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Results: 1 to 20 of 109

Similar articles for PubMed (Select 17904873)

1.

Epilepsy in Angelman syndrome.

Pelc K, Boyd SG, Cheron G, Dan B.

Seizure. 2008 Apr;17(3):211-7. Epub 2007 Sep 29. Review.

2.

Implications of slow waves and shifting epileptiform discharges in Angelman syndrome.

Yum MS, Lee EH, Kim JH, Ko TS, Yoo HW.

Brain Dev. 2013 Mar;35(3):245-51. doi: 10.1016/j.braindev.2012.04.006. Epub 2012 Jun 15.

PMID:
22704603
3.

Epilepsy in patients with angelman syndrome caused by deletion of the chromosome 15q11-13.

Valente KD, Koiffmann CP, Fridman C, Varella M, Kok F, Andrade JQ, Grossmann RM, Marques-Dias MJ.

Arch Neurol. 2006 Jan;63(1):122-8.

PMID:
16401744
4.

Parental imprinting and Angelman syndrome.

Lalande M, Minassian BA, DeLorey TM, Olsen RW.

Adv Neurol. 1999;79:421-9. Review.

PMID:
10514831
5.

Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome.

Galván-Manso M, Campistol J, Conill J, Sanmartí FX.

Epileptic Disord. 2005 Mar;7(1):19-25.

PMID:
15741136
6.

Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms.

Guerrini R, Carrozzo R, Rinaldi R, Bonanni P.

Paediatr Drugs. 2003;5(10):647-61. Review.

PMID:
14510623
7.

From electrophysiology to chromatin: a bottom-up approach to Angelman syndrome.

Dan B, Servais L, Boyd SG, Wagstaff J, Cheron G.

Ann N Y Acad Sci. 2004 Dec;1030:599-611.

PMID:
15659843
8.

Epilepsy in patients with Angelman syndrome.

Fiumara A, Pittalà A, Cocuzza M, Sorge G.

Ital J Pediatr. 2010 Apr 16;36:31. doi: 10.1186/1824-7288-36-31. Review.

9.

Are there distinctive sleep problems in Angelman syndrome?

Pelc K, Cheron G, Boyd SG, Dan B.

Sleep Med. 2008 May;9(4):434-41. Epub 2007 Aug 31.

PMID:
17765640
10.

Atypical absences and recurrent absence status in an adult with Angelman syndrome due to the UBE3A mutation.

Espay AJ, Andrade DM, Wennberg RA, Lang AE.

Epileptic Disord. 2005 Sep;7(3):227-30.

PMID:
16162432
11.

Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL.

PLoS One. 2010 Aug 20;5(8):e12278. doi: 10.1371/journal.pone.0012278.

12.

Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling.

Moncla A, Malzac P, Livet MO, Voelckel MA, Mancini J, Delaroziere JC, Philip N, Mattei JF.

J Med Genet. 1999 Jul;36(7):554-60.

13.

Neurologic manifestations of Angelman syndrome.

Thibert RL, Larson AM, Hsieh DT, Raby AR, Thiele EA.

Pediatr Neurol. 2013 Apr;48(4):271-9. doi: 10.1016/j.pediatrneurol.2012.09.015. Review.

PMID:
23498559
14.

Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion.

Neubert G, von Au K, Drossel K, Tzschach A, Horn D, Nickel R, Kaindl AM.

Gene. 2013 Jan 10;512(2):453-5. doi: 10.1016/j.gene.2012.10.061. Epub 2012 Nov 1.

PMID:
23124039
15.

Angelman syndrome: correlations between epilepsy phenotypes and genotypes.

Minassian BA, DeLorey TM, Olsen RW, Philippart M, Bronstein Y, Zhang Q, Guerrini R, Van Ness P, Livet MO, Delgado-Escueta AV.

Ann Neurol. 1998 Apr;43(4):485-93.

PMID:
9546330
16.

[Neurogenetic dialogue illustrated by the "pantin hilare" of angelman syndrome].

Dan B.

Bull Mem Acad R Med Belg. 2010;165(7-9):327-33; discussion 334-7. French.

PMID:
21513093
17.
18.

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

DeLorey TM, Handforth A, Anagnostaras SG, Homanics GE, Minassian BA, Asatourian A, Fanselow MS, Delgado-Escueta A, Ellison GD, Olsen RW.

J Neurosci. 1998 Oct 15;18(20):8505-14.

19.

Angelman syndrome in Denmark. birth incidence, genetic findings, and age at diagnosis.

Mertz LG, Christensen R, Vogel I, Hertz JM, Nielsen KB, Grønskov K, Østergaard JR.

Am J Med Genet A. 2013 Sep;161A(9):2197-203. doi: 10.1002/ajmg.a.36058. Epub 2013 Aug 2.

PMID:
23913711
20.

Clinical and genetic aspects of Angelman syndrome.

Williams CA, Driscoll DJ, Dagli AI.

Genet Med. 2010 Jul;12(7):385-95. doi: 10.1097/GIM.0b013e3181def138. Review.

PMID:
20445456
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