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Number of items: 113.

A

Aguirregomozcorta, M; Schwingenschuh, P; Katschnig, P; Paisan-Ruiz, C; Wood, N; Bhatia, K; (2009) Familial adult-onset tremulous segmental dystonia associated with epilepsy, a new phenotype? In: EUROPEAN JOURNAL OF NEUROLOGY. (pp. 169 - 169). WILEY-BLACKWELL PUBLISHING, INC

Ahmed, S; King, C; Dorward, N; Warner, T; (2009) Cerebral abscess as a complication of a halo fixation device. BMJ Case Rep , 2009 10.1136/bcr.06.2009.2024. Gold open access

Alafuzoff, I; Al-Sarraj, S; Arzberger, T; Bodi, I; Bogdanovic, N; Budka, H; Bugiani, O; ... Kretzschmar, H; + view all (2009) Reproducibility in the assessment of Alzheimer's disease and Lewy body disease-related pathologies: a study by Brain Net Europe. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 12 - 13). BLACKWELL PUBLISHING

Andrade, LAF; Selikhova, M; Lees, AJ; (2009) Konstantin N. Tretiakoff in Brazil a historical perspective and discussion of his contribution to Brazilian neuroscience. Arquivos de Neuro-Psiquiatria , 67 (2A) 322 - 327. 10.1590/S0004-282X2009000200032. Green open access
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Andreou, A.; (2009) Involvement of kainate glutamate receptors in the modulation of neuronal transmission in brain areas involved in migraine pathophysiology. Doctoral thesis , UCL (University College London). Green open access
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B

Bajaj, NNPS; Gontu, VK; Birchall, J; Grosset, DG; Lees, AJ; (2009) Dystonic features in adult sporadic tremor dominant Parkinson's disease: A case series. In: (pp. S83-S83).

Bajaj, NPS; Gontu, VK; Birchall, J; Patterson, J; Grosset, DG; Lees, AJ; (2009) Can handwriting distinguish dystonic pseudoparkinsonism front Parkinson's disease? In: (pp. S83-S84).

Bajaj, NPS; Gontu, VK; Birchall, J; Patterson, J; Grosset, DG; Lees, AJ; (2009) The accuracy of clinical diagnosis of tremor dominant Parkinson's disease in a specialist hospital setting: A blinded videotape study. MOVEMENT DISORDERS , 24 S521-S521.

Benevieste, O; Hilton-Jones, D; Hanna, MG; Group, IBMS; (2009) First international 'Institute of Myology' workshop on Inclusion Body Myositis.

Bhidayasiri, R; Ling, H; (2009) Treatment of Parkinson's disease in Thailand: review of the literature and practical recommendations. J Med Assoc Thai , 92 (1) pp. 142-154.

Biagioli, M; Pinto, M; Cesselli, D; Zaninello, M; Lazarevic, D; Roncaglia, P; Simone, R; ... Gustincich, S; + view all (2009) Unexpected expression of alpha- and beta-globin in mesencephalic dopaminergic neurons and glial cells. Proceedings of the National Academy of Sciences , 106 (36) pp. 15454-15459. 10.1073/pnas.0813216106.

Bunn, LM; Giunti, P; Marsden, JF; Day, BL; (2009) Vestibular processing for balance control in spino-cerebellar ataxia type 6 (SCA6). In: MOVEMENT DISORDERS. (pp. S9 - S9). WILEY-LISS

Bunn, LM; Marsden, JF; Giunti, P; Day, BL; (2009) The pattern of instability and its dependence on posture in spino-cerebellar ataxia type 6 (SCA6). In: MOVEMENT DISORDERS. (pp. S8 - S9). WILEY-LISS

C

Chio, A.; Schymick, J. C.; Restagno, G.; Scholz, S. W.; Lombardo, F.; Lai, S.-L.; Mora, G.; ... Traynor, B. J.; + view all (2009) A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Human Molecular Genetics , 18 (8) pp. 1524-1532. 10.1093/hmg/ddp059. Green open access
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Clarimon, J; Djaldetti, R; Lleo, A; Guerreiro, RJ; Molinuevo, JL; Paisan-Ruiz, C; Gomez-Isla, T; ... Hardy, J; + view all (2009) Whole genome analysis in a consanguineous family with early onset Alzheimer's disease. Neurobiology of Aging , 30 (12) pp. 1986-1991. 10.1016/j.neurobiolaging.2008.02.008.

