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Items: 1 to 20 of 161

1.

Long-term effect of thymectomy plus prednisone versus prednisone alone in patients with non-thymomatous myasthenia gravis: 2-year extension of the MGTX randomised trial.

Wolfe GI, Kaminski HJ, Aban IB, Minisman G, Kuo HC, Marx A, Ströbel P, Mazia C, Oger J, Cea JG, Heckmann JM, Evoli A, Nix W, Ciafaloni E, Antonini G, Witoonpanich R, King JO, Beydoun SR, Chalk CH, Barboi AC, Amato AA, Shaibani AI, Katirji B, Lecky BRF, Buckley C, Vincent A, Dias-Tosta E, Yoshikawa H, Waddington-Cruz M, Pulley MT, Rivner MH, Kostera-Pruszczyk A, Pascuzzi RM, Jackson CE, Verschuuren JJGM, Massey JM, Kissel JT, Werneck LC, Benatar M, Barohn RJ, Tandan R, Mozaffar T, Silvestri NJ, Conwit R, Sonett JR, Jaretzki A 3rd, Newsom-Davis J, Cutter GR; MGTX Study Group.

Lancet Neurol. 2019 Mar;18(3):259-268. doi: 10.1016/S1474-4422(18)30392-2. Epub 2019 Jan 25.

PMID:
30692052
2.

Evaluation of Left-Sided Heart Chambers With Novel Echocardiographic Techniques in Men With Duchenne or Becker Muscular Dystrophy.

Cirino RHD, Scola RH, Ducci RD, Camarozano AC, Kay CSK, Lorenzoni PJ, Werneck LC, Carmes ER, da Cunha CLP.

Am J Cardiol. 2019 Mar 15;123(6):972-978. doi: 10.1016/j.amjcard.2018.12.011. Epub 2018 Dec 19.

PMID:
30638960
3.

Clinical variability of children with anti-N-methyl-D-aspartate receptor encephalitis in southern Brazil: a cases series and review of the literature.

do Valle DA, Galeazzi JSP, Machado MR, Dos Santos VCSAR, da Silva AF, Lohr Júnior A, Santos MLSF, Scola RH.

Neurol Sci. 2019 Feb;40(2):351-356. doi: 10.1007/s10072-018-3648-z. Epub 2018 Nov 20. Review.

PMID:
30460460
4.

Multiple sclerosis: disease modifying therapy and the human leukocyte antigen.

Werneck LC, Lorenzoni PJ, Kay CSK, Scola RH.

Arq Neuropsiquiatr. 2018 Oct;76(10):697-704. doi: 10.1590/0004-282X20180103.

5.

Single-centre experience on genotypic and phenotypic features of southern Brazilian patients with McArdle disease.

Lorenzoni PJ, Werneck LC, Kay CSK, Arndt RC, Silvado CES, Scola RH.

Acta Neurol Belg. 2018 Nov 10. doi: 10.1007/s13760-018-1038-1. [Epub ahead of print]

PMID:
30415384
6.

A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis.

Fornari G, Gomes RR, Degenhardt-Goldbach J, Dos Santos SS, de Almeida SR, Dos Santos GD, Muro MD, Bona C, Scola RH, Trindade ES, Bini IH, Ferreira-Maba LS, Kestring DR, do Nascimento MMF, Lima BJFS, Voidaleski MF, Steinmacher DA, Soley BDS, Deng S, Bocca AL, da Silva MB, Salgado CG, de Azevedo CMPES, Vicente VA, de Hoog S.

Front Microbiol. 2018 Oct 9;9:2211. doi: 10.3389/fmicb.2018.02211. eCollection 2018.

7.

Motor neuron disease in patients with HIV infection: Report of two cases and brief review of the literature.

Lorenzoni PJ, Ducci RD, Dalledone GO, Kay CSK, de Almeida SM, Werneck LC, Scola RH.

Clin Neurol Neurosurg. 2018 Aug;171:139-142. doi: 10.1016/j.clineuro.2018.06.006. Epub 2018 Jun 10. Review.

PMID:
29909186
8.

Late-onset Pompe disease: what is the prevalence of limb-girdle muscular weakness presentation?

Lorenzoni PJ, Kay CSK, Higashi NS, D'Almeida V, Werneck LC, Scola RH.

Arq Neuropsiquiatr. 2018 Apr;76(4):247-251. doi: 10.1590/0004-282x20180018.

9.

Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness.

Owen D, Töpf A, Preethish-Kumar V, Lorenzoni PJ, Vroling B, Scola RH, Dias-Tosta E, Geraldo A, Polavarapu K, Nashi S, Cox D, Evangelista T, Dawson J, Thompson R, Senderek J, Laurie S, Beltran S, Gut M, Gut I, Nalini A, Lochmüller H.

