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11 |
Material Type: Artigo
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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 |
12 |
Material Type: Artigo
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Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutationsROZE, E ; APARTIS, E ; ANDRE-OBADIA, N ; MALTETE, D ; ECHANIZ-LAGUNA, A ; PEREON, Y ; BEAUGENDRE, Y ; DUPONT, S ; DE GRESLAN, T ; JEDYNAK, C. P ; PONSOT, G ; DUSSAULE, J. C ; CLOT, F ; BRICE, A ; DÜRR, A ; VIDAILHET, M ; DORISON, N ; THOBOIS, S ; GUYANT-MARECHAL, L ; TRANCHANT, C ; DAMIER, P ; DOUMMAR, D ; BAHI-BUISSON, NNeurology, 2008-03, Vol.70 (13), p.1010-1016 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Material Type: Artigo
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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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Material Type: Artigo
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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 |
15 |
Material Type: Artigo
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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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Material Type: Artigo
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IS THE COMMON LRRK2 G2019S MUTATION RELATED TO DYSKINESIAS IN NORTH AFRICAN PARKINSON DISEASE?LESAGE, S ; BELARBI, S ; TAZIR, M ; BRICE, A ; TROIANO, A ; CONDROYER, C ; HECHAM, N ; POLLAK, P ; LOHMAN, E ; BENHASSINE, T ; YSMAIL-DAHLOUK, F ; DÜRR, ANeurology, 2008-11, Vol.71 (19), p.1550-1552 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
17 |
Material Type: Artigo
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Efficacy of subthalamic nucleus stimulation in C9ORF72 expansion related parkinsonismDanaila, T ; Polo, G ; Klinger, H ; Broussolle, E ; Mertens, P ; Lesage, S ; Brice, A ; Thobois, SParkinsonism & related disorders, 2014-10, Vol.20 (10), p.1104-1105 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
18 |
Material Type: Artigo
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Predominant dystonia with marked cerebellar atrophy : A rare phenotype in familial dystoniaLE BER, I ; CLOT, F ; BRICE, A ; DÜRR, A ; VERCUEIL, L ; CAMUZAT, A ; VIEMONT, M ; BENAMAR, N ; DE LIEGE, P ; OUVRARD-HERNANDEZ, A.-M ; POLLAK, P ; STEVANIN, GNeurology, 2006-11, Vol.67 (10), p.1769-1773 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
19 |
Material Type: Artigo
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Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutationsVAN DE WARRENBURG, B. P. C ; LAMMENS, M ; LÜCKING, C. B ; DENEFLE, P ; WESSELING, P ; BOOIJ, J ; PRAAMSTRA, P ; QUINN, N ; BRICE, A ; HORSTINK, M. W. I. MNeurology, 2001-02, Vol.56 (4), p.555-557 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
20 |
Material Type: Artigo
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SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyHANNIBAL, M. C ; RUZZO, E. K ; BEDFORD, H. M ; WORRALL, B. B ; LOVITT, S ; APPEL, S. H ; ANDERMANN, E ; BIRD, T. D ; CHANCE, P. F ; MILLER, L. R ; BETZ, B ; BUCHAN, J. G ; KNUTZEN, D. M ; BARNETT, K ; LANDSVERK, M. L ; BRICE, A ; LEGUERN, ENeurology, 2009-05, Vol.72 (20), p.1755-1759 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |