Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 64

1.

The leukodystrophies.

Gordon HB, Letsou A, Bonkowsky JL.

Semin Neurol. 2014 Jul;34(3):312-20. doi: 10.1055/s-0034-1386769. Epub 2014 Sep 5. Review.

PMID:
25192509
2.

Congenital genetic inborn errors of metabolism presenting as an adult or persisting into adulthood: neuroimaging in the more common or recognizable disorders.

Krishna SH, McKinney AM, Lucato LT.

Semin Ultrasound CT MR. 2014 Apr;35(2):160-91. doi: 10.1053/j.sult.2013.10.008. Epub 2013 Oct 23. Review.

PMID:
24745891
3.

Exon-skipping antisense oligonucleotides to correct missplicing in neurogenetic diseases.

Siva K, Covello G, Denti MA.

Nucleic Acid Ther. 2014 Feb;24(1):69-86. doi: 10.1089/nat.2013.0461. Review.

4.

[MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature].

López-Marín L, Martín-Belinchón M, Gutiérrez-Solana LG, Morte-Molina B, Duat-Rodríguez A, Bernal J.

Rev Neurol. 2013 Jun 16;56(12):615-22. Review. Spanish.

5.

[Clinical and molecular manifestations of congenital cerebral hypomyelination].

Osaka H, Inoue K, Saitsu H.

No To Hattatsu. 2013 Mar;45(2):127-31. Review. Japanese. No abstract available.

PMID:
23650817
6.

[Congenital hypomyelinating leukodystrophies--from genomic dissection to molecular diagnosis and potential therapies].

Inoue K, Iwaki A, Kurosawa K, Takanashi J, Deguchi K, Yamamoto T, Osaka H.

No To Hattatsu. 2013 Mar;45(2):122-6. Review. Japanese. No abstract available.

PMID:
23650816
7.

Inborn errors of brain myelin formation.

Boespflug-Tanguy O.

Handb Clin Neurol. 2013;113:1581-92. doi: 10.1016/B978-0-444-59565-2.00027-7. Review.

PMID:
23622380
8.

Pelizaeus-Merzbacher disease as a chromosomal disorder.

Yamamoto T, Shimojima K.

Congenit Anom (Kyoto). 2013 Mar;53(1):3-8. doi: 10.1111/cga.12005. Review.

PMID:
23480352
9.

[Effects on oligodendrocytic function resulting from proteolipid protein 1 gene mutations].

Wang JM, Jiang YW, Wu XR.

Sheng Li Ke Xue Jin Zhan. 2012 Aug;43(4):271-4. Review. Chinese. No abstract available.

PMID:
23189621
10.

Pelizaeus-Merzbacher disease, Pelizaeus-Merzbacher-like disease 1, and related hypomyelinating disorders.

Hobson GM, Garbern JY.

Semin Neurol. 2012 Feb;32(1):62-7. doi: 10.1055/s-0032-1306388. Epub 2012 Mar 15. Review.

PMID:
22422208
11.

Leukodystrophies.

Perlman SJ, Mar S.

Adv Exp Med Biol. 2012;724:154-71. doi: 10.1007/978-1-4614-0653-2_13. Review.

PMID:
22411242
12.

[Congenital cerebral hypomyelination---Pelizaeus-Merzbacher disease and associated disorders].

Inoue K, Iwaki A, Kurosawa K, Takanashi J, Deguchi K, Yamamoto T, Osaka H.

No To Hattatsu. 2011 Nov;43(6):435-42. Review. Japanese.

PMID:
22180957
13.

The myelin mutants as models to study myelin repair in the leukodystrophies.

Duncan ID, Kondo Y, Zhang SC.

Neurotherapeutics. 2011 Oct;8(4):607-24. doi: 10.1007/s13311-011-0080-y. Review.

14.

Gap junctions in inherited human disorders of the central nervous system.

Abrams CK, Scherer SS.

Biochim Biophys Acta. 2012 Aug;1818(8):2030-47. doi: 10.1016/j.bbamem.2011.08.015. Epub 2011 Aug 16. Review.

15.

Gap junction disorders of myelinating cells.

Kleopa KA, Orthmann-Murphy J, Sargiannidou I.

Rev Neurosci. 2010;21(5):397-419. Review.

PMID:
21280457
16.

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
17.

Axonal damage in leukodystrophies.

Mar S, Noetzel M.

Pediatr Neurol. 2010 Apr;42(4):239-42. doi: 10.1016/j.pediatrneurol.2009.08.011. Review.

PMID:
20304325
18.

Gap junctions in inherited human disease.

Zoidl G, Dermietzel R.

Pflugers Arch. 2010 Jul;460(2):451-66. doi: 10.1007/s00424-010-0789-1. Epub 2010 Feb 7. Review.

PMID:
20140684
19.

The myelin proteolipid DMα in fishes.

Brösamle C.

Neuron Glia Biol. 2010 May;6(2):109-12. doi: 10.1017/S1740925X09000131. Epub 2009 Jun 10. Review.

PMID:
19508742
20.

Myelin under stress.

D'Antonio M, Feltri ML, Wrabetz L.

J Neurosci Res. 2009 Nov 15;87(15):3241-9. doi: 10.1002/jnr.22066. Review.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk