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Number of items: 81.

A

Antcliff, RJ and Hussain, AA and Hodgetts, A and Marshall, J (2000) Cystoid macular edema: Barriers limiting protein movement in the retina. INVEST OPHTH VIS SCI , 41 (4) S653 - S653.

B

Baker, M and Graff-Radford, D and DeVrieze, FW and Graff-Radford, N and Petersen, RC and Kokmen, E and Boeve, B and Myllykangas, L and Polvikoski, T and Sulkava, R and Verkoniemmi, A and Tienari, P and Haltia, M and Hardy, J and Hutton, M and Perez-Tur, J (2000) No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease. NEUROSCIENCE LETTERS , 285 (2) 147 - 149. 10.1016/S0304-3940(00)01057-0.

Bandmann, O and Vaughan, JR and Holmans, P and Marsden, CD and Wood, NW (2000) Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease. MOVEMENT DISORD , 15 (1) 30 - 35.

Bhatia, KP and Lee, MS and Rinne, JO and Revesz, T and Scaravilli, F and Davies, L and Marsden, CD (2000) Corticobasal degeneration look-alikes. In: UNSPECIFIED (169 - 182). LIPPINCOTT WILLIAMS & WILKINS

C

Carmichael, J and Conron, M and Beynon, H and Crow, J and Warner, TT (2000) Churg-Strauss syndrome presenting with visual loss. RHEUMATOLOGY , 39 (12) 1433 - 1434.

Cottrell, DA and Blakely, EL and Johnson, MA and Chinnery, PF and Hanna, M and Turnbull, DM (2000) Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder. J NEUROPATH EXP NEUR , 59 (7) 621 - 627.

D

Davies, NP and Eunson, LH and Gregory, RP and Mills, KR and Morrison, PJ and Hanna, MG (2000) Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenita. J NEUROL NEUROSUR PS , 68 (4) 504 - 507.

de Silva, HA and Khan, NL and Wood, NW (2000) The genetics of Parkinson's disease. CURR OPIN GENET DEV , 10 (3) 292 - 298.

E

Elson, GCA and Lelievre, E and Guillet, C and Chevalier, S and Plun-Favreau, H and Froger, J and Suard, I and de Coignac, AB and Delneste, Y and Bonnefoy, JY and Gauchat, JF and Gascan, H (2000) CLF associates with CLC to form a functional heteromeric ligand for the CNTF receptor complex. NAT NEUROSCI , 3 (9) 867 - 872.

Eunson, LH and Rea, R and Zuberi, SM and Youroukos, S and Panayiotopoulos, CP and Liguori, R and Avoni, P and McWilliam, RC and Stephenson, JBP and Hanna, MG and Kullmann, DM and Spauschus, A (2000) Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability. ANN NEUROL , 48 (4) 647 - 656.

F

Farrer, M and Destee, T and Becquet, E and Wavrant-De Vrieze, F and Mouroux, V and Richard, F and Defebvre, L and Lincoln, S and Hardy, J and Amouyel, S and Chartier-Harlin, MC (2000) Linkage exclusion in French families with probable Parkinson's disease. MOVEMENT DISORDERS , 15 (6) 1075 - 1083. 10.1002/1531-8257(200011)15:6<1075::AID-MDS1004>3.0.CO;2-2.

G

Geddes, JF and Jansen, GH and Robinson, SFD and Gomori, E and Holton, JL and Monson, JP and Besser, GM and Revesz, T (2000) 'Gangliocytomas' of the pituitary - A heterogeneous group of lesions with differing histogenesis. AM J SURG PATHOL , 24 (4) 607 - 613.

Ghiso, J and Vidal, R and Rostagno, A and Mead, S and Revesz, T and Plant, G and Frangione, B (2000) A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementia. VASCULAR FACTORS IN ALZHEIMER'S DISEASE , 903 129 - 137.

Ghiso, J and Vidal, R and Rostagno, A and Miravalle, L and Holton, JL and Mead, S and Revesz, T and Plant, G and Frangione, B (2000) Amyloidogenesis in familial British dementia is associated with a genetic defect on chromosome 13. MOLECULAR BASIS OF DEMENTIA , 920 84 - 92.

