This bibliography consists of citations to articles in books and journals. It includes pointers to abstracts on the Internet or in other sources when they are known.
Almqvist, E.; Andrew, S.; Theilmann, J.; Goldberg, P.; Zeisler, J.; Drugge, U.; Grandell, U.; Tapper-Persson, M.; Winblad, B.; Hayden, M.; Anvret, M. "Geographical distribution of haplotypes in Swedish families with Huntington's disease." Hum. Genet. 94: 124-128, 1994.
Altherr, M. R.; Wasmuth, J. J.; Seldin, M. F.; Nadeau, J. H.; Baehr, W.; Pittler, S. J. "Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3)." Genomics 12: 750-754, 1992.
Ambrose, C. M.; Duyao, M. P.; Barnes, G.; Bates, G. P.; Lin, C. S.; Srinidhi, J.; Baxendale, S.; Hummerich, H.; Lehrach, H.; Altherr, M.; Wasmuth, J.; Buckler, A.; Church, D.; Housman, D.; Berks, M.; Micklem, G.; Durbin, R.; Dodge, A.; Read, A.; Gusella, J.; MacDonald, M. E. "Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat." Somat. Cell Molec. Genet. 20: 27-38, 1994.
Andrew, S. E.; Goldberg, Y. P.; Kremer, B.; Squitieri, F.; Theilmann, J.; Zeisler, J.; Telenius, H.; Adam, S.; Almquist, E.; Anvret, M.; Lucotte, G.; Stoessl, A. J.; Campanella, G.; Hayden, M. R. "Huntington disease without CAG expansion: phenocopies or errors in assignment?" Am. J. Hum. Genet. 54: 852-863, 1994.
Andrew, S. E.; Goldberg, Y. P.; Kremer, B.; Telenius, H.; Theilmann, J.; Adam, S.; Starr, E.; Squitieri, F.; Lin, B.; Kalchman, M. A.; Graham, R. K.; Hayden, M. R. "The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease." Nature Genet. 4: 398-403, 1993.
Andrew, S.E.; Hayden, M.R. "Origins and evolution of Huntington disease chromosomes." Neurodegeneration, 1995 Sep; 4 (3): 239-44
Angier, Natalie. "Team Pinpoints Genetic Cause of Huntington's." The New York Times, March 24, 1993.
Ansari, A.A., Sundstrom, J.B., "Transplantation of fetal tissues." Immunology and Allergy Clinics of North America, 1996, Vol 16, Iss 2, pp 333. Address: A.A. Ansari, Emory Univ, Sch Med, Winship Canc Ctr, Room 4008, 1365B Clifton Rd NE, Atlanta, GA 30322 USA. Abstract available in Current Contents.
Aronin, N.; Chase, K.; Young, C.; Sapp, E.; Schwarz, C.; Matta, N.; Kornreich, R.; Landwehrmeyer, B.; Bird, E.; Beal, M. F.; Vonsattel, J.-P.; Smith, T.; Carraway, R.; Boyce, F. M.; Young, A. B.; Penney, J. B.; DiFiglia, M. "CAG expansion affects the expression of mutant huntingtin in Huntington's disease brain." Neuron 15: 1193-1201, 1995.
Aronin, N., M. Kim, et al. (1999). "Are there multiple pathways in the pathogenesis of Huntington's disease?." Philos Trans R Soc Lond B Biol Sci 354(1386): 995-1003.
Ashizawa, T., Jankovic, J., "Cervical dystonia as the initial presentation of Huntington's disease." Movement Disorders, 1996, Vol 11, Iss 4, pp 457-459. Address: T. Ashizawa, Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA.
Babul, Riyana ; Adam, Shelin ; Kremer, Berry ; Dufrasne, Suzanne ; Wiggins, Sandi ; Huggins, Marlene ; Theilmann, Jane ; Bloch, Maurice ; Hayden, Michael R. : Canadian Collaborative Group on Predictive Testing for Huntington Disease. "Attitudes toward direct predictive testing for the Huntington disease gene: relevance for other adult-onset disorders." JAMA. 1993 Nov 17; 270(19): 2321-2325.
Baetge EE. "Neural stem cells for CNS transplantation." Ann N Y Acad Sci, 1993 Sep 24; 695 285-91
Ball, David M. ; Harper, Peter S. "Pre-symptomatic testing for late-onset genetic disorders: lessons from Huntington's disease." FASEB (Federation of American Societies for Experimental Biology) Journal. 1992 Jul; 6(10): 2818-2819.
