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Number of items: 104.

A

Aguirregomozcorta, M; Edwards, MJ; Prvulovich, E; Schneider, SA; Quinn, NP; Lees, AJ; Dickson, JC; (2010) Why do clinicians request DaT scans? An analysis of requesting practice and outcome in 455 consecutive scans. In: (pp. S369-S369).

Ahmed, Z; Asi, YT; Lees, AJ; Revesz, T; Holton, JL; (2010) Oligodendrocyte precursor cells do not contain pathological inclusions in multiple system atrophy or progressive supranuclear palsy. In: BRAIN PATHOLOGY. (pp. 28 - 29). WILEY-BLACKWELL PUBLISHING, INC

Ahmed, Z; Tabrizi, S; Li, A; Houlden, H; Sailer, A; Lees, AJ; Revesz, T; (2010) A case of Huntington's disease phenocopy characterised by pallido-nigro-luysian degeneration with brain-iron accumulation and p62-positive glial inclusions. In: EUROPEAN JOURNAL OF NEUROLOGY. (pp. 379 - 379). WILEY-BLACKWELL

Ahmed, Z; Tabrizi, SJ; Li, A; Houlden, H; Sailer, A; Lees, AJ; Revesz, T; (2010) A Huntington's disease phenocopy characterized by pallido-nigro-luysian degeneration with brain iron accumulation and p62-positive glial inclusions. NEUROPATH APPL NEURO , 36 (6) 551 - 557. 10.1111/j.1365-2990.2010.01093.x.

Ali, N; Woodward, CE; Sweeney, M; Phadke, R; Holton, JL; Acheson, J; Plant, GT; (2010) Pupillary Dysfunction in an Atypical Case of Mitochondrial Myopathy With Tubular Aggregates. JOURNAL OF NEURO-OPHTHALMOLOGY , 30 (2) pp. 153-156. 10.1097/WNO.0b013e3181dbfdcd.

Anaya, FJ; Vandrovcova, J; Lees, A; de Silva, R; (2010) Investigation of the role of tau gene transcriptional regulation in neurodegeneration. In: MOVEMENT DISORDERS. (pp. S200 - S201). WILEY-LISS

B

Bandopadhyay, R; Phan, B; Mamais, A; Lashley, T; Lees, A; (2010) Validation of 4E-BP1 as a Putative LRRK2 Substrate: In Vivo Evidence. In: MOVEMENT DISORD. (pp. S629 - S629). WILEY-LISS

C

Compta, Y; Parkkinen, L; Vandrovcova, J; O'Sullivan, S; Holton, J; de Silva, R; Lashley, T; ... Revesz, T; + view all (2010) Lewy-and Alzheimer-type pathologies in Parkinson's disease with dementia: A comprehensive brain-bank study. In: MOVEMENT DISORDERS. (pp. S317 - S317). WILEY-LISS

D

Dale, RC; Melchers, A; Fung, VSC; Grattan-Smith, P; Houlden, H; Earl, J; (2010) Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency. DEV MED CHILD NEUROL , 52 (6) 583 - 586. 10.1111/j.1469-8749.2010.03619.x.

Davidson, G; Murphy, SM; Polke, JM; Davis, MB; Reilly, M; Houlden, H; MRC Ctr Neuromuscular Dis, ; (2010) Genes for hereditary sensory and autonomic neuropathies: frequency in a UK series and genotype-phenotype correlations. In: NEUROMUSCULAR DISORDERS. (pp. S22 - S22). PERGAMON-ELSEVIER SCIENCE LTD

Doherty, KMC; Ahmed, Z; Revesz, T; Holton, JL; Lees, AJ; (2010) A clinicopathological study of a case of parkin disease. In: MOVEMENT DISORDERS. (pp. S471 - S471). WILEY-LISS

Dressler, D; Warner, T; (2010) Dystonia Europe: Hamburg 2008. European Journal of Neurology , 17 (SUPPL. 1) 10.1111/j.1468-1331.2010.03062.x.

Dressler, D; Warner, T; (2010) Dystonia Europe: Hamburg 2008. Foreword. Eur J Neurol , 17 Sup v-. 10.1111/j.1468-1331.2010.03062.x.

de las Cuevas, N; Muñoz, U; Bartolomé, F; Esteras, N; Alquezar, C; Martín-Requero, A; (2010) Cell cycle and Alzheimer's disease: Studies in non-neuronal cells. Journal of Applied Biomedicine , 8 (3) pp. 121-130. 10.2478/v10136-009-0015-7.

