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Number of items: 70.

A

An, SF and Giometto, B and Groves, M and Miller, RF and Beckett, AAJ and Gray, F and Tavolato, B and Scaravilli, F (1997) Axonal damage revealed by accumulation of beta-APP in HIV-positive individuals without AIDS. J NEUROPATH EXP NEUR , 56 (11) 1262 - 1268.

An, SF and Scaravilli, F (1997) Early HIV-1 infection of the central nervous system. Arch Anat Cytol Pathol , 45 (2-3) 94 - 105.

B

Baker, M and Kwok, JBJ and Kucera, S and Crook, R and Farrer, M and Houlden, H and Isaacs, A and Lincoln, S and Onstead, L and Hardy, J and Wittenberg, L and Dodd, P and Webb, S and Hayward, N and Tannenberg, T and Andreadis, A and Hallupp, M and Schofield, P and Dark, F and Hutton, M (1997) Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22. ANN NEUROL , 42 (5) 794 - 798.

Bandmann, O and Marsden, CD and Wood, NW (1997) Atypical presentations of DRD mutations. Advances in Neurology

Bandmann, O and Sweeney, MG and Daniel, SE and Marsden, CD and Wood, NW (1997) Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease. J NEUROL , 244 (4) 262 - 265.

Bandmann, O and Sweeney, MG and Daniel, SE and Wenning, GK and Quinn, N and Marsden, CD and Wood, NW (1997) Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration. NEUROLOGY , 49 (6) 1598 - 1604.

Bandmann, O and Vaughan, J and Holmans, P and Marsden, CD and Wood, NW (1997) Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. LANCET , 350 (9085) 1136 - 1139.

Bandmann, O and Vaughan, J and Holmans, P and Marsden, CD and Wood, NW (1997) NAT2 slow acetylator phenotype is associated with familial Parkinson's disease. The Lancet , 350 1142 - 1145.

Bandmann, O and Vaughan, JR and Holmans, P and Marsden, CD and Wood, NW (1997) The role of NAT2 in Parkinson's disease. Advances in Neurology

Bandopadhyay, R and Sinha, A and Pickard, MR and Evans, I and Ekins, RP (1997) Maternal hypothyroxinemia and RXRb mRNA expression in developing rat fetal brain. In: Journal of Endocrinology. (pp. Abst - ?).

C

Cavanagh, JB and Holton, JL and Nolan, CC (1997) Selective damage to the cerebellar vermis in chronic alcoholism: a contribution from neurotoxicology to an old problem of selective vulnerability. Neuropathol Appl Neurobiol , 23 (5) 355 - 363.

Chalmers, RM and RiordanEva, P and Wood, NW (1997) Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy. J NEUROL NEUROSUR PS , 62 (4) 385 - 387.

Crook, R and Ellis, R and Shanks, M and Thal, LJ and PerezTur, J and Baker, M and Hutton, M and Haltia, T and Hardy, J and Galasko, D (1997) Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation. ANNALS OF NEUROLOGY , 42 (1) 124 - 128. 10.1002/ana.410420121.

D

Darling, JL and Warr, TJ and Ashmore, SM and Luxsuwong, M and Revesz, T (1997) Non-isotopic molecular cytogenetics in neuro-oncology. NEUROPATH APPL NEURO , 23 (6) 441 - 456.

daSilva, HAR and Patel, AJ (1997) Presenilins and early-onset familial Alzheimer's disease. NEUROREPORT , 8 (8) R1 - R12.

David, G and Abbas, N and Stevanin, G and Durr, A and Yvert, G and Cancel, G and Weber, C and Imbert, G and Saudou, F and Antoniou, E and Drabkin, H and Gemmill, R and Giunti, P and Benomar, A and Wood, N and Ruberg, M and Agid, Y and Mandel, JL and Brice, A (1997) Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. NAT GENET , 17 (1) 65 - 70.

deSilva, HAR and Jen, A and Wickenden, C and Jen, LS and Wilkinson, SL and Patel, AJ (1997) Cell-specific expression of beta-amyloid precursor protein isoform mRNAs and proteins in neurons and astrocytes. MOLECULAR BRAIN RESEARCH , 47 (1-2) 147 - 156.

E

Eckman, CB and Mehta, ND and Crook, R and Pereztur, J and Prihar, G and Pfeiffer, E and GraffRadford, N and Hinder, P and Yager, D and Zenk, B and Refolo, LM and Prada, CM and Younkin, SG and Hutton, M and Hardy, J (1997) A new pathogenic mutation in the APP gene (1716V) increases the relative proportion of A beta 42(43). HUMAN MOLECULAR GENETICS , 6 (12) 2087 - 2089. 10.1093/hmg/6.12.2087.

