21206709 17095305 12848455 15668046 12773895 10701065 14510623 10025538 10536901 20635355 34203304 12566516 24311297 23416059 10396298 12162161 10226746 24288033 10891793 26835328 10982040 11140414 10424818 15057988 25379297 20445456 9714017 10592081 - Search Results

Year	Number of Results
1998	1
1999	7
2000	5
2002	1
2003	4
2004	2
2005	1
2006	1
2007	1
2009	1
2010	3
2011	1
2012	1
2013	3
2014	4
2021	1
2022	0

1

Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?

Hamzi K, Itto AB, Nassereddine S, Nadifi S. Hamzi K, et al. Indian J Hum Genet. 2010 Sep;16(3):172-4. doi: 10.4103/0971-6866.73417. Indian J Hum Genet. 2010. PMID: 21206709 Free PMC article.

2

Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.

Camprubí C, Coll MD, Villatoro S, Gabau E, Kamli A, Martínez MJ, Poyatos D, Guitart M. Camprubí C, et al. Eur J Med Genet. 2007 Jan-Feb;50(1):11-20. doi: 10.1016/j.ejmg.2006.10.001. Epub 2006 Oct 10. Eur J Med Genet. 2007. PMID: 17095305

3

Molecular genetic testing for prenatal diagnosis.

Tantravahi U, Wheeler P. Tantravahi U, et al. Clin Lab Med. 2003 Jun;23(2):481-502. doi: 10.1016/s0272-2712(03)00035-0. Clin Lab Med. 2003. PMID: 12848455 Review.

4

Neurological aspects of the Angelman syndrome.

Williams CA. Williams CA. Brain Dev. 2005 Mar;27(2):88-94. doi: 10.1016/j.braindev.2003.09.014. Brain Dev. 2005. PMID: 15668046 Review.

5

[Angelman syndrome: clinical and genetic model].

Dan B, Chéron G. Dan B, et al. Rev Neurol (Paris). 2003 May;159(5 Pt 1):499-510. Rev Neurol (Paris). 2003. PMID: 12773895 Review. French.

6

[What is new in pediatric neurology?].

Landrieu P. Landrieu P. Arch Pediatr. 2000 Feb;7(2):185-95. doi: 10.1016/s0929-693x(00)88090-2. Arch Pediatr. 2000. PMID: 10701065 Review. French.

7

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

Guerrini R, Carrozzo R, Rinaldi R, Bonanni P. Guerrini R, et al. Paediatr Drugs. 2003;5(10):647-61. doi: 10.2165/00148581-200305100-00001. Paediatr Drugs. 2003. PMID: 14510623 Review.

8

Ion channels and the genetic contribution to epilepsy.

Ryan SG. Ryan SG. J Child Neurol. 1999 Jan;14(1):58-66. doi: 10.1177/088307389901400104. J Child Neurol. 1999. PMID: 10025538 Review.

9

Angelman syndrome: a review of clinical and genetic aspects.

Laan LA, v Haeringen A, Brouwer OF. Laan LA, et al. Clin Neurol Neurosurg. 1999 Sep;101(3):161-70. doi: 10.1016/s0303-8467(99)00030-x. Clin Neurol Neurosurg. 1999. PMID: 10536901 Review.

10

Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid.

Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA. Peters SU, et al. Am J Med Genet A. 2010 Aug;152A(8):1994-2001. doi: 10.1002/ajmg.a.33509. Am J Med Genet A. 2010. PMID: 20635355 Free PMC article. Clinical Trial.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results