Matte U - Search Results

1

Mutations, clinical findings and survival estimates in South American patients with X-linked adrenoleukodystrophy.

Pereira Fdos S, Matte U, Habekost CT, de Castilhos RM, El Husny AS, Lourenço CM, Vianna-Morgante AM, Giuliani L, Galera MF, Honjo R, Kim CA, Politei J, Vargas CR, Jardim LB. Pereira Fdos S, et al. Among authors: matte u. PLoS One. 2012;7(3):e34195. doi: 10.1371/journal.pone.0034195. Epub 2012 Mar 29. PLoS One. 2012. PMID: 22479560 Free PMC article.

2

Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients.

Matte U, Yogalingam G, Brooks D, Leistner S, Schwartz I, Lima L, Norato DY, Brum JM, Beesley C, Winchester B, Giugliani R, Hopwood JJ. Matte U, et al. Mol Genet Metab. 2003 Jan;78(1):37-43. doi: 10.1016/s1096-7192(02)00200-7. Mol Genet Metab. 2003. PMID: 12559846

3

CNS involvement in Fabry disease: clinical and imaging studies before and after 12 months of enzyme replacement therapy.

Jardim L, Vedolin L, Schwartz IV, Burin MG, Cecchin C, Kalakun L, Matte U, Aesse F, Pitta-Pinheiro C, Marconato J, Giugliani R. Jardim L, et al. Among authors: matte u. J Inherit Metab Dis. 2004;27(2):229-40. doi: 10.1023/B:BOLI.0000028794.04349.91. J Inherit Metab Dis. 2004. PMID: 15159654 Clinical Trial.

4

Adult derived mononuclear bone marrow cells improve survival in a model of acetaminophen-induced acute liver failure in rats.

Belardinelli MC, Pereira F, Baldo G, Vicente Tavares AM, Kieling CO, da Silveira TR, Meurer L, Soares Duarte ME, Giugliani R, Matte U. Belardinelli MC, et al. Among authors: matte u. Toxicology. 2008 May 2;247(1):1-5. doi: 10.1016/j.tox.2008.01.015. Epub 2008 Feb 1. Toxicology. 2008. PMID: 18336983

5

Fabry disease in hemodialysis patients in southern Brazil: prevalence study and clinical report.

Porsch DB, Nunes AC, Milani V, Rossato LB, Mattos CB, Tsao M, Netto C, Burin M, Pereira F, Matte U, Giugliani R, Barros EJ. Porsch DB, et al. Among authors: matte u. Ren Fail. 2008;30(9):825-30. doi: 10.1080/08860220802353777. Ren Fail. 2008. PMID: 18925518

6

Kidney function and 24-hour proteinuria in patients with Fabry disease during 36 months of agalsidase alfa enzyme replacement therapy: a Brazilian experience.

Thofehrn S, Netto C, Cecchin C, Burin M, Matte U, Brustolin S, Nunes AC, Coelho J, Tsao M, Jardim L, Giugliani R, Barros EJ. Thofehrn S, et al. Among authors: matte u. Ren Fail. 2009;31(9):773-8. doi: 10.3109/08860220903150296. Ren Fail. 2009. PMID: 19925283 Clinical Trial.

7

Genotypic and phenotypic characterization of Brazilian patients with GM1 gangliosidosis.

Sperb F, Vairo F, Burin M, Mayer FQ, Matte U, Giugliani R. Sperb F, et al. Among authors: matte u. Gene. 2013 Jan 1;512(1):113-6. doi: 10.1016/j.gene.2012.09.106. Epub 2012 Oct 6. Gene. 2013. PMID: 23046582 Free article.

8

Mucolipidosis II and III alpha/beta in Brazil: analysis of the GNPTAB gene.

Cury GK, Matte U, Artigalás O, Alegra T, Velho RV, Sperb F, Burin MG, Ribeiro EM, Lourenço CM, Kim CA, Valadares ER, Galera MF, Acosta AX, Schwartz IV. Cury GK, et al. Among authors: matte u. Gene. 2013 Jul 15;524(1):59-64. doi: 10.1016/j.gene.2013.03.105. Epub 2013 Apr 6. Gene. 2013. PMID: 23566849 Free article.

9

Neurological impairment among heterozygote women for X-linked Adrenoleukodystrophy: a case control study on a clinical, neurophysiological and biochemical characteristics.

Habekost CT, Schestatsky P, Torres VF, de Coelho DM, Vargas CR, Torrez V, Oses JP, Portela LV, Pereira Fdos S, Matte U, Jardim LB. Habekost CT, et al. Among authors: matte u. Orphanet J Rare Dis. 2014 Jan 13;9:6. doi: 10.1186/1750-1172-9-6. Orphanet J Rare Dis. 2014. PMID: 24410807 Free PMC article.

10

Progression rate of myelopathy in X-linked adrenoleukodystrophy heterozygotes.

Habekost CT, Pereira FS, Vargas CR, Coelho DM, Torrez V, Oses JP, Portela LV, Schestatsky P, Felix VT, Matte U, Torman VL, Jardim LB. Habekost CT, et al. Among authors: matte u. Metab Brain Dis. 2015 Oct;30(5):1279-84. doi: 10.1007/s11011-015-9672-2. Epub 2015 Apr 30. Metab Brain Dis. 2015. PMID: 25920484

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