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Items: 1 to 20 of 118

1.

Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population.

Gitaí LL, de Almeida DH, Born JP, Gameleira FT, de Andrade TG, Machado LC, Gitaí DL.

Neurol India. 2012 Nov-Dec;60(6):585-8. doi: 10.4103/0028-3886.105191.

2.

GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures.

Balan S, Sathyan S, Radha SK, Joseph V, Radhakrishnan K, Banerjee M.

Pharmacogenet Genomics. 2013 Nov;23(11):605-10. doi: 10.1097/FPC.0000000000000000.

PMID:
24061200
3.

Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy.

Born JP, Santos BP, Secolin R, Gameleira FT, Andrade TG, Machado LC, Gitaí LL, Gitaí DL.

Arq Neuropsiquiatr. 2015 Apr;73(4):289-92. doi: 10.1590/0004-282X20150010. Epub 2015 Apr 1.

4.

The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy.

Rozycka A, Steinborn B, Trzeciak WH.

Seizure. 2009 Oct;18(8):601-3. doi: 10.1016/j.seizure.2009.06.007. Epub 2009 Jul 3.

5.

GABRG2 rs211037 polymorphism and epilepsy: a systematic review and meta-analysis.

Haerian BS, Baum L.

Seizure. 2013 Jan;22(1):53-8. doi: 10.1016/j.seizure.2012.10.007. Epub 2012 Nov 7. Review.

6.

Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity.

Gennaro E, Veggiotti P, Malacarne M, Madia F, Cecconi M, Cardinali S, Cassetti A, Cecconi I, Bertini E, Bianchi A, Gobbi G, Zara F.

Epileptic Disord. 2003 Mar;5(1):21-5.

7.

Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.

Izzi C, Barbon A, Toliat MR, Heils A, Becker C, Nürnberg P, Sander T, Barlati S.

Am J Med Genet B Neuropsychiatr Genet. 2003 Nov 15;123B(1):59-63.

PMID:
14582146
8.

Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis.

Haerian BS, Baum L, Kwan P, Cherny SS, Shin JG, Kim SE, Han BG, Tan HJ, Raymond AA, Tan CT, Mohamed Z.

Mol Neurobiol. 2016 Oct;53(8):5457-67. doi: 10.1007/s12035-015-9457-y. Epub 2015 Oct 9.

PMID:
26452361
9.

Juvenile myoclonic epilepsy is not associated with the DRPLA gene in a European population.

Yapijakis C, Gatzonis S, Youroukos S, Kollia V, Karachristianou S, Anagnostouli M.

In Vivo. 2014 Nov-Dec;28(6):1193-6.

PMID:
25398822
10.

PER2 rs2304672, CLOCK rs1801260, and PER3 rs57875989 polymorphisms are not associated with juvenile myoclonic epilepsy.

Santos B, Marques T, Malta M, Gameleira F, Secolin R, Andrade T, Gitaí L, Gitaí D.

Epilepsy Behav. 2014 Jul;36:82-5. doi: 10.1016/j.yebeh.2014.04.024. Epub 2014 Jun 2.

11.

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.

Ma S, Blair MA, Abou-Khalil B, Lagrange AH, Gurnett CA, Hedera P.

Epilepsy Res. 2006 Oct;71(2-3):129-34. Epub 2006 Jul 12.

PMID:
16839746
12.

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK.

Epilepsy Res. 2005 Aug-Sep;66(1-3):91-8.

PMID:
16112844
13.

BRD2 and TAP-1 genes and juvenile myoclonic epilepsy.

Layouni S, Buresi C, Thomas P, Malafosse A, Dogui M.

Neurol Sci. 2010 Feb;31(1):53-6. doi: 10.1007/s10072-009-0190-z. Epub 2009 Dec 2.

PMID:
19953286
14.

Absence of GABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India.

Kapoor A, Vijai J, Ravishankar HM, Satishchandra P, Radhakrishnan K, Anand A.

J Genet. 2003 Apr-Aug;82(1-2):17-21.

15.

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF.

Epilepsia. 2004 May;45(5):467-78.

16.

Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.

Lenzen KP, Heils A, Lorenz S, Hempelmann A, Sander T.

Epilepsy Res. 2005 Jun;65(1-2):53-7.

PMID:
16023832
17.

The genetic variant "C588T" of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs.

Abou El Ella SS, Tawfik MA, Abo El Fotoh WMM, Soliman OAM.

Seizure. 2018 Aug;60:39-43. doi: 10.1016/j.seizure.2018.06.004. Epub 2018 Jun 6.

PMID:
29894917
18.

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.

Hempelmann A, Cobilanschi J, Heils A, Muhle H, Stephani U, Weber Y, Lerche H, Sander T.

Epilepsy Res. 2007 Apr;74(1):28-32. Epub 2007 Jan 9.

PMID:
17215107
19.

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.

Mumoli L, Tarantino P, Michelucci R, Bianchi A, Labate A, Franceschetti S, Marini C, Striano P, Gagliardi M, Ferlazzo E, Sofia V, Pennese L, Annesi G, Aguglia U, Guerrini R, Zara F, Gambardella A; Genetic Commission, Italian League Against Epilepsy.

Epilepsia. 2015 Apr;56(4):e40-3. doi: 10.1111/epi.12944. Epub 2015 Mar 6.

20.

Association of alpha subunit of GABAA receptor subtype gene polymorphisms with epilepsy susceptibility and drug resistance in north Indian population.

Kumari R, Lakhan R, Kalita J, Misra UK, Mittal B.

Seizure. 2010 May;19(4):237-41. doi: 10.1016/j.seizure.2010.02.009. Epub 2010 Mar 30.

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