E

Evans, AH; Lawrence, AD; Cresswell, SA; Katzenschlager, R; Lees, AJ; (2010) Compulsive use of dopaminergic drug therapy in Parkinson's disease: reward and anti-reward. Mov Disord , 25 (7) pp. 867-876. 10.1002/mds.22898.

F

Finegold, J; Giunti, P; Mckenna, W; Elliott, P; Pantazis, A; (2010) Description of the cardiomyopathy associated with friedreich's ataxia. In: EUROPEAN HEART JOURNAL. (pp. 37 - 37). OXFORD UNIV PRESS

Fratter, C; Gorman, GS; Stewart, JD; Buddles, M; Smith, C; Evans, J; Seller, A; ... Taylor, RW; + view all (2010) The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO. NEUROLOGY , 74 (20) 1619 - 1626.

G

Gallagher, D; Lees, A; Schrag, A; (2010) Clinical characteristics of patients with visual hallucinations (VH) in PD. In: (Proceedings) 14th International Congress of Parkinsons Disease and Movement Disorders. (pp. S279-S280). WILEY-LISS

Gallagher, D; Lees, A; Schrag, A; (2010) Testing an aetiological model of visual hallucinations in Parkinson's disease. In: (Proceedings) 14th International Congress of Parkinson's Disease and Movement Disorders. (pp. S280-S280). WILEY-BLACKWELL

Gallagher, D; Spratt, A; Shah, A; Bremmer, F; Davey, C; Lees, A; Schrag, A; (2010) Ophthalmic pathology and visual hallucinations (VH) in PD. In: (Proceedings) 14th International Congress of Parkinson's Disease and Movement Disorders. (pp. S280-S280). WILEY-BLACKWELL

Garcia, IL; Darquie, B; Curtis, EA; Sinclair, CDJ; Hinds, EA; (2010) Experiments on a videotape atom chip: fragmentation and transport studies. NEW J PHYS , 12 , Article 093017. 10.1088/1367-2630/12/9/093017. Gold open access

Granata A, WTT; (2010) The role of TorsinA in dystonia. Eur J Neurol , 17 (Suppl.1) pp. 81-87.

H

Hansson, O; Zetterberg, H; Blennow, K; (2010) Evaluation of plasma A beta 40 and A beta 42 as predictors of conversion to Alzheimer's disease in patients with mild cognitive impairment Response. NEUROBIOLOGY OF AGING , 31 (4) p. 541. 10.1016/j.neurobiolaging.2008.09.006.

Hardy, J; (2010) Genetics of tauopathies. In: EUROPEAN NEUROPSYCHOPHARMACOLOGY. (pp. S163 - S163). ELSEVIER SCIENCE BV

Hardy, J; (2010) The genetics of parkinsonisms. In: JOURNAL OF NEUROLOGY. (pp. S8 - S8). SPRINGER HEIDELBERG

Houlden, HP; Favaregh, AL; Hemsch, MJ; (2010) Quantification of the uncertainties for the Ares I A106 ascent aerodynamic database. 27th AIAA Aerodynamic Measurement Technology and Ground Testing Conference 2010

I

Innes, A; Kalmar, B; Houlden, H; Reilly, MM; Greensmith, L; (2010) Characterisation of novel mutations within HSP27 causing Charcot-Marie-Tooth disease 2F and distal hereditary motor neuropathy II. In: NEUROMUSCULAR DISORDERS. (pp. S21 - S22). PERGAMON-ELSEVIER SCIENCE LTD

Isaacs, JD; Adams, M; Lees, AJ; (2010) Noncompressive myelopathy associated with violent axial tics of tourette syndrome. Neurology , 74 (8) pp. 697-698. 10.1212/WNL.0b013e3181d0cc77.

