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Number of items: 56.

A

Abou-Sleiman, PM; Healy, DG; Ahmadi, K; Goldstein, DB; Wood, NW; (2003) Population genetic approaches to Parkinsons disease. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 541 - 541). UNIV CHICAGO PRESS

Abramov, A.Y.; Canevari, L.; Duchen, M.R.; (2003) Changes in intracellular calcium and glutathione in astrocytes as the primary mechanism of amyloid neurotoxicity. Nature Chemical Biology , 23 (12) pp. 5088-5095. Green open access
file

Alves, JD; Ames, PRJ; Donohue, S; Stanyer, L; Nourooz-Zadeh, J; Ravirajan, C; Isenberg, DA; (2003) Antibodies to high-density lipoprotein and beta(2)-glycoprotein I are inversely correlated with paraoxonase activity in systematic lupus erythematosus (vol 46, pg 2686, 2002). ARTHRITIS RHEUM , 48 (1) 284 - 284. 10.1002/art.539.

B

Baumann, M; Mamais, A; McBlane, F; Xiao, H; Boyes, J; (2003) Regulation of V(D)J recombination by nucleosome positioning at recombination signal sequences. EMBO J , 22 (19) 5197 - 5207.

C

Cheung, KK; Ryten, M; Burnstock, G; (2003) Abundant and dynamic expression of G protein-coupled P2Y receptors in mammalian development. DEVELOPMENTAL DYNAMICS , 228 (2) pp. 254-266. 10.1002/dvdy.10378.

Colosimo, C; Osaki, Y; Vanacore, N; Lees, AJ; (2003) Lack of association between progressive supranuclear palsy and arterial hypertension: a clinicopathological study. Mov Disord , 18 (6) pp. 694-697. 10.1002/mds.10392.

Cordivari, C; Vincent, A; Misra, VP; Catania, S; Murray, NMF; Bhatia, KP; Lees, AJ; (2003) Failure to identify change in the cervical dystonia muscle pattern is the main cause of reduced response to BTXA. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 408 - 409). BRITISH MED JOURNAL PUBL GROUP

D

Davies, NA; Cochrane, G; Hanna, M; (2003) Muscle disorders. In: Greenwood, RJ and Barnes, MP and McMillan, TM and Ward, CD, (eds.) Handbook of neurological rehabilitation. (pp. 705-725). Psychology Press: Hove.

Davies, NP; Hanna, MG; (2003) The skeletal muscle channelopathies: distinct entities and overlapping syndromes. CURR OPIN NEUROL , 16 (5) 559 - 568. 10.1097/01.wco.0000093098.34793.09.

de Silva, R.; Lashley, T.; Gibb, G.; Hanger, D.; Hope, A.; Reid, A.; Bandopadhyay, R.; ... Lees, A.; + view all (2003) Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies. Neuropathology and Applied Neurobiology , 29 (3) pp. 288-302. 10.1046/j.1365-2990.2003.00463.x.

E

Edwards, M.J.; Huang, Y.-Z.; Wood, N.W.; Rothwell, J.C.; Bhatia, K.P.; (2003) Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation. Brain , 126 (9) pp. 2074-2080. 10.1093/brain/awg209.

Emre, M; Lees, AJ; (2003) Parkinsonism and dementia: Synucleinopathies, tauopathies and beyond - Introduction. MOVEMENT DISORDERS , 18 S1-S1. 10.1002/mds.10556.

G

GEWINNER, C; Mueller, CW; Soler-Lopez, M; Groner, B; (2003) Signal transducers and activators of transcription (STATs): Activation and Biology. [Book]. X-ray cristal structure of Stat proteins and structure activity relationship. (1st ed.). Springer

Gasser, T; Wood, NW; (2003) Molecular Genetic Diagnosis of Neurological Diseases. In: Neurological Disorders: Course and Treatment: Second Edition. (pp. 1525-1538).

Goldstein, D.B.; Ahmadi, K.R.; Weale, M.E.; Wood, N.W.; (2003) Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends in Genetics , 19 (11) pp. 615-622. 10.1016/j.tig.2003.09.006.

Groves, MJ; Schanzer, A; Simpson, AJ; An, SF; Kuo, LT; Scaravilli, F; (2003) Profile of adult rat sensory neuron loss, apoptosis and replacement after sciatic nerve crush. J NEUROCYTOL , 32 (2) 113 - 122.

H

Hardy, J; (2003) Impact of genetic analysis on Parkinson's disease research. In: MOVEMENT DISORDERS. (pp. S96 - S98). WILEY-LISS

Hardy, J; (2003) The relationship between Lewy body disease, Parkinson's disease, and Alzheimer's disease. Annals of the New York Academy of Sciences , 991 pp. 167-170.

Holton, JL; Beesley, C; Winchester, B; Al-Memar, A; (2003) Vacuolar myopathy in twin girls. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY , 29 (5) p. 525.

