Torthaí cuardaigh - Proukakis, Christos

Somatic mutations may contribute to asymmetry in neurodegenerative disorders de réir Proukakis, Christos

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Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia? de réir Crosby, Andrew H., Proukakis, Christos

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Somatic Alpha-Synuclein Mutations in Parkinson's Disease: Hypothesis and Preliminary Data de réir Proukakis, Christos, Houlden, Henry, Schapira, Anthony H

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The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder de réir Benger, Matthew, Mankad, Kshitij, Proukakis, Christos, Mazarakis, Nicholas D., Kinali, Maria

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α-Synuclein mutations cluster around a putative protein loop() de réir Kara, Eleanna, Lewis, Patrick A., Ling, Helen, Proukakis, Christos, Houlden, Henry, Hardy, John

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Investigation of Somatic Mutations in Human Brains Targeting Genes Associated With Parkinson's Disease de réir Leija-Salazar, Melissa, Pittman, Alan, Mokretar, Katya, Morris, Huw, Schapira, Anthony H., Proukakis, Christos

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Evolution of prodromal clinical markers of Parkinson disease in a glucocerebrosidase mutation positive cohort de réir Beavan, Michelle, McNeill, Alisdair, Proukakis, Christos, Hughes, Derralynn A, Mehta, Atul, Schapira, Anthony H V

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Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia de réir Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.

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α-Synuclein structural features inhibit harmful polyunsaturated fatty acid oxidation, suggesting roles in neuroprotection de réir De Franceschi, Giorgia, Fecchio, Chiara, Sharon, Ronit, Schapira, Anthony H. V., Proukakis, Christos, Bellotti, Vittorio, de Laureto, Patrizia Polverino

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Selective vulnerability in α-synucleinopathies de réir Alegre-Abarrategui, Javier, Brimblecombe, Katherine R., Roberts, Rosalind F., Velentza-Almpani, Elisavet, Tilley, Bension S., Bengoa-Vergniory, Nora, Proukakis, Christos

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A novel α-synuclein missense mutation in Parkinson disease de réir Proukakis, Christos, Dudzik, Christopher G., Brier, Timothy, MacKay, Donna S., Cooper, J. Mark, Millhauser, Glenn L., Houlden, Henry, Schapira, Anthony H.

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Hyposmia and Cognitive Impairment in Gaucher Disease Patients and Carriers de réir McNeill, Alisdair, Duran, Raquel, Proukakis, Christos, Bras, Jose, Hughes, Derralyn, Mehta, Atuhl, Hardy, John, Wood, Nicholas W., Schapira, Anthony H.V.

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Evolution and clustering of prodromal parkinsonian features in GBA1 carriers de réir Mullin, Stephen, Beavan, Michelle, Bestwick, Jonathan, McNeill, Alisdair, Proukakis, Christos, Cox, Timothy, Hughes, Derralynn, Mehta, Atul, Zetterberg, Henrik, Schapira, Anthony H.V.

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Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's Disease de réir Toffoli, Marco, Higgins, Abigail, Lee, Chiao, Koletsi, Sofia, Chen, Xiao, Eberle, Michael, Sedlazeck, Fritz J., Mullin, Stephen, Proukakis, Christos, Schapira, Anthony H.V.

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Analysis of Parkinson's disease brain–derived DNA for alpha-synuclein coding somatic mutations de réir Proukakis, Christos, Shoaee, Maryiam, Morris, James, Brier, Timothy, Kara, Eleanna, Sheerin, Una-Marie, Charlesworth, Gavin, Tolosa, Eduardo, Houlden, Henry, Wood, Nicholas W, Schapira, Anthony H

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CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype de réir Dewan, Ramita, Jaunmuktane, Zane, Garcia‐Segura, Monica Emili, Strand, Catherine, Wild, Edward, Villar, Joaquin, Dalgard, Clifton L., Tabrizi, Sarah J., Traynor, Bryan J., Proukakis, Christos

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Visual short-term memory deficits associated with GBA mutation and Parkinson’s disease de réir Zokaei, Nahid, McNeill, Alisdair, Proukakis, Christos, Beavan, Michelle, Jarman, Paul, Korlipara, Prasad, Hughes, Derralynn, Mehta, Atul, Hu, Michele T. M., Schapira, Anthony H. V., Husain, Masud

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Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION de réir Leija‐Salazar, Melissa, Sedlazeck, Fritz J., Toffoli, Marco, Mullin, Stephen, Mokretar, Katya, Athanasopoulou, Maria, Donald, Aimee, Sharma, Reena, Hughes, Derralynn, Schapira, Anthony H.V., Proukakis, Christos

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α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy? de réir Kiely, Aoife P., Asi, Yasmine T., Kara, Eleanna, Limousin, Patricia, Ling, Helen, Lewis, Patrick, Proukakis, Christos, Quinn, Niall, Lees, Andrew J., Hardy, John, Revesz, Tamas, Houlden, Henry, Holton, Janice L.

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DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation de réir Nacheva, Elizabeth, Mokretar, Katya, Soenmez, Aynur, Pittman, Alan M., Grace, Colin, Valli, Roberto, Ejaz, Ayesha, Vattathil, Selina, Maserati, Emanuela, Houlden, Henry, Taanman, Jan-Willem, Schapira, Anthony H., Proukakis, Christos

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