K

Kay, V; Vandrovcova, J; Pittmann, A; Lees, A; de Silva, R; (2010) Tau gene polymorphism influences risk of sporadic tauopathy by allele-specific changes in transcription and alternative splicing. In: MOVEMENT DISORDERS. (pp. S475 - S475). WILEY-LISS

Kruer, MC; Paisan-Ruiz, C; Yoon, MY; Gregory, A; Woltjer, RL; Malandrini, A; Polster, BJ; ... Hayflick, SJ; + view all (2010) Defective Fatty Acid Hydroxylase Leads to a Novel Subtype of Neurodegeneration with Brain Iron Accumulation (NBIA). In: (Proceedings) 39th Annual Meeting of the Child-Neurology-Society. (pp. S30-S31). WILEY-LISS

Kruer, MC; Paisan-Ruiz, C; Yoon, MY; Hama, H; Gregory, A; Malandrini, A; Woltjer, RL; ... Hayflick, SJ; + view all (2010) Mutation in FA2H leads to Fatty Acid Hydroxylase-associated Neurodegeneration (FAHN). In: (Proceedings) 39th Annual Meeting of the Child-Neurology-Society. (pp. S91-S91). WILEY-LISS

L

Lashley, T; Rohrer, J; Bandopadhyay, R; Ahmed, Z; Borroni, B; Warren, J; Troakes, C; ... Revesz, T; + view all (2010) Frontotemporal lobar degeneration with FUS-positive inclusions. In: BRAIN PATHOLOGY. (pp. 24 - 24). WILEY-BLACKWELL PUBLISHING, INC

Lees, A; (2010) Clinical Neuropathologic Correlation. MOVEMENT DISORDERS , 25 S575-S575.

Lees, AJ; (2010) Chronic manganism clinical features and causes. In: (pp. p. 633).

Lees, AJ; (2010) Expanding the links between Brazilian and British neurology. Arq Neuropsiquiatr , 68 (4) pp. 493-494. Gold open access

Limongelli, G; Rahman, S; Pitceathly, RDS; Hanna, MG; Elliott, PM; (2010) Cardiac manifestations of mitochondrial disorders reply. EUR J HEART FAIL , 12 (6) 637 - 638. 10.1093/eurjhf/hfq046.

Limongelli, G; Tome-Esteban, M; Dejthevaporn, C; Rahman, S; Hanna, MG; Elliott, PM; (2010) Prevalence and natural history of heart disease in adults with primary mitochondrial respiratory chain disease (vol 12, pg 114, 2010). EUROPEAN JOURNAL OF HEART FAILURE , 12 (9) p. 1017. 10.1093/eurjhf/hfq143.

Lindgren, HS; O'Sullivan, SS; Lees, AJ; Cenci, MA; (2010) Immunohistochemical Detection of Fosb/Delta fosb-Like Proteins Maps Areas of Maladaptive Neuroplasticity in the Post-Mortem Parkinsonian Brain. MOVEMENT DISORDERS , 25 S673-S673.

Ling, H; Braschinsky, M; Taba, P; Luus, S; Lees, A; (2010) A decade of delayed diagnosis in two cases of monogenetic parkinsonism. In: (pp. S358-S358).

Ling, H; Lees, AJ; (2010) How can neuroimaging help in the diagnosis of movement disorders? Neuroimaging Clinics of North America , 20 (1) pp. 111-123. 10.1016/j.nic.2009.08.004.

Ling, H; Massey, L; Lees, A; Brown, P; Schwingenschuh, P; Bhatia, K; Day, BL; (2010) Bradykinesia in Parkinson's disease and related conditions. In: (pp. S358-S359).

Ling, H; Massey, LM; Lees, AJ; Brown, P; Schwingenschuh, P; Bhatia, K; Day, BL; (2010) Bradykinesia in Parkinson's Disease and Related Conditions. MOVEMENT DISORDERS , 25 S641-S642.

Ling, H; O'Sullivan, SS; Holton, JL; Revesz, T; Massey, LA; Williams, DR; Paviour, DC; (2010) Does corticobasal degeneration exist? A clinicopathological re-evaluation. Brain: a journal of neurology , 133 (Pt 7) pp. 2045-2057.

Luk, C; Vandrovcova, J; Malzer, E; Lees, AJ; de Silva, R; (2010) Brain Tau Isoform mRNA and Protein Correlation in PSP Brain. Translational Neuroscience , 1 (1) pp. 30-36. 10.2478/v10134-010-0009-8.

