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 *

510 related articles for article (PubMed ID: 33096746)

  • 81. Overlap cases of eyelid myoclonia with absences and juvenile myoclonic epilepsy.
    Destina Yalçin A; Forta H; Kiliç E
    Seizure; 2006 Sep; 15(6):359-65. PubMed ID: 16793291
    [TBL] [Abstract][Full Text] [Related]  

  • 82. When should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?
    Lebon S; Suarez P; Alija S; Korff CM; Fluss J; Mercati D; Datta AN; Poloni C; Marcoz JP; Campos-Xavier AB; Bonafé L; Roulet-Perez E
    Eur J Paediatr Neurol; 2015 Mar; 19(2):170-5. PubMed ID: 25532859
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Generalized spike-and-wave patterns in children: clinical correlates.
    Martínez-Menéndez B; Sempere AP; Mayor PP; Heras RS; Alvarez-Tejerina J; Mateos-Beato F
    Pediatr Neurol; 2000 Jan; 22(1):23-8. PubMed ID: 10669201
    [TBL] [Abstract][Full Text] [Related]  

  • 84. [The clinical utility of genetic testing in epilepsy].
    Kelemen A; Gál A
    Ideggyogy Sz; 2011 Sep; 64(9-10):321-4. PubMed ID: 22059368
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Idiopathic generalized epilepsies of adolescence.
    Beghi M; Beghi E; Cornaggia CM; Gobbi G
    Epilepsia; 2006; 47 Suppl 2():107-10. PubMed ID: 17105478
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Antiepileptic drug monotherapy for epilepsy: a network meta-analysis of individual participant data.
    Nevitt SJ; Sudell M; Weston J; Tudur Smith C; Marson AG
    Cochrane Database Syst Rev; 2017 Jun; 6(6):CD011412. PubMed ID: 28661008
    [TBL] [Abstract][Full Text] [Related]  

  • 87. [New classifications of epilepsies and seizure types created by the International League against Epilepsy (2017)].
    Belousova ED; Zavadenko NN; Kholin AA; Sharkov AA
    Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(7):99-106. PubMed ID: 28805769
    [TBL] [Abstract][Full Text] [Related]  

  • 88. [Epilepsy and genetics].
    Picard F
    Rev Med Suisse Romande; 2003 May; 123(5):317-21. PubMed ID: 15095716
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Treatment of pediatric epilepsy: European expert opinion, 2007.
    Wheless JW; Clarke DF; Arzimanoglou A; Carpenter D
    Epileptic Disord; 2007 Dec; 9(4):353-412. PubMed ID: 18077226
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Seizure-suppressor genes: can they help spearhead the discovery of novel therapeutic targets for epilepsy?
    Silva-Cardoso GK; N'Gouemo P
    Expert Opin Ther Targets; 2023; 27(8):657-664. PubMed ID: 37589085
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
    Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R
    Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Idiopathic generalized epilepsies.
    Caraballo RH; Dalla Bernardina B
    Handb Clin Neurol; 2013; 111():579-89. PubMed ID: 23622205
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Monogenic Epilepsies: Disease Mechanisms, Clinical Phenotypes, and Targeted Therapies.
    Guerrini R; Balestrini S; Wirrell EC; Walker MC
    Neurology; 2021 Oct; 97(17):817-831. PubMed ID: 34493617
    [TBL] [Abstract][Full Text] [Related]  

  • 94. [Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions].
    Gourfinkel-An I; Baulac S; Nabbout R; Brice A; Baulac M; Leguern E
    Rev Neurol (Paris); 2004 May; 160(5 Pt 2):S90-7. PubMed ID: 15269666
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies.
    Jähn JA; von Spiczak S; Muhle H; Obermeier T; Franke A; Mefford HC; Stephani U; Helbig I
    Epilepsy Res; 2014 Jan; 108(1):109-16. PubMed ID: 24246141
    [TBL] [Abstract][Full Text] [Related]  

  • 96. New paradigms for the treatment of pediatric monogenic epilepsies: Progressing toward precision medicine.
    Specchio N; Pietrafusa N; Perucca E; Cross JH
    Epilepsy Behav; 2022 Jun; 131(Pt B):107961. PubMed ID: 33867301
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Myoclonic-astatic epilepsy.
    Doose H
    Epilepsy Res Suppl; 1992; 6():163-8. PubMed ID: 1418479
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approach.
    Castellotti B; Ragona F; Freri E; Messina G; Magri S; Previtali R; Solazzi R; Franceschetti S; Taroni F; Canafoglia L; Gellera C; Granata T; DiFrancesco JC
    Epilepsia Open; 2024 Oct; 9(5):1922-1930. PubMed ID: 39215763
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Unraveling the shared genetics of common epilepsies and general cognitive ability.
    Karadag N; Hagen E; Shadrin AA; van der Meer D; O'Connell KS; Rahman Z; Kutrolli G; Parker N; Bahrami S; Fominykh V; Heuser K; Taubøll E; Ueland T; Steen NE; Djurovic S; Dale AM; Frei O; Andreassen OA; Smeland OB
    Seizure; 2024 Nov; 122():105-112. PubMed ID: 39388989
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Unraveling the shared genetics of common epilepsies and general cognitive ability.
    Karadag N; Hagen E; Shadrin AA; van der Meer D; O'Connell KS; Rahman Z; Kutrolli G; Parker N; Bahrami S; Fominykh V; Heuser K; Taubøll E; Ueland T; Steen NE; Djurovic S; Dale AM; Frei O; Andreassen OA; Smeland OB
    medRxiv; 2024 Mar; ():. PubMed ID: 38585944
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 26.