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Number of items: 131.

A

Adlkofer, F; Aguzzi, A; Baumeister, R; Haass, C; Silva, ODE; DeStrooper, B; Dotti, C; ... Wiltfang, J; + view all (2002) Early diagnosis of Alzheimer's disease and related dementia (DIADEM) - A research network funded by the European Union. NEUROBIOL AGING , 23 (1) S383 - S383.

B

Bandmann, O; Wood, NW; (2002) Dopa-responsive dystonia - The story so far. NEUROPEDIATRICS , 33 (1) pp. 1-5. 10.1055/s-2002-23590.

Bensimon, G; Leigh, PN; Ludolph, A; Lacomblez, L; Vidailhet, M; Landwehrmeyer, B; Burn, D; ... Grp, NNIPPSS; + view all (2002) Neuroprotection and Natural History in Parkinson Plus Syndromes (NNIPPS): Design and progress report of a clinical trial of the efficacy and safety of riluzole in Progressive Supranuclear Palsy (PSP) and Multiple System Atrophy (MSA). In: (pp. S256-S256).

Bloem, BR; Mazibrada, G; Schrag, A; Viswanathan, R; Lees, AJ; Quinn, NP; (2002) Falls and injuries in Progressive Supranuclear Palsy (PSP). In: (Proceedings) 7th International Congress of Parkinsons Disease and Movement Disorders. (pp. S252-S252). WILEY-LISS

Brealey, D.; Brand, M.; Hargreaves, I.; Heales, S.; Land, J.; Smolenski, R.; Davies, N.A.; ... Singer, M.; + view all (2002) Association between mitochondrial dysfunction and severity and outcome of septic shock. The Lancet , 360 (9328) pp. 219-223. 10.1016/S0140-6736(02)09459-X.

C

Camfield, L; Ben-Shlomo, Y; Warner, TT; Epidemiological Study Dystonia Eur, ; (2002) Impact of cervical dystonia on quality of life. MOVEMENT DISORD , 17 (4) 838 - 841. 10.1002/mds.10127.

Caselli, RJ; Hentz, JG; Osborne, D; Graff-Radford, NR; Barbieri, CJ; Alexander, GE; Hall, GR; ... Saunders, AM; + view all (2002) Apolipoprotein E and intellectual achievement. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY , 50 (1) pp. 49-54. 10.1046/j.1532-5415.2002.50007.x.

Cenci, AM; Andersson, M; Daniel, SE; Kingsbury, AE; Kilford, L; Lees, AJ; (2002) Striatal expression of FosB-related transcription factors in human Parkinson's disease: Relation to L-dopa-induced dyskinesia. In: (pp. S98-S98).

Colosimo, C; Hughes, AJ; Kilford, L; Lees, AJ; (2002) Lewy body cortical involvement may not always predict dementia in Parkinson's disease. In: (pp. S134-S134).

Colosimo, C; Osaki, Y; Vanacore, N; Lees, AJ; (2002) Lack of association between progressive supranuclear palsy and arterial hypertension: A clinico-pathological study. In: (pp. S254-S255).

Cordivari, C; (2002) Botulinum toxins in the treatment of limb dystonia. In: (pp. pp. 55-63).

Cordivari, C; Lees, AJ; Misra, P; Brown, P; (2002) EMG-EMG coherence in writer's cramp. MOVEMENT DISORD , 17 (5) 1011 - 1016. 10.1002/mds.10212.

Cordivari, C; Vincent, A; Misra, VP; Catania, S; Bhatia, KP; Lees, AJ; (2002) Patients with cervical dystonia thought to be secondary non responders to botulinum toxin treatment should be given a trial of EMG guided injections. In: MOVEMENT DISORDERS. (pp. S295 - S296). WILEY-LISS

Costa, DC; Lees, AJ; (2002) Dopamine neurotransmission, Parkinson's disease and SPET. EUR J NUCL MED , 29 (1) 163 - 163.

Cowan, DA; Russell, NJ; Mamais, A; Sheppard, DM; (2002) Antarctic Dry Valley mineral soils contain unexpectedly high levels of microbial biomass. EXTREMOPHILES , 6 (5) 431 - 436. 10.1007/s00792-002-002-0276-5.

D

Dale, RC; Church, AJ; Surtees, RA; Lees, AJ; Neville, AG; Giovannoni, G; (2002) Re-emergence of encephalitis lethargica-like syndrome: Evidence of CNS autoimmunity. In: (Proceedings) 7th International Congress of Parkinsons Disease and Movement Disorders. (pp. S260-S260). WILEY-LISS

Dale, RC; Church, AJ; Surtees, RAH; Lees, AJ; Neville, BGR; Giovanni, G; (2002) Re-emergence of encephalitis lethargica: New evidence of an autoimmune CNS disease. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 73 (2) p. 214.

Davies, NP; Weber, A; Mueller, R; Hilton-Jones, D; Chinnery, PF; Hanna, MG; (2002) Andersen's syndrome: A skeletal muscle potassium channel disorder. In: (Proceedings) 10th International Congress on Neuromuscular Diseases. (pp. S54-S54). ELSEVIER SCIENCE BV

Davies, NP; Weber, A; Mueller, R; Hilton-Jones, D; Chinnery, PF; Hanna, MG; (2002) Periodic paralysis, malignant ventricular arrhythmia and dysmorphism (Andersen's syndrome): A skeletal muscle potassium channel disorder. J NEUROL NEUROSUR PS , 73 (2) 221 - 221.

De Carvalho, M; Houlden, H; Goizet, C; Lacombe, D; (2002) Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation [4] (multiple letters). Neurology , 59 (11) 1823-.

Dobson-Stone, C; Danek, A; Rampoldi, L; Hardie, RJ; Chalmers, RM; Wood, NW; Bohlega, S; ... Monaco, AP; + view all (2002) Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. Eur J Hum Genet , 10 (11) pp. 773-781. 10.1038/sj.ejhg.5200866.

de Carvalho, M; Houlden, H; (2002) Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation. NEUROLOGY , 59 (11) 1823 - 1823.

de Silva, R; (2002) Functional aspects of alpha-synuclein. In: Neurodgenerative Disorders Associated with α-Synuclein Pathology. (pp. 1-10). Medicina stm Editores, S.L.: Barcelona.

de Silva, R; Lashley, T; Gibb, G; Hanger, D; Revesz, T; Lees, A; (2002) Dissection of tau isoform composition of tauopathy lesions using novel isoform-specific monoclonal antibodies. In: MOVEMENT DISORDERS. (pp. S20 - S20). WILEY-LISS

E

Eapen, V; Lees, AJ; Lakke, JPWF; Trimble, MR; Robertson, MM; (2002) Adult-onset tic disorders. MOVEMENT DISORD , 17 (4) 735 - 740. 10.1002/mds.10180.

Edwards, MJ; Wood, NW; Bhatia, KP; (2002) Unusual phenotypes in DYT1 dystonia: A report of 5 cases and review of the literature. In: MOVEMENT DISORDERS. (pp. S309 - S309). WILEY-LISS

Eunson, L; Khan, NL; Quinn, N; Bhatia, K; Wood, NW; Davis, MB; (2002) Novel parkin mutations in early-onset parkinsonism. In: JOURNAL OF MEDICAL GENETICS. (pp. S71 - S71). BRITISH MED JOURNAL PUBL GROUP

Everett, CM; Saveliev, A; Webster, Z; Wood, NW; Festenstein, R; (2002) The molecular basis for aberrant gene regulation in Friedreich's ataxia. J NEUROL NEUROSUR PS , 73 (2) 225 - 225.

F

Fidani, L; Goulas, A; Mirtsou, V; Petersen, RC; Tangalos, E; Crook, R; Hardy, J; (2002) Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease. NEUROSCIENCE LETTERS , 323 (1) pp. 81-83. 10.1016/S0304-3940(02)00114-3.

G

Garrard, P; Blake, J; Stinton, V; Hanna, M; Reilly, M; Holton, J; Landon, D; (2002) Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA? Journal of Neurology, Neurosurgery and Psychiatry , 73 (2) pp.207-208.

