Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 145

Related Citations for PubMed (Select 18541117)

1.

Genes involved in leukodystrophies: a glance at glial functions.

Boespflug-Tanguy O, Labauge P, Fogli A, Vaurs-Barriere C.

Curr Neurol Neurosci Rep. 2008 May;8(3):217-29. Review.

PMID:
18541117
2.

Update on genetic disorders affecting white matter.

Kaye EM.

Pediatr Neurol. 2001 Jan;24(1):11-24. Review.

PMID:
11182276
3.

The ovarioleukodystrophy.

Mathis S, Scheper GC, Baumann N, Petit E, Gil R, van der Knaap MS, Neau JP.

Clin Neurol Neurosurg. 2008 Dec;110(10):1035-7. doi: 10.1016/j.clineuro.2008.06.002. Epub 2008 Aug 3.

PMID:
18678442
4.

[Leukodystrophies: diseases of white matter of the nervous system].

Gärtner J, Kohlschütter A, Gieselmann V.

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2007 Dec;50(12):1531-40. Review. German.

PMID:
18026884
5.

Tools for diagnosis of leukodystrophies and other disorders presenting with white matter disease.

Vanderver A.

Curr Neurol Neurosci Rep. 2005 Mar;5(2):110-8. Review.

PMID:
15743548
6.

Leukodystrophies: clinical and genetic aspects.

Lyon G, Fattal-Valevski A, Kolodny EH.

Top Magn Reson Imaging. 2006 Aug;17(4):219-42. Review.

PMID:
17414998
7.

Developmental splicing deregulation in leukodystrophies related to EIF2B mutations.

Huyghe A, Horzinski L, Hénaut A, Gaillard M, Bertini E, Schiffmann R, Rodriguez D, Dantal Y, Boespflug-Tanguy O, Fogli A.

PLoS One. 2012;7(6):e38264. doi: 10.1371/journal.pone.0038264. Epub 2012 Jun 21.

8.

Canavan disease: a white matter disorder.

Kumar S, Mattan NS, de Vellis J.

Ment Retard Dev Disabil Res Rev. 2006;12(2):157-65. Review.

PMID:
16807907
9.

Diagnosing "undiagnosed" leukodystrophies: The role of molecular genetics.

Noetzel MJ.

Neurology. 2004 Mar 23;62(6):847-8. Review. No abstract available.

PMID:
15037679
10.

Familial multiple sclerosis and other inherited disorders of the white matter.

Kalman B, Leist TP.

Neurologist. 2004 Jul;10(4):201-15. Review.

PMID:
15245586
11.

The latest on leukodystrophies.

Schiffmann R, van der Knaap MS.

Curr Opin Neurol. 2004 Apr;17(2):187-92. Review.

PMID:
15021247
12.

Leukodystrophies with late disease onset: an update.

Köhler W.

Curr Opin Neurol. 2010 Jun;23(3):234-41. doi: 10.1097/WCO.0b013e328338313a. Review.

PMID:
20216214
13.

Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.

Kohlschütter A, Bley A, Brockmann K, Gärtner J, Krägeloh-Mann I, Rolfs A, Schöls L.

Brain Dev. 2010 Feb;32(2):82-9. doi: 10.1016/j.braindev.2009.03.014. Epub 2009 May 7. Review.

PMID:
19427149
14.

The spectrum of mutations for the diagnosis of vanishing white matter disease.

Scali O, Di Perri C, Federico A.

Neurol Sci. 2006 Sep;27(4):271-7. Review.

PMID:
16998732
15.

An update on the leukodsytrophies.

Schiffmann R, Boespflüg-Tanguy O.

Curr Opin Neurol. 2001 Dec;14(6):789-94. Review.

PMID:
11723390
16.

Diagnostic algorithm for the differentiation of leukodystrophies in early MS.

Köhler W.

J Neurol. 2008 Dec;255 Suppl 6:123-6. doi: 10.1007/s00415-008-6023-9.

PMID:
19300973
17.

Neuroimaging in leukodystrophies.

Barker PB, Horská A.

J Child Neurol. 2004 Aug;19(8):559-70. Review.

PMID:
15605464
18.

Diffusion-weighted MR imaging in leukodystrophies.

Patay Z.

Eur Radiol. 2005 Nov;15(11):2284-303. Epub 2005 Jul 15. Review.

PMID:
16021451
19.

Update on white matter genetic disorders.

Messing A, Brenner M, Johnson AB, Goldman JE.

Pediatr Neurol. 2001 Oct;25(4):347-8; author reply 348. No abstract available.

PMID:
11704412
20.

Where has all the white matter gone? Unraveling the mysteries of leukoencephalopathies.

Kaye EM, Moser H.

Neurology. 2004 May 11;62(9):1464-5. No abstract available.

PMID:
15136665
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk