Results
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1.
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Analysis of the genetic variability in Parkinson's disease from Southern Spain. [electronic resource] by
- Bandrés-Ciga, Sara
- Mencacci, Niccolò Emmanuele
- Durán, Raquel
- Barrero, Francisco Javier
- Escamilla-Sevilla, Francisco
- Morgan, Sarah
- Hehir, Jason
- Vives, Francisco
- Hardy, John
- Pittman, Alan M
Producer: 20160926
In:
Neurobiology of aging vol. 37
Availability: No items available.
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2.
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C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. [electronic resource] by
- Hensman Moss, Davina J
- Poulter, Mark
- Beck, Jon
- Hehir, Jason
- Polke, James M
- Campbell, Tracy
- Adamson, Garry
- Mudanohwo, Ese
- McColgan, Peter
- Haworth, Andrea
- Wild, Edward J
- Sweeney, Mary G
- Houlden, Henry
- Mead, Simon
- Tabrizi, Sarah J
Producer: 20140320
In:
Neurology vol. 82
Availability: No items available.
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3.
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Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled Trial. [electronic resource] by
- Mullin, Stephen
- Smith, Laura
- Lee, Katherine
- D'Souza, Gayle
- Woodgate, Philip
- Elflein, Josh
- Hällqvist, Jenny
- Toffoli, Marco
- Streeter, Adam
- Hosking, Joanne
- Heywood, Wendy E
- Khengar, Rajeshree
- Campbell, Philip
- Hehir, Jason
- Cable, Sarah
- Mills, Kevin
- Zetterberg, Henrik
- Limousin, Patricia
- Libri, Vincenzo
- Foltynie, Tom
- Schapira, Anthony H V
Producer: 20200706
In:
JAMA neurology vol. 77
Availability: No items available.
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4.
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A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations. [electronic resource] by
- Kara, Eleanna
- Kiely, Aoife P
- Proukakis, Christos
- Giffin, Nicola
- Love, Seth
- Hehir, Jason
- Rantell, Khadija
- Pandraud, Amelie
- Hernandez, Dena G
- Nacheva, Elizabeth
- Pittman, Alan M
- Nalls, Mike A
- Singleton, Andrew B
- Revesz, Tamas
- Bhatia, Kailash P
- Quinn, Niall
- Hardy, John
- Holton, Janice L
- Houlden, Henry
Producer: 20141124
In:
JAMA neurology vol. 71
Availability: No items available.
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5.
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Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study. [electronic resource] by
- Tan, Manuela M X
- Malek, Naveed
- Lawton, Michael A
- Hubbard, Leon
- Pittman, Alan M
- Joseph, Theresita
- Hehir, Jason
- Swallow, Diane M A
- Grosset, Katherine A
- Marrinan, Sarah L
- Bajaj, Nin
- Barker, Roger A
- Burn, David J
- Bresner, Catherine
- Foltynie, Thomas
- Hardy, John
- Wood, Nicholas
- Ben-Shlomo, Yoav
- Grosset, Donald G
- Williams, Nigel M
- Morris, Huw R
Producer: 20200512
In:
Brain : a journal of neurology vol. 142
Availability: No items available.
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