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Number of items: 37.

A

AN, SF and GRAY, F and SCARAVILLI, F (1995) PROGRAMMED CELL-DEATH IN BRAINS OF HIV-1-POSITIVE PRE-AIDS PATIENTS. LANCET , 346 (8979) 911 - 912.

B

BANDOPADHYAY, R and DEBELLEROCHE, J (1995) DEPLETION OF CORTICAL CHOLECYSTOKININ LEVELS AFTER EXCITOTOXIN INJECTION INTO THE NUCLEUS BASALIS - SENSITIVITY TO MK-801. EUR J PHARMACOL , 275 (1) 53 - 59.

BROWN, J and ASHWORTH, A and GYDESEN, S and SORENSEN, A and ROSSOR, M and HARDY, J and COLLINGE, J (1995) FAMILIAL NONSPECIFIC DEMENTIA MAPS TO CHROMOSOME-3. HUM MOL GENET , 4 (9) 1625 - 1628.

C

CEBALLOSBAUMANN, AO and PASSINGHAM, RE and WARNER, T and PLAYFORD, ED and MARSDEN, CD and BROOKS, DJ (1995) OVERACTIVE PREFRONTAL AND UNDERACTIVE MOTOR CORTICAL AREAS IN IDIOPATHIC DYSTONIA. ANN NEUROL , 37 (3) 363 - 372.

CHEN, X and DESILVA, H and PETTENATI, M and RAO, P and STGEORGEHYSLOP, P and ROSES, A and XIA, Y and HORSBURGH, K and UEDA, K and SAITOH, T (1995) THE HUMAN NACP/ALPHA-SYNUCLEIN GENE - CHROMOSOME ASSIGNMENT TO 4Q21.3-Q22 AND TAQI RFLP ANALYSIS. GENOMICS , 26 (2) 425 - 427. 10.1016/0888-7543(95)80237-G.

CLARK, RF and HUTTON, M and FULDNER, RA and FROELICH, S and KARRAN, E and TALBOT, C and CROOK, R and LENDON, C and PRIHAR, G and HE, C and KORENBLAT, K and MARTINEZ, A and WRAGG, M and BUSFIELD, F and BEHRENS, MI and MYERS, A and NORTON, J and MORRIS, J and MEHTA, N and PEARSON, C and LINCOLN, S and BAKER, M and DUFF, K and ZEHR, C and PEREZTUR, J and HOULDEN, H and RUIZ, A and OSSA, J and LOPERA, F and ARCOS, M and MADRIGAL, L and COLLINGE, J and HUMPHREYS, C and ASHWORTH, A and SARNER, S and FOX, N and HARVEY, R and KENNEDY, A and ROQUES, P and CLINE, RT and PHILLIPS, CA and VENTER, JC and FORSELL, L and AXELMAN, K and LILIUS, L and JOHNSTON, J and COWBURN, R and VIITANEN, M and WINBLAD, B and KOSIK, K and HALTIA, M and POYHONEN, M and DICKSON, D and MANN, D and NEARY, D and SNOWDEN, J and LANTOS, P and LANNFELT, L and ROSSOR, M and ROBERTS, GW and ADAMS, MD and HARDY, J and GOATE, A (1995) THE STRUCTURE OF THE PRESENILIN-1 (S182) GENE AND IDENTIFICATION OF 6 NOVEL MUTATIONS IN EARLY-ONSET AD FAMILIES. NAT GENET , 11 (2) 219 - 222.

COMI, G and CIAFALONI, E and DESILVA, H and PRELLE, A and BARDONI, A and RIGOLETTO, C and ROBOTTI, M and BRESOLIN, N and MOGGIO, M and FORTUNATO, F and CISCATO, P and TURCONI, A and ROSE, A and SCARLATO, G (1995) A G(+1)-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT. HUMAN MOLECULAR GENETICS , 4 (11) 2171 - 2174. 10.1093/hmg/4.11.2171.

COMPSTON, DAS and WOOD, HK and ROBERTSON, N and SAWCER, S and WOOD, NW (1995) GENES AND SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS. ACTA NEUROLOGICA SCANDINAVICA , 91 43 - 51.

