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Number of items: 261.

A

Abramov, AY; Duchen, MR; (2008) Mechanisms underlying the loss of mitochondrial membrane potential in glutamate excitotoxicity. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS , 1777 (7-8) 953 - 964. 10.1016/j.bbabio.2008.04.017.

Abramov, AY; Kasymov, VA; Zinchenko, VP; (2008) Beta amyloid activates synthesis of nitric oxide in hyppocampal astrocytes and causes death of neurons. BIOL MEMBRANY , 25 (1) 11 - 17.

Al-Mahdawi, S; Pinto, RM; Ismail, O; Varshney, D; Lymperi, S; Sandi, C; Trabzuni, D; (2008) The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues. HUMAN MOLECULAR GENETICS , 17 (5) pp. 735-746. 10.1093/hmg/ddm346.

Anckarsater, R; Zetterberg, H; Mansson, J-E; Blennow, K; Anckarsater, H; (2008) Non-neurological surgery results in a neurochemical stress response. JOURNAL OF NEURAL TRANSMISSION , 115 (3) pp. 397-399. 10.1007/s00702-007-0849-7.

Anderson, JM; Hampton, DW; Patani, R; Pryce, G; Crowther, RA; Reynolds, R; Franklin, RJM; ... Chandran, S; + view all (2008) Abnormally phosphorylated tau is associated with neuronal and axonal loss in experimental autoimmune encephalomyelitis and multiple sclerosis. BRAIN , 131 pp. 1736-1748. 10.1093/brain/awn119.

Andreasen, N; Zetterberg, H; (2008) Amyloid-related biomarkers for Alzheimer's disease. CURRENT MEDICINAL CHEMISTRY , 15 (8) pp. 766-771. 10.2174/092986708783955572.

Appel, S; Evans, A; Lees, AJ; (2008) Neuropsychiatric inventory (NPI) useful instrument in dopamine dysregulation syndrome (DDS). In: (pp. S288-S288).

Aschar-Sobbi, R; Abramov, AY; Diao, C; Kargacin, ME; Kargacin, GJ; French, RJ; Pavlov, E; (2008) High sensitivity, quantitative measurements of polyphosphate using a new DAPI-Based approach. J FLUORESC , 18 (5) 859 - 866. 10.1007/s10895-008-0315-4.

B

Bandopadhyay, R; Kumaran, R; Vandrovcova, J; Kingsbury, A; Lees, A; (2008) DJ-1 (PARK7) mRNA levels in idiopathic Parkinson's disease. In: MOVEMENT DISORDERS. (pp. S11 - S11). WILEY-LISS

Bandopadhyay, R; Kumaran, R; Vandrovcova, J; Kingsbury, A; Lees, A; (2008) DJ-1 (PARK7) mRNA levels in idiopathic Parkinson's disease. In: MOVEMENT DISORDERS. (pp. S11 - S11). WILEY-LISS

Baum, AE; Akula, N; Cabanero, M; Cardona, I; Corona, W; Klemens, B; Schulze, TG; ... McMahon, FJ; + view all (2008) A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. MOLECULAR PSYCHIATRY , 13 (2) pp. 197-207. 10.1038/sj.mp.4002012.

Bayot, A; Basse, N; Lee, I; Gareil, M; Pirotte, B; Bulteau, A-L; Friguet, B; (2008) Towards the control of intracellular protein turnover: mitochondrial Lon protease inhibitors versus proteasome inhibitors. Biochimie , 90 (2) pp. 260-269. 10.1016/j.biochi.2007.10.010.

Beck, J; Rohrer, JD; Campbell, T; Isaacs, A; Morrison, KE; Goodall, EF; Warrington, EK; ... Mead, S; + view all (2008) A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. BRAIN , 131 706 - 720. 10.1093/brain/awm320. Gold open access

Bennett, DLH; Groves, M; Blake, J; Holton, JL; King, RHM; Orrell, RW; Ginsberg, L; (2008) The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study. J NEUROL NEUROSUR PS , 79 (12) 1376 - 1381.

