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Material Type: Artigo
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277 Disentangling corticobasal syndrome from corticobasal degenerationRuth, Lamb ; Jonathan, Rohrer ; Steven, Lubbe ; Rimona, Weil ; Tammaryn, Lashley ; Janice, Holten ; Tamas, Revesz ; Andrew, Lees ; Huw, MorrisJournal of neurology, neurosurgery and psychiatry, 2018-10, Vol.89 (10), p.A40-A41 [Periódico revisado por pares]London: BMJ Publishing Group LTDTexto completo disponível |
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Material Type: Artigo
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A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disordersLamb, Ruth ; Rohrer, Jonathan D ; Real, Raquel ; Lubbe, Steven J ; Waite, Adrian J ; Blake, Derek J ; Walters, R Jon ; Lashley, Tammaryn ; Revesz, Tamas ; Holton, Janice L ; Morris, Huw RCold Spring Harbor molecular case studies, 2019-06, Vol.5 (3), p.a003913 [Periódico revisado por pares]United States: Cold Spring Harbor Laboratory PressTexto completo disponível |
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3 |
Material Type: Artigo
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PO184 Analysis of copy number variants in familial and sporadic parkinson’s diseaseJoseph, Theresita ; Hehir, Jason ; Tan, Manuela ; Zhang, Wei ; Houlden, Henry ; Lubbe, Steven ; Morris, HuwJournal of neurology, neurosurgery and psychiatry, 2017-12, Vol.88 (Suppl 1), p.A59-A60 [Periódico revisado por pares]London: BMJ Publishing Group LTDTexto completo disponível |
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4 |
Material Type: Artigo
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PARKINSON'S FAMILIES PROJECT: RECRUITMENT OF FAMILIAL PD PATIENTS VIA THE BNSUHong, James ; Tan, Manuela ; Rizig, Mie ; Brugaletta, Concetta ; Cable, Sarah ; Lubbe, Steven ; Morris, HuwJournal of neurology, neurosurgery and psychiatry, 2016-12, Vol.87 (12), p.e1-e1 [Periódico revisado por pares]London: BMJ Publishing Group LTDTexto completo disponível |
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5 |
Material Type: Artigo
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Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s diseaseLeonard, Hampton ; Blauwendraat, Cornelis ; Krohn, Lynne ; Faghri, Faraz ; Iwaki, Hirotaka ; Ferguson, Glen ; Day-Williams, Aaron G ; Stone, David J ; Singleton, Andrew B ; Nalls, Mike A ; Gan-Or, ZivJournal of medical genetics, 2020-05, Vol.57 (5), p.331-338 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |
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6 |
Material Type: Artigo
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PO187 Parkinson’s families project recruiting via the bnsu: baseline dataTan, Manuela MX ; Hong, James S ; Bras, Jose ; Lubbe, Steven J ; Grosset, Donald G ; Wood, Nick W ; Schapira, Anthony H ; Hardy, John ; Houlden, Henry ; Morris, Huw RJournal of neurology, neurosurgery and psychiatry, 2017-12, Vol.88 (Suppl 1), p.A60-A61 [Periódico revisado por pares]London: BMJ Publishing Group LTDTexto completo disponível |
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7 |
Material Type: Artigo
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Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations:Evidence for oligogenic inheritanceLubbe, Steven J ; Escott-Price, Valentina ; Gibbs, J. Raphael ; Nalls, Mike A ; Bras, Jose ; Price, T. Ryan ; Nicolas, Aude ; Jansen, Iris E ; Mok, Kin Y ; Pittman, Alan M ; Tomkins, James E ; Lewis, Patrick A ; Noyce, Alastair J ; Lesage, Suzanne ; Sharma, Manu ; Schiff, Elena R ; Levine, Adam P ; Brice, Alexis ; Gasser, Thomas ; Hardy, John ; Heutink, Peter ; Wood, Nicholas W ; Singleton, Andrew B ; Williams, Nigel M ; Morris, Huw R2016-12Texto completo disponível |
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8 |
Material Type: Artigo
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A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disordersLamb, Ruth ; Rohrer, Jonathan D ; Real, Raquel ; Lubbe, Steven J ; Waite, Adrian J ; Blake, Derek J ; Walters, R Jon ; Lashley, Tammaryn ; Revesz, Tamas ; Holton, Janice L ; Morris, Huw RCold Spring Harbor molecular case studies, 2019-06, Vol.5 (3), p.1 [Periódico revisado por pares]Cold Spring Harbor: Cold Spring Harbor Laboratory PressTexto completo disponível |