Garrard, P; Blake, J; Stinton, V; Hanna, MG; Reilly, MM; Holton, JL; Landon, DN; (2002) Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA? J NEUROL NEUROSUR PS , 73 (2) 207 - 208. Green open access
file

Goldstein, DB; Ramachandran, V; Wood, N; Shorvon, S; (2002) Pharmacogenomics of neurological disorders. In: Pharmacogenomics: The search for Individualised Therapies.

H

Hanna, MG; Wood, NW; (2002) Running a neurogenetic clinic. J NEUROL NEUROSUR PS , 73 2 - 4.

Hardy, J; (2002) Pathways to primary neurodegenerative disease. NEUROLOGIA , 17 (8) pp. 399-401.

Hardy, J; (2002) The real problem in association studies. AMERICAN JOURNAL OF MEDICAL GENETICS , 114 (2) p. 253. 10.1002/ajmg.10294.

Hawthorne, M; (2002) Botulinum toxins in the treatment of laryngeal and oromandibular dystonia. In: (pp. pp. 40-46).

Henderson, JN; Crook, R; Crook, J; Hardy, J; Onstead, L; Carson-Henderson, L; Mayer, P; ... Williams, B; + view all (2002) Apolipoprotein E4 and tau allele frequencies among Choctaw Indians. NEUROSCIENCE LETTERS , 324 (1) pp. 77-79. 10.1016/S0304-3940(02)00150-7.

Holton, J; Lashley, T; Revesz, T; Rostagno, A; Frangione, B; Ghiso, J; (2002) Morphological evidence of the activation of the classical complement pathway in the BRI gene-related dementias. NEUROBIOL AGING , 23 (1) S205 - S206.

Holton, J.L.; Lashley, T.; Ghiso, J.; Braendgaard, H.; Vidal, R.; Guerin, C.; Gibb, G.; ... Revesz, T.; + view all (2002) Familial Danish dementia: a novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta. Journal of Neuropathology and Experimental Neurology , 61 (3) pp. 254-267.

Holton, JL; Revesz, T; Crooks, R; Scaravilli, F; (2002) Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia. ACTA NEUROPATHOL , 103 (3) 221 - 227. 10.1007/s004010100457.

Houlden, H; Roper, H; Willis, T; Schenone, A; Di Battista, C; Wood, NW; Reilly, M; (2002) Giant axonal neuropathy is caused by mutations in the gigaxonin gene: Clinical, genetic, and pathological characterisation of three families. J NEUROL NEUROSUR PS , 73 (2) 225 - 225.

Houlden, H; Smith, S; de Carvalho, M; Mathias, C; Blake, J; Wood, NW; Reilly, M; (2002) Clinical and genetic characterisation of families with triple a (Allgrove) syndrome. J NEUROL NEUROSUR PS , 73 (2) 225 - 225.

Houlden, H.; Smith, S.; de Carvalho, M.; Blake, J.; Mathias, C.; Wood, N.W.; Reilly, M.M.; (2002) Clinical and genetic characterization of families with triple A (Allgrove) syndrome. Brain , 125 (12) pp. 2681-2690. 10.1093/brain/awf270.

Hughes, AJ; Lees, AJ; (2002) The evolution of the acute response to L-dopa in Parkinson's disease. In: (pp. S97-S98).

Hyman, N; (2002) Botulinum toxins in the treatment of cervical dystonia. In: (pp. pp. 10-15).

J

Jacques, TS; Holton, J; Watts, PM; Wills, AJ; Smith, SE; Hanna, MG; (2002) Tubular agaregate myopathy with abnormal pupils and skeletal deformities. J NEUROL NEUROSUR PS , 73 (3) 324 - 326.

Janssen, JC; Fox, NC; Harvey, RJ; Houlden, H; Rossor, MN; Beck, JA; Campbell, TA; ... Collinge, J; + view all (2002) Early-onset familial Alzheimer's disease: Mutation frequency in 31 families. NEUROBIOL AGING , 23 (1) S311 - S311.

