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Items: 1 to 50 of 208

1.

Sleep Disorders in Hereditary Ataxias.

Huebra L, Coelho FM, Filho FMR, Barsottini OG, Pedroso JL.

Curr Neurol Neurosci Rep. 2019 Jul 25;19(8):59. doi: 10.1007/s11910-019-0968-1. Review.

PMID:
31342187
2.

Teaching Video NeuroImages: Hepatic myelopathy: An unusual neurologic complication of hepatic encephalopathy.

Ciarlariello VB, Fujino MVT, Almeida MD, Barsottini OGP, Pedroso JL.

Neurology. 2019 Jul 16;93(3):e320-e321. doi: 10.1212/WNL.0000000000007782. No abstract available.

PMID:
31308174
3.

The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force.

Beaudin M, Matilla-Dueñas A, Soong BW, Pedroso JL, Barsottini OG, Mitoma H, Tsuji S, Schmahmann JD, Manto M, Rouleau GA, Klein C, Dupre N.

Cerebellum. 2019 Jul 2. doi: 10.1007/s12311-019-01052-2. [Epub ahead of print] Review.

PMID:
31267374
4.

Late-onset hummingbird sign in a woman with fragile X premutation.

Salomão RP, Vale TC, Marussi VHR, Barsottini OGP, Pedroso JL.

J Neurol Sci. 2019 Jun 20;403:75-77. doi: 10.1016/j.jns.2019.06.016. [Epub ahead of print] No abstract available.

PMID:
31229851
5.

Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach.

Barsottini OG, Pedroso JL, Martins CR Jr, França MC Jr, Albernaz PM.

Cerebellum. 2019 Jun 1. doi: 10.1007/s12311-019-01042-4. [Epub ahead of print] Review.

PMID:
31154624
6.

Septo-optic dysplasia with late-onset seizure: MRI and ophthalmological features.

Freitas JL, Rezende Filho FM, Lucato LT, Sallum JM, Pedroso JL, Barsottini OG.

Arq Neuropsiquiatr. 2019 May 13;77(4):294-295. doi: 10.1590/0004-282X20190039. No abstract available.

7.

Cognitive and Psychiatric Evaluation in SYNE1 Ataxia.

Gama MTD, Braga-Neto P, Dutra LA, Alessi H, Maria LA, Gadelha AA, Ortiz BB, Kunii I, Correia-Silva SR, Dias da Silva MR, Dion PA, Rouleau GA, França MC Jr, Barsottini OGP, Pedroso JL.

Cerebellum. 2019 Aug;18(4):731-737. doi: 10.1007/s12311-019-01033-5.

PMID:
31049853
8.

Acute cerebellar ataxia: differential diagnosis and clinical approach.

Pedroso JL, Vale TC, Braga-Neto P, Dutra LA, França MC Jr, Teive HAG, Barsottini OGP.

Arq Neuropsiquiatr. 2019 Mar;77(3):184-193. doi: 10.1590/0004-282X20190020.

9.

Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia.

Godeiro Junior CO, Vale TC, Afonso COM, Kok F, Pedroso JL, Barsottini OG.

Mov Disord Clin Pract. 2018 Mar 30;5(3):330-332. doi: 10.1002/mdc3.12610. eCollection 2018 May-Jun. No abstract available.

10.

Arm Levitation as Initial Manifestation of Creutzfeldt-Jakob Disease: Case Report and Review of the Literature.

Ciarlariello VB, Barsottini OGP, Espay AJ, Pedroso JL.

Tremor Other Hyperkinet Mov (N Y). 2018 Dec 10;8:572. doi: 10.7916/D80C6CGX. eCollection 2018. Review.

11.

Transcranial Doppler findings in antiphospholipid syndrome.

Ricarte IF, Dutra LA, Barsottini OGP, Souza AWS, Andrade DCO, Mangueira C, Silva GS.