Houlden, H.; Lincoln, S.; Farrer, M.; Cleland, P.G.; Hardy, J.; Orrell, R.W.; (2003) Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic. Neurology , 61 (10) pp. 1423-1426.

J

Josephs, K.A.; Holton, J.L.; Rossor, M.N.; Braendgaard, H.; Ozawa, T.; Fox, N.C.; Petersen, R.C.; ... Revesz, T.; + view all (2003) Neurofilament inclusion body disease: a new proteinopathy? Brain , 126 (10) pp. 2291-2303. 10.1093/brain/awg231.

Josephs, KA; Holton, JL; Rossor, MN; Braendgaard, H; Ozawa, T; Fox, NC; Petersen, RC; ... Revesz, T; + view all (2003) Neurofilament inclusion body disease. In: ANNALS OF NEUROLOGY. (pp. S51 - S51). WILEY-LISS

Josephs, KA; Holton, JL; Rossor, MN; Braendgaard, H; Petersen, RC; Pearl, GS; Ganguly, M; ... Revesz, T; + view all (2003) Neurofilament inclusion body disease: a new proteinopathy. NEUROPATH APPL NEURO , 29 (5) 521 - 521.

K

Katzenschlager, R; Cardozo, A; Cobo, MRA; Tolosa, E; Lees, AJ; (2003) Unclassifiable parkinsonism in two European tertiary referral centres for movement disorders. MOVEMENT DISORD , 18 (10) 1123 - 1131. 10.1002/mds.10523.

Katzenschlager, R; Costa, D; Gerschlager, W; O'Sullivan, J; Zijlmans, J; Gacinovic, S; Pirker, W; ... Brown, P; + view all (2003) [I-12]-FP-CIT-SPECT demonstrates dopaminergic deficit in orthostatic tremor. (vol 53, pg 489, 2003). ANNALS OF NEUROLOGY , 54 (2) p. 278.

Khan, N.L.; Graham, E.; Critchley, P.; Schrag, A.E.; Wood, N.W.; Lees, A.J.; Bhatia, K.P.; (2003) Parkin disease: a phenotypic study of a large case series. Brain , 126 (6) pp. 1279-1292. 10.1093/brain/awg142.

Khan, NL; Wood, NW; Bhatia, KP; (2003) Autosomal recessive, DYT2-like primary torsion dystonia - A new family. NEUROLOGY , 61 (12) 1801 - 1803.

Kuoppamaki, M; Giunti, P; Quinn, N; Wood, NW; Bhatia, KP; (2003) Slowly progressive cerebellar ataxia and cervical dystonia: Clinical presentation of a new form of spinocerebellar ataxia? MOVEMENT DISORD , 18 (2) 200 - 206. 10.1002/mds.10308.

L

Lang, AE; (2003) Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike? MOVEMENT DISORDERS , 18 (3) pp. 351-352. 10.1002/mds.10367.

Lang, AE; Lees, AJ; (2003) Untitled. MOVEMENT DISORDERS , 18 (1) p. 1. 10.1002/mds.10410.

Lee, M.-J.; Stephenson, D.A.; Groves, M.J.; Sweeney, M.G.; Davis, M.B.; An, S.-F.; Houlden, H.; ... Reilly, M.M.; + view all (2003) Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene. Human Molecular Genetics , 12 (15) pp. 1917-1925. 10.1093/hmg/ddg198.

Lee, MJ; Stephenson, DA; Groves, MJ; Sweeney, MG; Davis, MB; An, SF; Houlden, H; ... Reilly, MM; + view all (2003) Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene. HUM MOL GENET , 12 (15) 1917 - 1925. 10.1093/hmg/ddg198.

Lees, AJ; (2003) Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings. In: MOVEMENT DISORDERS. (pp. S28 - S33). WILEY-LISS

Lees, AJ; (2003) Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings. Mov Disord , 18 Sup S28-S33. 10.1002/mds.10560.

Lees, AJ; Grosset, DG; (2003) Dopamine transporter imaging. Movement Disorders , 18 (Suppl.) S1-S2.

Lees, AJ; Grosset, DG; (2003) Dopamine transporter imaging. Mov Disord , 18 Sup S1-S2. 10.1002/mds.10570.

Leigh, PN; Ludolph, AC; Payan, CAM; Graf, M; Lacomblez, L; Vidailhet, M; Landwehrmeyer, B; ... Grp, NNIPPSS; + view all (2003) Cross-sectional clinical description of a large prospective cohort of patients with progressive supranuclear palsy or multiple system atrophy: The NNIPPS project. In: (pp. S70-S71).

M

Marques, W; Sweeney, MG; Wood, NW; (2003) Thr(118)met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplication. BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH , 36 (10) pp. 1403-1407. 10.1590/S0100-879X2003001000018.

