UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Browse by UCL Departments and Centres

Up a level
Export as [feed] RSS 2.0 [feed] RSS 1.0 [feed] Atom
Group by: Author | Type
Jump to: B | C | F | G | H | K | M | N | P | R | S | W | Y | Z
Number of items: 40.

B

BALL, JA and KENNEDY, AM and ROQUES, P and STEVENS, J and ROSSOR, MN (1993) MRI FINDINGS IN AN INDIVIDUAL AT RISK FOR FAMILIAL ALZHEIMERS-DISEASE. DEMENTIA , 4 (2) 120 - 120.

BALL, JA and LANTOS, PL and JACKSON, M and MARSDEN, CD and SCADDING, JW and ROSSOR, MN (1993) ALIEN HAND SIGN IN ASSOCIATION WITH ALZHEIMERS HISTOPATHOLOGY. J NEUROL NEUROSUR PS , 56 (9) 1020 - 1023.

BROWN, J and GYDESEN, S and SORENSEN, SA and BRUN, A and DUFF, K and HOULDEN, H and FIDANI, L and KULLKARNI, S and CUMMINGS, J and GOATE, A and ROSSOR, M and HARDY, J (1993) EXCLUSION MAPPING IN FAMILIAL NONSPECIFIC DEMENTIA. DEMENTIA , 4 (3-4) 163 - 166.

BROWN, J and GYDESEN, S and SORENSEN, SA and BRUN, A and SMITH, S and HOULDEN, H and TWELLS, R and MULLAN, M and ROSSOR, M and COLLINGE, J and PALMER, M and GOATE, A and HARDY, J (1993) GENETIC-CHARACTERIZATION OF A FAMILIAL NONSPECIFIC DEMENTIA ORIGINATING IN JUTLAND, DENMARK. J NEUROL SCI , 114 (2) 138 - 143.

Brown, J and Lantos, P and Stratton, M and Roques, P and Rossor, M (1993) Familial progressive supranuclear palsy. J Neurol Neurosurg Psychiatry , 56 (5) 473 - 476.

C

CAIRNS, NJ and CHADWICK, A and LANTOS, PL and LEVY, R and ROSSOR, MN (1993) BETA-A4 PROTEIN DEPOSITION IN FAMILIAL ALZHEIMERS-DISEASE WITH THE MUTATION IN CODON 717 OF THE BETA-A4 AMYLOID PRECURSOR PROTEIN GENE AND SPORADIC ALZHEIMERS-DISEASE. NEUROSCI LETT , 149 (2) 137 - 140.

Cairns, NJ and Chadwick, A and Lantos, PL and Levy, R and Rossor, MN (1993) βA4 protein deposition in familial Alzheimer's disease with the mutation in codon 717 of the βA4 amyloid precursor protein gene and sporadic Alzheimer's disease. Neuroscience Letters , 149 (2) 137 - 140.

CHAMBERS, TJ and OWENS, JM and HATTERSLEY, G and JAT, PS and NOBLE, MD (1993) GENERATION OF OSTEOCLAST-INDUCTIVE AND OSTEOCLASTOGENIC CELL-LINES FROM THE H-2K(B)TSA58 TRANSGENIC MOUSE. P NATL ACAD SCI USA , 90 (12) 5578 - 5582.

Collinge, J (1993) Inherited prion diseases. In: Harding, AE, (ed.) Advances in neurology: inherited ataxias. (155 - 165). Raven Press: New York, USA.

COLLINGE, J (1993) INHERITED PRION DISEASES. INHERITED ATAXIAS , 61 155 - 165.

COLLINGE, J and PALMER, MS (1993) PRION DISEASES IN HUMANS AND THEIR RELEVANCE TO OTHER NEURODEGENERATIVE DISEASES. DEMENTIA , 4 (3-4) 178 - 185.