Lupus. 2019 Apr;28(4):483-491. doi: 10.1177/0961203319828833. Epub 2019 Feb 12.

PMID:
30755144
12.

Tractography study in a patient with hemidystonia-hemiatrophy syndrome.

Barcellos I, Vale TC, Pedroso JL, Tibana LAT, Barsottini OGP.

Mov Disord Clin Pract. 2018 Jan 18;5(2):200-202. doi: 10.1002/mdc3.12579. eCollection 2018 Mar-Apr. No abstract available.

13.

Movement Disorders in Metabolic Disorders.

Pedroso JL, Barsottini OG, Espay AJ.

Curr Neurol Neurosci Rep. 2019 Feb 9;19(2):7. doi: 10.1007/s11910-019-0921-3. Review.

PMID:
30739241
14.

Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.

da Graça FF, de Rezende TJR, Vasconcellos LFR, Pedroso JL, Barsottini OGP, França MC Jr.

Front Neurol. 2019 Jan 16;9:1117. doi: 10.3389/fneur.2018.01117. eCollection 2018. Review.

15.

Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS.

Rezende Filho FM, Parkinson MH, Pedroso JL, Poh R, Faber I, Lourenço CM, Júnior WM, França Junior MC, Kok F, Sallum JMF, Giunti P, Barsottini OGP.

Parkinsonism Relat Disord. 2019 May;62:148-155. doi: 10.1016/j.parkreldis.2018.12.024. Epub 2018 Dec 23.

PMID:
30638817
16.

Facial grimacing and clinical correlates in spinocerebellar ataxia type 3.

Rezende Filho FM, Vale TC, Pedroso JL, Braga-Neto P, Barsottini OG.

J Neurol Sci. 2019 Feb 15;397:138-140. doi: 10.1016/j.jns.2019.01.001. Epub 2019 Jan 2.

PMID:
30616057
17.

Autonomic dysfunction in hereditary spastic paraplegia type 4.

González-Salazar C, Takazaki KAG, Martinez ARM, Pimentel-Silva LR, Jacinto-Scudeiro LA, Nakagawa ÉY, Fujiwara Murakami CE, Saute JAM, Pedroso JL, Barsottini OGP, Teive HAG, França MC Jr.

Eur J Neurol. 2019 Apr;26(4):687-693. doi: 10.1111/ene.13878. Epub 2019 Jan 10.

PMID:
30489674
18.

Cross-cultural adaptation and validation of the International Cooperative Ataxia Rating Scale (ICARS) to Brazilian Portuguese.

Maggi FA, Braga-Neto P, Chien HF, Gama MTD, Rezende Filho FM, Saraiva-Pereira ML, Jardim LB, Voos MC, Pedroso JL, Barsottini OGP.

Arq Neuropsiquiatr. 2018 Oct;76(10):674-684. doi: 10.1590/0004-282X20180098.

19.

An Unusual Fundus Finding in a Teenage Girl.

Rezende Filho FM, Pedroso JL, Barsottini OGP.

JAMA Neurol. 2018 Dec 1;75(12):1566-1567. doi: 10.1001/jamaneurol.2018.3108. No abstract available.

PMID:
30326009
20.

Structural signature in SCA1: clinical correlates, determinants and natural history.

Martins Junior CR, Martinez ARM, Vasconcelos IF, de Rezende TJR, Casseb RF, Pedroso JL, Barsottini OGP, Lopes-Cendes Í, França MC Jr.

J Neurol. 2018 Dec;265(12):2949-2959. doi: 10.1007/s00415-018-9087-1. Epub 2018 Oct 15.

PMID:
30324307
21.

SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response.

Faber I, Martinez ARM, Martins CR Jr, Maia ML, Souza JP, Lourenço CM, Marques W Jr, Montecchiani C, Orlacchio A, Pedroso JL, Barsottini OGP, Ramos CD, Lopes-Cendes Í, Friedman JH, Amorim BJ, França MC Jr.