Bergmans, BA; Dotti, CG; Strooper, BD; (2008) Neuronal differentiation of murine embryonic stem cells. Journal of Stem Cells , 3 (3) pp. 183-194.

Bertfield, DL; Jumma, O; Pitceathly, RDS; Sussman, JD; (2008) Copper deficiency: an unusual case of myelopathy with neuropathy. ANN CLIN BIOCHEM , 45 434 - 435. 10.1258/acb.2008.007218.

Bhidayasiri, R; Ling, H; (2008) Multiple system atrophy. Neurologist , 14 (4) pp. 224-237. 10.1097/NRL.0b013e318167b93f.

Blazquez, L; Azpitarte, M; Saenz, A; Goicoechea, M; Otaegui, D; Ferrer, X; Illa, I; ... de Munain, AL; + view all (2008) Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis. NEUROGENETICS , 9 (3) pp. 173-182. 10.1007/s10048-008-0129-1.

Blennow, K; Zetterberg, H; (2008) What is the future for CSF biomarkers in the prediction of cognitive decline and Alzheimer's disease? Aging Health , 4 (3) pp. 213-215. 10.2217/1745509X.4.3.213.

Blom, ES; Holmans, P; Arepalli, S; Adighibe, O; Hamshere, ML; Gatz, M; Pedersen, NL; ... Glaser, A; + view all (2008) Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 147B (6) pp. 778-783. 10.1002/ajmg.b.30681.

Blomstedt, P; Hariz, MI; Lees, A; Silberstein, P; Limousin, P; Yelnik, J; Agid, Y; (2008) Acute severe depression induced by intraoperative stimulation of the substantia nigra: A case report. PARKINSONISM RELAT D , 14 (3) 253 - 256. 10.1016/j.parkreldis.2007.04.005.

Bras, J; Guerreiro, R; Ribeiro, M; Morgadinho, A; Januario, C; Dias, M; Calado, A; ... Singleton, A; + view all (2008) Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2. BMC Neurology , 8 , Article 1. 10.1186/1471-2377-8-1. Green open access
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Bras, J; Singleton, A; Cookson, MR; Hardy, J; (2008) Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease. FEBS J , 275 (23) 5767 - 5773. 10.1111/j.1742-4658.2008.06709.x.

Bras, J; Singleton, A; Cookson, MR; Hardy, J; (2008) Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease. FEBS J , 275 (23) pp. 5767-5773. 10.1111/j.1742-4658.2008.06709.x.

Brundin, P; Li, JY; Holton, JL; Lindvall, O; Revesz, T; (2008) Research in motion: the enigma of Parkinson's disease pathology spread. NAT REV NEUROSCI , 9 (10) 741 - 745. 10.1038/nrn2477.

C

Camargos, S; Scholz, S; Simon-Sanchez, J; Paisan-Ruiz, C; Lewis, P; Hernandez, D; Ding, J; ... Singleton, AB; + view all (2008) DYT16, a novel young-onset dystonia-parkinson ism disorder: identification of a segregating mutation in the stress-response protein PRKRA. LANCET NEUROL , 7 (3) 207 - 215. 10.1016/S1474-4422(08)70022-X.

Camargos, S; Scholz, S; Simón-Sánchez, J; Paisán-Ruiz, C; Lewis, P; Hernandez, D; Ding, J; ... Singleton, AB; + view all (2008) DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. The Lancet Neurology , 7 (3) pp. 207-215. 10.1016/S1474-4422(08)70022-X.

Camargos, ST; Cardoso, F; Momeni, P; Gianetti, JG; Lees, A; Hardy, J; Singleton, A; (2008) Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia. MOVEMENT DISORD , 23 (2) 299 - 302. 10.1002/mds.21842.

