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: A | B | C | D | H | J | K | L | M | P | R | S | T | W
Number of items: 39.

A

ADROER, R and LOPEZACEDO, C and OLIVA, R and HARDY, J and FIDANI, L (1993) A NOVEL SILENT VARIANT AT CODON-711 AND A VARIANT AT CODON-708 OF THE APP SEQUENCE DETECTED IN SPANISH ALZHEIMER AND CONTROL CASES. NEUROSCIENCE LETTERS , 150 (1) 33 - 34. 10.1016/0304-3940(93)90101-P.

AN, SF and GOULD, S and KEELING, JW and FLEMING, KA (1993) ROLE OF RESPIRATORY VIRAL-INFECTION IN SIDS - DETECTION OF VIRAL NUCLEIC-ACID BY IN-SITU HYBRIDIZATION. J PATHOL , 171 (4) 271 - 278.

B

BANDOPADHYAY, R and DEBELLEROCHE, J (1993) REGULATION OF CORTICAL CHOLECYSTOKININ NEURONS BY NMDA RECEPTORS. J NEUROCHEM , 61 S208 - S208.

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.

C

CHARTIER-HARLIN, M and CRAWFORD, F and PERL, D and STEELE, J and HARDY, J (1993) SEQUENCING OF EXON-16 AND EXON-17 OF THE BETA-AMYLOID PRECURSOR PROTEIN GENE REVEALS THE BETA-AMYLOID SEQUENCE TO BE NORMAL IN CASES OF THE PARKINSON DEMENTIA COMPLEX OF GUAM. JOURNAL OF NEURAL TRANSMISSION-PARKINSONS DISEASE AND DEMENTIA SECTION , 5 (1) 63 - 65. 10.1007/BF02260915.

Conway, D and Bain, PG and Warner, TT and Davis, MB and Findley, LJ and Thompson, PD and Marsden, CD and Harding, AE (1993) Linkage analysis with chromosome 9 markers in hereditary essential tremor. Mov Disord , 8 (3) 374 - 376. 10.1002/mds.870080324.

CRAWFORD, FC and HOULDEN, H and CROOK, R and MULLAN, MJ (1993) LINKAGE ANALYSIS AND DIRECT SEQUENCING OF CANDIDATES FOR THE CHROMOSOME-14 LOCUS IN FAMILIAL EARLY-ONSET ALZHEIMERS-DISEASE. AM J HUM GENET , 53 (3) 1725 - 1725.

D

DEMAEREL, P and BROWN, P and KENDALL, BE and REVESZ, T and PLANT, G (1993) ALLERGIC ASPERGILLOSIS OF THE SPHENOID SINUS - PITFALL ON MRI. BRIT J RADIOL , 66 (783) 260 - 263.

Demaerel, P and Brown, P and Kendall, BE and Revesz, T and Plant, G (1993) Case report: allergic aspergillosis of the sphenoid sinus: pitfall on MRI. Br J Radiol , 66 (783) 260 - 263.

H

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

HARDY, J and DUFF, K (1993) HETEROGENEITY IN ALZHEIMERS-DISEASE. ANNALS OF MEDICINE , 25 (5) 437 - 440. 10.3109/07853899309147308.

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.

HARDY, J and ROBERTS, G (1993) SMOKING AND NEUROGENERATIVE DISEASES. LANCET , 342 (8881) 1238 - 1238. 10.1016/0140-6736(93)92219-J.

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 CRAWFORD, F and ROSSOR, M and HARDY, J and MULLAN, M (1993) GENETIC-LINKAGE ANALYSIS IN LATE-ONSET ALZHEIMERS-DISEASE. AM J HUM GENET , 53 (3) 1017 - 1017.

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.

HOULDEN, H and MULLAN, M (1993) ALZHEIMERS-DISEASE ETIOLOGY - AMYLOID AND CHROMOSOME-14. BRIT J HOSP MED , 49 (8) 535 - 536.

J

JODICE, C and FRONTALI, M and PERSICHETTI, F and NOVELLETTO, A and PANDOLFO, M and SPADARO, M and GIUNTI, P and SCHINAIA, G and LULLI, P and MALASPINA, P and PLASMATI, R and TOLA, R and ANTONELLI, A and DIDONATO, S and MOROCUTTI, C and WEISSENBACH, J and CANN, HM and TERRENATO, L (1993) THE GENE FOR SPINAL CEREBELLAR ATAXIA-1 (SCA1) IS FLANKED BY 2 CLOSELY LINKED HIGHLY POLYMORPHIC MICROSATELLITE LOCI. HUM MOL GENET , 2 (9) 1383 - 1387.

JODICE, C and LISPI, M and MALASPINA, P and NOVELLETTO, A and PERSICHETTI, F and SCHINAIA, G and FRONTALI, M and GIUNTI, P and SPADARO, M and TERRENATO, L (1993) GENETIC-MAP SURROUNDING THE SCA1 LOCUS. CYTOGENET CELL GENET , 62 (2-3) 80 - 80.

K

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.

KING, A and HOULDEN, H and HARDY, J and LANE, R and CHANCELLOR, A and DEBELLEROCHE, J (1993) ABSENCE OF LINKAGE BETWEEN CHROMOSOME-21 LOCI AND FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS. J MED GENET , 30 (4) 318 - 318.

L

LANE, RJM and BANDOPADHYAY, R and DEBELLEROCHE, J (1993) ABNORMAL GLYCINE METABOLISM IN MOTOR-NEURON DISEASE - STUDIES ON PLASMA AND CEREBROSPINAL-FLUID. J ROY SOC MED , 86 (9) 501 - 505.

LANNFELT, L and FOLKESSON, R and MOHAMMED, A and WINBLAD, B and HELLGREN, D and DUFF, K and HARDY, J (1993) ALZHEIMERS-DISEASE - MOLECULAR-GENETICS AND TRANSGENIC ANIMAL-MODELS. BEHAVIOURAL BRAIN RESEARCH , 57 (2) 207 - 213. 10.1016/0166-4328(93)90137-F.

M

MALANDRINI, A and VILLANOVA, M and PIOMBONI, P and COLLODEL, G and SPADARO, M and GIUNTI, P and SALVADORI, C and MOROCUTTI, C and GUAZZI, GC (1993) ULTRASTRUCTURAL SPERM ABNORMALITIES AND CEREBELLAR ATROPHY - DOES A CORRELATION EXIST - REPORT OF 2 CASES WITHOUT ENDOCRINE HYPOGONADISM. J SUBMICR CYTOL PATH , 25 (3) 371 - 375.

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.

MULLAN, M and TSUJI, S and MIKI, T and KATSUYA, T and NARUSE, S and KANEKO, K and SHIMIZU, T and KOJIMA, T and NAKANO, I and OGIHARA, T and MIYATAKE, T and OVENSTONE, I and CRAWFORD, F and GOATE, A and HARDY, J and ROQUES, P and ROBERTS, G and LUTHERT, P and LANTOS, P and CLARK, C and GASKELL, P and CRAIN, B and ROSES, A (1993) CLINICAL COMPARISON OF ALZHEIMERS-DISEASE IN PEDIGREES WITH THE CODON-717 VAL-]ILE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE. NEUROBIOLOGY OF AGING , 14 (5) 407 - 419. 10.1016/0197-4580(93)90099-W.

P

PRINEAS, JW and BARNARD, RO and REVESZ, T and KWON, EE and SHARER, L and CHO, ES (1993) MULTIPLE-SCLEROSIS - PATHOLOGY OF RECURRENT LESIONS. BRAIN , 116 681 - 693.

R

REVESZ, T and ALSANJARI, N and DARLING, JL and SCARAVILLI, F and LANE, DP and THOMAS, DGT (1993) PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) - EXPRESSION IN SAMPLES OF HUMAN ASTROCYTIC GLIOMAS. NEUROPATH APPL NEURO , 19 (2) 152 - 158.

REVESZ, T and SCARAVILLI, F and COUTINHO, L and COCKBURN, H and SACARES, P and THOMAS, DGT (1993) RELIABILITY OF HISTOLOGICAL DIAGNOSIS INCLUDING GRADING IN GLIOMAS BIOPSIED BY IMAGE-GUIDED STEREOTAXIC TECHNIQUE. BRAIN , 116 781 - 793.

ROOKE, K and TALBOT, C and JAMES, L and ANAND, R and HARDY, J and GOATE, A (1993) A PHYSICAL MAP OF THE HUMAN APP GENE IN YACS. MAMMALIAN GENOME , 4 (11) 662 - 669. 10.1007/BF00360904.

S

SPADARO, M and GIUNTI, P and COLAZZA, GB and NASO, F and BIANCO, F and MOROCUTTI, C (1993) CLINICAL-STUDY OF LARGE KINDREDS WITH AUTOSOMAL DOMINANT HLA-LINKED SPINOCEREBELLAR ATAXIA (SCA1) OF LATE ONSET. ITAL J NEUROL SCI , 14 (1) 17 - 21.

SPADARO, M and SOLDATI, G and TERRACCIANO, ME and GIUNTI, P and ACCORINTI, M and LACAVA, M and PIVETTIPEZZI, P (1993) A NEUROLOGICAL AND ELECTROPHYSIOLOGICAL STUDY ON BEHCETS-DISEASE PATIENTS. In: Wechsler, B and Godeau, P, (eds.) BEHCETS DISEASE. (pp. 425 - 428). ELSEVIER SCIENCE PUBL B V

T

TANAKA, H and NARUSE, S and SEKI, K and ONODERA, O and KOBAYASHI, H and MIYATAKE, T and SHIBATA, A and SAKAKI, Y and KAMINO, K and MIKI, T and NUKINA, N and IMAGAWA, M and NAKANO, I and SHIMIZU, T and KOJIMA, T and HARDY, J and TSUJI, S (1993) ABSENCE OF LINKAGE DISEQUILIBRIUM AT AMYLOID PRECURSOR PROTEIN GENE LOCUS IN JAPANESE FAMILIAL ALZHEIMERS-DISEASE WITH 717VAL-]ILE MUTATION. NEUROSCIENCE LETTERS , 162 (1-2) 63 - 66. 10.1016/0304-3940(93)90560-8.

TERRENATO, L and JODICE, C and MALASPINA, P and NOVELLETTO, A and PERSICHETTI, F and SCHINAIA, G and FRONTALI, M and LULLI, P and CAPPELLACCI, S and GIUNTI, P and SPADARO, M and ANTONELLI, A and PANDOLFO, M (1993) LINKAGE DISEQUILIBRIUM BETWEEN SPINOCEREBELLAR ATAXIA (SCA1) AND D6S89 LOCI. CYTOGENET CELL GENET , 62 (2-3) 80 - 80.

W

Warner, TT and Fletcher, NA and Davis, MB and Ahmad, F and Conway, D and Feve, A and Rondot, P and Marsden, CD and Harding, AE (1993) Linkage analysis in British and French families with idiopathic torsion dystonia. Brain , 116 ( Pt 3) 739 - 744.

WARNER, TT and MOSSMAN, S and MURRAY, NMF (1993) HYPOKALEMIA MIMICKING GUILLAIN-BARRE-SYNDROME. J NEUROL NEUROSUR PS , 56 (10) 1134 - 1135.

WATKINS, L and KHUDADOS, ES and KALEOGLU, M and REVESZ, T and SACARES, P and CROCKARD, HA (1993) SKULL BASE CHORDOMAS - A REVIEW OF 38 PATIENTS, 1958-88. BRIT J NEUROSURG , 7 (3) 241 - 248.

WEBSTER, A and ROTBART, H and WARNER, T and RUDGE, P and HYMAN, N (1993) DIAGNOSIS OF ENTEROVIRUS BRAIN DISEASE IN HYPOGAMMAGLOBULINEMIC PATIENTS BY POLYMERASE CHAIN-REACTION. CLINICAL INFECTIOUS DISEASES , 17 (4) 657 - 661.

This list was generated on Wed May 22 07:33:32 2013 BST.