Mov Disord. 2018 Oct;33(10):1650-1656. doi: 10.1002/mds.27491. Epub 2018 Oct 10.

PMID:
30306626
22.

Twenty-five years since the identification of the first SCA gene: history, clinical features and perspectives for SCA1.

Martins Junior CR, Borba FC, Martinez ARM, Rezende TJR, Cendes IL, Pedroso JL, Barsottini OGP, França Júnior MC.

Arq Neuropsiquiatr. 2018 Aug;76(8):555-562. doi: 10.1590/0004-282X20180080. Review.

23.

Neurological manifestations of xeroderma pigmentosum due to XPA gene mutation.

Salomão RPA, Pedroso JL, Barsottini OGP.

Pract Neurol. 2018 Dec;18(6):489-491. doi: 10.1136/practneurol-2018-001888. Epub 2018 Aug 4. No abstract available.

PMID:
30077970
24.

MR Imaging Features of Adult-Onset Neuronal Intranuclear Inclusion Disease May Be Indistinguishable from Fragile X-Associated Tremor/Ataxia Syndrome.

Padilha IG, Nunes RH, Scortegagna FA, Pedroso JL, Marussi VH, Rodrigues Gonçalves MR, Barsottini OGP, da Rocha AJ.

AJNR Am J Neuroradiol. 2018 Sep;39(9):E100-E101. doi: 10.3174/ajnr.A5729. Epub 2018 Aug 2. No abstract available.

PMID:
30072371
25.

The cerebellar histiocytosis: Progressive ataxia is not always a genetic disease.

de Assis Franco I, Aragão MM, Braga-Neto P, Avelino MA, Pedroso JL, Marussi VHR, Freitas LF, Masruha MR, Barsottini OGP.

Neurology. 2018 Aug 21;91(8):357-359. doi: 10.1212/WNL.0000000000006036. Epub 2018 Jul 18. No abstract available.

PMID:
30021921
26.

Structural signature of SCA3: From presymptomatic to late disease stages.

Rezende TJR, de Paiva JLR, Martinez ARM, Lopes-Cendes I, Pedroso JL, Barsottini OGP, Cendes F, França MC Jr.

Ann Neurol. 2018 Sep;84(3):401-408. doi: 10.1002/ana.25297. Epub 2018 Sep 4.

PMID:
30014526
27.

SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage.

Faber I, Martinez ARM, de Rezende TJR, Martins CR Jr, Martins MP, Lourenço CM, Marques W Jr, Montecchiani C, Orlacchio A, Pedroso JL, Barsottini OGP, Lopes-Cendes Í, França MC Jr.

Neuroimage Clin. 2018 Jun 9;19:848-857. doi: 10.1016/j.nicl.2018.05.031. eCollection 2018.

28.

Sleep apnea in Machado-Joseph disease: a clinical and polysomnographic evaluation.

Folha Santos FA, de Carvalho LBC, Prado LFD, do Prado GF, Barsottini OG, Pedroso JL.

Sleep Med. 2018 Aug;48:23-26. doi: 10.1016/j.sleep.2018.04.002. Epub 2018 Apr 25.

PMID:
29852360
29.

Multimodal neuroimaging analysis in patients with SYNE1 Ataxia.

Gama MTD, Piccinin CC, Rezende TJR, Dion PA, Rouleau GA, França Junior MC, Barsottini OGP, Pedroso JL.

J Neurol Sci. 2018 Jul 15;390:227-230. doi: 10.1016/j.jns.2018.05.003. Epub 2018 May 4.

PMID:
29801895
30.

Neurologic manifestations of antiphospholipid syndrome.

Ricarte IF, Dutra LA, Abrantes FF, Toso FF, Barsottini OGP, Silva GS, de Souza AWS, Andrade D.

Lupus. 2018 Aug;27(9):1404-1414. doi: 10.1177/0961203318776110. Epub 2018 May 17. Review.

