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Results: 1 to 20 of 95

Similar articles for PubMed (Select 18316686)

1.

Gap junction protein 12: "connexing" the pieces in the puzzle of myelination and leukodystrophy.

Mar S, Noetzel MJ.

Neurology. 2008 Mar 4;70(10):744-5. doi: 10.1212/01.wnl.0000304252.66303.23. No abstract available.

PMID:
18316686
2.

GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease.

Henneke M, Combes P, Diekmann S, Bertini E, Brockmann K, Burlina AP, Kaiser J, Ohlenbusch A, Plecko B, Rodriguez D, Boespflug-Tanguy O, Gärtner J.

Neurology. 2008 Mar 4;70(10):748-54. Epub 2007 Dec 19.

PMID:
18094336
3.

Interruption of SOX10 function in myelinopathies.

Lupski JR.

Ann Neurol. 2010 Aug;68(2):121-3. doi: 10.1002/ana.22123. No abstract available.

PMID:
20695004
4.

X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease.

Isoardo G, Di Vito N, Nobile M, Benetton G, Fassio F.

Neurology. 2005 Nov 22;65(10):1672-3. No abstract available.

PMID:
16301507
5.

Hereditary leukodystrophies without identified mutations.

Robitaille Y.

J Neurol Sci. 2005 Feb 15;228(2):208-9. Epub 2004 Dec 2. Review. No abstract available.

PMID:
15694209
6.

Molecular mechanisms of gap junction mutations in myelinating cells.

Sargiannidou I, Markoullis K, Kleopa KA.

Histol Histopathol. 2010 Sep;25(9):1191-206. Review.

PMID:
20607661
7.

Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.

Sanahuja J, Franco E, Rojas-García R, Gallardo E, Combarros O, Begué R, Granés P, Illa I.

Arch Neurol. 2005 Dec;62(12):1911-4.

PMID:
16344349
8.

Gap junctions couple astrocytes and oligodendrocytes.

Orthmann-Murphy JL, Abrams CK, Scherer SS.

J Mol Neurosci. 2008 May;35(1):101-16. doi: 10.1007/s12031-007-9027-5. Review.

9.

Connexins are critical for normal myelination in the CNS.

Menichella DM, Goodenough DA, Sirkowski E, Scherer SS, Paul DL.

J Neurosci. 2003 Jul 2;23(13):5963-73.

10.

Connexin32 is a myelin-related protein in the PNS and CNS.

Scherer SS, Deschênes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL.

J Neurosci. 1995 Dec;15(12):8281-94.

11.

Connexin26 in adult rodent central nervous system: demonstration at astrocytic gap junctions and colocalization with connexin30 and connexin43.

Nagy JI, Li X, Rempel J, Stelmack G, Patel D, Staines WA, Yasumura T, Rash JE.

J Comp Neurol. 2001 Dec 24;441(4):302-23.

PMID:
11745652
12.

Clinical neurophysiology in GJA12-related hypomyelination vs Pelizaeus-Merzbacher disease.

Henneke M, Gegner S, Hahn A, Plecko-Startinig B, Weschke B, Gärtner J, Brockmann K.

Neurology. 2010 Jun 1;74(22):1785-9. doi: 10.1212/WNL.0b013e3181e0f820.

PMID:
20513814
13.

Four classes of intercellular channels between glial cells in the CNS.

Altevogt BM, Paul DL.

J Neurosci. 2004 May 5;24(18):4313-23.

14.

The gap junction proteome and its relationship to disease.

Laird DW.

Trends Cell Biol. 2010 Feb;20(2):92-101. doi: 10.1016/j.tcb.2009.11.001. Epub 2009 Nov 26. Review.

PMID:
19944606
15.

The role of connexins in human disease.

Chang EH, Van Camp G, Smith RJ.

Ear Hear. 2003 Aug;24(4):314-23. Review.

PMID:
12923422
16.

Molecular analysis of glial cell development in the canine 'shaking pup' mutant.

Nadon NL, Duncan ID.

Dev Neurosci. 1996;18(3):174-84.

PMID:
8894446
17.

[Effects on astrocytic function from MLC1 gene mutation with megalencephalic leukoencephalopathy with subcortical cysts].

Wang JM, Jiang YW, Wu XR.

Sheng Li Ke Xue Jin Zhan. 2010 Feb;41(1):69-71. Review. Chinese. No abstract available.

PMID:
21417022
18.

Myelin mishaps.

Barkovich AJ.

Ann Neurol. 2007 Aug;62(2):107-9. No abstract available.

PMID:
17683086
19.

Gap junction diseases of the skin.

van Steensel MA.

Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):12-9. Review. Erratum in: Am J Med Genet C Semin Med Genet. 2006 Feb 15;142(1):58.

PMID:
15468169
20.

PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1.

Combes P, Bonnet-Dupeyron MN, Gauthier-Barichard F, Schiffmann R, Bertini E, Rodriguez D, Armour JA, Boespflug-Tanguy O, Vaurs-Barrière C.

Neurogenetics. 2006 Mar;7(1):31-7. Epub 2006 Jan 17.

PMID:
16416265
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