Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 53

1.

We need a new concept: from complementary examination to a source of value.

Vedolin L.

Radiol Bras. 2019 Jul-Aug;52(4):VII. doi: 10.1590/0100-3984.2019.52.4e2. No abstract available.

2.

Predictors of objective cognitive impairment and subjective cognitive complaints in patients with Fabry disease.

Körver S, Geurtsen GJ, Hollak CEM, van Schaik IN, Longo MGF, Lima MR, Vedolin L, Dijkgraaf MGW, Langeveld M.

Sci Rep. 2019 Jan 17;9(1):188. doi: 10.1038/s41598-018-37320-0.

3.

Methylphenidate Alters Functional Connectivity of Default Mode Network in Drug-Naive Male Adults With ADHD.

Picon FA, Sato JR, Anés M, Vedolin LM, Mazzola AA, Valentini BB, Cupertino RB, Karam RG, Victor MM, Breda V, Silva K, da Silva N Jr, Bau CHD, Grevet EH, Rohde LAP.

J Atten Disord. 2018 Dec 10:1087054718816822. doi: 10.1177/1087054718816822. [Epub ahead of print]

PMID:
30526190
4.

Reproducibility of a quantitative system for assessing the quality of diagnostic ultrasound.

Iared W, Puchnick A, Bancovsky E, Bettini PR, Vedolin LM, Chammas MC.

Radiol Bras. 2018 May-Jun;51(3):172-177. doi: 10.1590/0100-3984.2017.0021.

5.

Therapeutic hypothermia for neonatal hypoxic-ischemic encephalopathy: magnetic resonance imaging findings and neurological outcomes in a Brazilian cohort.

Procianoy RS, Corso AL, Longo MG, Vedolin L, Silveira RC.

J Matern Fetal Neonatal Med. 2019 Aug;32(16):2727-2734. doi: 10.1080/14767058.2018.1448773. Epub 2018 Mar 13.

PMID:
29504433
6.

Globus pallidus restricted diffusion associated with vigabatrin therapy.

Trindade RAR, Wainstein B, Campos LG, Pérez JA, Bianchin MM, Vedolin LM, Duarte JÁ.

Arq Neuropsiquiatr. 2018 Feb;76(2):127-128. doi: 10.1590/0004-282X20170192. No abstract available.

7.

Surgical management of neurological manifestations of mucopolysaccharidosis disorders.

Alden TD, Amartino H, Dalla Corte A, Lampe C, Harmatz PR, Vedolin L.

Mol Genet Metab. 2017 Dec;122S:41-48. doi: 10.1016/j.ymgme.2017.09.011. Epub 2017 Sep 28. Review.

8.

Quantitative neuroimaging in mucopolysaccharidoses clinical trials.

Nestrasil I, Vedolin L.

Mol Genet Metab. 2017 Dec;122S:17-24. doi: 10.1016/j.ymgme.2017.09.006. Epub 2017 Sep 15. Review.

9.

Correction to: Correlation of CSF flow using phase-contrast MRI with ventriculomegaly and CSF opening pressure in mucopolysaccharidoses.

Corte AD, de Souza CFM, Anés M, Maeda FK, Lokossou A, Vedolin LM, Longo MG, Ferreira MM, Perrone SGP, Balédent O, Giugliani R.

Fluids Barriers CNS. 2017 Oct 13;14(1):28. doi: 10.1186/s12987-017-0076-z.

10.

Breast cancer mammographic diagnosis performance in a public health institution: a retrospective cohort study.

Mello JMRB, Bittelbrunn FP, Rockenbach MABC, May GG, Vedolin LM, Kruger MS, Soldatelli MD, Zwetsch G, de Miranda GTF, Teixeira SIP, Arruda BS.

Insights Imaging. 2017 Dec;8(6):581-588. doi: 10.1007/s13244-017-0573-2. Epub 2017 Oct 4.

11.

Correlation of CSF flow using phase-contrast MRI with ventriculomegaly and CSF opening pressure in mucopolysaccharidoses.