F

Fox, NC and Kennedy, AM and Harvey, RJ and Lantos, PL and Roques, PK and Collinge, J and Hardy, J and Hutton, M and Stevens, JM and Warrington, EK and Rossor, MN (1997) Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene - Pedigree but not mutation specific age at onset provides evidence for a further genetic factor. BRAIN , 120 491 - 501.

G

Gasser, T and MullerMyhsok, B and Wszolek, ZK and Durr, A and Vaughan, JR and Bonifati, V and Meco, G and Bereznai, B and Oehlmann, R and Agid, Y and Brice, A and Wood, N (1997) Genetic complexity and Parkinson's disease. SCIENCE , 277 (5324) 388 - 389.

Giometto, B and An, SF and Groves, M and Scaravilli, T and Geddes, JF and Miller, R and Tavolato, B and Beckett, AA and Scaravilli, F (1997) Accumulation of beta-amyloid precursor protein in HIV encephalitis: relationship with neuropsychological abnormalities. Ann Neurol , 42 (1) 34 - 40. 10.1002/ana.410420108.

Giometto, B and An, SF and Groves, M and Scaravilli, T and Geddes, JF and Miller, R and Tavolato, B and Beckett, AAJ and Scaravilli, F (1997) Accumulation of beta-amyloid precursor. ANN NEUROL , 42 (1) 34 - 40.

Giometto, B and Miotto, D and Botteri, M and Alessio, L and Scanarini, M and An, SF and Tavolato, B (1997) Folliculo-stellate cells of human pituitary adenomas: Immunohistochemical study of the monocyte/macrophage phenotype expression. NEUROENDOCRINOLOGY , 65 (1) 47 - 52.

Giometto, B and Scaravilli, T and Nicolao, P and An, SF and Groves, M and Tavolato, B and Beckett, AAJ and Scaravilli, F (1997) Detection of paraneoplastic anti-neuronal autoantibodies on paraffin-embedded tissues. BRAIN PATHOL , 7 (4) 1146 - 1146.

Giometto, B and Scaravilli, T and Nicolao, P and An, SF and Groves, M and Tavolato, B and Beckett, AAJ and Scaravilli, F (1997) The use of paraffin-embedded tissue for detection of antineuronal antibodies - Reply. ACTA NEUROPATHOL , 94 (3) 301 - 301.

Giunti, P and Sweeney, MG and Davis, MB and Wood, NW (1997) Characterization of the SCA2 CAG repeat expansion in ADCA type I families. J MED GENET , 34 548 - 548.

H

Hand, KSP and Baird, VH and VanPaesschen, W and Koepp, MJ and Revesz, T and Thom, M and Harkness, WFJ and Duncan, JS and Bowery, NG (1997) Central benzodiazepine receptor autoradiography in hippocampal sclerosis. BRIT J PHARMACOL , 122 (2) 358 - 364.

Hanna, M and Mills, K and Pazdera, L and Newsom-Davis, J (1997) Primary orthostatic tremor with prominent muscle hypertrophy. Neurology , 49 (3) 872 - 874.

Hanna, MG and Bhatia, KP (1997) Movement disorders and mitochondrial dysfunction. CURR OPIN NEUROL , 10 (4) 351 - 356.

Hanna, MG and Davis, MB and Sweeney, MG and Nousanjani, M and Ellis, C and Elliott, P and Wood, NW (1997) Generalised chorea in two patients harbouring Friedrich's ataxia trinucleotide repeat expansion. Movement Disorders

Hanna, MG and Vaughan, JR and Silburn, PA and Davis, PTG and Greenhall, RCD and Squier, MV and Mills, KR and Renowden, S and Sellar, A (1997) Two unusual clinical presentations of the mitochondrial DNP, A3243G point mutation in adult neurological practice. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 62 (5) 544 - 546. 10.1136/jnnp.62.5.544.

Hardy, J (1997) Amyloid, the presenilins and Alzheimer's disease. TRENDS IN NEUROSCIENCES , 20 (4) 154 - 159. 10.1016/S0166-2236(96)01030-2.

Hardy, J (1997) The 'amyloid cascade hypothesis' of AD: decoy or real McCoy? Reply. TRENDS IN NEUROSCIENCES , 20 (12) 559 - 559.

Hardy, J (1997) The Alzheimer family of diseases: Many etiologies, one pathogenesis? PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 94 (6) 2095 - 2097. 10.1073/pnas.94.6.2095.

Holton, JL and Nolan, CC and Burr, SA and Ray, DE and Cavanagh, JB (1997) Increasing or decreasing nervous activity modulates the severity of the glio-vascular lesions of 1,3-dinitrobenzene in the rat: effects of the tremorgenic pyrethroid, Bifenthrin, and of anaesthesia. Acta Neuropathol , 93 (2) 159 - 165.

