Vedolin LM - Search Results

1

White matter lesions in Fabry disease before and after enzyme replacement therapy: a 2-year follow-up.

Jardim LB, Aesse F, Vedolin LM, Pitta-Pinheiro C, Marconato J, Burin MG, Cecchin C, Netto CB, Matte US, Pereira F, Kalakun L, Giugliani R. Jardim LB, et al. Among authors: vedolin lm. Arq Neuropsiquiatr. 2006 Sep;64(3B):711-7. doi: 10.1590/s0004-282x2006000500002. Arq Neuropsiquiatr. 2006. PMID: 17057872 Free article.

2

Neurological outcomes after hematopoietic stem cell transplantation for cerebral X-linked adrenoleukodystrophy, late onset metachromatic leukodystrophy and Hurler syndrome.

Saute JA, Souza CF, Poswar FO, Donis KC, Campos LG, Deyl AV, Burin MG, Vargas CR, Matte UD, Giugliani R, Saraiva-Pereira ML, Vedolin LM, Gregianin LJ, Jardim LB. Saute JA, et al. Among authors: vedolin lm. Arq Neuropsiquiatr. 2016 Dec;74(12):953-966. doi: 10.1590/0004-282X20160155. Arq Neuropsiquiatr. 2016. PMID: 27991992 Free article.

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. 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

Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression.

Munoz-Rojas MV, Vieira T, Costa R, Fagondes S, John A, Jardim LB, Vedolin LM, Raymundo M, Dickson PI, Kakkis E, Giugliani R. Munoz-Rojas MV, et al. Among authors: vedolin lm. Am J Med Genet A. 2008 Oct 1;146A(19):2538-44. doi: 10.1002/ajmg.a.32294. Am J Med Genet A. 2008. PMID: 18792977

5

Brain imaging and genetic risk in the pediatric population, part 1: inherited metabolic diseases.

Longo MG, Vairo F, Souza CF, Giugliani R, Vedolin LM. Longo MG, et al. Among authors: vedolin lm. Neuroimaging Clin N Am. 2015 Feb;25(1):31-51. doi: 10.1016/j.nic.2014.09.004. Neuroimaging Clin N Am. 2015. PMID: 25476511 Review.

6

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a family report from South Brazil.

Burguêz D, Oliveira CM, Rockenbach MABC, Fussiger H, Vedolin LM, Winckler PB, Maestri MK, Finkelsztejn A, Santorelli FM, Jardim LB, Saute JAM. Burguêz D, et al. Among authors: vedolin lm. Arq Neuropsiquiatr. 2017 Jun;75(6):339-344. doi: 10.1590/0004-282X20170044. Arq Neuropsiquiatr. 2017. PMID: 28658401 Free article.

7

Conventional MRI and MR spectroscopy in nonclassical mitochondrial disease: report of three patients with mitochondrial DNA deletion.

Vedolin L, de Souza CF, Silveira RS, Lopes BC, Laybauer LS, Saraiva Pereira ML, Giugliani R. Vedolin L, et al. Childs Nerv Syst. 2006 Oct;22(10):1355-9. doi: 10.1007/s00381-006-0082-y. Epub 2006 Mar 22. Childs Nerv Syst. 2006. PMID: 16552564

8

Brain magnetic resonance imaging findings in patients with mucopolysaccharidosis VI.

Azevedo AC, Artigalás O, Vedolin L, Komlós M, Pires A, Giugliani R, Schwartz IV. Azevedo AC, et al. J Inherit Metab Dis. 2013 Mar;36(2):357-62. doi: 10.1007/s10545-012-9559-x. Epub 2012 Nov 21. J Inherit Metab Dis. 2013. PMID: 23179553

9

Are MPS II heterozygotes actually asymptomatic? A study based on clinical and biochemical data, X-inactivation analysis and imaging evaluations.

de Camargo Pinto LL, Maluf SW, Leistner-Segal S, Zimmer da Silva C, Brusius-Facchin A, Burin MG, Brustolin S, Llerena J, Moraes L, Vedolin L, Schuch A, Giugliani R, Schwartz IV. de Camargo Pinto LL, et al. Am J Med Genet A. 2011 Jan;155A(1):50-7. doi: 10.1002/ajmg.a.33770. Am J Med Genet A. 2011. PMID: 21204210

10

Body mass index is inversely correlated with the expanded CAG repeat length in SCA3/MJD patients.

Saute JA, Silva AC, Souza GN, Russo AD, Donis KC, Vedolin L, Saraiva-Pereira ML, Portela LV, Jardim LB. Saute JA, et al. Cerebellum. 2012 Sep;11(3):771-4. doi: 10.1007/s12311-011-0326-6. Cerebellum. 2012. PMID: 22090366

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