Levade T - Search Results

1

A MANBA mutation resulting in residual beta-mannosidase activity associated with severe leukoencephalopathy: a possible pseudodeficiency variant.

Sabourdy F, Labauge P, Stensland HM, Nieto M, Garcés VL, Renard D, Castelnovo G, de Champfleur N, Levade T. Sabourdy F, et al. Among authors: levade t. BMC Med Genet. 2009 Sep 3;10:84. doi: 10.1186/1471-2350-10-84. BMC Med Genet. 2009. PMID: 19728872 Free PMC article.

2

Human beta-mannosidase deficiency associated with peripheral neuropathy.

Levade T, Graber D, Flurin V, Delisle MB, Pieraggi MT, Testut MF, Carrière JP, Salvayre R. Levade T, et al. Ann Neurol. 1994 Jan;35(1):116-9. doi: 10.1002/ana.410350119. Ann Neurol. 1994. PMID: 8285582 Review.

3

Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene.

Redonnet-Vernhet I, Ploos van Amstel JK, Jansen RP, Wevers RA, Salvayre R, Levade T. Redonnet-Vernhet I, et al. Among authors: levade t. J Med Genet. 1996 Aug;33(8):682-8. doi: 10.1136/jmg.33.8.682. J Med Genet. 1996. PMID: 8863162 Free PMC article.

4

[Adult leukoencephalopathy caused by alpha-mannosidosis deficiency].

Castelnovo G, Levade T, Riise Stensland HM, Nonnon MJ, Berges MA, Tollersrud OK, Labauge P. Castelnovo G, et al. Among authors: levade t. Rev Neurol (Paris). 2007 Mar;163(3):359-61. doi: 10.1016/s0035-3787(07)90408-7. Rev Neurol (Paris). 2007. PMID: 17404523 French.

5

Functions of sphingolipid metabolism in mammals--lessons from genetic defects.

Sabourdy F, Kedjouar B, Sorli SC, Colié S, Milhas D, Salma Y, Levade T. Sabourdy F, et al. Among authors: levade t. Biochim Biophys Acta. 2008 Apr;1781(4):145-83. doi: 10.1016/j.bbalip.2008.01.004. Epub 2008 Feb 2. Biochim Biophys Acta. 2008. PMID: 18294974 Review.

6

Beta-mannosidosis: a new cause of spinocerebellar ataxia.

Labauge P, Renard D, Castelnovo G, Sabourdy F, de Champfleur N, Levade T. Labauge P, et al. Among authors: levade t. Clin Neurol Neurosurg. 2009 Jan;111(1):109-10. doi: 10.1016/j.clineuro.2008.09.007. Epub 2008 Nov 5. Clin Neurol Neurosurg. 2009. PMID: 18980795

7

Palmitoyl protein thioesterase 1 modulates tumor necrosis factor alpha-induced apoptosis.

Tardy C, Sabourdy F, Garcia V, Jalanko A, Therville N, Levade T, Andrieu-Abadie N. Tardy C, et al. Among authors: levade t. Biochim Biophys Acta. 2009 Jul;1793(7):1250-8. doi: 10.1016/j.bbamcr.2009.03.007. Epub 2009 Apr 5. Biochim Biophys Acta. 2009. PMID: 19345705 Free article.

8

Danon disease: further clinical and molecular heterogeneity.

Sabourdy F, Michelakakis H, Anastasakis A, Garcia V, Mavridou I, Nieto M, Pons MC, Skiadas C, Moraitou M, Manta P, Elleder M, Levade T. Sabourdy F, et al. Among authors: levade t. Muscle Nerve. 2009 Jun;39(6):837-44. doi: 10.1002/mus.21252. Muscle Nerve. 2009. PMID: 19373884

9

Danon disease: intrafamilial phenotypic variability related to a novel LAMP-2 mutation.

Cottinet SL, Bergemer-Fouquet AM, Toutain A, Sabourdy F, Maakaroun-Vermesse Z, Levade T, Chantepie A, Labarthe F. Cottinet SL, et al. Among authors: levade t. J Inherit Metab Dis. 2011 Apr;34(2):515-22. doi: 10.1007/s10545-010-9251-y. Epub 2010 Dec 16. J Inherit Metab Dis. 2011. PMID: 21161685

10

Genetic disorders of simple sphingolipid metabolism.

Albinet V, Bats ML, Bedia C, Sabourdy F, Garcia V, Ségui B, Andrieu-Abadie N, Hornemann T, Levade T. Albinet V, et al. Among authors: levade t. Handb Exp Pharmacol. 2013;(215):127-52. doi: 10.1007/978-3-7091-1368-4_7. Handb Exp Pharmacol. 2013. PMID: 23579453 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

299 results

Search Page

Filters