Campanella, M; Casswell, E; Chong, S; Farah, Z; Wieckowski, MR; Abramov, AY; Tinker, A; (2008) Regulation of mitochondrial structure and function by the F1FO-ATPase inhibitor protein, IF1. CELL METAB , 8 (1) 13 - 25. 10.1016/j.cmet.2008.06.001.

Cano, SJ; Warner, TT; Thompson, AJ; Bhatia, KP; Fitzpatrick, R; Hobart, JC; (2008) The Cervical Dystonia Impact Profile (CDIP-58): Can a Rasch developed patient reported outcome measure satisfy traditional psychometric criteria? HEALTH QUAL LIFE OUT , 6 , Article 58. 10.1186/1477-7525-6-58. Gold open access

Carvajal-Carmona, L; Webb, E; Jaeger, E; Broderick, P; Spain, S; Howarth, K; Pittman, A; ... Tomlinson, I; + view all (2008) A genome-wide association study of tag SNPs identify five novel colorectal cancer susceptibility loci. In: (Proceedings) 20th Meeting of the European-Association-for-Cancer-Research. (pp. p. 10). PERGAMON-ELSEVIER SCIENCE LTD

Chavez-Gutierrez, L; Tolia, A; Maes, E; Li, T; Wong, PC; de Strooper, B; (2008) Glu(332) in the Nicastrin ectodomain is essential for gamma-secretase complex maturation but not for its activity. JOURNAL OF BIOLOGICAL CHEMISTRY , 283 (29) pp. 20096-20105. 10.1074/jbc.M803040200.

Cheeran, B; Talelli, P; Mori, F; Koch, G; Suppa, A; Edwards, M; Houlden, H; ... Rothwell, JC; + view all (2008) A common polymorphism in the brain-derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS. J PHYSIOL-LONDON , 586 (23) 5717 - 5725. 10.1113/jphysiol.2008.159905. Gold open access

Cheeran, BJ; Talelli, P; Mori, F; Koch, G; Schneider, SA; Suppa, A; Edwards, M; ... Bhatia, KP; + view all (2008) Stimulation genomics: Identifying functional polymorphisms modulating LTP and LTD in human cerebral cortex and implications for levodopa induced dyskinesia in Parkinson's disease (PD). In: MOVEMENT DISORDERS. (pp. S20 - S20). WILEY-LISS

Cheeran, BJ; Talelli, P; Mori, F; Koch, G; Schneider, SA; Suppa, A; Edwards, M; ... Bhatia, KP; + view all (2008) Stimulation genomics: Identifying functional polymorphisms modulating LTP and LTD in human cerebral cortex and implications for levodopa induced dyskinesia in Parkinson's disease (PD). In: MOVEMENT DISORDERS. (pp. S20 - S20). WILEY-LISS

Clarimon, J; Pagonabarraga, J; Paisan-Ruiz, C; Campolongo, A; Pascual-Sedano, B; Marti-Masso, JF; Singleton, AB; (2008) Tremor dominant parkinsonism: Clinical description and LRRK2 mutation screening. MOVEMENT DISORD , 23 (4) 518 - 523. 10.1002/mds.21771.

Cole, AR; Soutar, MPM; Rembutsu, M; van Aalten, L; Hastie, CJ; Mclauchlan, H; Peggie, M; ... Sutherland, C; + view all (2008) Relative resistance of Cdk5-phosphorylated CRMP2 to dephosphorylation. JOURNAL OF BIOLOGICAL CHEMISTRY , 283 (26) pp. 18227-18237. 10.1074/jbc.M801645200. Gold open access

Cookson, MR; Hardy, J; Lewis, PA; (2008) Genetic Neuropathology of Parkinson's Disease. INT J CLIN EXP PATHO , 1 (3) 217 - 231. Gold open access

D

Dejaegere, T; Serneels, L; Schaefer, MK; Van Biervliet, J; Horre, K; Depboylu, C; Alvarez-Fischer, D; ... De Strooper, B; + view all (2008) Deficiency of Aph1B/C-gamma-secretase disturbs Nrg1 cleavage and sensorimotor gating that can be reversed with antipsychotic treatment. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 105 (28) pp. 9775-9780. 10.1073/pnas.0800507105.