Bamford, K. A.; Caine, E. D.; Kido, D. K.; Cox, C.; Shoulson, I. "A prospective evaluation of cognitive decline in early Huntington's disease: functional and radiographic correlates." Neurology 45: 1867-1873, 1995.
Barinaga, M. "An intriguing new lead on Huntington's disease." Science 271: 1233-1234, 1996. Electronic version available at: http://www.interlog.com/~rlaycock/scimar96.htm
Barinaga, M. "Neurobiology - An intriguing new lead on Huntington's disease." Science, 1996, Vol 271, Iss 5253, pp 1233-1234. Abstract available in Current Contents. Electronic copy available at http://www.interlog.com/~rlaycock/scimar96.htm
Barnes, G. T.; Duyao, M. P.; Ambrose, C. M.; McNeil, S.; Perischetti, F.; Srinidhi, J.; Gusella, J. F.; MacDonald, M. E. "Mouse Huntington's disease gene homolog (Hdh)." Somat. Cell Molec. Genet. 20: 87-97, 1994.
Bates, G., "Expanded glutamines and neurodegeneration - A gain of insight." Bioessays, 1996, Vol 18, Iss 3, pp 175-178. Address: G. Bates, Guys Hosp, Sch Med, Umds, Div Med & Molec Genet, London SE1 9RT, ENGLAND. Abstract available in Current Contents.
Bates, G. P.; Valdes, J.; Hummerich, H.; Baxendale, S.; Le Paslier, D. L.; Monaco, A. P.; Tagle, D.; MacDonald, M. E.; Altherr, M.; Ross, M.; Brownstein, B. H.; Bentley, D.; Wasmuth, J. J.; Gusella, J. F.; Cohen, D.; Collins, F.; Lehrach, H. "Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region." Nature Genet. 1: 180-187, 1992.
Baxendale, S.; Abdulla, S.; Elgar, G.; Buck, D.; Berks, M.; Micklem, G.; Durbin, R.; Bates, G.; Brenner, S.; Beck, S.; Lehrach, H. "Comparative sequence analysis of the human and pufferfish Huntington's disease genes." Nature Genet. 10: 67-76, 1995.
Behrens, M.I., Koh, J.Y., Muller, M.C., Choi, D.W. "NADPH diaphorase-containing striatal or cortical neurons are resistant to apoptosis." Neurobiology of Disease, 1996, Vol 3, Iss 1, pp 72-75. Address: Choi DW, Washington Univ, Sch Med, Dept Neurol, 660 S Euclid Ave, St Louis, MO 63110 USA. Abstract available in Current Contents.
Beischlag, T.V., Nam, D., Ulpian, C., Seeman, P., Niznik, H.B. "A polymorphic dinucleotide repeat in the human dopamine D5 receptor gene promoter." Neuroscience Letters, 1996, Vol 205, Iss 3, pp 173-176. Address: Niznik HB, Univ Toronto, Dept Pharmacol, Toronto, ON M5S 1A8, CANADA. Abstract available in Current Contents.
Binedell, J., Soldan, J.R., Scourfield, J., Harper, P.S. "Huntington's disease predictive testing: The case for an assessment approach to requests from adolescents." Journal of Medical Genetics, 1996, Vol 33, Iss 11, pp 912-918. Address: Binedell J, Univ Wales Coll Med, Inst Med Genet, Heath Pk, Cardiff CF4 4XN, S Glam, WALES. Abstract available in Current Contents.
Bird, Thomas D. ; Bennett, Robin L. ; Lipe, Hillary P. ; Wiggins, Sandi ; Hayden, Michael R. "The consequences of testing for Huntington's disease." [Letter and response]. New England Journal of Medicine. 1993 Apr 8; 328(14): 1046.
Bishop, Kathleen Kirk. "Psychosocial Aspects of Genetic Disorders: Implications for Practice." The Journal of Contemporary Human Services, April 1993.
Bloch, M.; Hayden, M. R. "Predictive testing for Huntington disease in childhood: challenges and implications." Am. J. Hum. Genet. 46: 1-4, 1990.
Bloch, Maurice ; Adam, Shelin ; Wiggins, Sandy ; Huggins, Marlene ; Hayden, Michael R. "Predictive testing for Huntington disease in Canada: the experience of those receiving an increased risk." American Journal of Medical Genetics. 1992 Feb 15; 42(4): 499-507.
Bond, C.E., Hodes, M.E., "Direct amplification of the CAG repeat of huntingtin without amplification of CCG." Clinical Chemistry, 1996, Vol 42, Iss 5, pp 773-774. Address: M.E. Hodes, Indiana Univ, Sch Med, Dept Med & Molec Genet, 975 W Walnut St, Indianapolis, IN 46202 USA. Summary by Mary Price available at http://www.interlog.com/~rlaycock/abs_cag.html#BOND
Bonini, N. M. (1999). "A genetic model for human polyglutamine-repeat disease in Drosophila melanogaster." Philos Trans R Soc Lond B Biol Sci 354(1386): 1057-60.
Borlongan, C.V.; Cahill, D.W.; Freeman, T.B.; Sanberg, P.R. "Recent advances in neural transplantation. Relevance to neurodegenerative disorders." J Fla Med Assoc, 1994 Oct; 81 (10): 689-94
Borlongan, C.V.; Koutouzis, T.K.; Freeman, T.B.; Cahill, D.W.; Sanberg, P.R. "Behavioral pathology induced by repeated systemic injections of 3-nitropropionic acid mimics the motoric symptoms of Huntington's disease." Brain Res, 1995 Oct 30; 697 (1-2): 254-7
Borlongan, C.V., Polgar, S., Freeman, T.B., Hauser, R.A., Cahill, D.W., Sanberg, P.R., "Will fetal striatal transplants correct the akinetic end-stage of Huntington's disease?" Neurodegeneration, 1996, Vol 5, Iss 2, pp 189-192. Address: C.V. Borlongan, Univ S Florida, Coll Med, Dept Surg, Div Neurol Surg, 12901 Bruce B Downs Blvd, Tampa, FL 33612 USA.
Brandt, J., Bylsma, F.W., Gross, R., Stine, O.C., Ranen, N., Ross, C.A., "Trinucleotide repeat length and clinical progression in Huntington's disease." Neurology, 1996, Vol 46, Iss 2, pp 527-531. Address: J. Brandt, Johns Hopkins Univ Hosp, Dept Psychiat & Behav Sci, Meyer 218, 600 N Wolf St, Baltimore, MD 21287 USA. Abstract available in Current Contents.
Brandt, Jason. "Cognitive investigations in Huntington's disease." In Neuropsychological explorations of memory and cognition : essays in honor of Nelson Butters. New York : Plenum Press, 1994. xvii, 334 p. Series: Critical issues in neuropsychology. Includes bibliographical references and index. ISBN: 0306449838
Brandt, Jason "Ethical considerations in genetic testing: an empirical study of presymptomatic diagnosis of Huntington's disease." Fulford, K.W.M.; Gillett, Grant R.; Soskice, Janet Martin, eds. Medicine and Moral Reasoning. New York, NY: Cambridge University Press; 1994: 41-59.
Brundin, P., Fricker, R.A., Nakao, N. "Paucity of P-zones in striatal grafts prohibit commencement of clinical trials in Huntington's disease." Neuroscience, 1996, Vol. 71, no. 3, pp. 895-897
Brundin, Patrik and Klas Wictorin. "Neuronal transplantation in rat models of Parkinson's and Huntington's diseases." In Repairing the damaged nervous system. London : Saunders Scientific Publications/Academic Press, 1993. p. 383-459. Series: Seminars in the neurosciences, v. 5, issue 6. ISSN 1044-5765.
Buetow, K. H.; Shiang, R.; Yang, P.; Nakamura, Y.; Lathrop, G. M.; White, R.; Wasmuth, J. J.; Wood, S.; Berdahl, L. D.; Leysens, N. J.; Ritty, T. M.; Wise, M. E.; Murray, J. C. "A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates." Am. J. Hum. Genet. 48: 911-925, 1991.
Burgess, M.M., Hayden, M.R. "Patients' rights to laboratory data: Trinucleotide repeat length in huntington disease." American Journal of Medical Genetics, 1996, Vol 62, Iss 1, pp 6-9. Address: Burgess MM, Univ British Columbia, Ctr Appl Eth, Chair Bioeth, 6356 Agr Rd, Vancouver, BC V6T 1Z2, CANADA. Abstract available in Current Contents.
Burke, J. R.; Enghild, J. J.; Martin, M. E.; Jou, Y.-S.; Myers, R. M.; Roses, A. D.; Vance, J. M.; Strittmatter, W. J. "Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH." Nature Med. 2: 347-350, 1996. Abstract available in Current Contents.