D

DANIEL, SE and GEDDES, JF and REVESZ, T (1995) GLIAL CYTOPLASMIC INCLUSIONS ARE NOT EXCLUSIVE TO MULTIPLE SYSTEM ATROPHY. J NEUROL NEUROSUR PS , 58 (2) 262 - 262.

DUFF, K and HARDY, J (1995) ALZHEIMERS-DISEASE - MOUSE MODEL MADE. NATURE , 373 (6514) 476 - 477. 10.1038/373476a0.

G

GHISO, J and PLANT, GT and REVESZ, T and WISNIEWSKI, T and FRANGIONE, B (1995) FAMILIAL CEREBRAL AMYLOID ANGIOPATHY (BRITISH TYPE) WITH NONNEURITIC AMYLOID PLAQUE-FORMATION MAY BE DUE TO A NOVEL AMYLOID PROTEIN. J NEUROL SCI , 129 (1) 74 - 75.

GIUNTI, P and SWEENEY, MG and HARDING, AE (1995) DETECTION OF THE MACHADO-JOSEPH DISEASE SPINOCEREBELLAR ATAXIA 3 TRINUCLEOTIDE REPEAT EXPANSION IN FAMILIES WITH AUTOSOMAL-DOMINANT MOTOR DISORDERS, INCLUDING THE DREW FAMILY OF WALWORTH. BRAIN , 118 1077 - 1085.

H

HAMMANS, SR and SWEENEY, MG and HANNA, MG and BROCKINGTON, M and MORGANHUGHES, JA and HARDING, AE (1995) THE MITOCHONDRIAL-DNA TRANSFER RNA(LEU(UUR)) A-]G((3243)) MUTATION - A CLINICAL AND GENETIC-STUDY. BRAIN , 118 721 - 734.

Hanna, MG and Nelson, I and Sweeney, MG and Cooper, JM and Watkins, PJ and Morgan-Hughes, JA and Harding, AE (1995) Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: Different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation. American Journal of Human Genetics , 56 (5) 1026 - 1033.

HANNA, MG and NELSON, I and SWEENEY, MG and COOPER, JM and WATKINS, PJ and MORGANHUGHES, JA and HARDING, AE (1995) CONGENITAL ENCEPHALOMYOPATHY AND ADULT-ONSET MYOPATHY AND DIABETES-MELLITUS - DIFFERENT PHENOTYPIC ASSOCIATIONS OF A NEW HETEROPLASMIC MTDNA TRANSFER-RNA GLUTAMIC-ACID MUTATION. AM J HUM GENET , 56 (5) 1026 - 1033.

Hanna, MG and Nelson, IP and Morgan-Hughes, JA and Harding, AE (1995) Erratum: Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: Relationship to proportion of mutant mitochondrial DNA (J. Neurol. Sci. (1995) 130 (154-160)). Journal of the Neurological Sciences , 132 (1) 95 - 95.

HANNA, MG and NELSON, IP and MORGANHUGHES, JA and HARDING, AE (1995) IMPAIRED MITOCHONDRIAL TRANSLATION IN HUMAN MYOBLASTS HARBORING THE MITOCHONDRIAL-DNA TRANSFER-RNA LYSINE-8344 A-]G (MERRF) MUTATION - RELATIONSHIP TO PROPORTION OF MUTANT MITOCHONDRIAL-DNA. J NEUROL SCI , 130 (2) 154 - 160.

HANNA, MG and NELSON, IP and MORGANHUGHES, JA and HARDING, AE (1995) IMPAIRED MITOCHONDRIAL TRANSLATION IN HUMAN MYOBLASTS HARBORING THE MITOCHONDRIAL-DNA TRANSFER-RNA LYSINE-8344 A-]G (MERRF) MUTATION - RELATIONSHIP TO PROPORTION OF MUTANT MITOCHONDRIAL-DNA (VOL 130, PG 154, 1995). J NEUROL SCI , 132 (1) 95 - 95.