M

Maennikkoe, R; Jefferies, C; Flanagan, SE; Hattersley, A; Ellard, S; Ashcroft, FM; (2010) Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptoms. HUMAN MOLECULAR GENETICS , 19 (6) pp. 963-972. 10.1093/hmg/ddp554.

Mamais, A.; (2010) Investigation of an N5-glutamine methyltranferase, a novel partner of α2-chimaerin. Doctoral thesis , UCL (University College London). Green open access
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Massey, L; Paviour, DC; Fox, NC; Micallef, C; Burn, DJ; Holton, JL; Lees, AJ; ... O'Sullivan, SS; + view all (2010) BLINDED ANALYSIS OF CONVENTIONAL MRI IN A COHORT OF PATHOLOGICALLY CONFIRMED PARKINSONIAN ILLNESSES. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. E57 - E57). B M J PUBLISHING GROUP

Massey, LA; Micallef, CD; Paviour, DC; O'Sullivan, SS; Burn, DJ; Holton, JL; Revesz, TA; ... Jager, HR; + view all (2010) Blinded analysis of conventional MR images in a cohort of pathologically confirmed parkinsonian illnesses at the QSBB. In: (Proceedings) 14th International Congress of Parkinson's Disease and Movement Disorders. (pp. S386-S387). WILEY-BLACKWELL

Massey, LA; Sinclair, CD; Mancini, LC; White, MJ; Thornton, JS; Lees, AJ; Yousry, TA; (2010) A multimodal assessment of the brainstem using 3T MRI in PSP and PD. In: MOVEMENT DISORDERS. (pp. S386 - S386). WILEY-LISS

Matthews, E; Sud, R; Labrum, R; Strycharczuk, L; Sinclair, CDJ; Yousry, TA; Hanna, MG; (2010) Using MRI as a diagnostic tool in the skeletal muscle channelopathies. In: NEUROMUSCULAR DISORDERS. (pp. S29 - S30). PERGAMON-ELSEVIER SCIENCE LTD

Miller, A; Ahmed, M; Hanna, MG; Greensmith, L; (2010) AUGMENTATION OF THE HEAT SHOCK RESPONSE IN AN IN VITRO MODEL OF SPORADIC INCLUSION BODY MYOSITIS. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 81 (11) E64 - E64. 10.1136/jnnp.2010.226340.190.

Moglia, C; Calvo, A; Lai, SL; Abramzon, Y; Schymick, JC; Guerreiro, RJ; Stephan, DA; ... Chio, A; + view all (2010) FUS Mutations in a Large Series of Sporadic and Familial ALS. In: NEUROLOGY. (pp. A334 - A334). LIPPINCOTT WILLIAMS & WILKINS

Momeni, P; Wickremaratchi, MM; Bell, J; Arnold, R; Beer, R; Hardy, J; Revesz, T; ... Morris, HR; + view all (2010) Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia. CLIN NEUROL NEUROSUR , 112 (10) 917 - 920. 10.1016/j.clineuro.2010.07.015.

Murphy, SM; Counihan, T; (2010) Cerebrovascular disorders. In: Andreoli, TE and Benjamin, IJ and Griggs, RC and Wing, EJ, (eds.) Andreoli and Carpenter's Cecil essentials of medicine. (pp. 1123-1135). Saunders Elsevier: Philadelphia.

Murphy, SM; Counihan, T; (2010) Cortical syndromes. In: Andreoli, TE and Benjamin, IJ and Griggs, RC and Wing, EJ, (eds.) Andreoli and Carpenter's Cecil essentials of medicine. (pp. 1068-1071). Saunders Elsevier: Philadelphia.

N

Nicaretta, DH; Rosso, ALZ; Mattos, JP; Brandao, L; Pimentel, MLV; Cunha, FC; Novis, SAP; (2010) Dystonia induced by peripheral trauma: Organic or psychogenic? In: (pp. S245-S245).

O

O'Sullivan, S.S.; (2010) Non-motor symptons in Parkinson's disease including the dopamine dysregulation syndrome and impulse control. Doctoral thesis , UCL (University College London).

O'Sullivan, SS; Evans, AH; Quinn, NP; Lawrence, AD; Lees, AJ; (2010) Reckless Generosity in Parkinson's Disease. MOVEMENT DISORD , 25 (2) 221 - 223. 10.1002/mds.22687.

