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Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's diseaseBrockmann, K. ; Schulte, C. ; Schneiderhan‐Marra, N. ; Apel, A. ; Pont‐Sunyer, C. ; Vilas, D. ; Ruiz‐Martinez, J. ; Langkamp, M. ; Corvol, J.‐C. ; Cormier, F. ; Knorpp, T. ; Joos, T. O. ; Bernard, A. ; Gasser, T. ; Marras, C. ; Schüle, B. ; Aasly, J. O. ; Foroud, T. ; Marti‐Masso, J. F. ; Brice, A. ; Tolosa, E. ; Berg, D. ; Maetzler, W.European journal of neurology, 2017-02, Vol.24 (2), p.427-e6 [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseLE BER, I ; CAMUZAT, A ; HEATH, S ; CAMU, W ; MARTINAUD, O ; LACOMBLEZ, L ; VERCELLETTO, M ; SALACHAS, F ; SELLAL, F ; DIDIC, M ; THOMAS-ANTERION, C ; PUEL, M ; BERGER, E ; MICHEL, B.-F ; BESSE, C ; DUYCKAERTS, C ; MEININGER, V ; CAMPION, D ; DUBOIS, B ; BRICE, A ; HANNEQUIN, D ; LAQUERRIERE, A ; GOLFIER, V ; SEILHEAN, D ; VIENNET, G ; COURATIER, P ; VERPILLAT, PNeurology, 2009-05, Vol.72 (19), p.1669-1676 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismBonifati, V ; Rizzu, P ; Squitieri, F ; Krieger, E ; Vanacore, N ; van Swieten, J C ; Brice, A ; van Duijn, C M ; Oostra, B ; Meco, G ; Heutink, PNeurological sciences, 2003-10, Vol.24 (3), p.159-160 [Periódico revisado por pares]Italy: Springer Nature B.VTexto completo disponível |
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MUTATIONS IN THE GLUCOCEREBROSIDASE GENE CONFER A RISK FOR PARKINSON DISEASE IN NORTH AFRICALESAGE, S ; CONDROYER, C ; TAZIR, M ; BRICE, A ; HECHAM, N ; ANHEIM, M ; BELARBI, S ; LOHMAN, E ; VIALLET, F ; POLLAK, P ; ABADA, M ; DÜRR, ANeurology, 2011-01, Vol.76 (3), p.301-303 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsAZZEDINE, H ; RAVISE, N ; HAMADOUCHE, T ; BOUHOUCHE, A ; GUILBOT, A ; STENDEL, C ; RUBERG, M ; BRICE, A ; BIROUK, N ; DUBOURG, O ; TAZIR, M ; LEGUERN, E ; VERNY, C ; GABRËELS-FESTEN, A ; LAMMENS, M ; GRID, D ; VALLAT, J. M ; DUROSIER, G ; SENDEREK, J ; NOUIOUA, SNeurology, 2006-08, Vol.67 (4), p.602-606 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1LE BER, I ; DUBOURG, O ; BENOIST, J.-F ; JARDEL, C ; MOCHEL, F ; KOENIG, M ; BRICE, A ; LOMBES, A ; DÜRR, ANeurology, 2007-01, Vol.68 (4), p.295-297 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG geneKoht, J. ; Stevanin, G. ; Durr, A. ; Mundwiller, E. ; Brice, A. ; Tallaksen, C. M. E.Acta neurologica Scandinavica, 2012-02, Vol.125 (2), p.116-122 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type VDUBOURG, O ; AZZEDINE, H ; BEN YAOU, R ; POUGET, J ; BAROIS, A ; MEININGER, V ; BOUTEILLER, D ; RUBERG, M ; BRICE, A ; LEGUERN, ENeurology, 2006-06, Vol.66 (11), p.1721-1726 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Unstable mutations and neurodegenerative disordersBRICE, AJournal of neurology, 1998-08, Vol.245 (8), p.505-510 [Periódico revisado por pares]Berlin: SpringerTexto completo disponível |
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Genetics of Parkinson's disease: LRRK2 on the riseBrice, AlexisBrain (London, England : 1878), 2005-12, Vol.128 (12), p.2760-2762 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |