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Items: 1 to 20 of 136

1.

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
2.

Parental imprinting and Angelman syndrome.

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

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

PMID:
10514831
3.

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
4.

Angelman syndrome: a review of clinical and genetic aspects.

Laan LA, v Haeringen A, Brouwer OF.

Clin Neurol Neurosurg. 1999 Sep;101(3):161-70. Review.

PMID:
10536901
5.

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
6.

Revisiting epilepsy and the electroencephalogram patterns in Angelman syndrome.

Leyser M, Penna PS, de Almeida AC, Vasconcelos MM, Nascimento OJ.

Neurol Sci. 2014 May;35(5):701-5. doi: 10.1007/s10072-013-1586-3.

PMID:
24395242
7.

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
8.

Distinct phenotypes distinguish the molecular classes of Angelman syndrome.

Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ.

J Med Genet. 2001 Dec;38(12):834-45.

9.

Angelman syndrome due to a novel splicing mutation of the UBE3A gene.

Sartori S, Anesi L, Polli R, Toldo I, Casarin A, Drigo P, Murgia A.

J Child Neurol. 2008 Aug;23(8):912-5. doi: 10.1177/0883073808316367.

PMID:
18487518
10.

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.

11.

Angelman syndrome - insights into a rare neurogenetic disorder.

Buiting K, Williams C, Horsthemke B.

Nat Rev Neurol. 2016 Oct;12(10):584-93. doi: 10.1038/nrneurol.2016.133. Review.

PMID:
27615419
12.

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.

13.

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.

PMID:
22704603
14.

Angelman syndrome.

Kyllerman M.

Handb Clin Neurol. 2013;111:287-90. doi: 10.1016/B978-0-444-52891-9.00032-4. Review.

PMID:
23622177
15.

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.

16.

[Angelman syndrome].

Moncla A, Livet MO, Malzac P, Voelckel MA, Mattei MG, Mattei JF, Giraud F.

Arch Pediatr. 1994 Dec;1(12):1118-26. Review. French.

PMID:
7849899
17.

[Clinical manifestation and EEG characteristics of Angelman syndrome].

Yang XY, Zou LP, Song F, Zhang LP, Zheng H, Wu HS, Xiao J.

Zhonghua Er Ke Za Zhi. 2010 Oct;48(10):783-6. Chinese.

PMID:
21176491
18.

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
19.

Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.

Wang PJ, Hou JW, Sue WC, Lee WT.

Brain Dev. 2005 Mar;27(2):101-7.

PMID:
15668048
20.

Another patient with MECP2 mutation without classic Rett syndrome phenotype.

Milani D, Pantaleoni C, D'Arrigo S, Selicorni A, Riva D.

Pediatr Neurol. 2005 May;32(5):355-7.

PMID:
15866439
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