Gwinn-Hardy, K and Chen, JY and Liu, HC and Liu, TY and Boss, M and Seltzer, W and Adam, A and Singleton, A and Koroshetz, W and Waters, C and Hardy, J and Farrer, M (2000) Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. NEUROLOGY , 55 (6) 800 - 805.

Gwinn-Hardy, K and Mehta, ND and Farrer, M and Maraganore, D and Muenter, M and Yen, SH and Hardy, J and Dickson, DW (2000) Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p. ACTA NEUROPATHOLOGICA , 99 (6) 663 - 672.

Gwinn-Hardy, KA and Crook, R and Lincoln, S and Adler, CH and Caviness, JN and Hardy, J and Farrer, M (2000) A kindred with Parkinson's disease not showing genetic linkage to established loci. NEUROLOGY , 54 (2) 504 - 507.

H

Hardy, J (2000) Pathways to primary neurodegenerative disease. In: ALZEHEIMER'S DISEASE: A COMPENDIUM OF CURRENT THEORIES. (pp. 29 - 34).

Hardy, J and Singleton, A (2000) The future of genetic analysis of neurological disorders. NEUROBIOLOGY OF DISEASE , 7 (2) 65 - 69. 10.1006/nbdi.2000.0291.

Hodgetts, A and Gauba, V and Warley, A and Marshall, J (2000) Changes in the fibre content of human Bruch's membrane with age. INVEST OPHTH VIS SCI , 41 (4) S25 - S25.

Holton, JL and Lashley, T and Vidal, R and Rostagno, A and Guerin, CJ and Houlden, H and Plant, G and Frangione, B and Ghiso, J and Revesz, T (2000) Familial British dementia: Immunohistochemical and immunoelectron microscopic study. BRAIN PATHOL , 10 (4) 713 - 714.

Holton, JL and Steel, T and Luxsuwong, M and Crockard, HA and Revesz, T (2000) Skull base chordomas: correlation of tumour doubling time with age, mitosis and Ki67 proliferation index. NEUROPATH APPL NEURO , 26 (6) 497 - 503.

Houlden, H and Baker, M and Bhatia, K and Hutton, M and Wood, N and Corticobasal Degeneration Collabor, (2000) Pathologically confirmed corticobasal degeneration shares the same tau haplotype association as progressive supranuclear palsy. ANN NEUROL , 48 (3) 436 - 436.

Houlden, H and Baker, M and McGowan, E and Lewis, P and Hutton, M and Crook, R and Wood, NW and Kumar-Singh, S and Geddes, J and Swash, M and Scaravilli, F and Holton, JL and Lashley, T and Tomita, T and Hashimoto, T and Verkkoniemi, A and Kalimo, H and Somer, M and Paetau, A and Martin, JJ and Van Broeckhoven, C and Golde, T and Hardy, J and Haltia, M and Revesz, T (2000) Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations. ANN NEUROL , 48 (5) 806 - 808.

J

Jarman, PR and Bhatia, KP and Davie, C and Heales, SJR and Turjanski, N and Taylor-Robinson, SD and Marsden, CD and Wood, NW (2000) Paroxysmal dystonic choreoathetosis: Clinical features and investigation of pathophysiology in a large family. MOVEMENT DISORD , 15 (4) 648 - 657.

Jenkins, R and Fox, NC and Rossor, AM and Harvey, RJ and Rossor, MN (2000) Intracranial volume and Alzheimer disease - Evidence against the cerebral reserve hypothesis. ARCH NEUROL-CHICAGO , 57 (2) 220 - 224.

Jouvenceau, A and Eunson, L and Spauschus, A and Ramesh, V and Hanna, MG and Kullmann, DM (2000) Non-functional alpha(1A) calcium channel in episodic ataxia type 2. J PHYSIOL-LONDON , 525 75P - 75P.

Jouvenceau, A and Eunson, L and Spauschus, A and Ramesh, V and Hanna, MG and Kullmann, DM (2000) Premature termination in the CACNA1A gene observed in episodic ataxia type 2 (EA2) results in a loss of alpha1A calcium channel function. EUR J NEUROSCI , 12 454 - 454.

