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Similar articles for PubMed (Select 21157375)

1.

Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis.

Damme M, Stroobants S, Walkley SU, Lüllmann-Rauch R, D'Hooge R, Fogh J, Saftig P, Lübke T, Blanz J.

J Neuropathol Exp Neurol. 2011 Jan;70(1):83-94. doi: 10.1097/NEN.0b013e31820428fa.

2.

Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.

Damme M, Morelle W, Schmidt B, Andersson C, Fogh J, Michalski JC, Lübke T.

Mol Cell Biol. 2010 Jan;30(1):273-83. doi: 10.1128/MCB.01143-09. Epub .

3.

Enzyme replacement therapy in alpha-mannosidosis guinea-pigs.

Crawley AC, King B, Berg T, Meikle PJ, Hopwood JJ.

Mol Genet Metab. 2006 Sep-Oct;89(1-2):48-57. Epub 2006 Jun 27.

PMID:
16807033
4.

Targeted disruption of the lysosomal alpha-mannosidase gene results in mice resembling a mild form of human alpha-mannosidosis.

Stinchi S, Lüllmann-Rauch R, Hartmann D, Coenen R, Beccari T, Orlacchio A, von Figura K, Saftig P.

Hum Mol Genet. 1999 Aug;8(8):1365-72.

5.

Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study.

Borgwardt L, Dali CI, Fogh J, Månsson JE, Olsen KJ, Beck HC, Nielsen KG, Nielsen LH, Olsen SO, Riise Stensland HM, Nilssen O, Wibrand F, Thuesen AM, Pearl T, Haugsted U, Saftig P, Blanz J, Jones SA, Tylki-Szymanska A, Guffon-Fouiloux N, Beck M, Lund AM.

J Inherit Metab Dis. 2013 Nov;36(6):1015-24. doi: 10.1007/s10545-013-9595-1. Epub 2013 Mar 14.

PMID:
23494656
6.

Behavioural characterisation of the alpha-mannosidosis guinea pig.

Robinson AJ, Crawley AC, Auclair D, Weston PF, Hirte C, Hemsley KM, Hopwood JJ.

Behav Brain Res. 2008 Jan 25;186(2):176-84. Epub 2007 Aug 10.

PMID:
17889945
7.

Neurocognitive and psychotiform behavioral alterations and enhanced hippocampal long-term potentiation in transgenic mice displaying neuropathological features of human alpha-mannosidosis.

D'Hooge R, Lüllmann-Rauch R, Beckers T, Balschun D, Schwake M, Reiss K, von Figura K, Saftig P.

J Neurosci. 2005 Jul 13;25(28):6539-49.

8.

Efficacy of enzyme replacement therapy in alpha-mannosidosis mice: a preclinical animal study.

Roces DP, Lüllmann-Rauch R, Peng J, Balducci C, Andersson C, Tollersrud O, Fogh J, Orlacchio A, Beccari T, Saftig P, von Figura K.

Hum Mol Genet. 2004 Sep 15;13(18):1979-88. Epub 2004 Jul 21.

9.

Developmental analysis of CNS pathology in the lysosomal storage disease alpha-mannosidosis.

Crawley AC, Walkley SU.

J Neuropathol Exp Neurol. 2007 Aug;66(8):687-97.

PMID:
17882013
10.

Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in alpha-mannosidosis mice.

Blanz J, Stroobants S, Lüllmann-Rauch R, Morelle W, Lüdemann M, D'Hooge R, Reuterwall H, Michalski JC, Fogh J, Andersson C, Saftig P.

Hum Mol Genet. 2008 Nov 15;17(22):3437-45. doi: 10.1093/hmg/ddn237. Epub 2008 Aug 19.

11.

Alpha-mannosidosis in the guinea pig: a new animal model for lysosomal storage disorders.

Crawley AC, Jones MZ, Bonning LE, Finnie JW, Hopwood JJ.

Pediatr Res. 1999 Nov;46(5):501-9.

PMID:
10541310
13.

Alpha-mannosidosis - a review of genetic, clinical findings and options of treatment.

Borgwardt L, Lund AM, Dali CI.

Pediatr Endocrinol Rev. 2014 Sep;12 Suppl 1:185-91. Review.

PMID:
25345101
14.

Beta-mannosidosis mice: a model for the human lysosomal storage disease.

Zhu M, Lovell KL, Patterson JS, Saunders TL, Hughes ED, Friderici KH.

Hum Mol Genet. 2006 Feb 1;15(3):493-500. Epub 2005 Dec 23.

15.

Over-expression of human lysosomal alpha-mannosidase in mouse embryonic stem cells.

Robinson AJ, Crawley AC, Hopwood JJ.

Mol Genet Metab. 2005 Jul;85(3):203-12. Epub 2005 Apr 26.

PMID:
15979032
16.
17.

Direct enzyme transfer from lymphocytes corrects a lysosomal storage disease.

Abraham D, Muir H, Olsen I, Winchester B.

Biochem Biophys Res Commun. 1985 Jun 14;129(2):417-25.

PMID:
4015639
18.

Intracellular transport of human lysosomal alpha-mannosidase and alpha-mannosidosis-related mutants.

Hansen G, Berg T, Riise Stensland HM, Heikinheimo P, Klenow H, Evjen G, Nilssen Ø, Tollersrud OK.

Biochem J. 2004 Jul 15;381(Pt 2):537-46.

19.

Diagnosis of alpha-mannosidosis by measuring alpha-mannosidase in plasma.

Prence EM, Natowicz MR.

Clin Chem. 1992 Apr;38(4):501-3.

20.

Bone marrow transplantation corrects the enzyme defect in neurons of the central nervous system in a lysosomal storage disease.

Walkley SU, Thrall MA, Dobrenis K, Huang M, March PA, Siegel DA, Wurzelmann S.

Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):2970-4.

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