Di Bernardo, MC; Crowther-Swanepoel, D; Broderick, P; Webb, E; Sellick, G; Wild, R; Sullivan, K; ... Houlston, RS; + view all (2008) A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NATURE GENETICS , 40 (10) pp. 1204-1210. 10.1038/ng.219.

Duncan, AJ; Sweeney, MG; Stern, E; Taylor, R; Woodward, C; Davis, MB; Hanna, MG; (2008) Comparative human mitochondrial genome analysis using the affymetrix Mitochip v2 and conventional cycle sequencing. In: NEUROMUSCULAR DISORDERS. (pp. 755 - 756). PERGAMON-ELSEVIER SCIENCE LTD

Duncan, AJ; Sweeney, MG; Stern, E; Taylor, RW; Woodward, C; Davis, MB; Hanna, MG; (2008) Identification of novel and recurrent mitochondrial DNA mutations in paediatric onset mitochondrial disease using the mitochip resequencing array. In: J INHERIT METAB DIS. (pp. 61 - 61). SPRINGER

Dunn, L; Vandrovcova, J; Malzer, E; Lees, AJ; Hardy, J; de Silva, R; (2008) Investigation of tau gene-specific natural antisense transcript expression and splicing. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 30 - 30). BLACKWELL PUBLISHING

E

Espinoza, M; de Silva, R; Dickson, DW; Davies, P; (2008) Differential incorporation of tau isoforms in Alzheimer's disease. J ALZHEIMERS DIS , 14 (1) 1 - 16.

Evans, A.H.; (2008) Compulsive use of dopaminergic drugs in Parkinson's disease: a window into the role of dopamine in addiction and impulse control disorders. Doctoral thesis , UCL (University College London).

F

Fialho, D; Kullmann, DM; Hanna, MG; Schorge, S; (2008) Non-genomic effects of sex hormones on CIC-1 may contribute to gender differences in myotonia congenita. In: NEUROMUSCULAR DISORDERS. (pp. 745 - 745). PERGAMON-ELSEVIER SCIENCE LTD

Fialho, D; Kullmann, DM; Hanna, MG; Schorge, S; (2008) Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita. Neuromuscular Disorders , 18 (11) 869 - 872. 10.1016/j.nmd.2008.07.004. Green open access
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Fitzgerald, JC; Plun-Favreau, H; (2008) Emerging pathways in genetic Parkinson's disease: Autosomal-recessive genes in Parkinson's disease - a common pathway? FEBS J , 275 (23) 5758 - 5766. 10.1111/j.1742-4658.2008.06708.x.

Fonteyn, EMR; Schmitz-Hubsch, T; Verstappen, CC; Baliko, L; Bloem, BR; Boesch, S; Bunn, L; ... van de Warrenburg, BPC; + view all (2008) Falls in spinocerebellar ataxias: Results of the EuroSCA fall study. In: MOVEMENT DISORDERS. (pp. S151 - S151). WILEY-LISS

G

Gallagher, DA; Lees, A; Schrag, A; (2008) Detection of non-motor symptoms in Parkinson's disease and impact on health-related quality of life. In: (Proceedings) 12th International Congress of Parkinsons Disease and Movement Disorders. (pp. S344-S344). WILEY-LISS

Gallagher, DA; Lees, A; Schrag, A; (2008) Unified Parkinson's disease rating scale (UPDRS) part I as a screening and diagnostic instrument for apathy in patients with Parkinson's disease. In: (Proceedings) 12th International Congress of Parkinsons Disease and Movement Disorders. (pp. S357-S357). WILEY-BLACKWELL

Gallagher, DA; Lees, AJ; Schrag, A; (2008) Unified Parkinson's Disease Rating Scale (UPDRS) part I as a screening and diagnostic instrument for apathy in patients with Parkinson's disease. PARKINSONISM RELAT D , 14 (7) 586 - 587. 10.1016/j.parkreldis.2008.01.005.

Gandhi, S; Hardie, RJ; Lees, AJ; (2008) An update on the Hardie neuroacanthocytosis series. In: (pp. pp. 43-51).

Garrard, P; Martin, NH; Giunti, P; Cipolotti, L; (2008) Cognitive and social cognitive functioning in spinocerebellar ataxia - A preliminary characterization. J NEUROL , 255 (3) 398 - 405. 10.1007/s00415-008-0680-6.

Garrard, P.; Martin, N.H.; Giunti, P.; Cipolotti, L.; (2008) Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization. Journal of Neurology , 255 (3) pp. 398-405. 10.1007/s00415-008-0680-6.

Gaston-Massuet, C; Andoniadou, CL; Signore, M; Sajedi, E; Bird, S; Turner, JMA; Martinez-Barbera, JP; (2008) Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development. DEV BIOL , 324 (2) 322 - 333. 10.1016/j.ydbio.2008.08.008.

Gilman, S; Wenning, G; Low, P; Brooks, D; Mathias, C; Trojanowski, J; Wood, NW; ... Vidailhet, M; + view all (2008) Second consensus statement on the diagnosis of multiple system atrophy. In: NEUROLOGY. (pp. A229 - A229). LIPPINCOTT WILLIAMS & WILKINS

Gilman, S; Wenning, GK; Low, PA; Brooks, DJ; Mathias, CJ; Troianowski, JQ; Wood, NW; ... Vidailhet, M; + view all (2008) Second consensus statement on the diagnosis of multiple system atrophy. In: MOVEMENT DISORDERS. (pp. S255 - S255). WILEY-LISS

Gilman, S; Wenning, GK; Low, PA; Brooks, DJ; Mathias, CJ; Trojanowski, JQ; Wood, NW; ... Vidailhet, M; + view all (2008) Second consensus statement on the diagnosis of multiple system atrophy. NEUROLOGY , 71 (9) 670 - 676.

Gilman, S; Wenning, GK; Low, PA; Brooks, DJ; Mathias, CJ; Trojanowski, JQ; Wood, NW; ... Vidailhet, M; + view all (2008) Second consensus statement on the diagnosis of multiple system atrophy. In: MOVEMENT DISORDERS. (pp. S255 - S255). WILEY-LISS

Goetz, CG; Tilley, BC; Shaftman, SR; Fahn, S; Martinez-Martin, P; Poewe, W; Sampaio, C; ... Stebbins, GT; + view all (2008) New version of the UPDRS (MDS-UPDRS): Factor analysis. In: (Proceedings) 60th Annual Meeting of the American-Academy-of-Neurology. (pp. A55-A56). LIPPINCOTT WILLIAMS & WILKINS

Goetz, CG; Tilley, BC; Shaftman, SR; Stebbins, GT; Fahn, S; Martinez-Martin, P; Poewe, W; ... LaPelle, N; + view all (2008) Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): Scale Presentation and Clinimetric Testing Results. MOVEMENT DISORDERS , 23 (15) pp. 2129-2170. 10.1002/mds.22340.

Granata, A; Watson, R; Collinson, LM; Schiavo, G; Warner, TT; (2008) The dystonia-associated protein torsinA modulates synaptic vesicle recycling. J BIOL CHEM , 283 (12) 7568 - 7579. 10.1074/jbc.M704097200. Gold open access

Graves, TD; Hanna, MG; (2008) Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity. J NEUROL , 255 (7) 1097 - 1099. 10.1007/s00415-008-0844-4.

Graves, TD; Imbrici, P; Kors, EE; Terwindt, GM; Eunson, LH; Frants, RR; Haan, J; ... Kullmann, DM; + view all (2008) Premature stop codons in a facilitating EF-hand splice variant of Ca(v)2.1 cause episodic ataxia type 2. NEUROBIOL DIS , 32 (1) 10 - 15. 10.1016/j.nbd.2008.06.002.