K

Ko, LW and Mehta, ND and Farrer, M and Easson, C and Hussey, J and Yen, S and Hardy, J and Yen, SHC (2000) Sensitization of neuronal cells to oxidative stress with mutated human alpha-synuclein. JOURNAL OF NEUROCHEMISTRY , 75 (6) 2546 - 2554. 10.1046/j.1471-4159.2000.0752546.x.

L

Lambert, JC and Goumidi, L and Wavrant-De Vrieze, F and Frigard, B and Harris, JM and Cummings, A and Coates, J and Pasquier, F and Cottel, D and Gaillac, M and St Clair, D and Mann, DMA and Hardy, J and Lendon, CL and Amouyel, P and Chartier-Harlin, MC (2000) The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease. HUMAN MOLECULAR GENETICS , 9 (15) 2275 - 2280.

Lewis, J and McGowan, E and Rockwood, J and Melrose, H and Nacharaju, P and Van Slegtenhorst, M and Gwinn-Hardy, K and Murphy, MP and Baker, M and Yu, X and Duff, K and Hardy, J and Corral, A and Lin, WL and Yen, SH and Dickson, DW and Davies, P and Hutton, M (2000) Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. NATURE GENETICS , 25 (4) 402 - 405.

Lewis, PA and Perez-Tur, J and Golde, TE and Hardy, J (2000) The presenilin 1 C92S mutation increases abeta 42 production. Biochem Biophys Res Commun , 277 (1) 261 - 263. 10.1006/bbrc.2000.3646.

Lodi, R and Schapira, AHV and Manners, D and Styles, P and Wood, NW and Taylor, DJ and Warner, TT (2000) Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy. ANN NEUROL , 48 (1) 72 - 76.

Lucking, CB and Durr, A and Bonifati, V and Vaughan, J and De Michele, G and Gasser, T and Harhangi, BS and Meco, G and Denefle, P and Wood, NW and Agid, Y and Brice, A and European Consortium Genetic Suscep, and French Parkinsons Dis Genetics Stu, (2000) Association between early-onset Parkinson's disease and mutations in the parkin gene. NEW ENGL J MED , 342 (21) 1560 - 1567.

M

Maraganore, DM and Farrer, MJ and Hardy, JA and McDonnell, SK and Schaid, DJ and Rocca, WA (2000) Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease. MOVEMENT DISORDERS , 15 (4) 714 - 719. 10.1002/1531-8257(200007)15:4<714::AID-MDS1018>3.0.CO;2-3.

McEntagart, M and Norton, N and Williams, H and Houlden, H and Donaghy, M and Boltshauser, E and Harper, PS and Williams, N and Rahman, N (2000) Localisation of the gene for distal Hereditary Motor Neuronopathy-VII to chromosome 2. J MED GENET , 37 S85 - S85.

McEntagart, ME and Norton, N and Williams, H and Houlden, H and Boltshauser, E and Donaghy, M and Harper, PS and Williams, N and Rahman, N (2000) Localization of the gene for distal Hereditary Motor Neuronopathy-VII to chromosome 2. AM J HUM GENET , 67 (4) 311 - 311.

McLendon, C and Xin, T and Ziani-Cherif, C and Murphy, MP and Findlay, KA and Lewis, PA and Pinnix, I and Sambamurti, K and Wang, R and Fauq, A and Golde, TE (2000) Cell-free assays for gamma-secretase activity. FASEB J , 14 (15) 2383 - 2386. 10.1096/fj.00-0286fje.

Mead, S and James-Galton, M and Revesz, T and Doshi, RB and Harwood, G and Pan, EL and Ghiso, J and Frangione, B and Plant, G (2000) Familial British dementia with amyloid angiopathy - Early clinical, neuropsychological and imaging findings. BRAIN , 123 975 - 991.

Meschia, JF and Brott, TG and Chukwudelunzu, FE and Hardy, J and Brown, RD and Meissner, I and Hall, LJ and Atkinson, EJ and O'Brien, PC (2000) Verifying the stroke-free phenotype by structured telephone interview. STROKE , 31 (5) 1076 - 1080.