Clarke, C.; Frackowiak, R.; Howard, R.; Rossor, M.; Shorvon, S.; (2009) The language of neurology: symptoms, signs and basic investigations. In: Clarke, C. and Howard, R. and Rossor, M. and Shorvon, S., (eds.) Neurology: a Queen Square textbook. (pp. 75-107). Wiley-Blackwell: Chichester, UK.

Coles, JL; Hallegger, M; Smith, CWJ; (2009) A nonsense exon in the Tpm1 gene is silenced by hnRNP H and F. RNA-A PUBLICATION OF THE RNA SOCIETY , 15 (1) pp. 33-43. 10.1261/rna.1225209.

D

Deriziotis, P.; (2009) Cellular mechanisms in prion-mediated neurodegeneration. Doctoral thesis , UCL (University College London). Green open access
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Dharmapuri, S; Aurisicchio, L; Biondo, A; Welsh, N; Ciliberto, G; La Monica, N; (2009) Antiapoptotic Small Interfering RNA as Potent Adjuvant of DNA Vaccination in a Mouse Mammary Tumor Model. HUMAN GENE THERAPY , 20 (6) pp. 589-597. 10.1089/hum.2008.210.

Dickey, C; Kraft, C; Jinwal, U; Koren, J; Johnson, A; Anderson, L; Lebson, L; ... Lewis, J; + view all (2009) Aging Analysis Reveals Slowed Tau Turnover and Enhanced Stress Response in a Mouse Model of Tauopathy. AM J PATHOL , 174 (1) 228 - 238. 10.2353/ajpath.2009.080764.

de Teixeira, AL; Cardoso, F; Maia, DP; Sacramento, DR; Mota, CDCC; Meira, ZMA; Lees, A; (2009) Frequency and significance of vocalizations in Sydenham's chorea. Parkinsonism Relat Disord , 15 (1) pp. 62-63. 10.1016/j.parkreldis.2008.01.014.

E

Evans, AH; Lawrence, AD; Lees, AJ; (2009) Changes in psychomotor effects of L-dopa and methylphenidate after sustained dopaminergic therapy in Parkinson's disease. J Neurol Neurosurg Psychiatry , 80 (3) pp. 267-272. 10.1136/jnnp.2006.108993.

F

Fialho, D.; (2009) Clinical, genetic and electrophysiological study of skeletal muscle channelopathies - new insights into Myotonia congenita and Andersen-Tawil syndrome. Doctoral thesis , UCL (University College London).

G

Gandhi, S; Tabrizi, SJ; Wood, NW; (2009) Neurogenetics. In: Scadding, J and Losseff, N, (eds.) Clinical Neurology. Hodder Arnold

Gandhi, S; Wood-Kaczmar, A; Wood, NW; Duchen, MR; Abramov, AY; (2009) PINK1 associated Parkinson's disease is caused by neuronal vulnerability to calcium induced cell death. In: MOVEMENT DISORDERS. (pp. S33 - S33). WILEY-LISS

Giunti, P; Loucas, MJ; Hurford, JL; Peplow, CA; Taylor, B; Wilkinson, H; (2009) Inter-disciplinary therapy assessment and intervention in ataxia: Current clinical model and case study. In: MOVEMENT DISORDERS. (pp. S13 - S13). WILEY-LISS

H

Hardy, J; (2009) GENETIC ANALYSIS OF NEURODEGENERATION. In: JOURNAL OF NEUROCHEMISTRY. (pp. 11 - 11). WILEY-BLACKWELL PUBLISHING, INC

Hardy, J; (2009) Genetic dissection of neurodegenerative disease. In: JOURNAL OF NEUROCHEMISTRY. (pp. 1 - 1). WILEY-BLACKWELL PUBLISHING, INC

Hardy, J; Coleman, PD; (2009) Genetic Analysis Publications in Neurobiology of Aging. NEUROBIOLOGY OF AGING , 30 (4) p. 506. 10.1016/j.neurobiolaging.2009.01.003.