Corte AD, de Souza CFM, Anés M, Maeda FK, Lokossou A, Vedolin LM, Longo MG, Ferreira MM, Perrone SGP, Balédent O, Giugliani R.

Fluids Barriers CNS. 2017 Sep 18;14(1):23. doi: 10.1186/s12987-017-0073-2. Erratum in: Fluids Barriers CNS. 2017 Oct 13;14 (1):28.

12.

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.

Arq Neuropsiquiatr. 2017 Jun;75(6):339-344. doi: 10.1590/0004-282X20170044.

13.

Pilomyxoid astrocytoma of the corpus callosum presenting with primary haemorrhage in an adolescent.

Longo M, Adams Perez J, Oliveira F, Antunes A, Vedolin L, Duarte JA.

BJR Case Rep. 2017 Jan 7;3(2):20150020. doi: 10.1259/bjrcr.20150020. eCollection 2017.

14.

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.

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

15.

Rhombencephalitis: pictorial essay.

Campos LG, Trindade RA, Faistauer Â, Pérez JA, Vedolin LM, Duarte JÁ.

Radiol Bras. 2016 Sep-Oct;49(5):329-336.

16.

Neuroimaging Findings in Patients with Mucopolysaccharidosis: What You Really Need to Know.

Reichert R, Campos LG, Vairo F, de Souza CF, Pérez JA, Duarte JÁ, Leiria FA, Anés M, Vedolin LM.

Radiographics. 2016 Sep-Oct;36(5):1448-62. doi: 10.1148/rg.2016150168. Review.

PMID:
27618324
17.

Intracranial extra-axial hemangioma in a newborn: A case report and literature review.

Dalsin M, Silva RS, Galdino Chaves JP, Oliveira FH, Martins Antunes ÁC, Vedolin LM.

Surg Neurol Int. 2016 May 13;7(Suppl 12):S314-6. doi: 10.4103/2152-7806.182414. eCollection 2016.

18.

MR Imaging in Spinocerebellar Ataxias: A Systematic Review.

Klaes A, Reckziegel E, Franca MC Jr, Rezende TJ, Vedolin LM, Jardim LB, Saute JA.

AJNR Am J Neuroradiol. 2016 Aug;37(8):1405-12. doi: 10.3174/ajnr.A4760. Epub 2016 May 12.

19.

Author Response.

Fernandes GC, Rieder CR, Vedolin L, Campos L, Koltermann T.

Neurology. 2015 Aug 18;85(7):655. No abstract available.

PMID:
26505051
20.

Identification of a premature stop codon mutation in the PHGDH gene in severe Neu-Laxova syndrome-evidence for phenotypic variability.

Mattos EP, Silva AA, Magalhães JA, Leite JC, Leistner-Segal S, Gus-Kessler R, Perez JA, Vedolin LM, Torreblanca-Zanca A, Lapunzina P, Ruiz-Perez VL, Sanseverino MT.

Am J Med Genet A. 2015 Jun;167(6):1323-9. doi: 10.1002/ajmg.a.36930. Epub 2015 Apr 25.

PMID:
25913727
21.

Teaching NeuroImages: the lentiform fork sign: an MRI pattern of metformin-associated encephalopathy.

Fernandes GC, Koltermann T, Campos L, Vedolin L, Rieder CR.

Neurology. 2015 Jan 20;84(3):e15. doi: 10.1212/WNL.0000000000001154. No abstract available.

PMID:
25601887
22.

Brain imaging and genetic risk in the pediatric population, part 2: congenital malformations of the central nervous system.

Longo MG, Félix TM, Ashton-Prolla P, Vedolin LM.

Neuroimaging Clin N Am. 2015 Feb;25(1):53-67. doi: 10.1016/j.nic.2014.09.003.

PMID:
25476512
23.

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

Longo MG, Vairo F, Souza CF, Giugliani R, Vedolin LM.

Neuroimaging Clin N Am. 2015 Feb;25(1):31-51. doi: 10.1016/j.nic.2014.09.004. Review.

PMID:
25476511
24.

Reproducibility of quantitative fiber tracking measurements in diffusion tensor imaging of frontal lobe tracts: A protocol based on the fiber dissection technique.

