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Number of items: 64.

A

An, SF and Giometto, B and Groves, M and Scaravilli, F (1998) Detection and localisation of HIV-1 in fixed adult AIDS brain tissue by in situ amplification. J NEUROPATH EXP NEUR , 57 (5) 490 - 490.

B

Bajaj, NPS and Shaw, C and Warner, T and RayChaudhuri, K (1998) The genetics of Parkinson's disease and parkinsonian syndromes. JOURNAL OF NEUROLOGY , 245 (10) 625 - 633. 10.1007/s004150050258.

Bandmann, O and Marsden, CD and Wood, NW (1998) Atypical presentations of dopa-responsive dystonia. Adv Neurol , 78 283 - 290.

Bandmann, O and Marsden, CD and Wood, NW (1998) Genetic aspects of Parkinson's disease. MOVEMENT DISORD , 13 (2) 203 - 211.

Bandmann, O and Valente, EM and Holmans, P and Surtees, RAH and Walters, JH and Wevers, RA and Marsden, CD and Wood, NW (1998) Dopa-responsive dystonia: A clinical and molecular genetic study. ANN NEUROL , 44 (4) 649 - 656.

Bandmann, O and Wood, NW (1998) Acetylator genotype and Parkinson's disease - Reply. LANCET , 351 (9096) 142 - 142.

Barker, RA and Revesz, T and Thom, M and Marsden, CD and Brown, P (1998) Review of 23 patients affected by the stiff man syndrome: Clinical subdivision into stiff trunk (man) syndrome, stiff limb syndrome, and progressive encephalomyelitis with rigidity. J NEUROL NEUROSUR PS , 65 (5) 633 - 640.

C

Cavanagh, JB and Holton, JL and Nolan, CC and Ray, DE and Naik, JT and Mantle, PG (1998) The effects of the tremorgenic mycotoxin penitrem A on the rat cerebellum. Vet Pathol , 35 (1) 53 - 63.

Crook, R and Verkkoniemi, A and Perez-Tur, J and Mehta, N and Baker, M and Houlden, H and Farrer, M and Hutton, M and Lincoln, S and Hardy, J and Gwinn, K and Somer, M and Paetau, A and Kalimo, H and Ylikoski, R and Poyhonen, M and Kucera, S and Haltia, M (1998) A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. NAT MED , 4 (4) 452 - 455.

Cruts, M and van Duijn, CM and Backhovens, H and Van den Broeck, M and Wehnert, A and Serneels, S and Sherrington, R and Hutton, M and Hardy, J and St George-Hyslop, PH and Hofman, A and Van Broeckhoven, C (1998) Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population based study of presenile Alzheimer disease. HUMAN MOLECULAR GENETICS , 7 (1) 43 - 51. 10.1093/hmg/7.1.43.

D

Dennis Lo, YM and An, SF (1998) Generation of labeled probes by PCR. Methods Mol Med , 16 93 - 100. 10.1385/0-89603-499-2:93.

F

Farrer, M and Wavrant-De Vrieze, F and Crook, R and Boles, L and Perez-Tur, J and Hardy, J and Johnson, WG and Steele, J and Maraganore, D and Gwinn, K and Lynch, T (1998) Low frequency of alpha-synuclein mutations in familial Parkinson's disease. ANNALS OF NEUROLOGY , 43 (3) 394 - 397. 10.1002/ana.410430320.

G

Geddes, JF and Revesz, T and Vowles, GH and Robinson, SFD and Nicoll, JAR (1998) Neocortical neurofibrillary tangles in the absence of amyloid deposition constitute the early pathology of repetitive head injury. Journal of Neuropathology and Experimental Neurology , 57 154 - ?.

Geddes, JF and Revesz, T and Vowles, GH and Robinson, SFD and Nicoll, JAR (1998) Neocortical neurofibrillary tangles in the absence of amyloid deposition constitute the early pathology of repetitive head injury. J NEUROPATH EXP NEUR , 57 (5) 507 - 507.

Giunti, P and Sabbadini, G and Sweeney, MG and Davis, MB and Veneziano, L and Mantuano, E and Federico, A and Plasmati, R and Frontali, M and Wood, NW (1998) The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families - Frequency, clinical and genetic correlates. BRAIN , 121 459 - 467.

Glynn, P and Holton, JL and Nolan, CC and Read, DJ and Brown, L and Hubbard, A and Cavanagh, JB (1998) Neuropathy target esterase: immunolocalization to neuronal cell bodies and axons. Neuroscience , 83 (1) 295 - 302.

Grunberg, J and Walter, J and Eckman, C and Capell, A and Schindzielorz, A and Younkin, S and Mehta, N and Hardy, J and Haass, C (1998) Truncated presenilin 2 derived from differentially spliced mRNAs does not affect the ratio of amyloid beta-peptide 1-42/1-40. NEUROREPORT , 9 (14) 3293 - 3299.