Morgan, D and Diamond, DM and Gottschall, PE and Ugen, KE and Dickey, C and Hardy, J and Duff, K and Jantzen, P and DiCarlo, G and Wilcock, D and Connor, K and Hatcher, J and Hope, C and Gordon, M and Arendash, GW (2000) A beta peptide vaccination prevents memory loss in an animal model of Alzheimer's disease. NATURE , 408 (6815) 982 - 985. 10.1038/35050116.

Morris, HR and Vaughan, JR and Datta, SR and Bandopadhyay, R and de Silva, HAR and Schrag, A and Cairns, NJ and Burn, D and Nath, U and Lantos, PL and Daniel, S and Lees, AJ and Quinn, NP and Wood, NW (2000) Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE. NEUROLOGY , 55 (12) 1918 - 1920.

Munchau, A and Valente, EM and Davis, MB and Stinton, V and Wood, NW and Quinn, NP and Bhatia, KP (2000) A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia. MOVEMENT DISORD , 15 (5) 954 - 959.

Munchau, A and Valente, EM and Shahidi, GA and Eunson, LH and Hanna, RG and Quinn, NP and Schapira, AHV and Wood, NW and Bhatia, KP (2000) A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study. J NEUROL NEUROSUR PS , 68 (5) 609 - 614.

Murphy, MP and Uljon, SN and Fraser, PE and Fauq, A and Lookingbill, HA and Findlay, KA and Smith, TE and Lewis, PA and McLendon, DC and Wang, R and Golde, TE (2000) Presenilin 1 regulates pharmacologically distinct gamma -secretase activities. Implications for the role of presenilin in gamma -secretase cleavage. J Biol Chem , 275 (34) 26277 - 26284. 10.1074/jbc.M002812200.
An open access publication

Myers, A and Holmans, P and Marshall, H and Kwon, J and Meyer, D and Ramic, D and Shears, S and Booth, J and DeVrieze, FW and Crook, R and Hamshere, M and Abraham, R and Tunstall, N and Rice, F and Carty, S and Lillystone, S and Kehoe, P and Rudrasingham, V and Jones, L and Lovestone, S and Perez-Tur, J and Williams, J and Owen, MJ and Hardy, J and Goate, AM (2000) Susceptibility locus for Alzheimer's disease on chromosome 10. SCIENCE , 290 (5500) 2304 - +. 10.1126/science.290.5500.2304.

Myllykangas, L and Polvikoski, T and Sulkava, R and Verkkoniemi, A and Tienari, P and Niinisto, L and Kontula, K and Hardy, J and Haltia, M and Perez-Tur, J (2000) Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over. NEUROSCIENCE LETTERS , 292 (3) 195 - 198. 10.1016/S0304-3940(00)01467-1.

N

Noury, AMS and Jackson, TL and Hodgetts, A and Scott, R and Sullivan, P and Marshall, J (2000) Scleral hydraulic conductivity in uveal effusion syndrome. INVEST OPHTH VIS SCI , 41 (4) S388 - S388.

O

Ostrerova-Golts, N and Petrucelli, L and Hardy, J and Lee, JM and Farer, M and Wolozin, B (2000) The A53T alpha-synuclein mutation increases iron-dependent aggregation and toxicity. JOURNAL OF NEUROSCIENCE , 20 (16) 6048 - 6054.

P

Pickering-Brown, S and Baker, M and Yen, SH and Liu, WK and Hasegawa, M and Cairns, N and Lantos, PL and Rossor, M and Iwatsubo, T and Davies, Y and Allsop, D and Furlong, R and Owen, F and Hardy, J and Mann, D and Hutton, M (2000) Pick's disease is associated with mutations in the tau gene. ANN NEUROL , 48 (6) 859 - 867.

Pulkes, T and Eunson, L and Patterson, V and Siddiqui, A and Wood, NW and Nelson, IP and Morgan-Hughes, JA and Hanna, MG (2000) Erratum: (Annals of Neurology (1999) 46 (916-919)). Annals of Neurology , 47 (6) 841 - 841.

Pulkes, T and Siddiqui, A and Morgan-Hughes, JA and Hanna, MG (2000) A novel mutation in the mitochondrial tRNA(Tyr) gene associated with exercise intolerance. NEUROLOGY , 55 (8) 1210 - 1212.

Pulkes, T and Sweeney, MG and Hanna, MG (2000) Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. LANCET , 356 (9247) 2068 - 2069.