Cariello, L., deCristofaro, T., Zanetti, L., Cuomo, T., DiMaio, L., Campanella, G., Rinaldi, S., Zanetti, P., DiLauro, R., Varrone, S. "Transglutaminase activity is related to CAG repeat length in patients with Huntington's disease." Human Genetics, 1996, Vol 98, Iss 6, pp 633-635. Language: English. Address: Cariello L, Stn Zool a Dohrn, Lab Biochim & Biol Mol, Villa Comunale, I-80121 Naples, ITALY. Abstract available in Current Contents.
Cha, J. H., A. S. Frey, et al. (1999). "Altered neurotransmitter receptor expression in transgenic mouse models of Huntington's disease." Philos Trans R Soc Lond B Biol Sci 354(1386): 981-9.
Chapman, Marguerite A. "Canadian experience with predictive testing for Huntington disease: lessons for genetic testing centers and policy makers." [Editorial]. American Journal of Medical Genetics. 1992 Feb 15; 42(4): 491-498.
Cicchetti, F., Parent, A. "Striatal interneurons in Huntington's disease: Selective increase in the density of calretinin-immunoreactive medium-sized neurons." Movement Disorders, 1996, Vol 11, Iss 6, pp 619-626. Language: English Address: Parent A, Hop Enfants Jesus, Ctr Rech Neurobiol, 1401 18E Rue, Quebec City, PQ G1J 1Z4, CANADA. Abstract available in Current Contents.
Cimons, Marlene. "It's all in the family." Los Angeles Times Magazine, February 10, 1991. 7 ff.
Claes, S., Legius, E., Dom, R., Cassiman, J.J. "Correlations between triplet repeat expansion and clinical features in Huntington's disease - Reply." Archives of Neurology, 1996, Vol 53, Iss 8, pp 715-715. Document type: Letter. Language: English. Address: Claes S, Univ Hosp Gasthuisberg, Ctr Human Genet, Herest 49, B-3000 Louvain, BELGIUM. Abstract available in Current Contents.
Connarty, M.; Dennis, N. R.; Patch, C.; Macpherson, J. N.; Harvey, J. F. "Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with denatorubral and pallidoluysian atrophy." Hum. Genet. 97: 76-78, 1996.
Cooke, Patrick. "Sentenced to live." Health 7 (July/August 1993) 80 ff.
Dalby, Shirley. "Behavioral and Sexual Problems in Huntington's Disease." Horizon, No. 64, 1992, Huntington Society of Canada.
Davies, S. W., M. Turmaine, et al. (1999). "From neuronal inclusions to neurodegeneration: neuropathological investigation of a transgenic mouse model of Huntington's disease." Philos Trans R Soc Lond B Biol Sci 354(1386): 971-9.
Decruyenaere, M., Evers-Kiebooms, G., Boogaerts, A., Cassiman, J.J., Cloostermans, T., Demyttenaere, K., Dom, R., Fryns, J.P., Van den Berghe, H. "Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making." J Med Genet, 1996 Sep; 33 (9): 737-43. Address: Centre for Human Genetics, UZ Gasthuisberg, University of Leuven, Belgium. Abstract available in Medline.
DeGrazia, David. "The ethical justification for minimal paternalism in the use of the predictive test for Huntington's disease." Journal of Clinical Ethics. 1991 Winter; 2(4): 219-228.
DeRooij, KE., Dorsman, JC., Smoor, MA., DenDunnen, JT., VanOmmen, GJB. "Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation." Human Molecular Genetics, 1996, Vol 5, Iss 8, pp 1093-1099. Address: VanOmmen GJB, Leiden Univ, Mgc Dept Human Genet, NL-2300 RA Leiden, NETHERLANDS. Abstract available in Current Contents.
De Wert, Guido. "Predictive testing for Huntington disease and the right not to know: some ethical reflections." Evers-Kiebooms, Gerry, et al., eds. Psychosocial Aspects of Genetic Counseling: Proceedings of a Conference. New York, NY: Wiley-Liss; 1992: 133-138.
Dorsman, J. C., M. A. Smoor, et al. (1999). "Analysis of the subcellular localization of huntingtin with a set of rabbit polyclonal antibodies in cultured mammalian cells of neuronal origin: comparison with the distribution of huntingtin in huntington's disease autopsy brain." Philos Trans R Soc Lond B Biol Sci 354(1386): 1061-7.