COLLINGE, J and PALMER, MS and CAMPBELL, T and SIDLE, KCL and CARROLL, D and HARDING, A (1993) INHERITED PRION DISEASE (PRP LYSINE-200) IN BRITAIN - 2 CASE-REPORTS. BRIT MED J , 306 (6873) 301 - 302.

COLLINGE, J and PALMER, MS and ROSSOR, MN and JANOTA, I and LANTOS, PL (1993) PRION DEMENTIA. LANCET , 341 (8845) 627 - 627.

F

Fisher, EMC (1993) Much ado about cloning. BMJ , 307 (6911) 1074 - 1075.

Fisher, EMC (1993) Working with the media. Physiological Society Magazine , 8 25 - 25.

G

GROVES, AK and ENTWISTLE, A and JAT, PS and NOBLE, M (1993) THE CHARACTERIZATION OF ASTROCYTE CELL-LINES THAT DISPLAY PROPERTIES OF GLIAL SCAR TISSUE. DEV BIOL , 159 (1) 87 - 104.

H

HARDY, J (1993) PRION DEMENTIA. LANCET , 341 (8845) 626 - 626.

HARDY, J and HOULDEN, H and COLLINGE, J and KENNEDY, A and NEWMAN, S and ROSSOR, M and LANNFELT, L and LILIUS, L and WINBLAD, B and CROOK, R and DUFF, K (1993) APOLIPOPROTEIN-E GENOTYPE AND ALZHEIMERS-DISEASE. LANCET , 342 (8873) 737 - 738.

HOULDEN, H and CRAWFORD, F and ROSSOR, M and MULLAN, M (1993) SCREENING FOR THE APP CODON 670-671 MUTATIONS IN ALZHEIMERS-DISEASE. NEUROSCI LETT , 154 (1-2) 161 - 162.

HOULDEN, H and CROOK, R and DUFF, K and COLLINGE, J and ROQUES, P and ROSSOR, M and HARDY, J (1993) CONFIRMATION THAT THE APOLIPOPROTEIN E4 ALLELE IS ASSOCIATED WITH LATE-ONSET, FAMILIAL ALZHEIMERS-DISEASE. NEURODEGENERATION , 2 (4) 283 - 286.

K

Kennedy, A and Rossor, M (1993) Management of dementia. Practitioner , 237 (1523) 103 - 107.

KENNEDY, AM and NEWMAN, S and MCCADDON, A and BALL, J and ROQUES, P and MULLAN, M and HARDY, J and CHARTIERHARLIN, MC and FRACKOWIAK, RSJ and WARRINGTON, EK and ROSSOR, MN (1993) FAMILIAL ALZHEIMERS-DISEASE - A PEDIGREE WITH A MIS-SENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE (AMYLOID PRECURSOR PROTEIN 717 VALINE -] GLYCINE). BRAIN , 116 309 - 324.

KENNEDY, AM and NEWMAN, SN and WARRINGTON, EK and ROQUES, P and FRACKOWIAK, RSJ and ROSSOR, MN (1993) FAMILIAL ALZHEIMERS-DISEASE VERSUS SPORADIC ALZHEIMERS-DISEASE - A CLINICAL, NEUROPSYCHOLOGICAL AND PET STUDY. NEUROLOGY , 43 (4) A192 - A192.

Khalili-Shirazi, A and Atkinson, P and Gregson, N and Hughes, RA (1993) Antibody responses to P0 and P2 myelin proteins in Guillain-Barré syndrome and chronic idiopathic demyelinating polyradiculoneuropathy. J Neuroimmunol , 46 (1-2) 245 - 251.

M

MULLAN, M and HOULDEN, H and CRAWFORD, F and KENNEDY, A and ROGUES, P and ROSSOR, M (1993) AGE-OF-ONSET IN FAMILIAL EARLY-ONSET ALZHEIMERS-DISEASE CORRELATES WITH GENETIC ETIOLOGY. AM J MED GENET , 48 (3) 129 - 130.