Dini LI, Vedolin LM, Bertholdo D, Grando RD, Mazzola A, Dini SA, Isolan GR, da Costa JC, Campero A.

Surg Neurol Int. 2013 Apr 12;4:51. doi: 10.4103/2152-7806.110508. Print 2013.

25.

Reply: To PMID 23328073.

Vedolin L.

AJNR Am J Neuroradiol. 2013 Feb;34(2):E23. No abstract available.

26.

Brain magnetic resonance imaging findings in patients with mucopolysaccharidosis VI.

Azevedo AC, Artigalás O, Vedolin L, Komlós M, Pires A, Giugliani R, Schwartz IV.

J Inherit Metab Dis. 2013 Mar;36(2):357-62. doi: 10.1007/s10545-012-9559-x. Epub 2012 Nov 21.

PMID:
23179553
27.

Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI.

González G, Vedolin L, Barry B, Poduri A, Walsh C, Barkovich AJ.

AJNR Am J Neuroradiol. 2013 Apr;34(4):877-83. doi: 10.3174/ajnr.A3312. Epub 2012 Oct 11.

28.

Guidelines for acute ischemic stroke treatment: part I.

Oliveira-Filho J, Martins SC, Pontes-Neto OM, Longo A, Evaristo EF, Carvalho JJ, Fernandes JG, Zétola VF, Gagliardi RJ, Vedolin L, Freitas GR; Executive Committee from Brazilian Stroke Society and the Scientific Department in Cerebrovascular Diseases.

Arq Neuropsiquiatr. 2012 Aug;70(8):621-9. No abstract available.

29.

Inherited cerebellar ataxia in childhood: a pattern-recognition approach using brain MRI.

Vedolin L, Gonzalez G, Souza CF, Lourenço C, Barkovich AJ.

AJNR Am J Neuroradiol. 2013 May;34(5):925-34, S1-2. doi: 10.3174/ajnr.A3055. Epub 2012 May 17. Review.

30.

Intra-arterial infusion of autologous bone marrow mononuclear cells in patients with moderate to severe middle cerebral artery acute ischemic stroke.

Friedrich MA, Martins MP, Araújo MD, Klamt C, Vedolin L, Garicochea B, Raupp EF, Sartori El Ammar J, Machado DC, Costa JC, Nogueira RG, Rosado-de-Castro PH, Mendez-Otero R, Freitas GR.

Cell Transplant. 2012;21 Suppl 1:S13-21. doi: 10.3727/096368912X612512.

PMID:
22507676
31.

Neuroimaging of Dandy-Walker malformation: new concepts.

Correa GG, Amaral LF, Vedolin LM.

Top Magn Reson Imaging. 2011 Dec;22(6):303-12. doi: 10.1097/RMR.0b013e3182a2ca77. Review.

PMID:
24132069
32.

Basic genetic principles applied to posterior fossa malformations.

Nunes RH, Littig IA, da Rocha AJ, Vedolin L.

Top Magn Reson Imaging. 2011 Dec;22(6):261-70. doi: 10.1097/RMR.0b013e3182a6d652. Review.

PMID:
24132065
33.

Congenital malformation of the posterior fossa: new insights.

Vedolin L.

Top Magn Reson Imaging. 2011 Dec;22(6):259. doi: 10.1097/RMR.0b013e3182a6e1e8. No abstract available.

PMID:
24132064
34.

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.

Cerebellum. 2012 Sep;11(3):771-4. doi: 10.1007/s12311-011-0326-6. Erratum in: Cerebellum. 2012 Sep;11(3):775-6.

PMID:
22090366
35.

Inherited white matter disorders of childhood: a magnetic resonance imaging-based pattern recognition approach.

Vedolin L.

Top Magn Reson Imaging. 2011 Oct;22(5):215-22. doi: 10.1097/RMR.0b013e318295b416.

PMID:
24562091
36.

The basis of inborn errors of metabolism for neuroradiologists.

Vairo F, Vedolin L.

Top Magn Reson Imaging. 2011 Oct;22(5):209-14. doi: 10.1097/RMR.0b013e31829689bd. Review.

