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Results: 18

1.

Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred.

Baba Y, Ghetti B, Baker MC, Uitti RJ, Hutton ML, Yamaguchi K, Bird T, Lin W, DeLucia MW, Dickson DW, Wszolek ZK.

Acta Neuropathol. 2006 Apr;111(4):300-11. Epub 2006 Mar 8.

PMID:
16523341
[PubMed - indexed for MEDLINE]
2.

Long tract degeneration in familial sudanophilic leukodystrophy with prominent spheroids.

Yazawa I, Nakano I, Yamada H, Oda M.

J Neurol Sci. 1997 Apr 15;147(2):185-91. Review.

PMID:
9106126
[PubMed - indexed for MEDLINE]
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.

PMID:
19487654
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Autosomal dominant late-onset leukoencephalopathy. Clinical report of a new Italian family.

Quattrocolo G, Leombruni S, Vaula G, Bergui M, Riva A, Bradac GB, Bergamini L.

Eur Neurol. 1997;37(1):53-61. Review.

PMID:
9018034
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

[CACH/VWM syndrome and leucodystrophies related to EIF2B mutations].

Labauge P, Fogli A, Niel F, Rodriguez D, Boespflug-Tanguy O.

Rev Neurol (Paris). 2007 Sep;163(8-9):793-9. Review. French.

PMID:
17878805
[PubMed - indexed for MEDLINE]
7.

[A Japanese family with probably autosomal dominant adult-onset leukodystrophy].

Asahara H, Yoshimura T, Sada S, Furuya H, Kobayashi T.

Rinsho Shinkeigaku. 1996 Aug;36(8):968-72. Review. Japanese.

PMID:
8958750
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
21986056
[PubMed - indexed for MEDLINE]
Free Article
9.

A novel type of familial proximal axonal dystrophy: three cases and a review of the axonal dystrophies.

Carpenter S, Soares H, Brandão O, Souto Moura C, Castro L, Rodrigues E, Cunha AL, Bartosch C.

Eur J Paediatr Neurol. 2012 May;16(3):292-300. doi: 10.1016/j.ejpn.2011.08.010. Epub 2011 Sep 16. Review.

PMID:
21925911
[PubMed - indexed for MEDLINE]
10.

The large spectrum of eIF2B-related diseases.

Fogli A, Boespflug-Tanguy O.

Biochem Soc Trans. 2006 Feb;34(Pt 1):22-9. Review.

PMID:
16246171
[PubMed - indexed for MEDLINE]
11.

Infantile neuroaxonal dystrophy and giant axonal neuropathy--overlap diseases of neuronal cytoskeletal elements in childhood?

Mahadevan A, Santosh V, Gayatri N, Ratnavalli E, NandaGopal R, Vasanth A, Roy AK, Shankar SK.

Clin Neuropathol. 2000 Sep-Oct;19(5):221-9. Review.

PMID:
11048747
[PubMed - indexed for MEDLINE]
12.

[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
[PubMed - indexed for MEDLINE]
13.

[Hereditary diffuse leukoencephalopathy with spheroids (HDLS): a review of the literature on its clinical characteristics and mutations in the colony-stimulating factor-1 receptor gene].

Konno T, Tada M, Tada M, Nishizawa M, Ikeuchi T.

Brain Nerve. 2014 May;66(5):581-90. Review. Japanese.

PMID:
24807373
[PubMed - indexed for MEDLINE]
14.

Childhood ataxia with CNS hypomyelination/vanishing white matter disease--a common leukodystrophy caused by abnormal control of protein synthesis.

Schiffmann R, Elroy-Stein O.

Mol Genet Metab. 2006 May;88(1):7-15. Epub 2006 Jan 18. Review.

PMID:
16378743
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

[HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy].

Seifried C, Sitzer M, Jen J, Auburger G.

Nervenarzt. 2005 Oct;76(10):1191-2, 1194-5. Review. German.

PMID:
15856153
[PubMed - indexed for MEDLINE]
17.

[Conformational diseases (neurological aspects)].

Zavalishin IA, Zakharova MN.

Zh Nevrol Psikhiatr Im S S Korsakova. 2003;103(1):54-60. Review. Russian. No abstract available.

PMID:
12616742
[PubMed - indexed for MEDLINE]
18.

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.

PMID:
23521113
[PubMed - indexed for MEDLINE]
Free PMC Article

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