Healy, D; Lees, A; (2009) Nineteenth century neurology: newly discovered photographs from the National Hospital, Queen Square. EUROPEAN JOURNAL OF NEUROLOGY , 16 p. 327.

Healy, DG; Goadsby, PJ; Kitchen, ND; Yousry, T; Hanna, MG; (2009) Spontaneous intracranial hypotension, hygromata and haematomata. BMJ Case Rep , 2009 bcr2007132019-. 10.1136/bcr.2007.132019.

Hornemann, T; Penno, A; Reilley, M; Houlden, H; Laura, M; Rentsch, K; Eichler, F; ... von Eckardstein, A; + view all (2009) ACCUMULATION OF TWO ATYPICAL SPHINGOLIPIDS IN HSAN I. In: JOURNAL OF NEUROCHEMISTRY. (pp. 88 - 89). WILEY-BLACKWELL PUBLISHING, INC

Houlden, H; (2009) The small, spastic, and furrowed tongue of Allgrove syndrome. NEUROLOGY , 72 (15) 1366 - 1366. 10.1212/WNL.0b013e3181a0fe97. Gold open access

I

Isaacs, JD; Adams, M; Lees, AJ; (2009) A NEW TIC-BORNE MYELOPATHY? In:

J

Justino, GC; Rodrigues, M; Florêncio, MH; Mira, L; (2009) Structure and antioxidant activity of brominated flavonols and flavanones. Journal of Mass Spectrometry , 44 (10) pp. 1459-1468. 10.1002/jms.1630.

K

Kalinderi, K; Bostantjopoulou, S; Paisan-Ruiz, C; Katsarou, Z; Hardy, J; Fidani, L; (2009) Complete screening for glucocerebrosidase mutations in Parkinson's disease patients from Greece. In: MOVEMENT DISORDERS. (pp. S138 - S138). WILEY-LISS

Kostareli, E; Gounari, M; Preza, E; Psatha, N; Kouvatsi, A; Anagnostopoulos, A; Thompson, K; (2009) ESTABLISHMENT OF HETEROHYBRIDOMAS FROM CHRONIC LYMPHOCYTIC LEUKEMIA (CLL) CELLS AND FUNCTIONAL ANALYSIS OF THE CLONOTYPIC B CELL RECEPTORS (BCRS). In: (Proceedings) 38th Annual Scientific Meeting of the ISEH-Society-for-Hematology-and-Stem-Cells. (pp. S42-S42). ELSEVIER SCIENCE INC

Kumaran, R; Vandrovcova, J; Lees, AJ; Bandopadhyay, R; (2009) DJ-1 (PARK7) gene expression and interactors: implications for idiopathic Parkinson's disease. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 14 - 14). BLACKWELL PUBLISHING

Kumaran, R.; (2009) Characterisation of DJ1 (PARK7) in human brain: possible involvement in idiopathic Parkinson's disease and other neurodegenerative disorders. Doctoral thesis , UCL (University College London). Green open access
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L

Labrum, R; Rajakulendran, S; Sweeney, MG; Bevan, R; Hanna, MG; Davis, MB; (2009) Screening for mutations causing episodic ataxia type 1 (EA1) and 2 (EA2). In: JOURNAL OF MEDICAL GENETICS. (pp. S71 - S71). B M J PUBLISHING GROUP

Lace, G; Forster, G; Savva, G; Matthews, F; Brayne, C; De Silva, R; Strong, MJ; ... Wharton, SB; + view all (2009) Variation in 4R and 3R tau isoforms in the ageing population. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 19 - 19). BLACKWELL PUBLISHING

Laura, M; Houlden, H; Blake, J; Ginsberg, L; Jungbluth, H; Robb, S; King, R; (2009) CHARCOT-MARIE-TOOTH TYPE 4C CAUSED BY MUTATION OF THE KIAA1985 GENE: REPORT OF SIX FAMILIES WITH VARIABLE PHENOTYPE. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 114 - 114). B M J PUBLISHING GROUP

