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Refinado por: autor: Gasser, Thomas remover autor: Lesage, Suzanne remover assunto: Parkinson Disease remover assunto: Adult 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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Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk

Moskvina, Valentina ; Harold, Denise ; Russo, Giancarlo ; Vedernikov, Alexey ; Sharma, Manu ; Saad, Mohamed ; Holmans, Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice

JAMA neurology, October 2013, Vol.70(10), pp.1268-76 [Periódico revisado por pares]

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Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease

Keller, Margaux F ; Saad, Mohamad ; Bras, Jose ; Bettella, Francesco ; Nicolaou, Nayia ; SimóN - SáNchez, Javier ; Mittag, Florian ; BüChel, Finja ; Sharma, Manu ; Gibbs, J. Raphael ; Schulte, Claudia ; Moskvina, Valentina ; Durr, Alexandra ; Holmans, Peter ; Kilarski, Laura L ; Guerreiro, Rita ; Hernandez, Dena G ; Brice, Alexis ; Ylikotila, Pauli ; StefáNsson, Hreinn ; Majamaa, Kari ; Morris, Huw R ; Williams, Nigel ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W ; Hardy, John ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A

Human Molecular Genetics, 2012, Vol. 21(22), pp.4996-5009 [Periódico revisado por pares]

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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

Mok, Kin Y ; Sheerin, Una ; Simón-Sánchez, Javier ; Salaka, Afnan ; Chester, Lucy ; Escott-Price, Valentina ; Mantripragada, Kiran ; Doherty, Karen M ; Noyce, Alastair J ; Mencacci, Niccolo E ; Lubbe, Steven J ; Williams-Gray, Caroline H ; Barker, Roger A ; van Dijk, Karin D ; Berendse, Henk W ; Heutink, Peter ; Corvol, Jean-Christophe ; Cormier, Florence

The Lancet Neurology, May 2016, Vol.15(6), pp.585-596 [Periódico revisado por pares]

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Deste Autor:

  1. Gasser, Thomas
  2. Morris, Huw R
  3. Hardy, John
  4. Brice, Alexis
  5. Plagnol, Vincent

Buscando em bases de dados remotas. Favor aguardar.