HARDY, J (1995) APOLIPOPROTEIN-E IN THE GENETICS AND EPIDEMIOLOGY OF ALZHEIMERS-DISEASE. AMERICAN JOURNAL OF MEDICAL GENETICS , 60 (5) 456 - 460. 10.1002/ajmg.1320600519.

HARDY, J and HUTTON, M (1995) 2 NEW GENES FOR ALZHEIMERS-DISEASE. TRENDS IN NEUROSCIENCES , 18 (10) 436 - 436. 10.1016/0166-2236(95)90092-6.

HOULDEN, H and CROOK, R and DUFF, K and HUTTON, M and COLLINGE, J and ROQUES, P and ROSSOR, M and HARDY, J (1995) APOLIPOPROTEIN-E ALLELES BUT NEITHER APOLIPOPROTEIN-B NOR APOLIPOPROTEIN AI/CIII ALLELES ARE ASSOCIATED WITH LATE-ONSET, FAMILIAL ALZHEIMERS-DISEASE. NEUROSCI LETT , 188 (3) 202 - 204.

I

IWAI, A and MASLIAH, E and YOSHIMOTO, M and GE, N and FLANAGAN, L and DESILVA, H and KITTEL, A and SAITOH, T (1995) THE PRECURSOR PROTEIN OF NON-A-BETA COMPONENT OF ALZHEIMERS-DISEASE AMYLOID IS A PRESYNAPTIC PROTEIN OF THE CENTRAL-NERVOUS-SYSTEM. NEURON , 14 (2) 467 - 475. 10.1016/0896-6273(95)90302-X.

K

KELLARWOOD, HF and WOOD, NW and HOLMANS, P and CLAYTON, D and ROBERTSON, N and COMPSTON, DAS (1995) MULTIPLE-SCLEROSIS AND THE HLA-D REGION - LINKAGE AND ASSOCIATION STUDIES. J NEUROIMMUNOL , 58 (2) 183 - 190.

L

LANNFELT, L and LILIUS, L and VIITANEN, M and HOULDEN, H and ROSSOR, M and HARDY, J and WINBLAD, B and BASUN, H (1995) MICROSATELLITE D21S210 (GT-12) ALLELE FREQUENCIES IN SPORADIC ALZHEIMERS-DISEASE. ACTA NEUROL SCAND , 91 (2) 145 - 148.

LIPPA, C and SMITH, T and SAUNDERS, A and CROOK, R and PULASKISALO, D and DAVIES, P and HARDY, J and ROSES, A and DICKSON, D (1995) APOLIPOPROTEIN-E GENOTYPE AND LEWY BODY DISEASE. NEUROLOGY , 45 (1) 97 - 103.

M

MULLAN, M and BENNETT, C and FIGUEREDO, C and HUGHES, D and MANT, R and OWEN, M and WARREN, A and MCINNIS, M and MARSHALL, A and LANTOS, P and COLLINGE, J and GOATE, A and HOULDEN, H and CRAWFORD, F (1995) CLINICAL-FEATURES OF EARLY-ONSET, FAMILIAL ALZHEIMERS-DISEASE LINKED TO CHROMOSOME-14. AM J MED GENET , 60 (1) 44 - 52.

N

NELSON, I and HANNA, MG and ALSANJARI, N and SCARAVILLI, F and MORGANHUGHES, JA and HARDING, AE (1995) A NEW MITOCHONDRIAL-DNA MUTATION ASSOCIATED WITH PROGRESSIVE DEMENTIA AND CHOREA - A CLINICAL, PATHOLOGICAL, AND MOLECULAR-GENETIC STUDY. ANN NEUROL , 37 (3) 400 - 403.

P

PerezTur, J and Froelich, S and Prihar, G and Crook, R and Baker, M and Duff, K and Wragg, M and Busfield, F and Lendon, C and Clark, RF and Roques, P and Fuldner, RA and Johnston, J and Cowburn, R and Forsell, C and Axelman, K and Lilius, L and Houlden, H and Karran, E and Roberts, GW and Rossor, M and Adams, MD and Hardy, J and Goate, A and Lannfelt, L and Hutton, M (1995) A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene. NEUROREPORT , 7 (1) 297 - 301.