Moorjani, N; Catarino, P; Westaby, S; Trabzuni, D; Al-Mohanna, F; Ahmad, M; (2003) Pressure overload induces activation of caspase enzymes 3, 8, and 9 in the transition to left ventricular failure. In: (Proceedings) Annual Scientific Conference of the British-Cardiac-Society. (pp. A32-A32). B M J PUBLISHING GROUP

P

Pitt, M.; Houlden, H.; Jacobs, J.; Mok, Q.; Harding, B.; Reilly, M.; Surtees, R.; (2003) Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1. Brain , 126 (12) pp. 2682-2692. 10.1093/brain/awg278.

Prime, KP; Edwards, SG; Pakianathan, MR; Holton, JL; Scaravilli, F; Miller, RF; (2003) Polymyositis masquerading as mitochondrial toxicity. SEX TRANSM INFECT , 79 (5) 417 - 418.

Proukakis, C; Crosby, AH; Auer-Grumbach, M; Wagner, K; Reid, E; Patton, MA; Warner, TT; (2003) Screening of the spastin gene in autosomal dominant hereditary spastic paraplegia reveals seven novel mutations. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 406 - 407). BRITISH MED JOURNAL PUBL GROUP

Pulkes, T; Liolitsa, D; Nelson, IP; Hanna, MG; (2003) Classical mitochondrial phenotypes without mtDNA mutations - The possible role of nuclear genes. NEUROLOGY , 61 (8) 1144 - 1147.

R

Revesz, T; Ghiso, J; Holton, JL; Frangione, B; (2003) Hereditary amyloidoses with neurodegeneration: familial British dementia and familial Danish dementia. In: Dickson, DW, (ed.) Neurodegeneration: the molecular pathology of dementia and movement disorders. (pp. 380-385). ISN Neuropath Press: Basel.

Revesz, T; Holton, JL; (2003) Anatamopathological spectrum of tauopathies. MOVEMENT DISORDERS , 18 S13 - S20. 10.1002/mds.10558.

S

Schott, JM; Paviour, DC; Fox, NC; Stevens, JM; Lees, AJ; Rossor, MN; (2003) Picturing the atrophy patterns of progressive supranuclear palsy and multiple system atrophy in vivo using fluid registered MRI. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 410 - 410). BRITISH MED JOURNAL PUBL GROUP

Sibbing, D; Trender-Gerhardt, I; Wood, NW; Oertel, WH; Bhatia, KP; Bandmann, O; Berg, D; ... Becker, G; + view all (2003) The promoter region of the menkes gene ATP7A is not altered in focal or generalized dystonia [2] (multiple letters). Annals of Neurology , 53 (2) pp. 278-280.

Simpson, RJ; Debnam, ES; Laftah, AH; Solanky, N; Beaumont, N; Bahram, S; Schumann, K; (2003) Duodenal nonheme iron content correlates with iron stores in mice, but the relationship is altered by Hfe gene knock-out. BLOOD , 101 (8) 3316 - 3318. 10.1182/blood-2002-10-3112.

Sultan, R; Hanna, MG; Rahman, S; Isenberg, DA; (2003) International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease. Journal of Rheumatology , 43 (1) pp. 49-54.

W

Weeks, R; Scaravilli, F; Lees, A; Carroll, C; Husain, M; Rudge, P; (2003) Cerebral amyloid angiopathy and motor neurone disease presenting with a progressive supranuclear palsy-like syndrome. Movement Disorders , 18 (3) pp.331-336.

Weeks, RA; Scaravilli, F; Lees, AJ; Carroll, C; Husain, M; Rudge, P; (2003) Cerebral amyloid angiopathy and motor neurone disease presenting with a progressive supranuclear palsy-like syndrome. MOVEMENT DISORD , 18 (3) 331 - 336. 10.1002/mds.10347.

Wilkinson, P.A.; Crosby, A.H.; Turner, C.; Patel, H.; Wood, N.W.; Schapira, A.H.; Warner, T.T.; (2003) A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia. Neurology , 61 (2) pp. 235-238.

Wilkinson, PA; Hart, PE; Patel, H; Warner, TT; Crosby, AH; (2003) SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia. J NEUROL SCI , 216 (1) 43 - 45. 10.1016/S0022-510X(03)00210-7.

Wood, N; (2003) Principles of genetic counselling. In: EPILEPSIA. (pp. 9 - 9). BLACKWELL PUBLISHING INC

Wood, NW; (2003) Neurogenetics. In: Fowler, TJ and Scadding, JW, (eds.) Clinical neurology. (pp. 119-129). Arnold: London.

Worth, PF; Wood, NW; (2003) A systematic and structured approach to the investigation of ataxia. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1166 - 1166). BRITISH MED JOURNAL PUBL GROUP

This list was generated on Sun Jun 17 01:55:43 2018 BST.