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
E-mail confirmado em fmrp.usp.br
TítuloCitado porAno
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
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
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
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
Ação popular constitucional: doutrina e processo
JA Silva
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
Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta type I‐IV
R Pollitt, R McMahon, J Nunn, R Bamford, A Afifi, N Bishop, A Dalton
Human mutation 27 (7), 716-716, 2006
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
Postsurgical idiopathic brachial neuritis
RI Malamut, W Marques, JD England, AJ Sumner
Muscle & Nerve: Official Journal of the American Association of …, 1994
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
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
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
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
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
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant
R Walz, R Castro, TR Velasco, V Alexandre, MH Lopes, JP Leite, ...
Neurology 61 (9), 1204-1210, 2003
Clinical aspects of hemolysis in patients with P. vivax malaria treated with primaquine, in the Brazilian Amazon
WMR Júnior, JFJ Sardinha, MRF Costa, MS Santana, MGC Alecrim, ...
The Brazilian Journal of Infectious Diseases 14 (4), 410-412, 2010
Dejerine‐Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible “hot spot” on Ser72
W Marques Jr, PK Thomas, MG Sweeney, L Carr, NW Wood
Annals of Neurology: Official Journal of the American Neurological …, 1998
Blastic CD4 NK cell leukemia/lymphoma: a distinct clinical entity
RP Falcão, AB Garcia, MG Marques, BP Simões, BA Fonseca, ...
Leukemia research 26 (9), 803-807, 2002
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 (11), 1809-1815, 2009
Central nervous system involvement in a novel connexin 32 mutation affecting identical twins
W Marques, MG Sweeney, NW Wood, SJ Wroe
Journal of Neurology, Neurosurgery & Psychiatry 66 (6), 803, 1999
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