Similar articles for PMID: 24114805

Year	Number of Results
1985	1
1991	1
1993	1
1996	5
1997	8
1998	1
1999	7
2000	3
2001	3
2002	4
2003	3
2004	3
2005	12
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2010	3
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2012	1
2013	4
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2015	4
2016	8
2018	3
2019	3
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2024	1

1

The α2B-adrenergic receptor is mutant in cortical myoclonus and epilepsy.

De Fusco M, Vago R, Striano P, Di Bonaventura C, Zara F, Mei D, Kim MS, Muallem S, Chen Y, Wang Q, Guerrini R, Casari G. De Fusco M, et al. Ann Neurol. 2014 Jan;75(1):77-87. doi: 10.1002/ana.24028. Epub 2014 Jan 2. Ann Neurol. 2014. PMID: 24114805 Free PMC article.

2

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Bonanni P, Patrignani A, Brown P, Parmeggiani L, Grosse P, Brovedani P, Moro F, Aridon P, Carrozzo R, Casari G. Guerrini R, et al. Brain. 2001 Dec;124(Pt 12):2459-75. doi: 10.1093/brain/124.12.2459. Brain. 2001. PMID: 11701600

3

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Parmeggiani L, Marini C, Brovedani P, Bonanni P. Guerrini R, et al. Adv Neurol. 2005;95:273-9. Adv Neurol. 2005. PMID: 15508930 No abstract available.

4

Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) in a unique south Indian community.

Mahadevan R, Viswanathan N, Shanmugam G, Sankaralingam S, Essaki B, Chelladurai RP. Mahadevan R, et al. Epilepsia. 2016 Mar;57(3):e56-9. doi: 10.1111/epi.13303. Epub 2016 Jan 8. Epilepsia. 2016. PMID: 26749494 Free article.

5

A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype.

Licchetta L, Pippucci T, Bisulli F, Cantalupo G, Magini P, Alvisi L, Baldassari S, Martinelli P, Naldi I, Vanni N, Liguori R, Seri M, Tinuper P. Licchetta L, et al. Epilepsia. 2013 Jul;54(7):1298-306. doi: 10.1111/epi.12216. Epub 2013 May 11. Epilepsia. 2013. PMID: 23663087 Free article.

6

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.

Striano P, Zara F, Striano S. Striano P, et al. Acta Neurol Scand. 2005 Apr;111(4):211-7. doi: 10.1111/j.1600-0404.2005.00385.x. Acta Neurol Scand. 2005. PMID: 15740570

7

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME.

de Falco FA, Striano P, de Falco A, Striano S, Santangelo R, Perretti A, Balbi P, Cecconi M, Zara F. de Falco FA, et al. Neurology. 2003 Apr 22;60(8):1381-5. doi: 10.1212/01.wnl.0000055874.24000.4a. Neurology. 2003. PMID: 12707452

8

Spinophilin Is Indispensable for the α2B Adrenergic Receptor-Elicited Hypertensive Response.

Che P, Chen Y, Lu R, Peng N, Gannon M, Wyss JM, Jiao K, Wang Q. Che P, et al. PLoS One. 2015 Aug 5;10(8):e0135030. doi: 10.1371/journal.pone.0135030. eCollection 2015. PLoS One. 2015. PMID: 26244553 Free PMC article.

9

Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family.

Magnin E, Vidailhet M, Depienne C, Saint-Martin C, Bouteiller D, LeGuern E, Apartis E, Rumbach L, Labauge P. Magnin E, et al. Rev Neurol (Paris). 2009 Oct;165(10):812-20. doi: 10.1016/j.neurol.2009.05.014. Epub 2009 Jul 18. Rev Neurol (Paris). 2009. PMID: 19616813

10

Role of arrestins in endocytosis and signaling of alpha2-adrenergic receptor subtypes.

DeGraff JL, Gagnon AW, Benovic JL, Orsini MJ. DeGraff JL, et al. J Biol Chem. 1999 Apr 16;274(16):11253-9. doi: 10.1074/jbc.274.16.11253. J Biol Chem. 1999. PMID: 10196213 Free article.

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