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W Marques OR W Marques Jr OR W Marques Junior OR Wilson Marques OR Wilson Marques Junior OR Marques
W Marques OR W Marques Jr OR W Marques Junior OR Wilson Marques OR Wilson Marques Junior OR Marques
Associate Professor of Neurology School of Medicine of Ribeirão Preto - USP
Dirección de correo verificada de fmrp.usp.br
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Mutations in ADAR1 cause Aicardi-Goutieres syndrome associated with a type I interferon signature
GI Rice, PR Kasher, GMA Forte, NM Mannion, SM Greenwood, ...
Nature Genetics, 2012
8332012
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ...
Brain 133 (3), 771-786, 2010
4362010
Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study
GI Rice, GMA Forte, M Szynkiewicz, DS Chase, A Aeby, MS Abdel-Hamid, ...
The lancet neurology 12 (12), 1159-1169, 2013
4152013
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia
A Cortese, R Simone, R Sullivan, J Vandrovcova, H Tariq, WY Yau, ...
Nature genetics 51 (4), 649-658, 2019
3952019
The phenotypic manifestations of chromosome 17p11. 2 duplication.
PK Thomas, W Marques Jr, MB Davis, MG Sweeney, RH King, JL Bradley, ...
Brain: a journal of neurology 120 (3), 465-478, 1997
3541997
PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum
M Synofzik, MA Gonzalez, CM Lourenco, M Coutelier, TB Haack, ...
Brain 137 (1), 69-77, 2014
2232014
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia
A Boukhris, R Schule, JL Loureiro, CM Lourenço, E Mundwiller, ...
The American Journal of Human Genetics 93 (1), 118-123, 2013
1812013
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion
A Cortese, S Tozza, WY Yau, S Rossi, SJ Beecroft, Z Jaunmuktane, ...
Brain 143 (2), 480-490, 2020
1752020
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study
D Adams, M Polydefkis, A González-Duarte, J Wixner, AV Kristen, ...
The Lancet Neurology 20 (1), 49-59, 2021
1112021
Damage to the superior gluteal nerve after direct lateral approach to the hip
CHF Picado, FL Garcia, W Marques Jr
Clinical Orthopaedics and Related Research® 455, 209-211, 2007
1102007
Postsurgical idiopathic brachial neuritis
RI Malamut, W Marques, JD England, AJ Sumner
Muscle & Nerve: Official Journal of the American Association of …, 1994
1071994
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial
L Schöls, TW Rattay, P Martus, C Meisner, J Baets, I Fischer, C Jägle, ...
Brain 140 (12), 3112-3127, 2017
1012017
Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12
G Landouré, PP Zhu, CM Lourenço, JO Johnson, C Toro, KV Bricceno, ...
Human mutation 34 (10), 1357-1360, 2013
982013
Expanding the phenotypes of the Pro56Ser VAPB mutation: Proximal SMA with dysautonomia
VD Marques, AA Barreira, MB Davis, PM Abou‐Sleiman, WA Silva Jr, ...
Muscle & Nerve: Official Journal of the American Association of …, 2006
902006
Role of ulnar nerve sonography in leprosy neuropathy with electrophysiologic correlation
J Elias Jr, MH Nogueira-Barbosa, LT Feltrin, RB Furini, NT Foss, ...
Journal of Ultrasound in Medicine 28 (9), 1201-1209, 2009
892009
Postural control and functional strength in patients with type 2 diabetes mellitus with and without peripheral neuropathy
MM Vaz, GC Costa, JG Reis, WM Junior, FJA de Paula, DC Abreu
Archives of physical medicine and rehabilitation 94 (12), 2465-2470, 2013
852013
17p duplicated Charcot–Marie–Tooth 1A
W Marques, MR Freitas, OJM Nascimento, AB Oliveira, L Calia, A Melo, ...
Journal of neurology 252 (8), 972-979, 2005
782005
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant
R Walz, R Castro, TR Velasco, V Alexandre Jr, MH Lopes, JP Leite, ...
Neurology 61 (9), 1204-1210, 2003
652003
Primary neural leprosy: systematic review
JA Garbino, W Marques Jr, JA Barreto, CO Heise, MMJ Rodrigues, ...
Arquivos de neuro-psiquiatria 71, 397-404, 2013
602013
Use of the frontal assessment battery in evaluating executive dysfunction in patients with Huntington’s disease
GR Rodrigues, CP Souza, RS Cetlin, DS de Oliveira, M Pena-Pereira, ...
Journal of neurology 256, 1809-1815, 2009
602009
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