O'Sullivan, SS; Johnson, M; Williams, DR; Revesz, T; Holton, JL; Lees, AJ; Perry, EK; (2010) The effect of drug treatment on neurogenesis in Parkinson's disease. Mov Disord 10.1002/mds.23340.

O'Sullivan, SS; Loane, CM; Lawrence, AD; Evans, AH; Piccini, P; Lees, AJ; (2010) Sleep Disturbance, Dreams, Mood and Impulsive-Compulsive Behaviours in Parkinson's Disease. In: (pp. A279-A279).

Ozawa, T; Holton, JL; Paviour, D; Lees, AJ; Tada, M; Kakita, A; Onodera, O; ... Revesz, T; + view all (2010) Disequilibrium in MSA phenotype distribution between populations: genetics or environment? In: BRAIN PATHOLOGY. (pp. 29 - 29). WILEY-BLACKWELL PUBLISHING, INC

P

Paisan-Ruiz, C; Houlden, H; (2010) Common pathogenic pathways in melanoma and Parkinson disease. NEUROLOGY , 75 (18) 1653 - 1655.

Paisán-Ruiz, C; Li, A; Schneider, S; Holton, JL; Johnson, R; Kidd, D; Chataway, J; ... Houlden, H; + view all (2010) Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations. Neurobiology of Aging

Parkkinen, L; O'Sullivan, SS; Kuoppamaki, M; Collins, C; Holton, JL; Revesz, T; Lees, AJ; (2010) Does L-dopa have toxic effects in Parkinson's disease brain? In: MOVEMENT DISORDERS. (pp. S418 - S418). WILEY-LISS

Pitceathly, RDS; Holton, JL; Miller, JAL; Quinlivan, R; Hanna, MG; (2010) The expanding histopathological profile of the myofibrillar myopathies. In: NEUROMUSCULAR DISORDERS. (pp. S28 - S28). PERGAMON-ELSEVIER SCIENCE LTD

Plessy, C; Bertin, N; Takahashi, H; Simone, R; Salimullah, M; Lassmann, T; Vitezic, M; ... Carninci, P; + view all (2010) Linking promoters to functional transcripts in small samples with nanoCAGE and CAGEscan. Nature Methods , 7 (7) pp. 528-534. 10.1038/nmeth.1470.

R

Rajakulendran, S; Kuntzer, T; Dunand, M; Yau, SC; Ashton, EJ; Storey, H; McCauley, J; ... Hanna, MG; + view all (2010) Marked Hemiatrophy in Carriers of Duchenne Muscular Dystrophy. ARCH NEUROL-CHICAGO , 67 (4) 497 - 500.

Rajakulendran, S; Matthews, E; Tan, SV; Dewar, L; Griggs, RC; Hanna, MG; CINCH Grp, ; (2010) The genetic skeletal muscle channelopathies: genotype-phenotype correlation and longitudinal studies. In: NEUROMUSCULAR DISORDERS. (pp. S16 - S17). PERGAMON-ELSEVIER SCIENCE LTD

Rajakulendran, S; Parton, M; Holton, JL; Hanna, MG; (2010) Clinical and pathological heterogeneity in partial merosin deficiency. In: NEUROMUSCULAR DISORDERS. (pp. S11 - S11). PERGAMON-ELSEVIER SCIENCE LTD

Rajakulendran, S; Tan, SV; Hanna, MG; (2010) Muscle weakness, palpitations and a small chin: the Andersen-Tawil syndrome. Pract Neurol , 10 (4) pp. 227-231. 10.1136/jnnp.2010.217794.

Renton, A.E.M.; (2010) Gene expression and genetic analyses in Parkinson’s disease with and without dementia. Doctoral thesis , UCL (University College London). Green open access
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Revesz, T; Lashley, T; Ahmed, Z; Rohrer, J; Warren, J; Al-Saraj, S; Fox, N; ... Holton, J; + view all (2010) The Spectrum of FUS-Positive Pathology in Frontotemporal Lobar Degenerations. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 552 - 552). LIPPINCOTT WILLIAMS & WILKINS

Rosser, GJ; Reitböck, PG; Gray, MC; Warwicker, P; (2010) Successful stabilisation of nephropathy in a patient with POEMS (polyneuropathy, organomegaly, endocrinopathy, M-band, skin changes) syndrome on treatment with mycophenolate and steroids: a case report. J Med Case Rep , 4 63-. 10.1186/1752-1947-4-63.