N

Noble, M and Groves, AK and Ataliotis, P and Morgan, J and Peckham, M and Partridge, T and Jat, PS (1993) Biological and Molecular Approaches to the Generation of Conditionally Immortal Neural Cells. Neuroprotocols , 3 (3) 189 - 199.

P

PALMER, MS and COLLINGE, J (1993) MUTATIONS AND POLYMORPHISMS IN THE PRION PROTEIN GENE. HUM MUTAT , 2 (3) 168 - 173.

PALMER, MS and MAHAL, SP and CAMPBELL, TA and HILL, AF and SIDLE, KC and LAPLANCHE, JL and COLLINGE, J (1993) DELETIONS IN THE PRION PROTEIN GENE ARE NOT ASSOCIATED WITH CJD. HUM MOL GENET , 2 (5) 541 - 544.

Parfitt, M and Crook, R and Roques, P and Rossor, M and Chartier-Harlin, MC (1993) The Cystatin-C gene is not linked to early onset familial Alzheimer's disease. Neurosci Lett , 154 (1-2) 81 - 83.

R

Rossor, M (1993) Alzheimer's disease. BMJ , 307 (6907) 779 - 782.

Rossor, M (1993) Fortnightly review: Alzheimer's disease. British Medical Journal , 307 (6907) 779 - 782.

ROSSOR, MN (1993) MOLECULAR PATHOLOGY OF ALZHEIMERS-DISEASE. J NEUROL NEUROSUR PS , 56 (6) 583 - 586.

ROSSOR, MN and NEWMAN, S and FRACKOWIAK, RSJ and LANTOS, P and KENNEDY, AM (1993) ALZHEIMERS-DISEASE FAMILIES WITH AMYLOID PRECURSOR PROTEIN MUTATIONS. ALZHEIMERS DISEASE: AMYLOID PRECUSOR PROTEINS, SIGNAL TRANSDUCTION, AND NEURONAL TRANSPLANTATION , 695 198 - 202.

S

Schmitt, K and Vollrath, D and Foote, S and Fisher, EMC and Page, DC and Arnheim, N (1993) Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes. Hum Mol Genet , 2 1978 - ?.

W

Warren, JD and Miles, TS and Türker, KS (1993) Properties of synaptic noise in tonically active human motoneurons. Journal of Electromyography and Kinesiology , 2 189 - 202.

WEBER, T and TUMANI, H and HOLDORFF, B and COLLINGE, J and PALMER, M and KRETZSCHMAR, HA and FELGENHAUER, K (1993) TRANSMISSION OF CREUTZFELDT-JAKOB DISEASE BY HANDLING OF DURA-MATER. LANCET , 341 (8837) 123 - 124.

WHITEHEAD, RH and VANEEDEN, PE and NOBLE, MD and ATALIOTIS, P and JAT, PS (1993) ESTABLISHMENT OF CONDITIONALLY IMMORTALIZED EPITHELIAL-CELL LINES FROM BOTH COLON AND SMALL-INTESTINE OF ADULT H-2KB-TSA58 TRANSGENIC MICE. P NATL ACAD SCI USA , 90 (2) 587 - 591.

WHITEHEAD, RH and VANEEDEN, PE and NOBLE, MD and ATALIOTIS, P and JAT, PS (1993) ESTABLISHMENT OF CONDITIONALLY IMMORTALIZED EPITHELIAL-CELL LINES FROM BOTH COLON AND SMALL-INTESTINE OF ADULT H-2KB-TSA58 TRANSGENIC MICE (VOL 90, PG 587, 1993). P NATL ACAD SCI USA , 90 (14) 6894 - 6894.

Y

Yulug, IG and Egan, SE and Pollock, PM and Fisher, EMC (1993) A homologue of the Drosophila Son of Sevenless gene maps to mouse chromosome 17. Genomics , 18 733 - 734.

Z

Zinn, AR and Page, DC and Fisher, EMC (1993) Turner syndrome: the case of the missing sex chromosome. Trends Genet , 9 90 - 93.

This list was generated on Thu May 23 09:45:17 2013 BST.