PMID:
29768970
31.

Video NeuroImages: Head titubation in anti-mGluR1 autoantibody-associated cerebellitis.

Pedroso JL, Dutra LA, Espay AJ, Höftberger R, Barsottini OGP.

Neurology. 2018 Apr 17;90(16):746-747. doi: 10.1212/WNL.0000000000005338. No abstract available.

PMID:
29661893
32.

Cerebellar degeneration and progressive ataxia associated with HIV-virus infection.

Pedroso JL, Vale TC, Gama MTD, Ribas G, Kristochik JCG, Germiniani FMB, Fink MCDDS, Oliveira ACP, Teive HAG, Barsottini OG.

Parkinsonism Relat Disord. 2018 Sep;54:95-98. doi: 10.1016/j.parkreldis.2018.04.007. Epub 2018 Apr 5.

PMID:
29643006
33.

Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK.

Arita JH, Barros MH, Ravagnani FG, Ziosi M, Sanches LR, Picosse FR, Lopes TO, de Carvalho Aguiar P, Macabelli CH, Chiaratti MR, Pedroso JL, Quinzii CM, Barsottini OGP, Ferreiro-Barros CC.

Biochim Biophys Acta Mol Basis Dis. 2018 May;1864(5 Pt A):1896-1903. doi: 10.1016/j.bbadis.2018.03.011. Epub 2018 Mar 8.

34.

Autoimmune encephalitis: a review of diagnosis and treatment.

Dutra LA, Abrantes F, Toso FF, Pedroso JL, Barsottini OGP, Hoftberger R.

Arq Neuropsiquiatr. 2018 Jan;76(1):41-49. doi: 10.1590/0004-282X20170176. Review.

35.

Dissecting superior cerebellar artery aneurysm: spontaneous resolution in a long-term follow-up.

Fujino MVT, Iquizli R, Abud T, Baccin CE, Silva GS, Barsottini OG, Pedroso JL.

Arq Neuropsiquiatr. 2017 Oct;75(10):758-759. doi: 10.1590/0004-282X20170143. No abstract available.

36.

SPG7 with parkinsonism responsive to levodopa and dopaminergic deficit.

Pedroso JL, Vale TC, Bueno FL, Marussi VHR, Amaral LLFD, França MC Jr, Barsottini OG.

Parkinsonism Relat Disord. 2018 Feb;47:88-90. doi: 10.1016/j.parkreldis.2017.12.004. Epub 2017 Dec 11.

PMID:
29246844
37.

Central nervous system vasculitis in a patient with HIV infection: a diagnostic challenge.

Amui NO, Silva RGF, Costa DMC, Barsottini OGP, Pedroso JL, Ferreira PRA.

Arq Neuropsiquiatr. 2017 Dec;75(12):897-898. doi: 10.1590/0004-282X20170163. No abstract available.

38.

Pontine calcification in late stage cerebellar multiple system atrophy: a marker of synucleinopathy neurodegeneration?

Pedroso JL, Barsottini OG, Knobel M, Handfas BW, Rocha AJ, Knobel E.

Arq Neuropsiquiatr. 2017 Nov;75(11):833-834. doi: 10.1590/0004-282X20170142. No abstract available.

39.

Neurological complications of solid organ transplantation.

Pedroso JL, Dutra LA, Braga-Neto P, Abrahao A, Andrade JBC, Silva GLD, Viana LA, Pestana JOM, Barsottini OG.

Arq Neuropsiquiatr. 2017 Oct;75(10):736-747. doi: 10.1590/0004-282X20170132. Review.

40.

Perioral and tongue fasciculations in Kennedy's disease.

Pedroso JL, Vale TC, Barsottini OG, Oliveira ASB, Espay AJ.

Neurol Sci. 2018 Apr;39(4):777-779. doi: 10.1007/s10072-017-3170-8. Epub 2017 Nov 4.

