Similar articles for PMID: 11761472

Year	Number of Results
1995	1
1997	1
1998	1
1999	5
2000	8
2001	7
2002	4
2003	6
2004	6
2005	7
2006	7
2007	6
2008	8
2009	5
2010	6
2011	6
2012	13
2013	12
2014	7
2015	8
2016	3
2017	3
2018	2
2019	7
2020	3
2021	2
2022	1
2023	1
2024	0

1

Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvement.

Inoue K, Tanaka H, Scaglia F, Araki A, Shaffer LG, Lupski JR. Inoue K, et al. Ann Neurol. 2001 Dec;50(6):747-54. doi: 10.1002/ana.10036. Ann Neurol. 2001. PMID: 11761472

2

Pelizaeus-Merzbacher disease.

Koeppen AH, Robitaille Y. Koeppen AH, et al. J Neuropathol Exp Neurol. 2002 Sep;61(9):747-59. doi: 10.1093/jnen/61.9.747. J Neuropathol Exp Neurol. 2002. PMID: 12230321 Review.

3

Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease.

Wolf NI, Sistermans EA, Cundall M, Hobson GM, Davis-Williams AP, Palmer R, Stubbs P, Davies S, Endziniene M, Wu Y, Chong WK, Malcolm S, Surtees R, Garbern JY, Woodward KJ. Wolf NI, et al. Brain. 2005 Apr;128(Pt 4):743-51. doi: 10.1093/brain/awh409. Epub 2005 Feb 2. Brain. 2005. PMID: 15689360

4

A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.

Hobson G, Stabley D, Funanage V, Marks H. Hobson G, et al. Hum Mutat. 2001 Feb;17(2):152. doi: 10.1002/1098-1004(200102)17:2<152::AID-HUMU9>3.0.CO;2-P. Hum Mutat. 2001. PMID: 11180600

5

Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease.

Wang PJ, Hwu WL, Lee WT, Wang TR, Shen YZ. Wang PJ, et al. Pediatr Neurol. 1997 Sep;17(2):125-8. doi: 10.1016/s0887-8994(97)00088-x. Pediatr Neurol. 1997. PMID: 9367291

6

Inoue K. Inoue K. Neurogenetics. 2005 Feb;6(1):1-16. doi: 10.1007/s10048-004-0207-y. Epub 2004 Dec 31. Neurogenetics. 2005. PMID: 15627202 Review.

7

Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.

Fattal-Valevski A, DiMaio MS, Hisama FM, Hobson GM, Davis-Williams A, Garbern JY, Mahoney MJ, Kolodny EH, Pastores GM. Fattal-Valevski A, et al. J Child Neurol. 2009 May;24(5):618-24. doi: 10.1177/0883073808327833. Epub 2009 Jan 16. J Child Neurol. 2009. PMID: 19151366

8

Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease.

Masliah-Planchon J, Dupont C, Vartzelis G, Trimouille A, Eymard-Pierre E, Gay-Bellile M, Renaldo F, Dorboz I, Pagan C, Quentin S, Elmaleh M, Kotsogianni C, Konstantelou E, Drunat S, Tabet AC, Boespflug-Tanguy O. Masliah-Planchon J, et al. BMC Med Genet. 2015 Sep 2;16:77. doi: 10.1186/s12881-015-0226-6. BMC Med Genet. 2015. PMID: 26329556 Free PMC article.

9

A novel PLP1 frameshift mutation causing a milder form of Pelizaeus-Merzbacher disease.

Shiihara T, Watanabe M, Moriyama K, Uematsu M, Sameshima K. Shiihara T, et al. Brain Dev. 2015 Apr;37(4):455-8. doi: 10.1016/j.braindev.2014.06.011. Epub 2014 Jul 16. Brain Dev. 2015. PMID: 25043250

10

Pelizaeus-Merzbacher disease and spastic paraplegia type 2: two faces of myelin loss from mutations in the same gene.

Hudson LD. Hudson LD. J Child Neurol. 2003 Sep;18(9):616-24. doi: 10.1177/08830738030180090801. J Child Neurol. 2003. PMID: 14572140 Review.

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