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MARIA-CEU MOREIRA
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Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
MC Moreira, S Klur, M Watanabe, AH Németh, IL Ber, JC Moniz, ...
Nature genetics 36 (3), 225-227, 2004
5922004
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
MC Moreira, C Barbot, N Tachi, N Kozuka, E Uchida, T Gibson, ...
Nature genetics 29 (2), 189-193, 2001
4882001
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies
I Le Ber, MC Moreira, S Rivaud‐Péchoux, C Chamayou, F Ochsner, ...
Brain 126 (12), 2761-2772, 2003
2702003
Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients
I Le Ber, N Bouslam, S Rivaud‐Péchoux, J Guimarães, A Benomar, ...
Brain 127 (4), 759-767, 2004
2342004
The ataxia–oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4
PM Clements, C Breslin, ED Deeks, PJ Byrd, L Ju, P Bieganowski, ...
DNA repair 3 (11), 1493-1502, 2004
2312004
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG) n allele at the SCA17 locus
I Silveira, C Miranda, L Guimaraes, MC Moreira, I Alonso, P Mendonca, ...
Archives of neurology 59 (4), 623-629, 2002
2082002
Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease
YZ Chen, SH Hashemi, SK Anderson, Y Huang, MC Moreira, DR Lynch, ...
Neurobiology of disease 23 (1), 97-108, 2006
1412006
Phenotypic variability of aprataxin gene mutations
C Tranchant, M Fleury, MC Moreira, M Koenig, JM Warter
Neurology 60 (5), 868-870, 2003
952003
Medium-term outcomes of digital versus conventional home-based rehabilitation after total knee arthroplasty: prospective, parallel-group feasibility study
FD Correia, A Nogueira, I Magalhães, J Guimarães, M Moreira, I Barradas, ...
JMIR rehabilitation and assistive technologies 6 (1), e13111, 2019
762019
Aprataxin gene mutations in Tunisian families
R Amouri, MC Moreira, M Zouari, G El Euch, C Barhoumi, M Kefi, S Belal, ...
Neurology 63 (5), 928-929, 2004
652004
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families
M Anheim, MC Fleury, J Franques, MC Moreira, JP Delaunoy, ...
Archives of neurology 65 (7), 958-962, 2008
542008
Digital versus conventional rehabilitation after total hip arthroplasty: a single-center, parallel-group pilot study
FD Correia, A Nogueira, I Magalhães, J Guimarães, M Moreira, I Barradas, ...
JMIR rehabilitation and assistive technologies 6 (1), e14523, 2019
522019
Clinical, biomarker, and molecular delineations and genotype-phenotype correlations of ataxia with oculomotor apraxia type 1
M Renaud, MC Moreira, BB Monga, D Rodriguez, R Debs, P Charles, ...
JAMA neurology 75 (4), 495-502, 2018
312018
Ataxia with oculomotor apraxia type 2
MC Moreira, M Koenig
252018
Sanar: A collaborative environment to support knowledge sharing with medical artifacts
A Moreira, V Vieira, JC del Arco
2012 Brazilian Symposium on Collaborative Systems, 35-42, 2012
112012
Né meth
MC Moreira, S Klur, M Watanabe
AH, Le Ber, I., Moniz, JC, Tranchant, C., Aubourg, P., Tazir, M., Schö ls, L …, 2004
112004
Recessive ataxia plus oculomotor apraxia syndromes
M Koenig, MC Moreira
Blue Books of Neurology 31, 244-254, 2007
42007
Mutation of the aprataxin gene presenting with Charcot-Marie-Tooth-like neuropathy and cerebellar ataxia
F Ochsner, I Le Ber, G Said, MC Moreira, P Michel, M Koenig, A Dürr, ...
Revue neurologique 161 (3), 331-336, 2005
42005
Autosomal recessive ataxias: a new gene-aprataxin-responsible for ataxia-ocular apraxia 1, and a new locus on 9q34
M Moreira, S Klur, C Barbot, N Tachi, P Bomont, M Watanabe, M Shoji, ...
42002
Measuring relevant information in health social network conversations and clinical diagnosis cases
A Moreira, R Alonso-Calvo, A Muñoz, J Crespo
International Journal of Environmental Research and Public Health 15 (12), 2787, 2018
22018
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