Similar articles for PMID: 12376950

Year	Number of Results
1998	1
2000	1
2001	2
2002	4
2003	3
2004	6
2005	9
2006	4
2007	6
2008	10
2009	5
2012	1
2016	1
2018	1
2024	0

1

Adjunct diagnostic test for Angelman syndrome: the tuning fork response.

Hall BD, Cadle RG. Hall BD, et al. Am J Med Genet. 2002 Nov 1;112(4):429. doi: 10.1002/ajmg.10668. Am J Med Genet. 2002. PMID: 12376950 No abstract available.

2

Adjunct diagnostic test for Angelman syndrome: the tuning fork response.

Hall BD. Hall BD. Am J Med Genet. 2002 May 1;109(3):238-40. doi: 10.1002/ajmg.10302. Am J Med Genet. 2002. PMID: 11977186 No abstract available.

3

What would the brain look like in Angelman syndrome?

Dan B, Pelc K, Christophe C. Dan B, et al. Eur J Paediatr Neurol. 2009 May;13(3):269-70. doi: 10.1016/j.ejpn.2008.08.005. Epub 2008 Sep 27. Eur J Paediatr Neurol. 2009. PMID: 18824378 No abstract available.

4

Benefit of corticosteroid therapy in Angelman syndrome.

Forrest KM, Young H, Dale RC, Gill DS. Forrest KM, et al. J Child Neurol. 2009 Aug;24(8):952-8. doi: 10.1177/0883073808331344. J Child Neurol. 2009. PMID: 19666884

5

Bone mineral density in angelman syndrome.

Coppola G, Verrotti A, Mainolfi C, Auricchio G, Fortunato D, Operto FF, Pascotto A. Coppola G, et al. Pediatr Neurol. 2007 Dec;37(6):411-6. doi: 10.1016/j.pediatrneurol.2007.07.004. Pediatr Neurol. 2007. PMID: 18021922

6

Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome.

Saitoh S, Wada T, Okajima M, Takano K, Sudo A, Niikawa N. Saitoh S, et al. Brain Dev. 2005 Aug;27(5):389-91. doi: 10.1016/j.braindev.2003.12.013. Brain Dev. 2005. PMID: 16023557

7

Angelman syndrome: uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patterns.

Valente KD, Fridman C, Varela MC, Koiffmann CP, Andrade JQ, Grossmann RM, Kok F, Marques-Dias MJ. Valente KD, et al. Epilepsy Res. 2005 Dec;67(3):163-8. doi: 10.1016/j.eplepsyres.2005.09.003. Epub 2005 Oct 14. Epilepsy Res. 2005. PMID: 16226874

8

Angelman syndrome revisited.

Paprocka J, Jamroz E, Szwed-Białozyt B, Jezela-Stanek A, Kopyta I, Marszał E. Paprocka J, et al. Neurologist. 2007 Sep;13(5):305-12. doi: 10.1097/01.nrl.0000253067.32759.aa. Neurologist. 2007. PMID: 17848870

9

Another patient with MECP2 mutation without classic Rett syndrome phenotype.

Milani D, Pantaleoni C, D'Arrigo S, Selicorni A, Riva D. Milani D, et al. Pediatr Neurol. 2005 May;32(5):355-7. doi: 10.1016/j.pediatrneurol.2004.12.012. Pediatr Neurol. 2005. PMID: 15866439

10

Late-treated phenylketonuria mimicking Angelman syndrome.

Dan B, Christiaens F, Mewasingh LD, De Laet C, Goyens P. Dan B, et al. Am J Med Genet. 2001 Dec 15;104(4):345-6. doi: 10.1002/ajmg.10075. Am J Med Genet. 2001. PMID: 11754074 No abstract available.

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