Hutton, M and Hardy, J (1997) The presenilins and Alzheimer's disease. HUMAN MOLECULAR GENETICS , 6 (10) 1639 - 1646. 10.1093/hmg/6.10.1639.

J

Jarman, PR and Bandmann, O and Marsen, CD and Wood, NW (1997) GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs. J NEUROL NEUROSUR PS , 63 (3) 304 - 308.

Jarman, PR and Davis, MB and Hodgson, SV and Marsden, CD and Wood, NW (1997) Paroxysmal dystonic choreoathetosis - Genetic linkage studies in a British family. BRAIN , 120 2125 - 2130.

Jarman, PR and Wood, NW and Davis, MT and Davis, PV and Bhatia, KP and Marsden, CD and Davis, MB (1997) Hereditary geniospasm: Linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity. AM J HUM GENET , 61 (4) 928 - 933.

Jen, A and Wickenden, C and de Silva, HAR and Patel, AJ (1997) Preparation and purification of antisera against different regions or isoforms of beta-amyloid precursor protein. BRAIN RES PROTOC , 2 (1) 23 - 30.

K

Kellett, MW and Fletcher, NA and Wood, N and Enevoldson, TP (1997) Trinucleotide (GAA)n repeat expansion in two families with Friedreich's ataxia with retained reflexes. J NEUROL NEUROSUR PS , 63 (6) 780 - 783.

Koepp, MJ and Richardson, MP and Labbe, C and Brooks, DJ and Cunningham, VJ and Ashburner, J and VanPaesschen, W and Revesz, T and Duncan, JS (1997) C-11-flumazenil PET, volumetric MRI, and quantitative pathology in mesial temporal lobe epilepsy. NEUROLOGY , 49 (3) 764 - 773.

Kompoliti, K and Pappert, EJ and Goetz, CG and Ford, B and Wood, NW (1997) Progressive cognitive decline with truncal/limb ataxia and ballistic movements. MOVEMENT DISORD , 12 (6) 1075 - 1084.

Kwok, JBJ and Taddei, K and Hallupp, M and Fisher, C and Brooks, WS and Broe, GA and Hardy, J and Fulham, MJ and Nicholson, GA and Stell, R and Hyslop, PHS and Fraser, PE and Kakulas, B and Clarnette, R and Relkin, N and Gandy, SE and Schofield, PR and Martins, RN (1997) Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype. NEUROREPORT , 8 (6) 1537 - 1542. 10.1097/00001756-199704140-00043.

L

Lambert, JC and PerezTur, J and Dupire, MJ and Galasko, D and Mann, D and Amouyel, P and Hardy, J and Delacourte, A and ChartierHarlin, MC (1997) Distortion of allelic expression of apolipoprotein E in Alzheimer's disease. HUMAN MOLECULAR GENETICS , 6 (12) 2151 - 2154. 10.1093/hmg/6.12.2151.

Lamont, PJ and Davis, MB and Wood, NW (1997) Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients - Clinical and genetic correlates. BRAIN , 120 673 - 680.

Lodi, R and Taylor, DJ and Tabrizi, SJ and Kumar, S and Sweeney, M and Wood, NW and Styles, P and Radda, GK and Schapira, AHV (1997) In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by P-31 magnetic resonance spectroscopy. ANN NEUROL , 42 (4) 573 - 579.

Lopes, J and Vandenberghe, A and Tardieu, S and Ionasecu, V and Levy, N and Wood, NW and Tachi, N and Bouche, P and Brice, A and Le Guern, E (1997) The 17p11.2 rearrangements resulting in CMT1A and HNPP are observed at different frequencies and occur by different sex-dependent mechanisms. Nature Genetics

N

Nelson, I and Hanna, MG and Wood, NW and Harding, AE (1997) Depletion of mitochondrial DNA by ddC in untransformed human cell lines. Somatic Cell and Molecular Genetics , 23 (4) 287 - 290.

Nelson, I and Hanna, MG and Wood, NW and Harding, AE (1997) Depletion of mitochondrial DNA by ddC in untransformed human cell lines. SOMAT CELL MOLEC GEN , 23 (4) 287 - 290.

P

Patel, AJ and Jen, A and Wickenden, C and Jen, LS and Gentleman, SM and deSilva, HAR (1997) Glia-derived cytokines and the biogenesis of amyloid plaques in Alzheimer's disease. MOLECULAR PSYCHIATRY , 2 (2) 130 - 132. 10.1038/sj.mp.4000226.