Graves, TD; Morris, H; Zuberi, S; Hanna, MG; Kullmann, DM; Schorge, S; (2008) Episodic ataxia type 1 in twins: Genotype-phenotype correlation. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 344 - 344). B M J PUBLISHING GROUP

Graves, TD; Zuberi, SM; Morris, H; Schorge, S; Kullmann, DM; Hanna, MG; (2008) Episodic ataxia type 1 in identical twins. In: NEUROMUSCULAR DISORDERS. (pp. 746 - 746). PERGAMON-ELSEVIER SCIENCE LTD

Graves, TD; Zuberi, SM; Morris, H; Schorge, S; Kullmann, DM; Hanna, MG; (2008) Episodic ataxia type 1 in identical twins: genotype-phenotype correlation. In: JOURNAL OF NEUROLOGY. (pp. 16 - 16). DR DIETRICH STEINKOPFF VERLAG

Greenfield, J; Treacy, C; Giunti, P; (2008) Centres of excellence for the care of people with progressive ataxias. British Journal of Neuroscience Nursing , 4 (11) pp. 544-548. 10.12968/bjnn.2008.4.11.31698.

Guerreiro, RJ; Santana, I; Bras, JM; Revesz, T; Rebelo, O; Ribeiro, MH; Santiago, B; ... Hardy, J; + view all (2008) Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases. MOVEMENT DISORD , 23 (9) 1269 - 1273. 10.1002/mds.22078.

Guerreiro, RJ; Schymick, JC; Crews, C; Singleton, A; Hardy, J; Traynor, BJ; (2008) TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis. PLOS ONE , 3 (6) , Article e2450. 10.1371/journal.pone.0002450. Green open access
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H

Hall, AM; Unwin, RJ; Hanna, MG; Duchen, MR; (2008) Renal function and mitochondrial cytopathy (MC): more questions than answers. QJM-INT J MED , 101 (10) 755 - 766. 10.1093/qjmed/hcn060.

Hampel, H; Bürger, K; Teipel, SJ; Bokde, ALW; Zetterberg, H; Blennow, K; (2008) Core candidate neurochemical and imaging biomarkers of Alzheimer's disease**This paper was presented in part by the 1st author at the 10th International Conference of Alzheimer's Disease and Related Disorders (ICAD), Madrid, Spain, July 2006, as an invited plenary lecture. Alzheimer's and Dementia , 4 (1) pp. 38-48. 10.1016/j.jalz.2007.08.006.

Hampel, H; Bürger, K; Teipel, SJ; Bokde, ALW; Zetterberg, H; Blennow, K; (2008) Core candidate neurochemical and imaging biomarkers of Alzheimer's disease. Alzheimers Dement , 4 (1) pp. 38-48. 10.1016/j.jalz.2007.08.006.

Hardy, J; (2008) Race, genetics, and medicine at a crossroads. LANCET S85 - S89.

Hardy, J; (2008) ALZHEIMER'S DISEASE: GENETICS TO PATHOGENESIS. In: Ragaini, R, (ed.) INTERNATIONAL SEMINAR ON NUCLEAR WAR AND PLANETARY EMERGENCIES - 38TH SESSION. (pp. 355 - 363). WORLD SCIENTIFIC PUBL CO PTE LTD

Hardy, J; Low, N; Singleton, A; (2008) Whole genome association studies: Deciding when persistence becomes perseveration. AM J MED GENET B , 147B (2) 131 - 133. 10.1002/ajmg.b.30568.

Hardy, J; Low, N; Singleton, A; (2008) Whole genome association studies: Deciding when persistence becomes perseveration. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , 147 (2) pp. 131-133. 10.1002/ajmg.b.30568.

Hardy, J; Singleton, A; (2008) The HapMap - Charting a course for genetic discovery in neurological diseases. ARCH NEUROL-CHICAGO , 65 (3) 319 - 321.