PMID:
24562090
37.

White matter disorders of childhood.

Vedolin L.

Top Magn Reson Imaging. 2011 Oct;22(5):207. doi: 10.1097/RMR.0b013e3182968005. No abstract available.

PMID:
24562089
38.

Topiramate is effective for status epilepticus and seizure control in neuraminidase deficiency.

Bragatti JA, Torres CM, Netto CB, Vedolin L, Garzon E, Rieder CR, Schwartz IV, Bianchin MM.

Arq Neuropsiquiatr. 2011 Jun;69(3):565-6. No abstract available.

39.

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.

Mov Disord. 2011 Mar;26(4):731-5. doi: 10.1002/mds.23428. Epub 2010 Nov 10.

PMID:
21506152
40.

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.

Am J Med Genet A. 2011 Jan;155A(1):50-7. doi: 10.1002/ajmg.a.33770.

PMID:
21204210
41.

Optic nerve enlargement and leukodystrophy: an unusual finding of the infantile form of Krabbe disease.

Garcia AM, Morais NM, Ohlweiler L, Winckler MI, Ranzan J, Artigalás OA, Pinto LL, Netto CB, Ashton-Prolla P, Vedolin L, Riesgo Rdos S, Rotta NT.

Arq Neuropsiquiatr. 2010 Oct;68(5):816-8. No abstract available.

42.

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.

Cerebellum. 2010 Dec;9(4):603-5; author reply 606-7. doi: 10.1007/s12311-010-0205-6. No abstract available.

PMID:
20734176
43.

X-linked adrenoleukodystrophy: clinical course and minimal incidence in South Brazil.

Jardim LB, da Silva AC, Blank D, Villanueva MM, Renck L, Costa ML, Vargas CR, Deon M, Coelho Dl, Vedolin L, de Castro CG Jr, Gregianin L, Bonfim C, Giugliani R.

Brain Dev. 2010 Mar;32(3):180-90. doi: 10.1016/j.braindev.2009.02.002. Epub 2009 Mar 6.

PMID:
19269120
44.

Progressive multifocal leukoencephalopathy in a kidney transplant recipient after conversion to mycophenolic acid therapy.

Manfro RC, Vedolin L, Cantarelli M, Oppitz P, Antunes AC, Rieder CR.

Transpl Infect Dis. 2009 Apr;11(2):189-90. doi: 10.1111/j.1399-3062.2009.00368.x. Epub 2009 Feb 5.

PMID:
19210690
45.

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.

Am J Med Genet A. 2008 Oct 1;146A(19):2538-44. doi: 10.1002/ajmg.a.32294.

PMID:
18792977
46.

Magnetic resonance imaging findings in Hunter syndrome.

Finn CT, Vedolin L, Schwartz IV, Giugliani R, Haws CA, Prescot AP, Renshaw PF.

Acta Paediatr. 2008 Apr;97(457):61-8. doi: 10.1111/j.1651-2227.2008.00646.x. Review.

PMID:
18339191
47.

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

Santos C, Wanderley H, Vedolin L, Pena SD, Jardim L, Sequeiros J.

Clin Genet. 2008 May;73(5):480-5. doi: 10.1111/j.1399-0004.2008.00981.x. Epub 2008 Mar 12.

PMID:
18341606
48.

Brain MRI in mucopolysaccharidosis: effect of aging and correlation with biochemical findings.

Vedolin L, Schwartz IV, Komlos M, Schuch A, Azevedo AC, Vieira T, Maeda FK, Marques da Silva AM, Giugliani R.

Neurology. 2007 Aug 28;69(9):917-24.

PMID:
17724296
49.

Correlation of MR imaging and MR spectroscopy findings with cognitive impairment in mucopolysaccharidosis II.

Vedolin L, Schwartz IV, Komlos M, Schuch A, Puga AC, Pinto LL, Pires AP, Giugliani R.

AJNR Am J Neuroradiol. 2007 Jun-Jul;28(6):1029-33.

50.

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.

Arq Neuropsiquiatr. 2006 Sep;64(3B):711-7.

Supplemental Content

Loading ...
Support Center