Laura, M; Houlden, H; Blake, J; Ginsberg, L; Jungbluth, H; Robb, S; King, RHM; ... Reilly, MM; + view all (2009) CHARCOT-MARIE-TOOTH TYPE 4C CAUSED BY MUTATION OF KIAA1985 GENE: REPORT OF 5 FAMILIES WITH VARIABLE PHENOTYPE. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 86 - 87). WILEY-BLACKWELL PUBLISHING, INC

Laura, M; Houlden, H; Blake, J; Reilly, MM; (2009) MUTATIONS IN THE HSP27 GENE CAUSE DOMINANT, RECESSIVE AND SPORADIC DISTAL HMN/CMT TYPE 2. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 101 - 101). B M J PUBLISHING GROUP

Lees, A; (2009) Impulse control disorders. Focus on Parkinson's Disease , 21 (1) pp. 2-3.

Lees, AJ; Hardy, J; Revesz, T; (2009) Parkinson's disease (vol 373, pg 2055, 2009). LANCET , 374 (9691) 684 - 684.

Li, A; Paisan-Ruiz, C; Holton, JL; Schneider, S; Hardy, J; Kidd, D; Chataway, J; ... Revesz, T; + view all (2009) A pathological genotype-phenotype study of four neuroaxonal dystrophy cases with PLA2G6 mutations. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 20 - 20). BLACKWELL PUBLISHING

Ling, H; O'Sullivan, S; Paviour, D; Massey, L; Holton, J; Revesz, T; Lees, A; (2009) Diagnostic accuracy in 18 cases of pathologically confirmed corticobasal degeneration. In: MOVEMENT DISORDERS. (pp. S409 - S410). WILEY-LISS

Ling, H; Unnwongse, K; Bhidayasiri, R; (2009) Complex Movement Disorders in a Sporadic Boucher-Neuhauser Syndrome: Phenotypic Manifestations Beyond the Triad. MOVEMENT DISORDERS , 24 (15) pp. 2304-2306. 10.1002/mds.22831.

Liu, W; Ding, JH; Gibbs, JR; Wang, SJ; Hardy, J; Singleton, A; (2009) A simple and efficient algorithm for genome-wide homozygosity analysis in disease. MOL SYST BIOL , 5 , Article 304. 10.1038/msb.2009.53. Gold open access

Ludtmann, MHR; Rollinson, D; Emery, AM; Walker, AJ; (2009) Protein kinase C signalling during miracidium to mother sporocyst development in the helminth parasite, Schistosoma mansoni. Int J Parasitol , 39 (11) pp. 1223-1233. 10.1016/j.ijpara.2009.04.002.

Lundin, JS; Vandrovcova, J; Song, B; Zhou, X; Zelada-Hedman, M; Werelius, B; Houlston, RS; (2009) TGFBR1 variants TGFBR1*6A and Int7G24A are not associated with an increased familial colorectal cancer risk. BRIT J CANCER , 100 (10) 1674 - 1679. 10.1038/sj.bjc.6605054.

Lunn, M; Hanna, M; Howard, R; Parton, M; Reilly, M; (2009) Nerve and Muscle Disease. In: Neurology: A Queen Square Textbook. (pp. 337-410).

M

Massey, L; Lashley, T; O'Sullivan, S; Phadke, R; Moriyama, L; Lees, AJ; Holton, JL; (2009) TAR DNA binding protein-43 (TDP-43) proteinopathy in association with progressive supranuclear palsy. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 29 - 29). BLACKWELL PUBLISHING

Massey, L; Paviour, D; O'Sullivan, S; Burn, D; Holton, J; Revesz, T; Lees, A; ... Micallef, C; + view all (2009) A systematic, comprehensive, blinded radiological study of MR findings in pathologically confirmed PSP, MSA and PD. In: MOVEMENT DISORDERS. (pp. S199 - S200). WILEY-LISS

Meola, G; Hanna, MG; Fontaine, B; (2009) Diagnosis and new treatment in muscle channelopathies. J NEUROL NEUROSUR PS , 80 (4) 360 - 365. 10.1136/jnnp.2008.164046.

Merrison, AFA; Hanna, MG; (2009) Muscle disease. Practical Neurology , 9 (1) pp. 54-65. 10.1136/jnnp.2008.167171.

