Որոնման արդյունքները - Proukakis, Christos
- Ցուցադրվում են 1 - 20 արդյունքները 32
- Գնացեք Հաջորդ էջ
-
1
-
2
-
3
-
4
The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder Benger, Matthew, Mankad, Kshitij, Proukakis, Christos, Mazarakis, Nicholas D., Kinali, Maria
Հրապարակվել է 2019Տեքստ -
5
-
6
Investigation of Somatic Mutations in Human Brains Targeting Genes Associated With Parkinson's Disease Leija-Salazar, Melissa, Pittman, Alan, Mokretar, Katya, Morris, Huw, Schapira, Anthony H., Proukakis, Christos
Հրապարակվել է 2020Տեքստ -
7
Evolution of prodromal clinical markers of Parkinson disease in a glucocerebrosidase mutation positive cohort Beavan, Michelle, McNeill, Alisdair, Proukakis, Christos, Hughes, Derralynn A, Mehta, Atul, Schapira, Anthony H V
Հրապարակվել է 2015Տեքստ -
8
Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.
Հրապարակվել է 2003Տեքստ -
9
α-Synuclein structural features inhibit harmful polyunsaturated fatty acid oxidation, suggesting roles in neuroprotection De Franceschi, Giorgia, Fecchio, Chiara, Sharon, Ronit, Schapira, Anthony H. V., Proukakis, Christos, Bellotti, Vittorio, de Laureto, Patrizia Polverino
Հրապարակվել է 2017Տեքստ -
10
Selective vulnerability in α-synucleinopathies Alegre-Abarrategui, Javier, Brimblecombe, Katherine R., Roberts, Rosalind F., Velentza-Almpani, Elisavet, Tilley, Bension S., Bengoa-Vergniory, Nora, Proukakis, Christos
Հրապարակվել է 2019Տեքստ -
11
A novel α-synuclein missense mutation in Parkinson disease Proukakis, Christos, Dudzik, Christopher G., Brier, Timothy, MacKay, Donna S., Cooper, J. Mark, Millhauser, Glenn L., Houlden, Henry, Schapira, Anthony H.
Հրապարակվել է 2013Տեքստ -
12
Hyposmia and Cognitive Impairment in Gaucher Disease Patients and Carriers McNeill, Alisdair, Duran, Raquel, Proukakis, Christos, Bras, Jose, Hughes, Derralyn, Mehta, Atuhl, Hardy, John, Wood, Nicholas W., Schapira, Anthony H.V.
Հրապարակվել է 2012Տեքստ -
13
Evolution and clustering of prodromal parkinsonian features in GBA1 carriers Mullin, Stephen, Beavan, Michelle, Bestwick, Jonathan, McNeill, Alisdair, Proukakis, Christos, Cox, Timothy, Hughes, Derralynn, Mehta, Atul, Zetterberg, Henrik, Schapira, Anthony H.V.
Հրապարակվել է 2019Տեքստ -
14
Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's Disease Toffoli, Marco, Higgins, Abigail, Lee, Chiao, Koletsi, Sofia, Chen, Xiao, Eberle, Michael, Sedlazeck, Fritz J., Mullin, Stephen, Proukakis, Christos, Schapira, Anthony H.V.
Հրապարակվել է 2021Տեքստ -
15
Analysis of Parkinson's disease brain–derived DNA for alpha-synuclein coding somatic mutations 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
Հրապարակվել է 2014Տեքստ -
16
CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype 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
Հրապարակվել է 2022Տեքստ -
17
Visual short-term memory deficits associated with GBA mutation and Parkinson’s disease 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
Հրապարակվել է 2014Տեքստ -
18
Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION 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
Հրապարակվել է 2019Տեքստ -
19
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy? 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.
Հրապարակվել է 2013Տեքստ -
20
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation 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
Հրապարակվել է 2017Տեքստ