Jarman, PR; Wood, NW; (2002) Genetics of movement disorders and ataxia. Journal of Neurology, Neurosurgery and Psychiatry , 73 (Suppl.2) II22-II26.

Jarman, PR; Wood, NW; (2002) Genetics of movement disorders and ataxia. J NEUROL NEUROSUR PS , 73 22 - 26.

K

Kambouris, M; Bohlega, SA; Trabzuni, D; Carroll, P; Meyer, BF; (2002) Localization of the gene for a novel autosomal recessive neuromuscular disease featuring tremulous and myoclonic dystonia with MRI white matter alterations. In: (Proceedings) 52nd Annual Meeting of the American-Society-of-Human-Genetics. (pp. p. 443). UNIV CHICAGO PRESS

Katzenschlager, R; Costa, D; Gacinovic, S; Lees, AJ; (2002) [I-123]-FP-CIT-SPECT in the early diagnosis of PD presenting as exercise-induced dystonia. NEUROLOGY , 59 (12) 1974 - 1976.

Katzenschlager, R; Costa, D; Gerschlager, W; O'Sullivan, JD; Lees, AJ; Brown, P; (2002) Dopamine transporter imaging with I-123-FP-CIT SPECT demonstrates marked presynaptic nigrostriatal dopaminergic deficit in orthostatic tremor. In: (pp. S346-S346).

Khan, N; Valente, EM; Brooks, DJ; Piccini, P; Bhatia, KP; Quinn, NP; Wood, NW; (2002) The genetic basis and phenotypic variability in early onset parkinsonism. J NEUROL NEUROSUR PS , 73 (2) 213 - 213.

Khan, NL; Brooks, DJ; Pavese, N; Wood, NW; Lees, AJ; Piccini, P; (2002) Progression of nigrostriatal dysfunction in a parkin kindred: An F-18-dopa PET and clinical study. J NEUROL NEUROSUR PS , 72 (1) 134 - 134.

Khan, NL; Wood, NW; Bhatia, KP; (2002) Autosomal recessive, DYT-2-like primary torsion dystonia: A new family. In: MOVEMENT DISORDERS. (pp. S275 - S275). WILEY-LISS

Koe, BM; Lees, A; (2002) Joint PSP (Europe) Association/Alzheimer's Society International Medical Workshop - Stowe School, Buckinghamshire, United Kingdom, October 2001 - Abstracts. MOVEMENT DISORDERS , 17 (6) pp. 1401-1402.

L

Lang, A; Lees, A; (2002) Untitled. MOVEMENT DISORDERS , 17 (1) p. 1. 10.1002/mds.10108.

Lang, AE; Lees, A; (2002) Management of Parkinson's disease: An evidence-based review. MOVEMENT DISORDERS , 17 I-I. 10.1002/mds.5554.

Lannuzel, A; Hermann, C; Yousry, C; Lees, A; Caparros-Lefebvre, D; (2002) Encephalomyelitis with rigidity complicating human immunodeficiency virus infection. Mov Disord , 17 (1) pp. 202-204.

Lee, MJ; Huang, YC; Sweeney, MG; Wood, NW; Reilly, MM; Yip, PK; (2002) Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis. J NEUROL , 249 (9) 1311 - 1312. 10.1007/s00415-002-0762-9.

Lees, A; (2002) Optimal patient management with botulinum toxins: evidence and experience. In: (pp. pp. 1-2).

Lees, AJ; (2002) Drugs for Parkinson's disease. Journal of Neurology Neurosurgery and Psychiatry , 73 (6) pp. 607-610. 10.1136/jnnp.73.6.607.

Lees, AJ; (2002) Drugs for Parkinson's disease - Oldies but goodies. J NEUROL NEUROSUR PS , 73 (6) 607 - 610.

Lees, AJ; (2002) Odd and unusual movement disorders. J NEUROL NEUROSUR PS , 72 I17 - I21.

Lees, AJ; (2002) Parkinson's Disease with Dementia (PDD) is the same clinicopathological entity as Dementia with Lewy Bodies (DLB). In: (pp. S9-S9).

