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 *

234 related articles for article (PubMed ID: 27888506)

  • 1. Rapid and safe response to low-dose carbamazepine in neonatal epilepsy.
    Sands TT; Balestri M; Bellini G; Mulkey SB; Danhaive O; Bakken EH; Taglialatela M; Oldham MS; Vigevano F; Holmes GL; Cilio MR
    Epilepsia; 2016 Dec; 57(12):2019-2030. PubMed ID: 27888506
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
    Zara F; Specchio N; Striano P; Robbiano A; Gennaro E; Paravidino R; Vanni N; Beccaria F; Capovilla G; Bianchi A; Caffi L; Cardilli V; Darra F; Bernardina BD; Fusco L; Gaggero R; Giordano L; Guerrini R; Incorpora G; Mastrangelo M; Spaccini L; Laverda AM; Vecchi M; Vanadia F; Veggiotti P; Viri M; Occhi G; Budetta M; Taglialatela M; Coviello DA; Vigevano F; Minetti C
    Epilepsia; 2013 Mar; 54(3):425-36. PubMed ID: 23360469
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early and effective treatment of KCNQ2 encephalopathy.
    Pisano T; Numis AL; Heavin SB; Weckhuysen S; Angriman M; Suls A; Podesta B; Thibert RL; Shapiro KA; Guerrini R; Scheffer IE; Marini C; Cilio MR
    Epilepsia; 2015 May; 56(5):685-91. PubMed ID: 25880994
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.
    Grinton BE; Heron SE; Pelekanos JT; Zuberi SM; Kivity S; Afawi Z; Williams TC; Casalaz DM; Yendle S; Linder I; Lev D; Lerman-Sagie T; Malone S; Bassan H; Goldberg-Stern H; Stanley T; Hayman M; Calvert S; Korczyn AD; Shevell M; Scheffer IE; Mulley JC; Berkovic SF
    Epilepsia; 2015 Jul; 56(7):1071-80. PubMed ID: 25982755
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical characteristics of KCNQ2 encephalopathy.
    Kim HJ; Yang D; Kim SH; Won D; Kim HD; Lee JS; Choi JR; Lee ST; Kang HC
    Brain Dev; 2021 Feb; 43(2):244-250. PubMed ID: 32917465
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome.
    Piro E; Nardello R; Gennaro E; Fontana A; Taglialatela M; Mangano GD; Corsello G; Mangano S
    Epileptic Disord; 2019 Feb; 21(1):87-91. PubMed ID: 30782577
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Benign familial neonatal convulsions: novel mutation in a newborn.
    Lee IC; Chen JY; Chen YJ; Yu JS; Su PH
    Pediatr Neurol; 2009 May; 40(5):387-91. PubMed ID: 19380078
    [TBL] [Abstract][Full Text] [Related]  

  • 8. KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
    Singh NA; Westenskow P; Charlier C; Pappas C; Leslie J; Dillon J; Anderson VE; Sanguinetti MC; Leppert MF;
    Brain; 2003 Dec; 126(Pt 12):2726-37. PubMed ID: 14534157
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation.
    Blumkin L; Suls A; Deconinck T; De Jonghe P; Linder I; Kivity S; Dabby R; Leshinsky-Silver E; Lev D; Lerman-Sagie T
    Eur J Paediatr Neurol; 2012 Jul; 16(4):356-60. PubMed ID: 22169383
    [TBL] [Abstract][Full Text] [Related]  

  • 10. KCNQ2 encephalopathy: delineation of the electroclinical phenotype and treatment response.
    Numis AL; Angriman M; Sullivan JE; Lewis AJ; Striano P; Nabbout R; Cilio MR
    Neurology; 2014 Jan; 82(4):368-70. PubMed ID: 24371303
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.
    Soldovieri MV; Boutry-Kryza N; Milh M; Doummar D; Heron B; Bourel E; Ambrosino P; Miceli F; De Maria M; Dorison N; Auvin S; Echenne B; Oertel J; Riquet A; Lambert L; Gerard M; Roubergue A; Calender A; Mignot C; Taglialatela M; Lesca G
    Hum Mutat; 2014 Mar; 35(3):356-67. PubMed ID: 24375629
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.
    Zeng Q; Yang X; Zhang J; Liu A; Yang Z; Liu X; Wu Y; Wu X; Wei L; Zhang Y
    J Hum Genet; 2018 Jan; 63(1):9-18. PubMed ID: 29215089
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Distinctive Ictal Amplitude-Integrated Electroencephalography Pattern in Newborns with Neonatal Epilepsy Associated with KCNQ2 Mutations.
    Vilan A; Mendes Ribeiro J; Striano P; Weckhuysen S; Weeke LC; Brilstra E; de Vries LS; Cilio MR
    Neonatology; 2017; 112(4):387-393. PubMed ID: 28926830
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions.
    Otto JF; Singh NA; Dahle EJ; Leppert MF; Pappas CM; Pruess TH; Wilcox KS; White HS
    Epilepsia; 2009 Jul; 50(7):1752-9. PubMed ID: 19453707
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel SCN2A mutation in family with benign familial infantile seizures.
    Striano P; Bordo L; Lispi ML; Specchio N; Minetti C; Vigevano F; Zara F
    Epilepsia; 2006 Jan; 47(1):218-20. PubMed ID: 16417554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sodium-channel defects in benign familial neonatal-infantile seizures.
    Heron SE; Crossland KM; Andermann E; Phillips HA; Hall AJ; Bleasel A; Shevell M; Mercho S; Seni MH; Guiot MC; Mulley JC; Berkovic SF; Scheffer IE
    Lancet; 2002 Sep; 360(9336):851-2. PubMed ID: 12243921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epileptic negative myoclonus induced by carbamazepine in a child with BECTS. Benign childhood epilepsy with centrotemporal spikes.
    Nanba Y; Maegaki Y
    Pediatr Neurol; 1999 Sep; 21(3):664-7. PubMed ID: 10513696
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distinctive Amplitude-Integrated EEG Ictal Pattern and Targeted Therapy with Carbamazepine in KCNQ2 and KCNQ3 Neonatal Epilepsy: A Case Series.
    Vilan A; Grangeia A; Ribeiro JM; Cilio MR; de Vries LS
    Neuropediatrics; 2024 Feb; 55(1):32-41. PubMed ID: 37827512
    [TBL] [Abstract][Full Text] [Related]  

  • 19. KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
    Weckhuysen S; Mandelstam S; Suls A; Audenaert D; Deconinck T; Claes LR; Deprez L; Smets K; Hristova D; Yordanova I; Jordanova A; Ceulemans B; Jansen A; Hasaerts D; Roelens F; Lagae L; Yendle S; Stanley T; Heron SE; Mulley JC; Berkovic SF; Scheffer IE; de Jonghe P
    Ann Neurol; 2012 Jan; 71(1):15-25. PubMed ID: 22275249
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Early recognition of characteristic conventional and amplitude-integrated EEG patterns of seizures in SCN2A and KCNQ3-related epilepsy in neonates.
    Pijpers JA; Au PYB; Weeke LC; Vein AA; Smit LS; Vilan A; Jacobs E; de Vries LS; Steggerda SJ; Cilio MR; Carapancea E; Cornet MC; Appendino JP; Peeters-Scholte CMPCD
    Seizure; 2023 Aug; 110():212-219. PubMed ID: 37429183
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.