Merrison, AFA; Hanna, MG; (2009) The bare essentials: muscle disease. Pract Neurol , 9 (1) pp. 54-65. 10.1136/jnnp.2008.167171.

Murphy, S; Gorman, G; Beetz, C; Byrne, P; Dytko, M; McMonagle, P; Kinsella, K; ... Hutchinson, M; + view all (2009) Dementia in hereditary spastic paraplegia: clinical, genetic, and neuropathologic evidence. Neurology , 73 pp. 378-384. 10.1212/ANL.0b013e3181b04c6c.

Murphy, SM; Delanty, N; (2009) Treatment of the epilepsy patient with concomitant medical conditions. In: French, JA and Delanty, N, (eds.) Therapeutic strategies in epilepsy. (pp. 229-249). Clinical Publishing: Oxford.

Murphy, SM; Farrell, MA; Hennessy, MJ; (2009) Postpartum relapsing sensory neuritis responsive to intravenous immunoglobulin. Journal of Neurology , 256 pp. 2085-2086. 10.1007/s00415-009-5276-2.

O

O'Sullivan, SS; Evans, AH; Quinn, NP; Lees, AJ; (2009) Reckless generosity in Parkinson's disease. In: (pp. S247-S247).

O'Sullivan, SS; Loane, CM; Lawrence, AD; Evans, AH; Piccini, P; Lees, AJ; (2009) Impulse control disorders in Parkinson's disease are associated with increased sleep disturbance. MOVEMENT DISORDERS , 24 S395-S395.

O'Sullivan, SS; Massey, LA; Williams, DR; Revesz, T; Lees, A; Holton, J; (2009) Parkinson's disease with Onuf's nucleus involvement mimicking multiple system atrophy. BMJ Case Reports 10.1136/bcr.08.2008.0774.

O'Sullivan, SS; Massey, LA; Williams, DR; Revesz, T; Lees, A; Holton, J; (2009) Parkinson's disease with Onuf's nucleus involvement mimicking multiple system atrophy. BMJ Case Rep , 2009 10.1136/bcr.08.2008.0774.

O'Sullivan, SS; Politis, M; Wu, K; Lawrence, AD; Evans, AH; Bose, SK; Lees, AJ; (2009) Increased dopamine neurotransmission in Parkinson's patients with Impulse control disorders in response to rewarding visual stimuli: A pilot study. In: (pp. S247-S247).

P

Paisan-Ruiz, C; Scopes, G; Lee, P; Houlden, H; (2009) Homozygosity Mapping Through Whole Genome Analysis Identifies a COL18A1 Mutation in an Indian Family Presenting With an Autosomal Recessive Neurological Disorder. AM J MED GENET B , 150B (7) 993 - 997. 10.1002/ajmg.b.30929.

Paisán-Ruiz, C; Scopes, G; Lee, P; Houlden, H; (2009) Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorder. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , 150 (7) pp. 993-997. 10.1002/ajmg.b.30929.

Parkkinen, L; O'Sullivan, S; Holton, JL; Kuoppamaki, M; Lees, A; Revesz, T; (2009) Does L-dopa have toxic effects in Parkinson's disease brain? In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 28 - 28). BLACKWELL PUBLISHING

Paudel, R; Laura, M; Lunn, MPT; Hammans, S; Katifi, H; Houlden, H; Reilly, MM; (2009) MUTATIONS IN THE FRABIN GENE CAN CAUSE A VARIABLE PHENOTYPE AND LEAD TO PROTEIN TRUNCATION. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 118 - 118). WILEY-BLACKWELL PUBLISHING, INC

Polke, J; Ling, H; Sweeney, MG; Haworth, A; Houlden, H; Foskett, P; Wood, N; ... Davis, M; + view all (2009) Single Exon Rearrangements of GTP Cyclohydrolase I in Two Families with Dopa-Responsive Dystonia. In: JOURNAL OF MEDICAL GENETICS. (pp. S73 - S73). B M J PUBLISHING GROUP

Proukakis, C; Moore, D; Labrum, R; Wood, NW; Houlden, H; (2009) A clinical and genetic study of hereditary spastic paraplegia caused by SPAST/SPG4 mutations, including 12 new mutations. In: EUROPEAN JOURNAL OF NEUROLOGY. (pp. 296 - 296). WILEY-BLACKWELL PUBLISHING, INC

Q

Quinn, N; Bhatia, K; Brown, P; Cordivari, C; Hariz, M; Lees, A; Limousin, P; ... Tabrizi, S; + view all (2009) Movement Disorders. In: Neurology: A Queen Square Textbook. (pp. 155-187).

