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Similar articles for PubMed (Select 23052294)

1.

Neural stem cell engraftment and myelination in the human brain.

Gupta N, Henry RG, Strober J, Kang SM, Lim DA, Bucci M, Caverzasi E, Gaetano L, Mandelli ML, Ryan T, Perry R, Farrell J, Jeremy RJ, Ulman M, Huhn SL, Barkovich AJ, Rowitch DH.

Sci Transl Med. 2012 Oct 10;4(155):155ra137. doi: 10.1126/scitranslmed.3004373. Erratum in: Sci Transl Med. 2012 Dec 19;4(165):165er8.

2.

Human neural stem cells induce functional myelination in mice with severe dysmyelination.

Uchida N, Chen K, Dohse M, Hansen KD, Dean J, Buser JR, Riddle A, Beardsley DJ, Wan Y, Gong X, Nguyen T, Cummings BJ, Anderson AJ, Tamaki SJ, Tsukamoto A, Weissman IL, Matsumoto SG, Sherman LS, Kroenke CD, Back SA.

Sci Transl Med. 2012 Oct 10;4(155):155ra136. doi: 10.1126/scitranslmed.3004371. Erratum in: Sci Transl Med. 2012 Dec 19;4(165):165er7.

3.

High-resolution diffusion tensor imaging of fixed brain in a mouse model of Pelizaeus-Merzbacher disease: comparison with quantitative measures of white matter pathology.

Ruest T, Holmes WM, Barrie JA, Griffiths IR, Anderson TJ, Dewar D, Edgar JM.

NMR Biomed. 2011 Dec;24(10):1369-79. doi: 10.1002/nbm.1700. Epub 2011 Mar 24.

PMID:
22223367
4.

Central nervous system stem cell transplantation for children with neuronal ceroid lipofuscinosis.

Selden NR, Al-Uzri A, Huhn SL, Koch TK, Sikora DM, Nguyen-Driver MD, Guillaume DJ, Koh JL, Gultekin SH, Anderson JC, Vogel H, Sutcliffe TL, Jacobs Y, Steiner RD.

J Neurosurg Pediatr. 2013 Jun;11(6):643-52. doi: 10.3171/2013.3.PEDS12397. Epub 2013 Apr 12.

PMID:
23581634
5.

Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvement.

Inoue K, Tanaka H, Scaglia F, Araki A, Shaffer LG, Lupski JR.

Ann Neurol. 2001 Dec;50(6):747-54.

PMID:
11761472
6.

Magnetic resonance imaging of a unique mutation in a family with Pelizaeus-Merzbacher disease.

Miller E, Widjaja E, Nilsson D, Yoon G, Banwell B, Blaser S.

Am J Med Genet A. 2010 Mar;152A(3):748-52. doi: 10.1002/ajmg.a.33305.

PMID:
20186781
7.

Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1.

Sima AA, Pierson CR, Woltjer RL, Hobson GM, Golden JA, Kupsky WJ, Schauer GM, Bird TD, Skoff RP, Garbern JY.

Acta Neuropathol. 2009 Oct;118(4):531-9. doi: 10.1007/s00401-009-0562-8. Epub 2009 Jun 27.

8.

Two autopsy cases with Pelizaeus-Merzbacher disease phenotype of adult onset, without mutation of proteolipid protein gene.

Sasaki A, Miyanaga K, Ototsuji M, Iwaki A, Iwaki T, Takahashi S, Nakazato Y.

Acta Neuropathol. 2000 Jan;99(1):7-13.

PMID:
10651021
9.

MR-revealed myelination in the cerebral corticospinal tract as a marker for Pelizaeus-Merzbacher's disease with proteolipid protein gene duplication.

Takanashi J, Sugita K, Tanabe Y, Nagasawa K, Inoue K, Osaka H, Kohno Y.

AJNR Am J Neuroradiol. 1999 Nov-Dec;20(10):1822-8.

10.

Familial Pelizaeus-Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus.

Kitsiou-Tzeli S, Konstantinidou A, Sofocleous C, Kosma K, Syrmou A, Giannikou K, Sifakis S, Makrythanasis P, Tzetis M.

Birth Defects Res A Clin Mol Teratol. 2012 Jun;94(6):494-8. doi: 10.1002/bdra.23015. Epub 2012 Apr 18.

PMID:
22511562
11.

Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher disease.

Laukka JJ, Stanley JA, Garbern JY, Trepanier A, Hobson G, Lafleur T, Gow A, Kamholz J.

J Neurol Sci. 2013 Dec 15;335(1-2):75-81. doi: 10.1016/j.jns.2013.08.030. Epub 2013 Aug 30.

12.

Quantitative proton MRS of Pelizaeus-Merzbacher disease: evidence of dys- and hypomyelination.

Hanefeld FA, Brockmann K, Pouwels PJ, Wilken B, Frahm J, Dechent P.

Neurology. 2005 Sep 13;65(5):701-6.

PMID:
16157902
13.

Effect of curcumin in a mouse model of Pelizaeus-Merzbacher disease.

Yu LH, Morimura T, Numata Y, Yamamoto R, Inoue N, Antalfy B, Goto Y, Deguchi K, Osaka H, Inoue K.

Mol Genet Metab. 2012 May;106(1):108-14. doi: 10.1016/j.ymgme.2012.02.016. Epub 2012 Mar 3.

PMID:
22436581
14.
15.

Astrocytic hypertrophy in dysmyelination influences the diffusion anisotropy of white matter.

Harsan LA, Poulet P, Guignard B, Parizel N, Skoff RP, Ghandour MS.

J Neurosci Res. 2007 Apr;85(5):935-44.

PMID:
17278151
16.
17.

Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication.

Shimojima K, Inoue T, Imai Y, Arai Y, Komoike Y, Sugawara M, Fujita T, Ideguchi H, Yasumoto S, Kanno H, Hirose S, Yamamoto T.

J Hum Genet. 2012 Sep;57(9):580-6. doi: 10.1038/jhg.2012.71. Epub 2012 Jun 14.

PMID:
22695888
18.

Pelizaeus-Merzbacher disease.

Koeppen AH, Robitaille Y.

J Neuropathol Exp Neurol. 2002 Sep;61(9):747-59. Review.

PMID:
12230321
19.

PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus-Merzbacher disease.

Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Kirkham D, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M.

Glia. 2007 Mar;55(4):341-51.

PMID:
17133418
20.

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

Kuan CC, Sano M, Kaga K, Kodama M, Kodama K.

Acta Otolaryngol. 2008 May;128(5):539-46. doi: 10.1080/00016480701258713.

PMID:
18421608
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