PMID:
29103179
41.

Teaching NeuroImages: Spinocerebellar ataxia type 3 presenting with a cock-walk gait phenotype.

Rocha E, Vale TC, Kok F, Pedroso JL, Barsottini OG.

Neurology. 2017 Oct 10;89(15):e192. doi: 10.1212/WNL.0000000000004497. Epub 2017 Oct 9. No abstract available.

PMID:
28993536
42.

Teaching NeuroImages: Typical neuroimaging features in high-altitude cerebral edema.

Marussi VHR, Pedroso JL, Piccolo AM, Barsottini OG, Moraes FM, Oliveira ASB, Freitas LF, Amaral LLFD.

Neurology. 2017 Oct 3;89(14):e176-e177. doi: 10.1212/WNL.0000000000004544. No abstract available.

PMID:
28972114
43.

Teaching NeuroImages: The Charcot shoulder: Chiari malformation with syringomyelia associated with arthropathy.

Bocca LF, Tonholo Silva TY, Ejnisman B, Pedroso JL, Barsottini OG.

Neurology. 2017 Jul 25;89(4):e38-e39. doi: 10.1212/WNL.0000000000004154. No abstract available.

PMID:
28739670
44.

LMNB1 mutation causes cerebellar involvement and a genome instability defect.

Pedroso JL, Munford V, Bastos AU, Castro LP, Marussi VHR, Silva GS, Arita JH, Menck CFM, Barsottini OG.

J Neurol Sci. 2017 Aug 15;379:249-252. doi: 10.1016/j.jns.2017.06.027. Epub 2017 Jun 16. No abstract available.

PMID:
28716252
45.

Anti-N-methyl-D-aspartate receptor encephalitis and Epstein-Barr virus: another tale on autoimmunity?

Danieli D, Moraes ACM, Alves MP, Dutra LA, Höftberger R, Barsottini OGP, Masruha MR.

Eur J Neurol. 2017 Aug;24(8):e46-e47. doi: 10.1111/ene.13332. No abstract available.

PMID:
28707812
46.

The relationship between the First World War and neurology: 100 years of "Shell Shock".

Pedroso JL, Linden SC, Barsottini OG, Maranhão P Filho, Lees AJ.

Arq Neuropsiquiatr. 2017 May;75(5):317-319. doi: 10.1590/0004-282X20170046.

47.

Structural signature of classical versus late-onset friedreich's ataxia by Multimodality brain MRI.

Rezende TJR, Martinez ARM, Faber I, Girotto K, Pedroso JL, Barsottini OG, Lopes-Cendes I, Cendes F, Faria AV, França MC.

Hum Brain Mapp. 2017 Aug;38(8):4157-4168. doi: 10.1002/hbm.23655. Epub 2017 May 23.

PMID:
28543952
48.

Frontal lobes white matter abnormalities mimicking cystic leukodystrophy in Wilson's disease.

Rezende Filho FM, Rocha E, Dutra LA, Pedroso JL, Barsottini OGP.

Arq Neuropsiquiatr. 2017 Apr;75(4):260-261. doi: 10.1590/0004-282X20170003. No abstract available.

49.

Professor Wadia's contributions to neurology and spinocerebellar ataxia type 2.

Tensini FS, Pedroso JL, Barsottini OGP, Teive HAG.

Arq Neuropsiquiatr. 2017 Apr;75(4):255-257. doi: 10.1590/0004-282X20170008.

50.

Dentatorubro-Pallidoluysian Atrophy (DRPLA) among 700 Families with Ataxia in Brazil.

Braga-Neto P, Pedroso JL, Furtado GV, Gheno TC, Saraiva-Pereira ML, Jardim LB, Barsottini OGP; Rede Neurogenetica.

Cerebellum. 2017 Aug;16(4):812-816. doi: 10.1007/s12311-017-0862-9.

PMID:
28432641

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