Leong, W; Cordivari, C; Houlden, H; Murray, N; Reilly, M; (2002) Point mutations in PMP22 are rare causes of hereditary neuropathy with liability to pressure palsies. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S90 - S91). ELSEVIER SCIENCE BV

Liolitsa, D; Hanna, MG; (2002) Models of mitochondrial disease. INT REV NEUROBIOL , 53 429 - 466.

Lisbonne, M; Plun-Favreau, H; (2002) French Society of Immunology: Cytokine Meeting May 16-17, 2002, Le Croisic, Port-aux-Rocs, France. Eur Cytokine Netw , 13 (4) pp. 474-476.

Littleton, ET; Man, WD; Holton, JL; Landon, DN; Hanna, MG; Polkey, MI; Taylor, GP; (2002) Human T cell leukaemia virus type I associated neuromuscular disease causing respiratory failure. J NEUROL NEUROSUR PS , 72 (5) 650 - 652.

Lovestone, S; Hardy, J; (2002) Psychotic genes or forgetful ones? NEUROLOGY , 59 (1) pp. 11-12. 10.1212/WNL.59.1.11.

Lowe, N; (2002) Botulinum toxins for cosmetic purposes and in the treatment of hyperhidrosis. In: (pp. pp. 23-30).

Ludolph, AC; Bensimon, G; Leigh, N; Lacomblez, L; Landwehrmeyer, B; Burn, D; Vidailhet, M; ... Grp, NNIPPSS; + view all (2002) The European neuroprotection and natural history in Parkinson plus syndromes trial - A natural history anti therapeutic approach to multisystem atrophy and progressive supranuclear palsy. ANNALS OF NEUROLOGY , 52 (3) S56-S56.

M

Misbahuddin, A; Placzek, MR; Chaudhuri, KR; Wood, NW; Bhatia, KP; Warner, TT; (2002) A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm. NEUROLOGY , 58 (1) 124 - 126.

Misbahuddin, A; Placzek, MR; Nemeth, A; Shaw-Smith, C; Warner, TT; (2002) Genetic heterogeneity in myoclonus dystonia syndrome (MDS). In: (Proceedings) 7th International Congress of Parkinsons Disease and Movement Disorders. (pp. S289-S289). WILEY-LISS

Misbahuddin, A.; Placzek, M.R.; Chaudhuri, K.R.; Wood, N.W.; Bhatia, K.P.; Warner, T.T.; (2002) A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm. Neurology , 58 (1) pp. 124-126.

Morris, H.R.; Gibb, G.; Katzenschlager, R.; Wood, N.W.; Hanger, D.P.; Strand, C.; Lashley, T.; ... Revesz, T.; + view all (2002) Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy. Brain , 125 (5) pp. 969-975. 10.1093/brain/awf109.

Myllykangas, L; Polvikoski, T; Reunanen, K; Wavrant-DeVrieze, F; Ellis, C; Hernandez, D; Sulkava, R; ... Tienari, PJ; + view all (2002) ApoE epsilon 3-haplotype modulates Alzheimer beta-amyloid deposition in the brain. AMERICAN JOURNAL OF MEDICAL GENETICS , 114 (3) pp. 288-291. 10.1002/ajmg.10202.

N

Nath, U; Ben-Shlomo, Y; Thomson, R; Lees, A; Burn, D; (2002) Quality of death certification in progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome). In: (pp. S259-S260).

Nicholl, DJ; Vaughan, JR; Khan, NL; Ho, SL; Aldous, DEW; Lincoln, S; Farrer, M; ... Wood, NW; + view all (2002) Two large British kindreds with familial Parkinson's disease: A clinico-pathological and genetic study. Brain , 125 (1) pp. 44-57.

O

O'Brien, C; (2002) Botulinum toxin type B: an overview. In: (pp. pp. 3-9).

O'Brien, C; (2002) Botulinum toxins in the treatment of upper and lower limb spasticity. In: (pp. pp. 16-22).