H

Hanna, MG and Davis, MB and Sweeney, MG and Noursadeghi, M and Ellis, CJ and Elliot, P and Wood, NW and Marsden, CD (1998) Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion. MOVEMENT DISORD , 13 (2) 339 - 340.

Hanna, MG and Nelson, IP and Morgan-Hughes, JA and Wood, NW (1998) MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity. J NEUROL NEUROSUR PS , 65 (4) 512 - 517.

Hanna, MG and Nelson, IP and Rahman, S and Lane, RJM and Land, J and Heales, S and Cooper, MJ and Schapira, AHV and Morgan-Hughes, JA and Wood, NW (1998) Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. AM J HUM GENET , 63 (1) 29 - 36.

Hanna, MG and Stewart, J and Schapira, AHV and Wood, NW and Morgan-Hughes, JA and Murray, NMF (1998) Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A). J NEUROL NEUROSUR PS , 65 (2) 248 - 250.

Hanna, MG and Wood, N and Kullmann, DM (1998) Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders. J NEUROL NEUROSUR PS , 65 (4) 427 - 431.

Hardy, J and Duff, K and Hardy, KG and Perez-Tur, J and Hutton, M (1998) Genetic dissection of Alzheimer's disease and related dementias: Amyloid and its relationship to tau. NATURE NEUROSCIENCE , 1 (5) 355 - 358. 10.1038/1565.

Hardy, J and Gwinn-Hardy, K (1998) Genetic classification of primary neurodegenerative disease. SCIENCE , 282 (5391) 1075 - 1079. 10.1126/science.282.5391.1075.

Hardy, J and Perez-Tur, J and Baker, M and Farrer, M and Crook, R and Hutton, M and Johnson, WG and Gwinn, K and Muenter, M and Rocca, WA and Maraganore, D (1998) Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism. AMERICAN JOURNAL OF MEDICAL GENETICS , 81 (2) 166 - 171. 10.1002/(SICI)1096-8628(19980328)81:2<166::AID-AJMG8>3.0.CO;2-U.

Harvey, RJ and Ellison, D and Hardy, J and Hutton, M and Rogues, PK and Collinge, J and Fox, NC and Rossor, MN (1998) Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine -> serine (L250S) substitution at codon 250 of the presenilin 1 gene. J NEUROL NEUROSUR PS , 64 (1) 44 - 49.

Holcomb, L and Gordon, MN and McGowan, E and Yu, X and Benkovic, S and Jantzen, P and Wright, K and Saad, I and Mueller, R and Morgan, D and Sanders, S and Zehr, C and O'Campo, K and Hardy, J and Prada, CM and Eckman, C and Younkin, S and Hsiao, K and Duff, K (1998) Accelerated Alzheimer-type phenotype in transgenic mice carrying both mutant amyloid precursor protein and presenilin 1 transgenes. NATURE MEDICINE , 4 (1) 97 - 100. 10.1038/nm0198-097.

Houlden, H and Crook, R and Backhovens, H and Prihar, G and Baker, M and Hutton, M and Rossor, M and Martin, JJ and Van Broeckhoven, C and Hardy, J (1998) ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families. AM J MED GENET , 81 (1) 117 - 121.

Howard, RS and Thorpe, J and Barker, R and Revesz, T and Hirsch, N and Miller, D and Williams, AJ (1998) Respiratory insufficiency due to high anterior cervical cord infarction. J NEUROL NEUROSUR PS , 64 (3) 358 - 361.

Hutton, M and Lendon, CL and Rizzu, P and Baker, M and Froelich, S and Houlden, H and Pickering-Brown, S and Chakraverty, S and Isaacs, A and Grover, A and Hackett, J and Adamson, J and Lincoln, S and Dickson, D and Davies, P and Petersen, RC and Stevens, M and de Graaff, E and Wauters, E and van Baren, J and Hillebrand, M and Joosse, M and Kwon, JM and Nowotny, P and Che, LK and Norton, J and Morris, JC and Reed, LA and Trojanowski, J and Basun, H and Lannfelt, L and Neystat, M and Fahn, S and Dark, F and Tannenberg, T and Dodd, PR and Hayward, N and Kwok, JBJ and Schofield, PR and Andreadis, A and Snowden, J and Craufurd, D and Neary, D and Owen, F and Oostra, BA and Hardy, J and Goate, A and van Swieten, J and Mann, D and Lynch, T and Heutink, P (1998) Association of missense and 5 '-splice-site mutations in tau with the inherited dementia FTDP-17. NATURE , 393 (6686) 702 - 705.

Hutton, M and Perez-Tur, J and Hardy, J (1998) Genetics of Alzheimer's disease. ESSAYS IN BIOCHEMISTRY, VOL 33, 1998 , 33 117 - 131.