Pickard, MR and Evans, IM and Bandopadhyay, R and Leonard, AJ and Sinha, AK and Ekins, RP (1997) Thyroid hormone action in rat brain from fetal to adult life. In: Hendrich, CE, (ed.) Recent Research Developments in Neuroendocrinology - Thyroid Hormone and Brain Maturation. (15 - 29). Research Signpost: Trivandrum.

Plante-Bordeneuve, V and Taussig, D and Thomas, F and Said, G and Wood, NW and Marsden, CD and Harding, AE (1997) Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele. Neurology , 48 1589 - 1593.

R

Revesz, T and Gibb, GM and Anderton, BH and Daniel, SE (1997) Tau-patterns in typical and atypical cases of the Steele-Richardson-Olszewski syndrome (SROS). J NEUROPATH EXP NEUR , 56 (5) 80 - 80.

Revesz, T and McLaughlin, JL and Rossor, MN and Lantos, PL (1997) Pathology of familial Alzheimer's disease with Lewy bodies. J NEURAL TRANSM-SUPP (51) 121 - 135.

Rubio, JP and Danek, A and Stone, C and Chalmers, R and Wood, N and Verellen, C and Ferrer, X and Malandrini, A and Fabrizi, GM and Manfredi, M and Vance, J and PericakVance, M and Brown, R and Rudolf, G and Picard, F and Alonso, E and Brin, M and Nemeth, AH and Farrall, M and Monaco, AP (1997) Chorea-acanthocytosis: Genetic linkage to chromosome 9q21. AM J HUM GENET , 61 (4) 899 - 908.

S

Scaravilli, F and An, SF and Giometto, B and Scaravilli, T and Tavolato, B (1997) Relationship between accumulation of beta-APP and neuropsychological abnormalities in HIV encephalitis. J NEUROPATH EXP NEUR , 56 (5) 108 - 108.

Schapira, AHV and Warner, T and Gash, MT and Cleeter, MWJ and Marinho, CFM and Copper, JM (1997) Complex I function in familial and sporadic dystonia. ANN NEUROL , 41 (4) 556 - 559.

Sweeney, M and Giunti, P and Wood, NW and Davis, MB (1997) Genetic analysis of late onset pure Cerebellar Ataxia (SCA6). J MED GENET , 34 549 - 549.

T

Teo, I and Veryard, C and Barnes, H and An, SF and Jones, M and Lantos, PL and Luthert, P and Shaunak, S (1997) Circular forms of unintegrated human immunodeficiency virus type 1 DNA and high levels of viral protein expression: Association with dementia and multinucleated giant cells in the brains of patients with AIDS. J VIROL , 71 (4) 2928 - 2933.

V

VanPaesschen, W and Revesz, T and Duncan, JS (1997) Corpora amylacea in hippocampal sclerosis. J NEUROL NEUROSUR PS , 63 (4) 513 - 515.

VanPaesschen, W and Revesz, T and Duncan, JS and King, MD and Connelly, A (1997) Quantitative neuropathology and quantitative magnetic resonance imaging of the hippocampus in temporal lobe epilepsy. ANN NEUROL , 42 (5) 756 - 766.

W

Warner, TT and Househam, E and Clough, C and Chaudhuri, R (1997) Movement disorders associated with xeroderma pigmentosum. In: ANNALS OF NEUROLOGY. (pp. M74 - M74).

Warner, TT and Schapira, AHV (1997) Genetic counselling in mitochondrial diseases. CURR OPIN NEUROL , 10 (5) 408 - 412.

WavrantDeVrieze, F and PerezTur, J and Lambert, JC and Frigard, B and Pasquier, F and Delacourte, A and Amouyel, P and Hardy, J and ChartierHarlin, MC (1997) Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease. NEUROSCIENCE LETTERS , 227 (1) 68 - 70. 10.1016/S0304-3940(97)00304-2.

Winblad, B and Hardy, O (1997) European research on Alzheimer's disease. LANCET , 350 (9070) 73 - 74. 10.1016/S0140-6736(05)66284-8.

Wood, N (1997) Genes and parkinsonism. J NEUROL NEUROSUR PS , 62 (4) 305 - 309.

Wood, N (1997) Genetic aspects of parkinsonism. BAILLIERE CLIN NEUR , 6 (1) 37 - 53.

Wood, NW (1997) Diagnosing Friedreich's ataxia. Archives of Disease in Childhood

Z

Zamaraeva, MV and Hagelgans, AI and Abramov, AY and Ternovsky, VI and Merzlyak, PG and Tashmukhamedov, BA and Saidkhodzjaev, AI (1997) Ionophoretic properties of ferutinin. CELL CALCIUM , 22 (4) 235 - 241.

This list was generated on Sat May 18 07:51:01 2013 BST.