O'Brien, C; (2002) Discussion: optimal doses for treatment with botulinum toxins. In: (pp. pp. 64-76).

O'Sullivan, JD; Turner, K; Marks, L; Lees, AJ; (2002) Controlled trial of speech therapy and intra-parotid botulinum toxin for the treatment of salivary drooling in Parkinson's disease. In: (pp. S94-S95).

Osaki, Y; Ben-Shlomo, Y; Wenning, G; Daniel, S; Lees, A; Quinn, N; (2002) Do published criteria improve diagnostic accuracy in multiple system atrophy? In: (pp. S251-S251).

Osaki, Y; Colosimo, C; Ben-Shlomo, Y; Wenning, G; Quinn, N; Lees, A; (2002) The accuracy of clinical diagnosis of progressive supranuclear palsy. In: (pp. S261-S261).

P

Parry, EM; Parry, JM; Corso, C; Doherty, A; Haddad, F; Hermine, TF; Johnson, G; ... Williamson, J; + view all (2002) Detection and characterization of mechanisms of action of aneugenic chemicals. Mutagenesis , 17 (6) pp. 509-521. 10.1093/mutage/17.6.509.

Paviour, DC; Schott, JM; Fox, NC; Stevens, JM; Lees, AJ; Rossor, MN; (2002) Picturing atrophy patterns of Progressive Supranuclear Palsy (PSP) in vivo using fluid registered MRI. In: MOVEMENT DISORDERS. (pp. S178 - S179). WILEY-LISS

Perry, EK; Burn, DJ; Kilford, L; Lees, AJ; Perry, RH; (2002) Increased Alzheimer pathology in Parkinson's disease is associated with chronic antimuscarinic drug treatment. In: (pp. S22-S22).

Placzek, MR; Warner, TT; (2002) Basic genetics for the clinical neurologist. J NEUROL NEUROSUR PS , 73 5 - 11.

Placzek, MR; Warner, TT; (2002) Basic genetics for the clinical neurologist. J Neurol Neurosurg Psychiatry , 73 Sup II5-I11.

Poewe, W; (2002) Botulinum toxins in the treatment of blepharospasm and hemifacial spasm. In: (pp. pp. 31-39).

Porta, M; Maggioni, G; (2002) Botulinum toxins in the treatment of tensiontype headache and hypersalivation. In: (pp. pp. 47-54).

Proukakis, C; Hart, PE; Cornish, A; Warner, TT; Crosby, AH; (2002) Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia. J NEUROL SCI , 201 (1-2) 65 - 69.

R

Reilly, M; Lee, MJ; Sweeney, M; Davis, M; Groves, M; Houlden, H; Wood, N; ... Stephenson, D; + view all (2002) The cytosolic chaperonin containing T-complex polypeptide 1 gene (CCT4) is mutated in the mutilated foot rat (MF), an animal model for human hereditary sensory neuropathy. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S10 - S10). ELSEVIER SCIENCE BV

Reilly, MM; Hanna, MG; (2002) Genetic neuromuscular disease. J NEUROL NEUROSUR PS , 73 12 - 21.

Reilly, MM; Hanna, MG; (2002) Genetic neuromuscular disease. J Neurol Neurosurg Psychiatry , 73 Sup II12-II21.

Remy, P; Doder, M; Lees, AJ; Turjanski, N; Hammers, A; Brooks, DJ; (2002) Depression in Parkinson's disease is associated with impaired catecholamine terminal function in the midbrain, thalamus, and anterior cingulate cortex. NEUROLOGY , 58 (7) A488-A488.

Rosenberg, RN; Aminoff, M; BoIler, F; Soerensen, PS; Griggs, RC; Hachinski, V; Hallett, M; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. J Neurol Neurosurg Psychiatry , 72 (2) 143-.

Rosenberg, RN; Aminoff, M; Boller, F; Griggs, RC; Hallett, M; Johnson, RT; Kennard, C; ... Zochodne, D; + view all (2002) Reporting clinical trials: Full access to all the data. CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES , 29 (1) p. 4.

Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hachinski, V; Hallett, M; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all of the data. Arch Neurol , 59 (1) pp. 27-28.

Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hachinski, V; Hallett, M; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. Brain , 125 (Pt 3) i-ii.

Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hachinski, V; Hallett, M; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. Author's right to access to all data obtained in their study. J Neurol , 249 (5) pp. 638-639. 10.1007/s004150200080.

Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hallett, M; Hachinski, V; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. Mov Disord , 17 (1) pp. 3-4.

Rosenberg, RN; Aminoff, M; Boller, F; Sørenson, PS; Griggs, RC; Hachinski, V; Hallett, M; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. Neurology , 58 (3) pp. 347-348.

Rosenberg, RN; Aminoff, MJ; Boller, F; Soerensen, PS; Griggs, RC; Hachinski, V; Hallett, M; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. Muscle Nerve , 25 (2) pp. 133-134.

Rosenberg, RR; Aminoff, M; Boller, F; Sørensen, PS; Griggs, RC; Hallett, M; Johnson, RT; ... Zochodne, D; + view all (2002) Reporting clinical trials: full access to all the data. Eur J Neurol , 9 (2) pp. 123-124.

Rostagno, A; Revesz, T; Lashley, T; Tomidokoro, Y; Magnotti, L; Braendgaard, H; Plant, G; ... Ghiso, J; + view all (2002) Complement activation in chromosome 13 dementias - Similarities with Alzheimer's disease. J BIOL CHEM , 277 (51) 49782 - 49790. 10.1074/jbc.M206448200. Gold open access

Ryten, M; Dunn, PM; Burnstock, G; (2002) ATP regulates the differentiation of mammalian skeletal muscle by activation of a P2X receptor on satellite cells. In: (Proceedings) 7th International Symposium on Adenosine and Adenine Nucleotides. (pp. p. 561). WILEY-BLACKWELL

Ryten, M; Dunn, PM; Neary, JT; Burnstock, G; (2002) ATP regulates the differentiation of mammalian skeletal muscle by activation of a P2X<inf>5</inf>receptor on satellite cells. In: (pp. pp. 345-355).

S

Sambamurti, K; Hardy, J; Refolo, LM; Lahiri, DK; (2002) Targeting APP metabolism for the treatment of Alzheimer's disease. DRUG DEVELOPMENT RESEARCH , 56 (2) pp. 211-227. 10.1002/ddr.10077.

Scherfler, C; Khan, NL; Pavese, N; Lees, AJ; Quinn, NP; Wood, NT; Brooks, DJ; (2002) Striatal and extrastriatal PET measurements of dopa metabolism and D2 receptor status in patients with parkin gene mutations. NEUROLOGY , 58 (7) A201-A201.

Schrag, A; Selai, C; Davis, J; Lees, A; Quinn, N; (2002) Health-related quality of life in patients with Progressive Supranuclear Palsy (PSP). In: MOVEMENT DISORDERS. (pp. S253 - S254). WILEY-LISS

Siddiqui, A; Johnson, M; Dixon, M; Koepp, M; Shorvon, SD; Sander, JWA; Gardiner, RM; ... Wood, NW; + view all (2002) A novel locus on chromosome 2p 14-21 in a British family with generalised epilepsy and febrile seizures. J NEUROL NEUROSUR PS , 73 (2) 224 - 224.

Singleton, AA; Subramony, SH; Hernandez, D; Smith-Jefferson, S; Hussey, J; Gwinn-Hardy, K; Lynch, T; ... Singleton, A; + view all (2002) Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 476 - 476). UNIV CHICAGO PRESS

Smith, CCT; Stanyer, L; Betteridge, DJ; (2002) Evaluation of methods for the extraction of nitrite and nitrate in biological fluids employing high-performance anion-exchange liquid chromatography for their determination. J CHROMATOGR B , 779 (2) 201 - 209.

Spacey, SD; Szczygielski, BI; McRory, JE; Wali, GM; Wood, NW; Snutch, TP; (2002) Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia. J NEURAL TRANSM , 109 (9) 1189 - 1194. 10.1007/s00702-002-0750-3.