Rowe, KC; Paulsen, JS; Langbehn, DR; Duff, K; Beglinger, LJ; Wang, C; O'Rourke, JJF; ... Moser, DJ; + view all (2010) Self-Paced Timing Detects and Tracks Change in Prodromal Huntington Disease. NEUROPSYCHOLOGY , 24 (4) pp. 435-442. 10.1037/a0018905.

Russou, M; Laura, M; Polke, JM; Davis, MB; Blake, J; Bradner, S; Houlden, H; ... Reilly, MM; + view all (2010) Diverse phenotypes are associated with missense mutations in the peripheral myelin protein 22 gene. In: NEUROMUSCULAR DISORDERS. (pp. S21 - S21). PERGAMON-ELSEVIER SCIENCE LTD

Ryan, D; Murphy, S; Hennessy, M; (2010) Bilateral posterior cerebral artery infarction. [Digital scholarly resource]. (In press).

S

Saidha, S; Murphy, S; McCartthy, P; Mayne, PD; Hennessy, M; (2010) L-2-hydroxyglutaric aciduria diagnosed in an adult presenting with acute deterioration. Journal of Neurology , 247 pp. 146-148. 10.1007/s00415-009-5319-8.

Saidha, S; Murphy, S; Ronayne, A; McCarthy, P; Hennessy, MJ; Counihan, T; (2010) Treatment of anti-glutamic acid decarboxylase antibody-associated limbic encephalitis with mycophenolate mofetil. Journal of Neurology , 257 pp. 1035-1038. 10.1007/s00415-010-5476-9.

Sailer, A; Kurzawa, M; Chinnery, PF; McKeith, IG; Morris, CM; Houlden, H; (2010) The SNCA locus in dementia with Lewy bodies. In: MOVEMENT DISORDERS. (pp. S488 - S488). WILEY-LISS

Sailer, A; Paisa-Puiz, C; Li, A; Paudel, R; Scholz, SW; Ahmed, Z; Revesz, T; ... Houlden, H; + view all (2010) Genetic analysis of the MAPT locus in multiple system atrophy. In: EUROPEAN JOURNAL OF NEUROLOGY. (pp. 598 - 598). WILEY-BLACKWELL

Scholz, S.W.; (2010) The promise of genome‐wide SNP genotyping: from population genetics to disease gene identification. Doctoral thesis , UCL (University College London). Green open access
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Schorge, S; Matthews, E; Kullmann, DM; Hanna, MG; (2010) VOLTAGE SENSOR CHARGE LOSS ACCOUNTS FOR MOST CASES OF HYPOKALEMIC PERIODIC PARALYSIS Reply. NEUROLOGY , 74 (3) 269 - 270.

Selikhova, M; O'Sullivan, SS; Guekht, A; Revesz, T; Lees, A; (2010) Clinico- Demographical Correlations of Dementia in Pathologically Confirmed PD. MOVEMENT DISORD , 25 S693 - S693.

Sewry, CA; Holton, JH; Dick, DJ; Jacques, TS; Muntoni, F; Hanna, MG; (2010) Zebra body myopathy resolved. In: (pp. p. 8).

Sharma, S.; (2010) LRRK2 genetics and expression in the Parkinsonian brain. Doctoral thesis , UCL (University College London). Green open access
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Sinclair, CDJ; Morrow, JM; Yousry, TA; Reilly, MM; Hanna, MG; Golay, X; Thornton, JS; (2010) Inter-scan reproducibility of quantitative neuromuscular MRI. In: NEUROMUSCULAR DISORDERS. (pp. S28 - S28). PERGAMON-ELSEVIER SCIENCE LTD

Sinclair, CDJ; Samson, RS; Thomas, DL; Weiskopf, N; Lutti, A; Thornton, JS; Golay, X; (2010) Quantitative magnetization transfer MRI: a potential new source of biomarkers in skeletal muscle? In: NEUROMUSCULAR DISORDERS. (pp. S28 - S29). PERGAMON-ELSEVIER SCIENCE LTD

Sokolovsky, N; Cook, A; Hunt, H; Giunti, P; Cipolotti, L; (2010) Erratum: A preliminary characterisation of cognition and social cognition in spinocerebellar ataxia types 2, 1, and 7 (Behavioural Neurology (2010) 23:1 (17-29) DOI: 10.3233/BEN20100270). Behavioural Neurology , 23 (3) 159-. 10.3233/BEN-2010-0280.