Pulkes, T and Wills, AJ and Hanna, MG (2000) Exercise intolerance associated with a novel stop codon mutation in the mitochondrial ND2 gene. ANNALS OF NEUROLOGY , 48 (3) 469 - 469.

R

Rahman, S and Lake, BD and Taanman, JW and Hanna, MG and Cooper, JM and Schapira, AHV and Leonard, JV (2000) Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms. BRAIN , 123 591 - 600.

Rea, R and Spauschus, A and Eunson, L and Hanna, MG and Kullmann, DM (2000) Functional analysis of interactions between wild-type and mutant subunits of hKv1.1 in episodic ataxia type 1. J PHYSIOL-LONDON , 525 76P - 76P.

Revesz, T (2000) Axonal lesions in multiple sclerosis: an old story revisited. BRAIN , 123 203 - 204.

Revesz, T and Houlden, H and Holton, JL and Baker, M and Vowles, GH and Lashley, T and Wood, NW and Scaravilli, F and Swash, M and Hardy, J and Geddes, JF (2000) Alzheimer's disease with spastic paraparesis due to deletion of exon 4 and a P436E point mutation of exon 12 of the presenilin 1 gene. BRAIN PATHOL , 10 (4) 633 - 633.

Rossor, MN and Revesz, T and Lantos, PL and Warrington, EK (2000) Semantic dementia with ubiquitin-positive tau-negative inclusion bodies. BRAIN , 123 267 - 276.

S

Scaravilli, F and Cordery, RJ and Kretzschmar, H and Gambetti, P and Brink, B and Fritz, V and Temlett, J and Kaplan, C and Fish, D and An, SF and Schulz-Schaeffer, WJ and Rossor, MN (2000) Sporadic fatal insomnia: A case study. ANN NEUROL , 48 (4) 665 - 668.

Scaravilli, F and Kretschmar, H and Gambetti, P and Brink, B and An, SF and Schulz-Schaeffer, WJ and Rossor, MN (2000) Sporadic fatal insomnia (sFI): Report of a case. J NEUROPATH EXP NEUR , 59 (5) 433 - 433.

Scaravilli, T and Pramstaller, PP and Salerno, A and Egarter-Vigl, E and Giometto, B and Vitaliani, R and An, SF and Revesz, T (2000) Neuronal loss in Onuf's nucleus in three patients with progressive supranuclear palsy. ANN NEUROL , 48 (1) 97 - 101.

Scaravilli, T and Pramstaller, PP and Salerno, A and Giometto, B and Revesz, T (2000) Involvement of the Onuf nucleus in progressive supranuclear palsy. NEUROLOGY , 54 (7) A392 - A392.

Schmitz-Valckenberg, S and Hodgetts, A and Hussein, AA and Jey, A and Marshall, J (2000) Predictive model of age-related changes in fluid movement through extrafibrillar space in Bruch's Membrane. INVEST OPHTH VIS SCI , 41 (4) S25 - S25.

Spauschus, A and Rea, R and Eunson, L and Hanna, MG and Kullmann, DM (2000) Mutations of Kv1.1 found in patients with episodic ataxia type 1 (EA1) affect the open probability of channels in vitro. EUR J NEUROSCI , 12 25 - 25.

Spauschus, A and Rea, R and Eunson, L and Wood, NW and Hanna, MG and Kullmann, DM (2000) Functional characterisation of mutant Kv1.1 subunits from two families with episodic ataxia type 1. J PHYSIOL-LONDON , 523 156P - 157P.

Steiner, H and Kostka, M and Romig, H and Basset, G and Pesold, B and Hardy, J and Capell, A and Meyn, L and Grim, ML and Baumeister, R and Fechteler, K and Haass, C (2000) Glycine 384 is required for presenilin-1 function and is conserved in bacterial polytopic aspartyl proteases. NATURE CELL BIOLOGY , 2 (11) 848 - 851.

T

Tabrizi, SJ and Orth, M and Wilkinson, JM and Taanman, JW and Warner, TT and Cooper, JM and Schapira, AHV (2000) Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity. HUM MOL GENET , 9 (18) 2683 - 2689.