R

Rahman, S; Hanna, MG; (2009) Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases. J Neurol Neurosurg Psychiatry , 80 (9) pp. 943-953. 10.1136/jnnp.2008.158279.

Rajakulendran, S; Graves, T; Kullmann, D; Schorge, S; Hanna, M; (2009) Variation in CACNA1A associated with episodic ataxia and epilepsy. In: EUROPEAN JOURNAL OF NEUROLOGY. (pp. 46 - 46). WILEY-BLACKWELL PUBLISHING, INC

Revesz, T; Holton, JL; Lashley, T; Plant, G; Frangione, B; Rostagno, A; Ghiso, J; (2009) Erratum: Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies (Acta Neuropathologica (2009) vol. 118 (115-130) 10.1007/s00401-009-0501-8). Acta Neuropathologica , 118 (2) 321-. 10.1007/s00401-009-0555-7.

Revesz, T; Holton, JL; Lashley, T; Plant, G; Frangione, B; Rostagno, A; Ghiso, J; (2009) Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies (vol 118, pg 115, 2009). ACTA NEUROPATHOL , 118 (2) 321 - 321. 10.1007/s00401-009-0555-7.

Roiser, JP; de Martino, B; Tan, GCY; Kumaran, D; Seymour, B; Wood, NW; Dolan, RJ; (2009) A Genetically Mediated Bias in Decision Making Driven by Failure of Amygdala Control. J NEUROSCI , 29 (18) 5985 - 5991. 10.1523/JNEUROSCI.0407-09.2009. Gold open access

Rolstad, S; Nordlund, A; Eckerstrom, C; Gustavsson, MH; Zetterberg, H; Wallin, A; (2009) Cognitive Reserve in Relation to Abeta42 in Patients Converting from MCI to Dementia - A Follow-Up Report. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS , 28 (2) pp. 110-115. 10.1159/000234912.

Rosso, ALZ; Nicaretta, DH; Costa, FHR; Silva, ML; Gondar, AFP; Miranda, CS; Pereira, JS; (2009) The clinical features of African-Brazilian patients with Parkinson's disease. MOVEMENT DISORDERS , 24 S536-S536.

Royal, E; Reynolds, FA; Houlden, H; (2009) What are the experiences of adults returning to work following recovery from Guillain-Barre syndrome? An interpretative phenomenological analysis. DISABIL REHABIL , 31 (22) 1817 - 1827. 10.1080/09638280902822294.

Ryten, M; Trabzuni, D; Hardy, J; (2009) Genotypic analysis of gene expression in the dissection of the aetiology of complex neurological and psychiatric diseases. Briefings in Functional Genomics , 8 (3) pp. 194-198. 10.1093/bfgp/elp028.

Ryten, M; Trabzuni, D; Hardy, J; (2009) Genotypic analysis of gene expression in the dissection of the aetiology of complex neurological and psychiatric diseases. Brief Funct Genomic Proteomic , 8 (3) pp. 194-198. 10.1093/bfgp/elp028.

S

Sanotsky, Y; Selikhova, M; Fedoryshyn, L; Matvienko, Y; Komnatska, I; Kyrylchuk, M; Friedman, A; (2009) Two year follow up in ephedrone induced parkinsonism with dystonia. MOVEMENT DISORDERS , 24 S70-S71.