J

Jarman, PR and Warner, TT (1998) The dystonias. J Med Genet , 35 (4) 314 - 318.

K

Kapoor, R and Miller, DH and Jones, SJ and Plant, GT and Brusa, A and Gass, A and Hawkins, CP and Page, R and Wood, NW and Compston, DAS and Moseley, IF and McDonald, WI (1998) Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis. NEUROLOGY , 50 (1) 230 - 237.

L

Lambert, JC and Berr, C and Pasquier, F and Delacourte, A and Frigard, B and Cottel, D and Perez-Tur, J and Mouroux, V and Mohr, M and Cecyre, D and Galasko, D and Lendon, C and Poirier, J and Hardy, J and Mann, D and Amouyel, P and Chartier-Harlin, MC (1998) Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease. HUMAN MOLECULAR GENETICS , 7 (9) 1511 - 1516. 10.1093/hmg/7.9.1511.

Lamont, PJ and Surtees, R and Woodward, CE and Leonard, JV and Wood, NW and Harding, AE (1998) Clinical and laboratory findings in referrals for mitochondrial DNA analysis. ARCH DIS CHILD , 79 (1) 22 - 27.

Leff, AP and McNabb, AW and Hanna, MG and Clarke, CRA and Larner, AJ (1998) Complex partial status epilepticus in late-onset MELAS. EPILEPSIA , 39 (4) 438 - 441.

Lopes, J and Ravise, N and Vandenberghe, A and Palau, F and Ionasescu, V and Mayer, M and Levy, N and Wood, N and Tachi, N and Bouche, P and Latour, P and Ruberg, M and Brice, A and LeGuern, E (1998) Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. HUM MOL GENET , 7 (1) 141 - 148.

Lucking, CB and Abbas, N and Durr, A and Bonifati, V and Bonnet, AM and de Broucker, T and De Michele, G and Wood, NW and Agid, Y and Brice, A and European Consortium Genetic Susceptibility Park, and French Parkinsons Dis Genetics Study Grp, (1998) Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. LANCET , 352 (9137) 1355 - 1356.

Luxsuwong, M and Revesz, T and Warr, T and Darling, JI (1998) Expression of the p53 protein in recurrent astrocytic gliomas. British Journal of Neurosurgery , 12 (2) 187 - 187.

M

Marques, W and Thomas, PK and Sweeney, MG and Carr, L and Wood, NW (1998) Dejerine-Sottas neuropathy and PMP22 point mutations: A new base pair substitution and a possible "hot spot" on Ser72. ANN NEUROL , 43 (5) 680 - 683.

Mehta, ND and Refolo, LM and Eckman, C and Sanders, S and Yager, D and Perez-Tur, J and Younkin, S and Duff, K and Hardy, J and Hutton, M (1998) Increased A beta 42(43) from cell lines expressing presenilin 1 mutations. ANNALS OF NEUROLOGY , 43 (2) 256 - 258. 10.1002/ana.410430217.

R

Ray, DE and Holton, JL and Nolan, CC and Cavanagh, JB and Harpur, ES (1998) Neurotoxic potential of gadodiamide after injection into the lateral cerebral ventricle of rats. AJNR Am J Neuroradiol , 19 (8) 1455 - 1462.

Revesz, T and Daniel, SE (1998) Corticobasal degeneration. In: Markesbery, WR, (ed.) Neuropathology of dementing disorders. (257 - 267). Arnold

S

Sagdullaev, BT and Abramov, AY and Gagelgans, AI and Dzhakhangirov, FN and Usmanov, PB (1998) Effect of a diterpene alkaloid series on calcium homeostases of rat cardiomyocites - Structure-activity bond. KHIM PRIR SOEDIN+ (4) 523 - 526.

Scaravilli, F and Lindsay, R and Groves, M and An, SF and Giometto, B (1998) Axotomy-induced apoptosis in adult rat primary sensory neurons and effect of administration of neurotrophins. J NEUROPATH EXP NEUR , 57 (5) 491 - 491.

Seery, JP and Bryant, DJ and Jenkinson, G and Schwieso, JE and Houlden, HJ and Changani, KK and Hodgson, HJF and Taylor-Robinson, SD (1998) Intravenous intralipid infusion in hepatic steatosis: an in vivo hepatic phosphorus-31 magnetic resonance spectroscopy study. HEPATOL RES , 12 (1) 50 - 58.

Stanyer, L and Cooper, MB and Betteridge, DJ and Smith, CCT (1998) Stimulatory actions of native and oxidised plasma lipoproteins on beta-amyloid fibrillogenesis in vitro. ATHEROSCLEROSIS , 141 (1) 183 - 183.

