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 *

218 related articles for article (PubMed ID: 28524225)

  • 1. [How must we manage epileptic encephalopathies in infants? Conclusions].
    Soto-Insuga V
    Rev Neurol; 2017 May; 64(s03):S77-S80. PubMed ID: 28524225
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Epileptic encephalopathies].
    Ramos-Lizana J
    Rev Neurol; 2017 May; 64(s03):S45-S48. PubMed ID: 28524219
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Infantile epileptic encephalopathies: what matters is genetics].
    Garcia-Penas JJ; Jimenez-Legido M
    Rev Neurol; 2017 May; 64(s03):S65-S69. PubMed ID: 28524223
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Trends and expectations the research on the molecular background of epileptic encephalopathies - state of the art in 2017].
    Hoffman-Zacharska D; Górka-Skoczylas P
    Dev Period Med; 2017; 21(4):317-327. PubMed ID: 29291359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Neuroimaging in epileptic encephalopathies in infants].
    Lopez-Pino MA; Garcia-Esparza E
    Rev Neurol; 2017 May; 64(s03):S61-S64. PubMed ID: 28524222
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Epileptic spasms in infants. Beyond hypsarrhythmia].
    Garcia-Fernandez M
    Rev Neurol; 2017 May; 64(s03):S55-S59. PubMed ID: 28524221
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deciphering the concepts behind "Epileptic encephalopathy" and "Developmental and epileptic encephalopathy".
    Scheffer IE; Liao J
    Eur J Paediatr Neurol; 2020 Jan; 24():11-14. PubMed ID: 31926847
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The epileptic encephalopathies of infancy and childhood.
    Wirrell E; Farrell K; Whiting S
    Can J Neurol Sci; 2005 Nov; 32(4):409-18. PubMed ID: 16408569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Neonatal epileptics syndromes].
    Guerrero Ruiz GDP
    Medicina (B Aires); 2024 Sep; 84 Suppl 3():75-80. PubMed ID: 39331780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Metabolic approach in epileptic encephalopathies in infants].
    Lopez-Marin L
    Rev Neurol; 2017 May; 64(s03):S49-S53. PubMed ID: 28524220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Developmental and epileptic encephalopathy due to SZT2 genomic variants: Emerging features of a syndromic condition.
    Trivisano M; Rivera M; Terracciano A; Ciolfi A; Napolitano A; Pepi C; Calabrese C; Digilio MC; Tartaglia M; Curatolo P; Vigevano F; Specchio N
    Epilepsy Behav; 2020 Jul; 108():107097. PubMed ID: 32402703
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Developmental and epileptic encephalopathies: recognition and approaches to care.
    Raga S; Specchio N; Rheims S; Wilmshurst JM
    Epileptic Disord; 2021 Feb; 23(1):40-52. PubMed ID: 33632673
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathies.
    Mastrangelo M; Celato A; Leuzzi V
    Eur J Paediatr Neurol; 2012 Mar; 16(2):179-91. PubMed ID: 21940184
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Febrile infection-related epilepsy syndrome (FIRES): therapeutic complications, long-term neurological and neuroimaging follow-up.
    Lee HF; Chi CS
    Seizure; 2018 Mar; 56():53-59. PubMed ID: 29453111
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Early onset epilepsy and inherited metabolic disorders: diagnosis and management.
    Prasad AN; Hoffmann GF
    Can J Neurol Sci; 2010 May; 37(3):350-8. PubMed ID: 20481269
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Impact of focal interictal epileptiform discharges on behaviour and cognition in children.
    Van Bogaert P; Urbain C; Galer S; Ligot N; Peigneux P; De Tiège X
    Neurophysiol Clin; 2012; 42(1-2):53-8. PubMed ID: 22200342
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CAD Deficiency-Another Treatable Early Infantile Epileptic Encephalopathy.
    Kamate M; Patil S
    Pediatr Neurol; 2020 Sep; 110():97-98. PubMed ID: 32654958
    [No Abstract]   [Full Text] [Related]  

  • 18. [Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2].
    Terczyńska I; Mierzewska H; Szczepanik E; Antczak-Marach D
    Przegl Lek; 2010; 67(9):757-61. PubMed ID: 21387820
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.
    Milh M; Villeneuve N; Chouchane M; Kaminska A; Laroche C; Barthez MA; Gitiaux C; Bartoli C; Borges-Correia A; Cacciagli P; Mignon-Ravix C; Cuberos H; Chabrol B; Villard L
    Epilepsia; 2011 Oct; 52(10):1828-34. PubMed ID: 21770924
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.
    Bayat A; Bayat M; Rubboli G; Møller RS
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356067
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.