BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 38636144)

  • 1. Predictors of genetic diagnosis in individuals with developmental and epileptic encephalopathies.
    Luiza Benevides M; de Moraes HT; Granados DMM; Bonadia LC; Sauma L; Augusta Montenegro M; Guerreiro MM; Lopes-Cendes Í; Carolina Coan A
    Epilepsy Behav; 2024 Jun; 155():109762. PubMed ID: 38636144
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Long-term outcome of developmental and epileptic encephalopathies.
    Van Bogaert P
    Rev Neurol (Paris); 2022 Sep; 178(7):659-665. PubMed ID: 35489823
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features.
    Aljaafari D; Fasano A; Nascimento FA; Lang AE; Andrade DM
    Epilepsia; 2017 Mar; 58(3):e44-e48. PubMed ID: 28186331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical evaluation and diagnosis of severe epilepsy syndromes of early childhood.
    Zupanc ML
    J Child Neurol; 2009 Aug; 24(8 Suppl):6S-14S. PubMed ID: 19666878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies.
    Zhou P; He N; Zhang JW; Lin ZJ; Wang J; Yan LM; Meng H; Tang B; Li BM; Liu XR; Shi YW; Zhai QX; Yi YH; Liao WP
    Genes Brain Behav; 2018 Nov; 17(8):e12456. PubMed ID: 29314583
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Defining Dravet syndrome: An essential pre-requisite for precision medicine trials.
    Li W; Schneider AL; Scheffer IE
    Epilepsia; 2021 Sep; 62(9):2205-2217. PubMed ID: 34338318
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Expanding Clinical Spectrum of Genetic Pediatric Epileptic Encephalopathies.
    Shbarou R; Mikati MA
    Semin Pediatr Neurol; 2016 May; 23(2):134-42. PubMed ID: 27544470
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epileptic encephalopathies: new genes and new pathways.
    Nieh SE; Sherr EH
    Neurotherapeutics; 2014 Oct; 11(4):796-806. PubMed ID: 25266964
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Myoclonic-astatic epilepsy of early childhood--clinical and EEG analysis of myoclonic-astatic seizures, and discussions on the nosology of the syndrome.
    Oguni H; Fukuyama Y; Tanaka T; Hayashi K; Funatsuka M; Sakauchi M; Shirakawa S; Osawa M
    Brain Dev; 2001 Nov; 23(7):757-64. PubMed ID: 11701290
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Outcomes and comorbidities of SCN1A-related seizure disorders.
    de Lange IM; Gunning B; Sonsma ACM; van Gemert L; van Kempen M; Verbeek NE; Sinoo C; Nicolai J; Knoers NVAM; Koeleman BPC; Brilstra EH
    Epilepsy Behav; 2019 Jan; 90():252-259. PubMed ID: 30527252
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy.
    Nabbout R; Chemaly N; Chipaux M; Barcia G; Bouis C; Dubouch C; Leunen D; Jambaqué I; Dulac O; Dellatolas G; Chiron C
    Orphanet J Rare Dis; 2013 Nov; 8():176. PubMed ID: 24225340
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Late infantile epileptic encephalopathy: A distinct developmental and epileptic encephalopathy syndrome.
    Kacker S; Phitsanuwong C; Oetomo A; Nordli DR
    Epileptic Disord; 2024 Feb; 26(1):98-108. PubMed ID: 38100275
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic Diagnosis of Dravet Syndrome Using Next Generation Sequencing-Based Epilepsy Gene Panel Testing.
    Lee J; Lee C; Park WY; Lee J
    Ann Clin Lab Sci; 2020 Sep; 50(5):625-637. PubMed ID: 33067208
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.
    Mei D; Cetica V; Marini C; Guerrini R
    Epilepsia; 2019 Dec; 60 Suppl 3():S2-S7. PubMed ID: 31904125
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures.
    Trivisano M; Striano P; Sartorelli J; Giordano L; Traverso M; Accorsi P; Cappelletti S; Claps DJ; Vigevano F; Zara F; Specchio N
    Epilepsy Behav; 2015 Oct; 51():53-6. PubMed ID: 26262932
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and genetic factors predicting Dravet syndrome in infants with
    Cetica V; Chiari S; Mei D; Parrini E; Grisotto L; Marini C; Pucatti D; Ferrari A; Sicca F; Specchio N; Trivisano M; Battaglia D; Contaldo I; Zamponi N; Petrelli C; Granata T; Ragona F; Avanzini G; Guerrini R
    Neurology; 2017 Mar; 88(11):1037-1044. PubMed ID: 28202706
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diagnosis switching and outcomes in a cohort of patients with potential epilepsy with myoclonic-atonic seizures.
    Eschbach K; Moss A; Joshi C; Angione K; Smith G; Dempsey A; Juarez-Colunga E; Demarest ST
    Epilepsy Res; 2018 Nov; 147():95-101. PubMed ID: 30286391
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut Syndrome.
    Lattanzi S; Trinka E; Striano P; Rocchi C; Salvemini S; Silvestrini M; Brigo F
    CNS Drugs; 2021 Mar; 35(3):265-281. PubMed ID: 33754312
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epidemiology of Developmental and Epileptic Encephalopathy and of Intellectual Disability and Epilepsy in Children.
    Poke G; Stanley J; Scheffer IE; Sadleir LG
    Neurology; 2023 Mar; 100(13):e1363-e1375. PubMed ID: 36581463
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Core Features Differentiate Dravet Syndrome from Febrile Seizures.
    Nordli DR; Nordli DR; Galan FN
    J Pediatr; 2023 Jul; 258():113416. PubMed ID: 37030608
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.