Thom, M and Holton, JL and D'Arrigo, C and Griffin, B and Beckett, A and Sisodiya, S and Alexiou, D and Sander, JW (2000) Microdysgenesis with abnormal cortical myelinated fibres in temporal lobe epilepsy: a histopathological study with calbindin D-28-K immunohistochemistry. NEUROPATH APPL NEURO , 26 (3) 251 - 257.

V

Valente, EM and Spacey, SD and Wali, GM and Bhatia, KP and Dixon, PH and Wood, NW and Davis, MB (2000) A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16. BRAIN , 123 2040 - 2045.

Verkkoniemi, A and Somer, M and Rinne, JO and Myllykangas, L and Crook, R and Hardy, J and Viitanen, M and Kalimo, H and Haltia, M (2000) Variant Alzheimer's disease with spastic paraparesis - Clinical characterization. NEUROLOGY , 54 (5) 1103 - 1109.

Vidal, R and Revesz, T and Rostagno, A and Kim, E and Holton, JL and Bek, T and Bojsen-Moller, M and Braendgaard, H and Plant, G and Ghiso, J and Frangione, B (2000) A decamer duplication in the 3 ' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred. P NATL ACAD SCI USA , 97 (9) 4920 - 4925.

W

Warner, T and Camfield, L and Marsden, CD and Nemeth, AH and Hyman, N and Harley, D and Wissel, J and Poewe, W and Marttila, RJ and Erjanti, H and Burbaud, P and Lagueny, A and Kamm, C and Gasser, T and Franz, D and Castelon-Konkiewitz, E and Trender, I and Ceballos-Baumann, A and Nebe, A and Freudenberg, B and Bentivoglio, A and Cassetta, E and Albanese, A and Curra, A and Vacca, L and Berardelli, A and Ferreira, J and Sampaio, C and Passao, V and Marti, F and Tolosa, E and Claveria, L and Duarte, J and Ben-Shlomo, Y and Newton, A and Eu, ESD (2000) A prevalence study of primary dystonia in eight European countries. JOURNAL OF NEUROLOGY , 247 (10) 787 - 792.

Weiler, M and de Silva, HAR and Morris, H and Wood, NW and Lees, AJ (2000) Strong association of novel tau promoter polymorphisms with progressive supranuclear palsy. AM J HUM GENET , 67 (4) 193 - 193.

Wilson, CJ and Wood, NW and Leonard, JV and Surtees, R and Rahman, S (2000) Mitochondrial DNA point mutation T9176C in Leigh syndrome. J CHILD NEUROL , 15 (12) 830 - 833.

Wood, NW and Harding, AE (2000) Ataxic disorders. In: Bradley, WG and Daroff, RB and Fenichel, GM and Marsden, CD, (eds.) Neurology in clinical practice: volume 1. Principles of diagnosis and management. (309 - 317). Butterworth Heinemann: Oxford.

Wood, NW and Harding, AE (2000) Cerebellar and spinocerebellar disorders. In: Bradley, WG and Daroff, RB and Fenichel, GM and Marsden, CD, (eds.) Neurology in clinical practice: volume 2. The neurological disorders. (1931 - 1951). Butterworth Heinemann: Oxford.

Worth, PF and Houlden, H and Giunti, P and Davis, MB and Wood, NW (2000) Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia. NAT GENET , 24 (3) 214 - 215.

Worth, PF and Houlden, H and Giunti, P and Davis, MB and Wood, NW and Moseley, ML and Schut, LJ and Bird, TD and Day, JW and Ranum, LPW (2000) Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia [2] (multiple letters). Nature Genetics , 24 (3) 214 - 215.

Z

Zhang, J and Hattori, N and Leroy, E and Morris, HR and Kubo, SI and Kobayashi, T and Wood, NW and Polymeropoulos, MH and Mizuno, Y (2000) Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease. PARKINSONISM RELAT D , 6 (4) 195 - 197.

Zimprich, F and Djamshidian, A and Hainfellner, JA and Budka, H and Zeitlhofer, J (2000) An autosomal dominant early adult-onset distal muscular dystrophy. MUSCLE NERVE , 23 (12) 1876 - 1879.

This list was generated on Fri May 24 10:45:39 2013 BST.