Srai, SK; Chung, BM; Marks, J; Pourvali, K; Solanky, N; Rapisarda, C; Chaston, TB; ... Sharp, PA; + view all (2010) Erythropoietin regulates intestinal iron absorption in a rat model of chronic renal failure. KIDNEY INT , 78 (7) 660 - 667. 10.1038/ki.2010.217.

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TT, DKPJBLLDWCSJRCAECNQSP-HIOTHSGIW; (2010) "Frontal" behaviors before the diagnosis of Huntington's disease and their relationship to markers of disease progression: evidence of early lack of awareness. J Neuropsychiatry Clin Neurosci , 22 pp. 196-207.

Tomidokoro, Y; Tamaoka, A; Holton, JL; Lashley, T; Frangione, B; Revesz, T; Rostagno, A; (2010) Pyroglutamate formation at the N-termini of ABri molecules in familial british dementia is not restricted to the central nervous system. Hirosaki Medical Journal , 61 (SUPPL.)

U

Ule, J; Wang, Z; Kayikci, M; Briese, M; Zarnack, K; Luscombe, NM; Rot, G; ... Curk, T; + view all (2010) iCLIP predicts the dual splicing effects of TIA-RNA interactions. PLoS Biology , 8 (10) 10.1371/journal.pbio.1000530. Gold open access

V

Vandrovcova, J; Anaya, F; Kay, V; Lees, A; Hardy, J; de Silva, R; (2010) Disentangling the Role of the Tau Gene Locus in Sporadic Tauopathies. CURR ALZHEIMER RES , 7 (8) 726 - 734.

W

Wain, LV; Shrine, NRG; Shaw, C; Powell, JF; Hardy, J; Shaw, P; Morrison, KE; ... Tobin, MD; + view all (2010) The Role of Common Copy Number Variation in Amyotrophic Lateral Sclerosis (ALS). In: GENETIC EPIDEMIOLOGY. (pp. 929 - 930). WILEY-BLACKWELL

Wedderburn, LR; Varsani, H; Charman, SC; Amato, AA; Banwell, B; Bove, KE; Corse, AM; ... UK JDM Res Grp, ; + view all (2010) VALIDATION OF A HISTOPATHOLOGICAL SCORE TOOL FOR THE MEASUREMENT OF SEVERITY IN MUSCLE BIOPSIES FROM PATIENTS WITH JUVENILE DERMATOMYOSITIS. In: RHEUMATOLOGY. (pp. I116 - I116). OXFORD UNIV PRESS

Wedderburn, LR; Varsani, H; Charman, SC; Amato, AA; Banwell, B; Bove, KE; Corse, AM; ... Holton, JL; + view all (2010) Validation of a histopathological score tool for the measurement of severity in muscle biopsies from patients with juvenile dermatomyositis. In: (pp. p. 7).

Willis, TA; Hollingsworth, KG; Sveen, ML; Morrow, J; Vandenheede, J; Mayhew, A; Eagle, M; ... Straub, V; + view all (2010) Assessing muscle pathology by MRI in LGMD2I. In: NEUROMUSCULAR DISORDERS. (pp. 666 - 666). PERGAMON-ELSEVIER SCIENCE LTD

Wray, S; Hardy, J; (2010) All MAPT out?: Well-travelled pathways into neurodegeneration. Biochemist , 32 (2) pp. 14-17.

Wu, K; O'Sullian, S; Politis, M; Bose, S; Lees, A; Piccini, P; (2010) REWARDING VISUAL CUES INCREASE DOPAMINE NEUROTRANSMISSION IN PARKINSON'S PATIENTS WITH IMPULSE CONTROL DISORDERS: A PET STUDY. In: (Proceedings) Annual Meeting of the Association-of-British-Neurologists. (pp. E29-E30). B M J PUBLISHING GROUP

Wu, K; Politis, M; O'Sullivan, S; Bose, S; Lees, A; Piccini, P; (2010) Impulse Control Disorders Subtypes in Parkinson's Disease: Clinical and PET Correlations. MOVEMENT DISORDERS , 25 S725-S726.

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Y

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