Steel, TR and Allibone, J and Revesz, T and D'Arrigo, C and Crockard, HA (1998) Intradural neurotropic spread of malignant mesothelioma - Case report and review of the literature. J NEUROSURG , 88 (1) 122 - 125.

Stevanin, G and David, G and Abbas, N and Durr, A and Holmberg, M and Duyckaerts, C and Giunti, P and Cancel, G and Ruberg, M and Mandel, JL and Brice, A (1998) Spinocerebellar ataxia 7. In: Rubinsztein, DC and Hayden, MR, (eds.) Analysis of triplet repeat disorders. Bios Scientific: Oxford.

Stevanin, G and Giunti, P and David, G and Belal, S and Durr, A and Ruberg, M and Wood, N and Brice, A (1998) De novo expansion of intermediate alleles in spinocerebellar ataxia 7. HUM MOL GENET , 7 (11) 1809 - 1813.

V

Valente, EM and Warner, TT and Jarman, PR and Mathen, D and Fletcher, NA and Marsden, CD and Bhatia, KP and Wood, NW (1998) The role of DYT1 in primary torsion dystonia in Europe. BRAIN , 121 2335 - 2339.

Van Paesschen, W and Revesz, T (1998) Hippocampal sclerosis. In: Scaravilli, F, (ed.) Neuropathology of epilepsy. (501 - 573). World Scientific: Singapore.

Vaughan, J and Durr, A and Tassin, J and Bereznai, B and Gasser, T and Bonifati, V and De Michele, G and Fabrizio, E and Volpe, G and Bandmann, O and Johnson, WG and Golbe, LI and Breteler, M and Meco, G and Agid, Y and Brice, A and Marsden, CD and Wood, NW (1998) The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease. Ann Neurol , 44 (2) 270 - 273. 10.1002/ana.410440221.

Vaughan, J and Durr, A and Tassin, J and Bereznai, B and Gasser, T and Bonifati, V and De Michele, G and Fabrizio, E and Volpe, G and Bandmann, O and Johnson, WG and Golbe, LI and Breteler, M and Meco, G and Agid, Y and Brice, A and Marsden, CD and Wood, NW and Eurpean Consortium Genetic Susceptibility Parki, (1998) The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases. ANN NEUROL , 44 (2) 270 - 273.

Vaughan, JR and Farrer, MJ and Wszolek, ZK and Gasser, T and Durr, A and Agid, Y and Bonifati, V and DeMichele, G and Volpe, G and Lincoln, S and Breteler, M and Meco, G and Brice, A and Marsden, CD and Hardy, J and Wood, NW (1998) Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. HUM MOL GENET , 7 (4) 751 - 753.

Vaughan, JR and Farrer, MJ and Wszolek, ZK and Gasser, T and Durr, A and Agid, Y and Bonifati, V and DeMichele, G and Volpe, G and Lincoln, S and Breteler, M and Meco, G and Brice, A and Marsden, CD and Hardy, J and Wood, NW (1998) Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD). Hum Mol Genet , 7 (4) 751 - 753.

W

Warner, TT and Jarman, P (1998) The molecular genetics of the dystonias. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 64 (4) 427 - 429. 10.1136/jnnp.64.4.427.

Warner, TT and Schapira, AHV (1998) The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom. J NEUROL NEUROSUR PS , 65 (3) 378 - 379.

Warr, TJ and Ward, SJ and Darling, JL and Thomas, DGT (1998) Identification of chromosomal gains and losses in paediatric malignant astrocytoma by comparative genomic hybridisation. British Journal of Cancer , 78 157 - ?.

Wood, NW (1998) Diagnosing Friedreich's ataxia. ARCH DIS CHILD , 78 (3) 204 - 207.

Wood, NW (1998) Genetic risk factors in Parkinson's disease. ANNALS OF NEUROLOGY , 44 (3) S58 - S62.

Wood, NW (1998) Genetic risk factors in Parkinson's disease. In: Olanow, CW and Jenner, P, (eds.) Beyond the decade of the brain: neuroprotection in Parkinson's disease. (115 - 120). Wells Medical: Tunbridge Wells.

Wu, WS and Holmans, P and Wavrant-Devrieze, F and Shears, S and Kehoe, P and Crook, R and Booth, J and Williams, N and Perez-Tur, J and Roehl, K and Fenton, L and Chartier-Harlin, MC and Lovestone, S and Williams, J and Hutton, M and Hardy, J and Owen, MJ and Goate, A (1998) Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION , 280 (7) 619 - 622. 10.1001/jama.280.7.619.

Z

Zori, RT and Gardner, JL and Zhang, J and Mullan, MJ and Shah, R and Osborn, AR and Houlden, H and Wallace, MR and Roberts, S and Yang, TP (1998) Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome. AM J MED GENET , 78 (5) 450 - 454.

This list was generated on Sat May 18 07:51:09 2013 BST.