Spacey, SD; Valente, EM; Wali, GM; Warner, TT; Jarman, PR; Schapira, AHV; Dixon, PH; ... Wood, NW; + view all (2002) Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene. MOVEMENT DISORD , 17 (4) 717 - 725. 10.1002/mds.10126.

T

Tabrizi, SJ; Rajagopalan, B; Styles, P; Manners, D; Schapira, AH; Warner, TT; (2002) Creatine therapy for Huntington's disease (HD): Clinical and-(31)phosphorous magnetic resonance spectroscopy (P-31 MRS) findings in a one year pilot. In: MOVEMENT DISORDERS. (pp. S319 - S319). WILEY-LISS

Thom, M.; Sisodiya, S.M.; Beckett, A.; Martinian, L.; L.in, W.-R.; Harkness, W.; Mitchell, T.N.; ... Scaravilli, F.; + view all (2002) Cytoarchitectural abnormalities in hippocampal sclerosis. Journal of Neuropathology and Experimental Neurology , 61 (6) pp. 510-519.

Thurrell, AE; Wijnberg, N; Bronstein, AM; Quinn, NP; Lees, AJ; Bloem, BR; (2002) Proprioceptive regulation of postural control in Parkinson's disease (PD). In: (pp. S163-S163).

Tijssen, MAJ; Munchau, A; Marsden, JF; Lees, A; Bhatia, KP; Brown, P; (2002) Descending control of muscles in patients with cervical dystonia. MOVEMENT DISORD , 17 (3) 493 - 500. 10.1002/mds.10121.

V

Vaughan, JR; Revesz, T; Petrucelli, L; Luecking, C; Farrer, M; Lees, AJ; (2002) Prominent neurolibrillary tangle pathology in a Parkin brain. In: MOVEMENT DISORDERS. (pp. S156 - S156). WILEY-LISS

Visvikis, D; Gacinovic, S; Erlandsson, K; Katzenschlager, R; O'Sullivan, JD; Lees, AJ; Costa, DC; (2002) Analysis of 123I-FPCIT 9DaTSCANTM) binding in normal volunteers and Parkinson's disease. In: (pp. pp. 378-379).

Vitaliani, R; Scaravilli, T; Egarter-Vigl, E; Giometto, B; Klein, C; Scaravilli, F; An, SF; (2002) The pathology of the spinal cord in progressive supranuclear palsy. J NEUROPATH EXP NEUR , 61 (3) 268 - 274.

W

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Wu, RM; Shan, DE; Sun, CM; Liu, RS; Hwu, WL; Tai, CH; Hussey, J; ... Lincoln, S; + view all (2002) Clinical, F-18-dopa PET, and genetic analysis of an ethnic chinese kindred with early-onset parkinsonism and parkin gene mutations. MOVEMENT DISORDERS , 17 (4) pp. 670-675. 10.1002/mds.10184.

Z

Zermansky, AJ; Ben-Shlomo, Y; Thomson, R; Lees, AJ; Burn, DJ; (2002) Anxiety and depression in PSP: Common, but unrelated to disease severity. In: (pp. S247-S247).

Zetterberg, H; Rymo, L; Coppola, A; D'Angelo, A; Spandidos, DA; Blennow, K; (2002) Reply to 'MTHFR C677T and A1298C polymorphisms and mutated sequences occurring in cis'. EUROPEAN JOURNAL OF HUMAN GENETICS , 10 (10) pp. 579-582. 10.1038/sj.ejhg.5200863.

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Zijlmans, J; Booij, J; Valk, J; Lees, A; Horstink, M; (2002) Posttraumatic tremor without parkinsonism in a patient with complete contralateral loss of the nigrostriatal pathway. MOVEMENT DISORD , 17 (5) 1086 - 1088. 10.1002/mds.10203.

Zijlmans, J; Daniel, S; Lees, A; (2002) Clinical features of patients with pathology confirmed vascular parkinsonism. In: (pp. S248-S249).

This list was generated on Sun Apr 15 02:06:27 2018 BST.