R

REVESZ, T and DANIEL, SE and LEES, AJ and WILL, RG (1995) A CASE OF PROGRESSIVE SUBCORTICAL GLIOSIS ASSOCIATED WITH DEPOSITION OF ABNORMAL PRION PROTEIN (PRP). J NEUROL NEUROSUR PS , 58 (6) 759 - 760.

S

SHERRINGTON, R and ROGAEV, E and LIANG, Y and ROGAEVA, E and LEVESQUE, G and IKEDA, M and CHI, H and LIN, C and LI, G and HOLMAN, K and TSUDA, T and MAR, L and FONCIN, J and BRUNI, A and MONTESI, M and SORBI, S and RAINERO, I and PINESSI, L and NEE, L and CHUMAKOV, I and POLLEN, D and BROOKES, A and SANSEAU, P and POLINSKY, R and WASCO, W and DASILVA, H and HAINES, J and PERICAKVANCE, M and TANZI, R and ROSES, A and FRASER, P and ROMMENS, J and STGEORGEHYSLOP, P (1995) CLONING OF A GENE BEARING MISSENSE MUTATIONS IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE. NATURE , 375 (6534) 754 - 760. 10.1038/375754a0.

Sherrington, R and Rogaev, EI and Liang, Y and Rogaeva, EA and Levesque, G and Ikeda, M and Chi, H and Lin, C and Li, G and Holman, K and Tsuda, T and Mar, L and Foncin, JF and Bruni, A and Montesi, MP and Sorbi, S and Rainero, I and Pinessi, L and Nee, L and Chumakov, I and Pollen, D and Brookes, A and Sanseau, P and Polinsky, RJ and Wasco, W and de Silva, R and Haines, JL and Pericak-Vance, M and Tanzi, RE and Roses, AD and Fraser, PE and Rommens, JM and St George-Hyslop, PH (1995) Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature , 375 (6534) 734 - 735. 10.1038/375754a0.

V

VanPaesschen, W and Sisodiya, S and Connelly, A and Duncan, JS and Free, SL and Raymond, AA and Grunewald, RA and Revesz, T and Shorvon, SD and Fish, DR and Stevens, JM and Johnson, CL and Scaravilli, F and Harkness, WFJ and Jackson, GD (1995) Quantitative hippocampal MRI and intractable temporal lobe epilepsy. NEUROLOGY , 45 (12) 2233 - 2240.

VANPAESSCHEN, WIM and REVESZ, T and SISODIYA, S and CONNELLY, A and JACKSON, GD and DUNCAN, JS (1995) QUANTITATIVE NEUROPATHOLOGY AND QUANTITATIVE MAGNETIC-RESONANCE-IMAGING OF THE HIPPOCAMPUS OF PATIENTS WITH INTRACTABLE TEMPORAL-LOBE EPILEPSY. EPILEPSIA , 36 S96 - S96.

W

Warner, TT and Williams, LD and Walker, RW and Flinter, F and Robb, SA and Bundey, SE and Honavar, M and Harding, AE (1995) A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families. Ann Neurol , 37 (4) 452 - 459. 10.1002/ana.410370407.

WOOD, NW and SAWCER, SJ and KELLARWOOD, HF and HOLMANS, P and CLAYTON, D and ROBERTSON, N and COMPSTON, DAS (1995) THE T-CELL RECEPTOR-BETA LOCUS AND SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS. NEUROLOGY , 45 (10) 1859 - 1863.

WOOD, NW and SAWCER, SJ and KELLERWOOD, HF and HOLMANS, P and CLAYTON, D and ROBERTSON, N and COMPSTON, DAS (1995) SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS AND THE IMMUNOGLOBULIN HEAVY-CHAIN VARIABLE REGION. J NEUROL , 242 (10) 677 - 682.

Y

Yue, KK and Holton, JL and Clarke, JP and Hyam, JL and Hashimoto, T and Chidgey, MA and Garrod, DR (1995) Characterisation of a desmocollin isoform (bovine DSC3) exclusively expressed in lower layers of stratified epithelia. J Cell Sci , 108 ( Pt 6) 2163 - 2173.

This list was generated on Fri May 24 10:43:13 2013 BST.