Am J Med Genet A. 2018 Jul;176(7):1594-1601. doi: 10.1002/ajmg.a.38707. Epub 2018 Apr 28.

PMID:
29704306
10.

How to Spot Congenital Myasthenic Syndromes Resembling the Lambert-Eaton Myasthenic Syndrome? A Brief Review of Clinical, Electrophysiological, and Genetics Features.

Lorenzoni PJ, Scola RH, Kay CSK, Werneck LC, Horvath R, Lochmüller H.

Neuromolecular Med. 2018 Jun;20(2):205-214. doi: 10.1007/s12017-018-8490-1. Epub 2018 Apr 25. Review.

PMID:
29696584
11.

Lambert-Eaton myasthenic syndrome: the 60th anniversary of Eaton and Lambert's pioneering article.

Lorenzoni PJ, Kay CSK, Werneck LC, Scola RH.

Arq Neuropsiquiatr. 2018 Feb;76(2):124-126. doi: 10.1590/0004-282X20170194.

12.

Predictors of early left ventricular systolic dysfunction in duchenne muscular dystrophy patients.

Cirino RHD, Scola RH, Ducci RD, Wermelinger ACC, Kay CSK, Lorenzoni PJ, Werneck LC, Carmes ER, Da Cunha CLP.

Muscle Nerve. 2018 Feb 14. doi: 10.1002/mus.26102. [Epub ahead of print]

PMID:
29443387
13.

Immune-mediated rippling muscle disease in a patient with treated hypothyroidism.

Ducci RD, Scola RH, Lorenzoni PJ, Kay CSK, Blood MRY, Leão LG, Vainzof M, Werneck LC.

J Neurol Sci. 2017 Dec 15;383:53-55. doi: 10.1016/j.jns.2017.10.016. Epub 2017 Oct 13. No abstract available.

PMID:
29246623
14.

Brazilian consensus on Duchenne muscular dystrophy. Part 1: diagnosis, steroid therapy and perspectives.

Araujo APQC, Carvalho AAS, Cavalcanti EBU, Saute JAM, Carvalho E, França MC Junior, Martinez ARM, Navarro MMM, Nucci A, Resende MBD, Gonçalves MVM, Gurgel-Giannetti J, Scola RH, Sobreira CFDR, Reed UC, Zanoteli E.

Arq Neuropsiquiatr. 2017 Aug;75(8):104-113. doi: 10.1590/0004-282x20170112.

15.

Treatment of epilepsy in patients with myasthenia gravis: Is really harder than it looks?

Lorenzoni PJ, Ducci RD, Tensini TS, Dalledone G, Kay CSK, de Paola L, Werneck LC, Scola RH, Silvado C.

J Clin Neurosci. 2017 Oct;44:353-356. doi: 10.1016/j.jocn.2017.06.067. Epub 2017 Jul 29.

PMID:
28765064
16.

Is there a relationship between narcolepsy, multiple sclerosis and HLA-DQB1*06:02?

Lorenzoni PJ, Werneck LC, Crippa ACS, Zanatta A, Kay CSK, Silvado CES, Scola RH.

Arq Neuropsiquiatr. 2017 Jun;75(6):345-348. doi: 10.1590/0004-282X20170063.

17.

Flavivirus cross-reactivity in serological tests and Guillain-Barré syndrome in a hematopoietic stem cell transplant patient: A case report.

Raboni SM, Bonfim C, Almeida BM, Zanluca C, Koishi AC, Rodrigues PRVP, Kay CK, Ribeiro LL, Scola RH, Duarte Dos Santos CN.

Transpl Infect Dis. 2017 Aug;19(4). doi: 10.1111/tid.12700. Epub 2017 Jul 3.

PMID:
28306183
18.

Clinical follow-up of pregnancy in myasthenia gravis patients.

Ducci RD, Lorenzoni PJ, Kay CS, Werneck LC, Scola RH.

Neuromuscul Disord. 2017 Apr;27(4):352-357. doi: 10.1016/j.nmd.2017.01.021. Epub 2017 Feb 1.

PMID:
28256306
19.

Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndrome.

Shen XM, Scola RH, Lorenzoni PJ, Kay CS, Werneck LC, Brengman J, Selcen D, Engel AG.

Ann Clin Transl Neurol. 2017 Jan 16;4(2):130-138. doi: 10.1002/acn3.387. eCollection 2017 Feb. Erratum in: Ann Clin Transl Neurol. 2017 May 08;4(5):356.

20.

Hereditary Neuropathy With Liability to Pressure Palsies: A Single-Center Experience in Southern Brazil.

Lorenzoni PJ, Kay CS, Cavalet C, Arndt RC, Werneck LC, Scola RH.

Neurol Int. 2016 Sep 30;8(3):6677. eCollection 2016 Sep 30.

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