Schneider, SAS; Paisan-Ruiz, C; Garcia-Gorostiaga, I; Quinn, NP; Weber, Y; Lerche, H; Hardy, J; (2009) GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias. In: MOVEMENT DISORDERS. (pp. S106 - S106). WILEY-LISS

Schrag, A; Sheikh, S; Quinn, N; Lees, A; Selai, C; Mathias, D; Litvan, I; ... Jahanshahi, M; + view all (2009) Comparison of depression, anxiety and quality of life in PSP and MSA. In: MOVEMENT DISORDERS. (pp. S375 - S375). WILEY-LISS

Selikhova, M; Williams, DR; Kempster, PA; Reverz, T; Lees, AJ; (2009) Clinical-pathological study of subtypes in Parkinson's disease. MOVEMENT DISORDERS , 24 S537-S537.

Sevastou, IG; Heales, SJ; Pocock, JM; (2009) MODULATION OF MICROGLIAL INDUCED OLIGODENDROCYTE TOXICITY IN MULTIPLE SCLEROSIS. In: GLIA. (pp. S68 - S68). WILEY-LISS

Shamovsky, I; de Graaf, C; Alderin, L; Bengtsson, M; Bladh, H; Borjesson, L; Connolly, S; ... Urbahns, K; + view all (2009) Increasing Selectivity of CC Chemokine Receptor 8 Antagonists by Engineering Nondesolvation Related Interactions with the Intended and Off-Target Binding Sites. JOURNAL OF MEDICINAL CHEMISTRY , 52 (23) pp. 7706-7723. 10.1021/jm900713y.

Sharma, S; Bandopadhyay, R; Kingsbury, AE; Lashley, TC; Lees, AJ; Revesz, T; Wood, NW; (2009) LRRK2 mRNA and protein expression in Parkinson's disease cases with LRRK2 G2019S mutation. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 27 - 28). BLACKWELL PUBLISHING

Silveira Moriyama, L.; (2009) Olfaction in Parkinson’s Disease. Doctoral thesis , UCL (University College London).

Simone, R; Plessy, C; Carninci, P; (2009) A method of manufacturing a mixture of amplified double-stranded nucleic acids comprising unknown sequence. WO 2009154303 A2.

Smyth, A; Murphy, SM; Counihan, T; (2009) An unusual cause of cavernous sinus syndrome. [Digital scholarly resource].

Song, YJC; Holton, JL; Lashley, T; O'Sullivan, S; McCann, H; Lockhart, PJ; Revesz, T; (2009) Astrocytic pathology in parkinsonian syndromes. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 27 - 27). BLACKWELL PUBLISHING

Steele, JC; Williams, DR; Lees, AJ; Wherrett, JR; (2009) J. CLIFFORD RICHARDSON AND 50 YEARS OF PROGRESSIVE SUPRANUCLEAR PALSY Reply. NEUROLOGY , 72 (2) pp. 199-200.

Sweeney, M; Woodward, CE; Mudanohwo, EE; Rahman, S; Hanna, MG; Davis, MB; (2009) Urine epithelial cells as an alternative to muscle biopsies in the detection of mitochondrial DNA mutations. In: JOURNAL OF MEDICAL GENETICS. (pp. S69 - S69). B M J PUBLISHING GROUP

T

Taanman, JW; Daras, M; Albrecht, J; Davie, CA; Mallam, EA; Muddle, JR; Weatherall, M; ... Ginsberg, L; + view all (2009) Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). NEUROMUSCULAR DISORD , 19 (2) 151 - 154. 10.1016/j.nmd.2008.11.002.

Tomlinson, SE; Hanna, MG; Holton, JL; Rahman, S; (2009) A novel POLG1 mutation resulting in severe cachexia and muscle wasting. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 16 - 16). BLACKWELL PUBLISHING

Tomlinson, SE; Tan, SV; Kullmann, DM; Burke, D; Hanna, MG; Bostock, H; (2009) AXONAL EXCITABILITY CHANGES IN GENETIC NEURONAL ION CHANNEL DISORDERS. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 144 - 145). WILEY-BLACKWELL PUBLISHING, INC

Tomlinson, SE; Tan, SV; Kullmann, DM; Burke, D; Hanna, MG; Bostock, H; (2009) Nerve Excitability Measurements Can Distingush Genetic Channelopathies in the Episodic Ataxias. In: NEUROLOGY. (pp. A266 - A266). LIPPINCOTT WILLIAMS & WILKINS

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This list was generated on Sun May 20 02:02:50 2018 BST.