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Progression of nigrostriatal dysfunction in a parkin kindred: an 18 Fdopa PET and clinical study

Khan, Naheed L ; Brooks, David J ; Pavese, Nicola ; Sweeney, Mary G ; Wood, Nicholas W ; Lees, Andrew J ; Piccini, Paola

Brain, 2002, Vol.125(10), pp.2248-2256 [Periódico revisado por pares]

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Parkin disease: a phenotypic study of a large case series

Khan, Naheed L ; Graham, Elizabeth ; Critchley, Peter ; Schrag, Anette E ; Wood, Nicholas W ; Lees, Andrew J ; Bhatia, Kailash P ; Quinn, Niall

Brain, 2003, Vol.126(6), pp.1279-1292 [Periódico revisado por pares]

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Striatal and cortical pre and postsynaptic dopaminergic dysfunction in sporadic parkin linked parkinsonism

Scherfler, Christoph ; Khan, Naheed L ; Pavese, Nicola ; Eunson, Louise ; Graham, Elizabeth ; Lees, Andrew J ; Quinn, Niall P ; Wood, Nicholas W ; Brooks, David J ; Piccini, Paola P

Brain, 2004, Vol.127(6), pp.1332-1342 [Periódico revisado por pares]

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Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases

Sailer, W., Anna ; Scholz, Raphael, Sonja ; Gibbs, O., J. ; Tucci, W., Arianna ; Johnson, J., Janel ; Wood, J., Nicholas ; Plagnol, B., Vincent ; Hummerich, B., Holger ; Ding, B., Jinhui ; Hernandez, B., Dena ; Hardy, B., John ; Federoff, B., Howard ; Traynor, B., Bryan ; Singleton, B., Andrew ; Houlden, B., Henry

Neurology, 2012, Vol.79(2), pp.127-131 [Periódico revisado por pares]

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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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Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus

Daniah Trabzuni ; Mina Ryten ; Warren Emmett ; Adaikalavan Ramasamy ; Karl J Lackner ; Tanja Zeller ; Robert Walker ; Colin Smith ; Patrick A Lewis ; Adamantios Mamais ; Rohan de Silva ; Jana Vandrovcova ; International Parkinson Disease Genomics Consortium (Ipdgc) ; Dena Hernandez ; Michael A Nalls ; Manu Sharma ; Sophie Garnier ; Suzanne Lesage ; Javier Simon-Sanchez ; Thomas Gasser ; Peter Heutink ; Alexis Brice ; Andrew Singleton ; Huaibin Cai ; Eric Schadt ; Nicholas W Wood ; Rina Bandopadhyay ; Michael E Weale ; John Hardy ; Vincent Plagnol

PLoS ONE, 01 January 2013, Vol.8(8), p.e70724 [Periódico revisado por pares]

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Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

Thomas, Anna c ; Williams, Hywel ; Setó-Salvia, Núria ; Bacchelli, Chiara ; Jenkins, Dagan ; O’sullivan, Mary ; Mengrelis, Konstantinos ; Ishida, Miho ; Ocaka, Louise ; Chanudet, Estelle ; James, Chela ; Lescai, Francesco ; Anderson, Glenn ; Morrogh, Deborah ; Ryten, Mina ; Duncan, Andrew j ; Pai, Yun jin ; Saraiva, Jorge m ; Ramos, Fabiana ; Farren, Bernadette ; Saunders, Dawn ; Vernay, Bertrand ; Gissen, Paul ; Straatmaan-Iwanowska, Anna ; Baas, Frank ; Wood, Nicholas w ; Hersheson, Joshua ; Houlden, Henry ; Hurst, Jane ; Scott, Richard ; Bitner-Glindzicz, Maria ; Moore, Gudrun e ; Sousa, Sérgio b ; Stanier, Philip

The American Journal of Human Genetics, 04 June 2015, Vol.96(6), pp.1008-1009 [Periódico revisado por pares]

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Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

Thomas, Anna c ; Williams, Hywel ; Setó-Salvia, Núria ; Bacchelli, Chiara ; Jenkins, Dagan ; O’sullivan, Mary ; Mengrelis, Konstantinos ; Ishida, Miho ; Ocaka, Louise ; Chanudet, Estelle ; James, Chela ; Lescai, Francesco ; Anderson, Glenn ; Morrogh, Deborah ; Ryten, Mina ; Duncan, Andrew j ; Pai, Yun jin ; Saraiva, Jorge m ; Ramos, Fabiana ; Farren, Bernadette ; Saunders, Dawn ; Vernay, Bertrand ; Gissen, Paul ; Straatmaan-Iwanowska, Anna ; Baas, Frank ; Wood, Nicholas w ; Hersheson, Joshua ; Houlden, Henry ; Hurst, Jane ; Scott, Richard ; Bitner-Glindzicz, Maria ; Moore, Gudrun e ; Sousa, Sérgio b ; Stanier, Philip

The American Journal of Human Genetics, 06 November 2014, Vol.95(5), pp.611-621 [Periódico revisado por pares]

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Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Zhou, Kaixin ; Bellenguez, Celine ; Spencer, Chris C A ; Bennett, Amanda J ; Coleman, Ruth L ; Tavendale, Roger ; Hawley, Simon A ; Donnelly, Louise A ; Schofield, Chris ; Groves, Christopher J ; Burch, Lindsay ; Carr, Fiona ; Strange, Amy ; Freeman, Colin ; Blackwell, Jenefer M ; Bramon, Elvira ; Brown, Matthew A ; Casas, Juan P ; Corvin, Aiden ; Craddock, Nicholas ; Deloukas, Panos ; Dronov, Serge ; Duncanson, Audrey ; Edkins, Sarah ; Gray, Emma ; Hunt, Sarah ; Jankowski, Janusz ; Langford, Cordelia ; Markus, Hugh S ; Mathew, Christopher G ; Plomin, Robert ; Rautanen, Anna ; Sawcer, Stephen J ; Samani, Nilesh J ; Trembath, Richard ; Viswanathan, Ananth C ; Wood, Nicholas W ; Harries, Lorna W ; Hattersley, Andrew T ; Doney, Alex S F ; Colhoun, Helen ; Morris, Andrew D ; Sutherland, Calum ; Hardie, D Grahame ; Peltonen, Leena ; Mccarthy, Mark I ; Holman, Rury R ; Palmer, Colin N A ; Donnelly, Peter ; Pearson, Ewan R

Nature genetics, February 2011, Vol.43(2), pp.117-20 [Periódico revisado por pares]

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Deste Autor:

  1. Wood, Nicholas W.
  2. Wood, N.W.
  3. Hardy, John
  4. Lees, Andrew
  5. Gasser, Thomas

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