Vedolin L - Search Results

1

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. Among authors: vedolin l. Cerebellum. 2012 Sep;11(3):771-4. doi: 10.1007/s12311-011-0326-6. Cerebellum. 2012. PMID: 22090366

2

Serum insulin-like system alterations in patients with spinocerebellar ataxia type 3.

Saute JA, da Silva AC, Muller AP, Hansel G, de Mello AS, Maeda F, Vedolin L, Saraiva-Pereira ML, Souza DO, Arpa J, Torres-Aleman I, Portela LV, Jardim LB. Saute JA, et al. Among authors: vedolin l. Mov Disord. 2011 Mar;26(4):731-5. doi: 10.1002/mds.23428. Epub 2010 Nov 10. Mov Disord. 2011. PMID: 21506152

3

Depressive mood is associated with ataxic and non-ataxic neurological dysfunction in SCA3 patients.

Saute JA, da Silva AC, Donis KC, Vedolin L, Saraiva-Pereira ML, Jardim LB. Saute JA, et al. Among authors: vedolin l. Cerebellum. 2010 Dec;9(4):603-5; author reply 606-7. doi: 10.1007/s12311-010-0205-6. Cerebellum. 2010. PMID: 20734176 No abstract available.

4

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. Arq Neuropsiquiatr. 2016 Dec;74(12):953-966. doi: 10.1590/0004-282X20160155. Arq Neuropsiquiatr. 2016. PMID: 27991992 Free article.

5

MR Imaging in Spinocerebellar Ataxias: A Systematic Review.

Klaes A, Reckziegel E, Franca MC Jr, Rezende TJ, Vedolin LM, Jardim LB, Saute JA. Klaes A, et al. Among authors: vedolin lm. AJNR Am J Neuroradiol. 2016 Aug;37(8):1405-12. doi: 10.3174/ajnr.A4760. Epub 2016 May 12. AJNR Am J Neuroradiol. 2016. PMID: 27173364 Free PMC article.

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. 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

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.

9

Huntington disease-like 2: the first patient with apparent European ancestry.

Santos C, Wanderley H, Vedolin L, Pena SD, Jardim L, Sequeiros J. Santos C, et al. Among authors: vedolin l. Clin Genet. 2008 May;73(5):480-5. doi: 10.1111/j.1399-0004.2008.00981.x. Epub 2008 Mar 12. Clin Genet. 2008. PMID: 18341606

10

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. 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

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