brodtkorb E; Røsby O; Rødningen OK; Selmer KK
    Epilepsy Res; 2013 Jul; 105(1-2):110-7. PubMed ID: 23415449
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lennox-Gastaut syndrome and phenotype: secondary network epilepsies.
    Archer JS; Warren AE; Stagnitti MR; Masterton RA; Abbott DF; Jackson GD
    Epilepsia; 2014 Aug; 55(8):1245-54. PubMed ID: 24902608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
    Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
    JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A genomic copy number variant analysis implicates the MBD5 and HNRNPU genes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion.
    Du X; An Y; Yu L; Liu R; Qin Y; Guo X; Sun D; Zhou S; Wu B; Jiang YH; Wang Y
    BMC Med Genet; 2014 May; 15():62. PubMed ID: 24885232
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lacosamide in Lennox-Gastaut syndrome: case report.
    Andrade-Machado R; Benjumea-Cuartas V; Jaramillo-Jimenez E
    Clin Neuropharmacol; 2012; 35(3):148-9. PubMed ID: 22592511
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lennox-Gastaut syndrome of unknown cause: phenotypic characteristics of patients in the Epilepsy Phenome/Genome Project.
    Widdess-Walsh P; Dlugos D; Fahlstrom R; Joshi S; Shellhaas R; Boro A; Sullivan J; Geller E;
    Epilepsia; 2013 Nov; 54(11):1898-904. PubMed ID: 24116958
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy.
    Epilepsy Phenome/Genome Project Epi4K Consortium
    Ann Neurol; 2015 Aug; 78(2):323-8. PubMed ID: 26068938
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The epilepsy phenotype in adult patients with intellectual disability and pathogenic copy number variants.
    d'Orsi G; Martino T; Palumbo O; Pascarella MG; Palumbo P; Di Claudio MT; Avolio C; Carella M
    Seizure; 2017 Dec; 53():86-93. PubMed ID: 29156220
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
    Striano P; Coppola A; Paravidino R; Malacarne M; Gimelli S; Robbiano A; Traverso M; Pezzella M; Belcastro V; Bianchi A; Elia M; Falace A; Gazzerro E; Ferlazzo E; Freri E; Galasso R; Gobbi G; Molinatto C; Cavani S; Zuffardi O; Striano S; Ferrero GB; Silengo M; Cavaliere ML; Benelli M; Magi A; Piccione M; Dagna Bricarelli F; Coviello DA; Fichera M; Minetti C; Zara F
    Arch Neurol; 2012 Mar; 69(3):322-30. PubMed ID: 22083797
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Development of Lennox-Gastaut syndrome in adulthood].
    Rodriguez-Rodriguez S; Salas-Puig J; Alvarez-Carriles JC; Temprano-Fernandez T; Anton-Gonzalez C; Garcia-Martinez A
    Rev Neurol; 2011 Mar; 52(5):257-63. PubMed ID: 21341220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Lennox-Gastaut syndrome--course and treatment].
    Lund C; Brodtkorb E; Nakken KO
    Tidsskr Nor Laegeforen; 2011 Jan; 131(1):24-7. PubMed ID: 21233883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Array CGH analysis of a cohort of Russian patients with intellectual disability.
    Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN
    Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cortical excitability decreases in Lennox-Gastaut syndrome.
    Badawy RA; Macdonell RA; Vogrin SJ; Lai A; Cook MJ
    Epilepsia; 2012 Sep; 53(9):1546-53. PubMed ID: 22813348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Infantile spasms are associated with abnormal copy number variations.
    Tiwari VN; Sundaram SK; Chugani HT; Huq AH
    J Child Neurol; 2013 Oct; 28(10):1191-6. PubMed ID: 22914377
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis.
    Hartmann C; von Spiczak S; Suls A; Weckhuysen S; Buyse G; Vilain C; Van Bogaert P; De Jonghe P; Cook J; Muhle H; Stephani U; Helbig I; Mefford HC
    Epilepsia; 2015 Mar; 56(3):e26-32. PubMed ID: 25690317
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clobazam for patients with Lennox-Gastaut syndrome and epilepsy.
    Seif-Eddeine H; Ng YT
    Expert Rev Neurother; 2012 Apr; 12(4):385-93. PubMed ID: 22449211
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel copy number variations and phenotypes of infantile epileptic spasms syndrome.
    Cheng M; Bai L; Yang Y; Liu W; Niu X; Chen Y; Tan Q; Yang X; Wu Q; Zhao HQ; Zhang Y
    Clin Genet; 2024 Aug; 106(2):161-179. PubMed ID: 38544467
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transition issues for children with diffuse cortical malformations, multifocal postnatal lesions, (infectious and traumatic) and Lennox-Gastaut and similar syndromes.
    Camfield PR; Bahi-Buisson N; Trinka E
    Epilepsia; 2014 Aug; 55 Suppl 3():24-8. PubMed ID: 25209082
    [TBL] [Abstract][Full Text] [Related]  

  • 19. All children who experience epileptic falls do not necessarily have Lennox-Gastaut syndrome... but many do.
    Arzimanoglou A; Resnick T
    Epileptic Disord; 2011 May; 13 Suppl 1():S3-13. PubMed ID: 21669558
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
    Lesch KP; Selch S; Renner TJ; Jacob C; Nguyen TT; Hahn T; Romanos M; Walitza S; Shoichet S; Dempfle A; Heine M; Boreatti-Hümmer A; Romanos J; Gross-Lesch S; Zerlaut H; Wultsch T; Heinzel S; Fassnacht M; Fallgatter A; Allolio B; Schäfer H; Warnke A; Reif A; Ropers HH; Ullmann R
    Mol Psychiatry; 2011 May; 16(5):491-503. PubMed ID: 20308990
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.