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Items: 1 to 20 of 28

1.

Adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia: report of five cases and a new mutation.

Kleinfeld K, Mobley B, Hedera P, Wegner A, Sriram S, Pawate S.

J Neurol. 2013 Feb;260(2):558-71. doi: 10.1007/s00415-012-6680-6. Epub 2012 Sep 30. Review.

PMID:
23052599
2.

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia can present as frontotemporal dementia syndrome.

Wong JC, Chow TW, Hazrati LN.

Dement Geriatr Cogn Disord. 2011;32(2):150-8. doi: 10.1159/000331422. Epub 2011 Oct 5. Review.

3.

Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): a single entity?

Wider C, Van Gerpen JA, DeArmond S, Shuster EA, Dickson DW, Wszolek ZK.

Neurology. 2009 Jun 2;72(22):1953-9. doi: 10.1212/WNL.0b013e3181a826c0. Review.

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An adult-onset leukoencephalopathy with axonal spheroids and pigmented glia accompanied by brain calcifications: a case report and a literature review of brain calcifications disorders.

Fujioka S, Broderick DF, Sundal C, Baker MC, Rademakers R, Wszolek ZK.

J Neurol. 2013 Oct;260(10):2665-8. doi: 10.1007/s00415-013-7093-x. Epub 2013 Sep 14. Review. No abstract available.

6.

[Recent advances of study on hereditary diffuse leukoencephalopathy with spheroids].

Cheng X, Xu J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):330-3. doi: 10.3760/cma.j.issn.1003-9406.2014.03.016. Review. Chinese.

PMID:
24928013
7.

[Neuropathology of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)].

Oyanagi K.

Rinsho Shinkeigaku. 2014;54(12):1165-7. doi: 10.5692/clinicalneurol.54.1165. Review. Japanese.

PMID:
25672734
8.

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia.

Sundal C, Wszolek Z.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2012 Aug 30 [updated 2014 Dec 18].

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[Infantile neuroaxonal dystrophy. A report of two new cases and a review of the literature published over the past ten years].

Rodríguez-Costa T, Cabello A, Recuero-Fernández E, Casas-Fernández C, Puche-Mira A, Domingo-Jiménez R, Ricoy JR.

Rev Neurol. 2001 Sep 1-15;33(5):443-7. Review. Spanish.

12.

Rapid onset frontal leukodystrophy with decreased diffusion coefficient and neuroaxonal spheroids.

Maillart E, Rousseau A, Galanaud D, Gray F, Polivka M, Labauge P, Hauw JJ, Lyon-Caen O, Gout O, Sedel F.

J Neurol. 2009 Oct;256(10):1649-54. doi: 10.1007/s00415-009-5172-9. Epub 2009 May 21. Review.

PMID:
19458985
13.

Update on several/certain adult-onset genetic leukoencephalopathies: clinical signs and molecular confirmation.

Di Donato I, Dotti MT, Federico A.

J Alzheimers Dis. 2014;42 Suppl 3:S27-35. doi: 10.3233/JAD-141026. Review.

PMID:
24958462
14.

A clinicopathological and genetic study of sporadic diffuse leukoencephalopathy with spheroids: a report of two cases.

Kimura T, Ishizawa K, Mitsufuji T, Abe T, Nakazato Y, Yoshida K, Sasaki A, Araki N.

Neuropathol Appl Neurobiol. 2013 Dec;39(7):837-43. doi: 10.1111/nan.12046. Review. No abstract available.

15.

Adult-onset Krabbe disease with homozygous T1853C mutation in the galactocerebrosidase gene. Unusual MRI findings of corticospinal tract demyelination.

Satoh JI, Tokumoto H, Kurohara K, Yukitake M, Matsui M, Kuroda Y, Yamamoto T, Furuya H, Shinnoh N, Kobayashi T, Kukita Y, Hayashi K.

Neurology. 1997 Nov;49(5):1392-9. Review.

PMID:
9371928
16.

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.

Pareyson D, Fancellu R, Mariotti C, Romano S, Salmaggi A, Carella F, Girotti F, Gattellaro G, Carriero MR, Farina L, Ceccherini I, Savoiardo M.

Brain. 2008 Sep;131(Pt 9):2321-31. doi: 10.1093/brain/awn178. Epub 2008 Aug 6. Review.

17.

Inherited leukoencephalopathies with clinical onset in middle and old age.

Nannucci S, Donnini I, Pantoni L.

J Neurol Sci. 2014 Dec 15;347(1-2):1-13. doi: 10.1016/j.jns.2014.09.020. Epub 2014 Sep 20. Review.

PMID:
25307983
18.

Mitochondrial membrane protein-associated neurodegeneration (MPAN).

Hartig M, Prokisch H, Meitinger T, Klopstock T.

Int Rev Neurobiol. 2013;110:73-84. doi: 10.1016/B978-0-12-410502-7.00004-1. Review.

PMID:
24209434
19.

Leukodystrophies with astrocytic dysfunction.

Rodriguez D.

Handb Clin Neurol. 2013;113:1619-28. doi: 10.1016/B978-0-444-59565-2.00030-7. Review.

PMID:
23622383
20.

Case definition and classification of leukodystrophies and leukoencephalopathies.

Vanderver A, Prust M, Tonduti D, Mochel F, Hussey HM, Helman G, Garbern J, Eichler F, Labauge P, Aubourg P, Rodriguez D, Patterson MC, Van Hove JL, Schmidt J, Wolf NI, Boespflug-Tanguy O, Schiffmann R, van der Knaap MS; GLIA Consortium.

Mol Genet Metab. 2015 Apr;114(4):494-500. doi: 10.1016/j.ymgme.2015.01.006. Epub 2015 Jan 29. Review.

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