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Jump to: A | B | C | D | E | F | G | H | J | K | L | M | O | R | S | V | W | Z
Number of items: 53.

A

Agid, Y; Ahlskog, E; Albanese, A; Calne, D; Chase, T; De Yebenes, J; Factor, S; ... Tolosa, E; + view all (1999) Levodopa in the treatment of Parkinson's disease: A consensus meeting. Movement Disorders , 14 (6) pp. 911-913. 10.1002/1531-8257(199911)14:6<911::AID-MDS1001>3.0.CO;2-H.

B

Bandmann, O; Vaughan, J; Holmans, PA; Marsden, CD; Wood, NW; (1999) Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2. In: UNSPECIFIED (pp. 199-204).

Barreira, AA; Marques, W; Sweeney, MG; Davis, MB; Chimelli, L; Paçó-Larson, ML; Wood, NW; (1999) A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve Biopsy. Ann N Y Acad Sci , 883 (1) pp. 466-468. 10.1111/j.1749-6632.1999.tb08612.x.

Ben-Shlomo, Y; Head, J; Lees, AJ; (1999) Mortality in DATATOP. Ann Neurol , 45 (1) pp. 138-139.

Burton, BJL; Burdon, MA; Holton, JL; Thom, M; Plant, GT; (1999) Fibrous dysplasia of the sphenoid associated with visual loss and optic disc oedema. NEURO-OPHTHALMOLOGY , 21 (4) 241 - 248.

C

Caparros-Lefebvre, D; Lees, A; Grp, CPS; (1999) Atypical parkinsonism in the French West Indies - reply. LANCET , 354 (9188) p. 1473. 10.1016/S0140-6736(05)77612-1.

Caparros-Lefebvre, D; Lees, A; Tolosa, E; (1999) Phenomenological study of Parkinsonism in the French West Indies. NEUROLOGY , 52 (6) A224-A224.

Costa, DC; Walker, Z; Gacinovic, S; Serra-Mestre, J; Walker, RWH; Doder, M; Livingstone, G; ... Katona, CLE; + view all (1999) Clinical applications of DaTSCAN (TM) and single photon emission tomography (SPET). In: (pp. p. 982).

Costa, DC; Walker, Z; Serra-Mestre, J; Gacinovic, S; Lees, A; (1999) Potential clinical applications of FP-CIT: Experience from studies of 140 subjects. In: (pp. 467-).

D

Dixon, PH; Stinton, VJ; Humphray, SJ; Hammond, S; Howard, PJ; Dunham, I; Wood, N; (1999) Physical and EST mapping on chromosome 9: Candidate Genes for the geniospasm (GSM1) locus. The American Journal of Human Genetics , 65 1241-.

Dixon, PH; Stinton, VJ; Humphray, SJ; Hammond, S; Howard, PJ; Dunham, I; Wood, N; (1999) Physical and EST mapping on chromosome 9: Candidate Genes for the geniospasm (GSM1) locus. AM J HUM GENET , 65 (4) A224 - A224.

E

Eunson, LH; Davis, MB; Wood, NW; Hanna, MG; (1999) The national DNA-based diagnostic service for periodic paralyses. J MED GENET , 36 S63 - S63.

F

Flowers, JM; Leigh, PN; Davies, AM; Ninkina, NN; Buchman, VL; Vaughan, J; Wood, NW; (1999) Mutations in the gene encoding human persyn are not associated with amyotrophic lateral sclerosis or familial Parkinson's disease. NEUROSCIENCE LETTERS , 274 (1) pp. 21-24. 10.1016/S0304-3940(99)00673-4.

G

Groves, MJ; Martinian, L; An, SF; Scaravilli, F; (1999) Expression of three oligosaccharide conjugates by neonatal rat dorsal root ganglion neurons: comparison with CGRP and GAP43 immunoreactivity. J ANAT , 195 271 - 280.

Gwinn-Hardy, K; Evidente, VGH; Waters, C; Muenter, MD; Hardy, J; (1999) L-dopa slows the progression of familial parkinsonism. LANCET , 353 (9167) pp. 1850-1851. 10.1016/S0140-6736(99)01398-7.

H

Hanna, MG; (1999) Case 22. In: Wills, AJ and Marsden, CD, (eds.) Fifty neurological cases from the National Hospital. (pp. 71-74). Martin Dunitz: London.

Hanna, MG; (1999) Case 8. In: Wills, AJ and Marsden, CD, (eds.) Fifty neurological cases from the National Hospital. (pp. 23-25). Martin Dunitz: London.

Hanna, MG; Nelson, IP; (1999) Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases. CELL MOL LIFE SCI , 55 (5) 691 - 706.

Hardy, J; Gwinn-Hardy, K; (1999) Neurodegenerative disease: a different view of diagnosis. MOLECULAR MEDICINE TODAY , 5 (12) pp. 514-517. 10.1016/S1357-4310(99)01604-4.

Hardy, J; Israel, A; (1999) Alzheimer's disease - In search of gamma-secretase. NATURE , 398 (6727) pp. 466-467. 10.1038/18979.

Hodgson, DJ; David, KM; Powell, M; Holton, JL; Pezzella, F; (1999) Intracranial extracerebral follicular lymphoma mimicking a sphenoid wing meningioma. J NEUROL NEUROSUR PS , 67 (2) 251 - 252.

Houlden, H; Lee, MJ; Sweeney, M; Davis, M; Jacobs, J; Love, S; Thomas, PK; ... Reilly, M; + view all (1999) Genetic linkage analysis in hereditary motor and sensory neuropathy type II: a five generation kindred with prominent sensory complication. J MED GENET , 36 S34 - S34.

Hu, HL; Bennett, N; Holton, JL; Nolan, CC; Lister, T; Cavanagh, JB; Ray, DE; (1999) Glutathione depletion increases brain susceptibility to m-dinitrobenzene neurotoxicity. NEUROTOXICOLOGY , 20 (1) pp. 83-90.

J

Jarman, P; Wood, N; (1999) Parkinson's disease genetics comes of age - Knowledge about genes in familial parkinsonism helps elucidate idiopathic disease. BRIT MED J , 318 (7199) 1641 - 1642.

K

Khan, NL; Wood, NW; (1999) Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities. Curr Opin Neurol , 12 (2) pp. 149-154.

L

Lee, MJ; Houlden, H; Sweeney, M; Davis, M; Thomas, PK; Manji, H; Wood, N; (1999) Sequencing of the peripheral myelin protein zero (MPZ) gene in hereditary motor and sensory neuropathy (HMSN): assessment of the frequency of MPZ gene mutations in HMSN type IIII. J MED GENET , 36 S20 - S20.

Lees, AJ; (1999) The treatment of the motor disorders of multiple system atrophy. In: Mathias, CJ and Bannister, R, (eds.) Autonomic failure: a textbook of clinical disorders of the autonomic nervous system. (pp. 357-363). Oxford University Press: Oxford.

Lees, AJ; (1999) Case 25. In: Wills, AJ and Marsden, CD, (eds.) Fifty neurological cases from the National Hospital. (pp. 83-84). Martin Dunitz: London.

Litvan, I; Lees, AJ; (1999) Progressive supranuclear palsy. In: Stern, GM, (ed.) Advances in Neurology, vol 80. (pp. 341-345). Lippincott Williams and Wilkins: Philadelphia.

M

Maraganore, DM; Farrer, MJ; Hardy, JA; Lincoln, SJ; McDonnell, SK; Rocca, WA; (1999) Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease. NEUROLOGY , 53 (8) pp. 1858-1860. 10.1212/WNL.53.8.1858.

Marques, W; Hanna, MG; Marques, SR; Sweeney, MG; Thomas, PK; Wood, NW; (1999) Phenotypic variation of a new P0 mutation in genetically identical twins. J NEUROL , 246 (7) 596 - 599.

Marques, W; Sweeney, MG; Wood, NW; Wroe, SJ; Marques, W; (1999) Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. J NEUROL NEUROSUR PS , 66 (6) 803 - 804.

Morris, HR; Baker, M; Lees, AJ; Hutton, M; Hardy, J; Wood, NW; (1999) Further analysis of the association of tau with progressive supranuclear palsy. The American Journal of Human Genetics , 65 2621-.

Morris, HR; Baker, M; Lees, AJ; Hutton, M; Hardy, J; Wood, NW; (1999) Further analysis of the association of tau with progressive supranuclear palsy. AM J HUM GENET , 65 (4) A462 - A462.

Morris, HR; Perez-Tur, J; Janssen, JC; Brown, J; Lees, AJ; Wood, NW; Hardy, J; ... Rossor, MN; + view all (1999) Mutation in the tau exon 10 splice site region in familiar frontotemporal dementia. ANN NEUROL , 45 (2) 270 - 271.

