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Refinado por: autor: Gasser, Thomas remover assunto: Abridged remover
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Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

Mencacci, Niccolò E ; Isaias, Ioannis U ; Reich, Martin M ; Ganos, Christos ; Plagnol, Vincent ; Polke, James M ; Bras, Jose ; Hersheson, Joshua ; Stamelou, Maria ; Pittman, Alan M ; Noyce, Alastair J ; Mok, Kin Y ; Opladen, Thomas ; Kunstmann, Erdmute ; Hodecker, Sybille ; Münchau, Alexander ; Volkmann, Jens ; Samnick, Samuel ; Sidle, Katie ; Nanji, Tina ; Sweeney, Mary G ; Houlden, Henry ; Batla, Amit ; Zecchinelli, Anna L ; Pezzoli, Gianni ; Marotta, Giorgio ; Lees, Andrew ; Alegria, Paulo ; Krack, Paul ; Cormier - Dequaire, Florence ; Lesage, Suzanne ; Brice, Alexis ; Heutink, Peter ; Gasser, Thomas ; Lubbe, Steven J ; Morris, Huw R ; Taba, Pille ; Koks, Sulev ; Majounie, Elisa ; Raphael Gibbs, J ; Singleton, Andrew ; Hardy, John ; Klebe, Stephan ; Bhatia, Kailash P ; Wood, Nicholas W

Brain, 2014, Vol. 137(9), pp.2480-2492 [Periódico revisado por pares]

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A genome-wide association study in multiple system atrophy

Sailer, W., Anna ; Scholz, A., Sonja ; Nalls, Ryan, Michael ; Schulte, A., Claudia ; Federoff, W., Monica ; Price, E., T. ; Lees, S., Andrew ; Ross, W., Owen ; Dickson, J., Dennis ; Mok, J., Kin ; Mencacci, R., Niccolo ; Schottlaender, R., Lucia ; Chelban, P., Viorica ; Ling, U., Helen ; Oʼsullivan, Teresa, Sean ; Wood, R., Nicholas ; Traynor, G., Bryan ; Ferrucci, A., Luigi ; Federoff, L., Howard ; Mhyre, K., Timothy ; Morris, B., Huw ; Deuschl, B., Günther ; Quinn, B., Niall ; Widner, B., Hakan ; Albanese, B., Alberto ; Infante, B., Jon ; Bhatia, B., Kailash ; Poewe, B., Werner ; Oertel, B., Wolfgang ; Höglinger, B., Günter ; Wüllner, B., Ullrich ; Goldwurm, B., Stefano ; Pellecchia, B., Maria ; Ferreira, B., Joaquim ; Tolosa, B., Eduardo ; Bloem, B., Bastiaan ; Rascol, B., Olivier ; Meissner, B., Wassilios ; Hardy, B., John ; Revesz, B., Tamas ; Holton, B., Janice ; Gasser, B., Thomas ; Wenning, B., Gregor ; Singleton, B., Andrew ; Houlden, B., Henry

Neurology, 2016, Vol.87(15), pp.1591-1598 [Periódico revisado por pares]

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Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

Witoelar, Aree ; Jansen, Iris E ; Wang, Yunpeng ; Desikan, Rahul S ; Gibbs, J Raphael ; Blauwendraat, Cornelis ; Thompson, Wesley K ; Hernandez, Dena G ; Djurovic, Srdjan ; Schork, Andrew J ; Bettella, Francesco ; Ellinghaus, David ; Franke, Andre ; Lie, Benedicte A ; Mcevoy, Linda K ; Karlsen, Tom H ; Lesage, Suzanne ; Morris, Huw R ; Brice, Alexis ; Wood, Nicholas W ; Heutink, Peter ; Hardy, John ; Singleton, Andrew B ; Dale, Anders M ; Gasser, Thomas ; Andreassen, Ole A ; Sharma, Manu

JAMA neurology, 01 July 2017, Vol.74(7), pp.780-792 [Periódico revisado por pares]

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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

Blauwendraat, Cornelis ; Reed, Xylena ; Kia, Demis A ; Gan-Or, Ziv ; Lesage, Suzanne ; Pihlstrøm, Lasse ; Guerreiro, Rita ; Gibbs, J Raphael ; Sabir, Marya ; Ahmed, Sarah ; Ding, Jinhui ; Alcalay, Roy N ; Hassin-Baer, Sharon ; Pittman, Alan M ; Brooks, Janet ; Edsall, Connor ; Hernandez, Dena G ; Chung, Sun Ju ; Goldwurm, Stefano ; Toft, Mathias ; Schulte, Claudia ; Bras, Jose ; Wood, Nicholas W ; Brice, Alexis ; Morris, Huw R ; Scholz, Sonja W ; Nalls, Mike A ; Singleton, Andrew B ; Cookson, Mark R

JAMA neurology, 01 November 2018, Vol.75(11), pp.1416-1422 [Periódico revisado por pares]

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Deste Autor:

  1. Gasser, Thomas
  2. Morris, Huw R
  3. Wood, Nicholas W
  4. Hardy, John
  5. Brice, Alexis

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