Harrower, T; Stewart, JD; Hudson, G; Houlden, H; Warner, G; O'Donovan, DG; Findlay, LJ; ... Chinnery, PF; + view all (2008) POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease. ARCH NEUROL-CHICAGO , 65 (1) 133 - 136.

Healy, DG; Falchi, M; O'Sullivan, SS; Bonifati, V; Durr, A; Bressman, S; Brice, A; ... Int LRRK2 Consortium, ; + view all (2008) Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. LANCET NEUROL , 7 (7) 583 - 590. 10.1016/S1474-4422(08)70117-0. Gold open access

Healy, DG; Goadsby, PJ; Kitchen, ND; Yousry, T; Hanna, MG; (2008) Spontaneous intracranial hypotension, hygromata and haematomata. J NEUROL NEUROSUR PS , 79 (4) 442 - 442. 10.1136/jnnp.2007.132019.

Healy, DG; Goadsby, PJ; Kitchen, ND; Yousry, T; Hanna, MG; (2008) Spontaneous intracranial hypotension, hygromata and haematomata. Journal of Neurology, Neurosurgery and Psychiatry , 79 (4) 442-. 10.1136/jnnp.2007.132019.

Healy, DG; Wood, NW; Schapira, AHV; (2008) Test for LRRK2 mutations in patients with Parkinson's disease. Pract Neurol , 8 (6) pp. 381-385. 10.1136/jnnp.2008.162420.

Hebert, SS; Horre, K; Nicolai, L; Papadopoulou, AS; Mandemakers, W; Silahtaroglu, AN; Kauppinen, S; ... De Strooper, B; + view all (2008) Loss of microRNA cluster miR-29a/b-1 in sporadic Alzheimer's disease correlates with increased BACE1/beta-secretase expression. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 105 (17) pp. 6415-6420. 10.1073/pnas.0710263105.

Hemsch, MJ; Hanke, JL; Walker, EL; Houlden, HP; (2008) Detailed uncertainty analysis for ares i ascent aerodynamics wind tunnel database. 26th AIAA Aerodynamic Measurement Technology and Ground Testing Conference

Hoglund, K; Hansson, O; Buchhave, P; Zetterberg, H; Lewczuk, P; Londos, E; Blennow, K; ... Wiltfang, J; + view all (2008) Prediction of Alzheimer's disease using a cerebrospinal fluid pattern of C-terminally truncated beta-amyloid peptides. NEURODEGENERATIVE DISEASES , 5 (5) pp. 268-276. 10.1159/000119457.

Holton, JL; Schneider, SA; Gandhi, S; Ganesharajah, T; Strand, C; Shashidharan, P; Barreto, J; ... Revesz, T; + view all (2008) Neuropathology of primary dystonia unrelated to DYT1 mutations. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 28 - 28). BLACKWELL PUBLISHING

Holton, JL; Schneider, SA; Ganesharajah, T; Gandhi, S; Strand, C; Shashidharan, P; Barreto, J; ... Revesz, T; + view all (2008) Neuropathology of primary adult-onset dystonia. NEUROLOGY , 70 (9) 695 - 699.

Holton, JL; Schneider, SA; Ganesharajah, T; Gandhi, S; Strand, C; Shashidharan, P; Barreto, J; ... Revesz, T; + view all (2008) Neuropathology of primary adult onset non-DYT1 dystonia. In: JOURNAL OF NEUROLOGY. (pp. 98 - 98). DR DIETRICH STEINKOPFF VERLAG

Houlden, H; Johnson, J; Gardner-Thorpe, C; Lashley, T; Hernandez, D; Singleton, AB; Holton, J; ... Wood, NW; + view all (2008) Tau tubulin kinase 2, implicated by tau phosphorylation, contains mutations that segregate with spinocerebellar ataxia type II. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 344 - 344). B M J PUBLISHING GROUP

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