O

O'Sullivan, J; Costa, DC; Lees, AJ; (1999) 123 I-FP-CIT SPECT in the confirmation of organic parkinsonism. Parkinsonism and Related Disorders , 5 (Sup 63-.

O'Sullivan, J; Costa, DC; Lees, AJ; (1999) Confirming Parkinson's disease with 123 I-FP-CIT SPECT. European Journal of Neurology , 6 (Sup 131-.

O'Sullivan, J; Lees, AJ; (1999) Oral dopamine agonists adverse drug reaction profile. Prescribers' Journal , 39 (3) pp. 166-173.

O'Sullivan, JD; Lees, AJ; Hughes, AJ; (1999) Yawning in Parkinson's disease. Neurology , 52 (2) 428-.

R

Rascol, O; Lees, AJ; (1999) Dyskinesias. MOVEMENT DISORDERS , 14 p. 1.

Revesz, T; Holton, JL; Crooks, R; Scaravilli, F; (1999) Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia. J NEUROPATH EXP NEUR , 58 (5) 547 - 547.

Rudel, R; Hanna, MG; Lehmann-Horn, F; (1999) Muscle channelopathies: malignant hyperthermia, periodic paralyses, paramyotonia, and myotonia. In: Schapira, AHV and Griggs, RC, (eds.) Muscle diseases. (pp. 135-175). Butterworth-Heinemann: Boston.

S

Smith, CCT; Stanyer, L; Cooper, MB; Betteridge, DJ; (1999) Platelet aggregation may not be a prerequisite for collagen-stimulated platelet generation of nitric oxide. BBA-GEN SUBJECTS , 1473 (2-3) 286 - 292.

Steele, JC; Morris, HR; Lees, AJ; Perez-Tur, J; McGeer, PL; (1999) Atypical parkinsonism in the French West Indies. LANCET , 354 (9188) 1474 - 1474.

Stevanin, G; David, G; Durr, A; Giunti, P; Benomar, A; Abada-Bendib, M; Lees, MS; ... Brice, A; + view all (1999) Multiple origins of the spinocerebellar ataxia (SCA7) mutation revealed by linkage disequllibrium studies with closely flanking markers, including an intragenic polymorphism (G(3145)TG/A(3145)TG). AM J HUM GENET , 65 (4) A447 - A447.

Sweeney, MG; Giunti, P; Stinton, VJ; Worth, PF; Hanna, MG; Wood, NW; Davis, MB; (1999) Population genetics of the SCA6 locus in British families with ADCA. AM J HUM GENET , 65 (4) A400 - A400.

V

Valente, EM; Povey, S; Warner, TT; Wood, NW; Davis, MB; (1999) Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: Evidence for a limited number of founder mutations. Annals of Human Genetics , 63 (1) pp. 1-8. 10.1017/S0003480099007265.

Valente, EM; Povey, S; Warner, TT; Wood, NW; Davis, MB; (1999) Detailed haplotype analysis in Ashkenazi Jews and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence of two new founder mutations. Annals of Human Genetics , 63 pp. 1-8.

Vaughan, JR; Farrer, M; De Michele, G; Volpe, G; Hardy, J; Wood, NW; (1999) Further evidence for a chromosome 4p haplotype segregating with Parkinson's disease in an independent Italian kindred. AM J HUM GENET , 65 (4) A496 - A496.

W

Warner, TT; (1999) Sex-related influences on the frequency and age of onset of Primary Dystonia. Neurology , 53 pp. 1871-1873.

Warner, TT; (1999) Sex-related influences on the frequency and age of onset of primary dystonia. Epidemiologic Study of Dystonia in Europe (ESDE) Collaborative Group. Neurology , 53 1871-.

Worth, PF; Dunne, E; Nemeth, AH; Wood, NW; (1999) Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene. AM J HUM GENET , 65 (4) A499 - A499.

Z

Zamaraeva, MV; Hagelgans, AI; Lubnina, LV; Abramov, AY; Ahmedhodjaeva, HS; Saidhodjaev, AI; Glazyrina, NG; (1999) Hormonal activity and membrane action of plants terpenoids. CELL MOL BIOL LETT , 4 (2) 189 - 201.

This list was generated on Sun Jun 17 01:55:04 2018 BST.