Dugan, L.L., Gabrielsen, J.K., Yu, S.P., Lin, T.S., Choi, D.W. "Buckminsterfullerenol free radical scavengers reduce excitotoxic and apoptotic death of cultured cortical neurons." Neurobiology of Disease, 1996, Vol 3, Iss 2, pp 129-135. Address: Choi DW, Washington Univ, Sch Med, Dept Neurol, 660 S Euclid Ave, St Louis,MO 63110 USA. Abstract available in Current Contents.
Dunnett, S.B.; Svendsen, C.N. "Huntington's disease: animal models and transplantation repair." Curr Opin Neurobiol, 1993 Oct; 3 (5): 790-6
Durbach, N.; Hayden, M. R. "George Huntington: the man behind the eponym." J. Med. Genet. 30: 406-409, 1993.
Dure, L. S., IV; Landwehrmeyer, G. B.; Golden, J.; McNeil, S. M.; Ge, P.; Aizawa, H.; Huang, Q.; Ambrose, C. M.; Duyao, M. P.; Bird, E. D.; DiFiglia, M.; Gusella, J. F.; MacDonald, M. E.; Penney, J. B.; Young, A. B.; Vonsattel, J.-P. "IT15 gene expression in fetal human brain." Brain Res. 659: 33-41, 1994.
Duyao, M.; Ambrose, C.; Myers, R.; Novelletto, A.; Persichetti, F.; Frontali, M.; Folstein, S.; Ross, C.; Franz, M.; Abbott, M.; Gray, J.; Conneally, P.; Young, A.; Penney, J.; Hollingsworth, Z.; Shoulson, I.; Lazzarini, A.; Falek, A.; Koroshetz, W.; Sax, D.; Bird, E.; Vonsattel, J.; Bonilla, E.; Alvir, J.; Bickman Conde, J.; Cha, J.-H.; Dure, L.; Gomez, F.; Ramos, M.; Sanchez-Ramos, J.; Snodgrass, S.; de Young, M.; Wexler, N.; Moscowitz, C.; Penchaszadeh, G.; MacFarlane, H.; Anderson, M.; Jenkins, B.; Srinidhi, J.; Barnes, G.; Gusella, J.; MacDonald, M. "Trinucleotide repeat length instability and age of onset in Huntington's disease." Nature Genet. 4: 387-392, 1993.
Duyao, M. P.; Auerbach, A. B.; Ryan, A.; Persichetti, F.; Barnes, G. T.; McNeil, S. M.; Ge, P.; Vonsattel, J.-P.; Gusella, J. F.; Joyner, A. L.; MacDonald, M. E. "Inactivation of the mouse Huntington's disease gene homolog Hdh." Science 269: 407-410, 1995.
Emerich, D.F., Lindner, M.D., Winn, S.R., Chen, E.Y., Frydel, B.R., Kordower, J.H. "Implants of encapsulated human CNTF-producing fibroblasts prevent behavioral deficits and striatal degeneration in a rodent model of Huntington's disease." Journal of Neuroscience, 1996, Vol 16, Iss 16, pp 5168-5181. Address: Emerich DF, Cytotherapeut Inc, 2 Richmond Sq, Providence,RI 02906 USA. Abstract available in Current Contents.
Emerich, Dwaine F., David W. Cahill, Paul R. Sandberg. "Excitotoxic lesions of the neostriatum as an animal model of Huntington's Disease." In Toxin-induced models of neurological disorders. New York : Plenum Press, 1994. 344 p. Includes bibliographical references and index. ISBN: 0306446146
Farrer, L. A.; Cupples, L. A.; Wiater, P.; Conneally, P. M.; Gusella, J. F.; Myers, R. H. "The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD." Am. J. Hum. Genet. 53: 125-130, 1993.
Faul, R.L.M. [et al.] "The distibution of GABAA- benzodiazepine receptors in the basal ganglia in Huntington's disease and in the quinolinic acid-lesioned rat." In Chemical signalling in the basal ganglia. Amsterdam ; New York : Elsevier, 1993. xv, 354 p. Series: Progress in brain research ; v. 99. Includes bibliographical references and index. ISBN: 0444815627 (alk. paper)
Feero, W.; Hoffman, E.P. "Huntington's disease. Their loss is our gain?" Curr Biol, 1995 Nov 1; 5 (11): 1229-31
Feigin, A., Kieburtz, K., Como, P., Hickey, C., Claude, K., Abwender, D., Zimmerman, C., Steinberg, K., Shoulson, I., "Assessment of coenzyme Q10 tolerability in Huntington's disease." Movement Disorders, 1996, Vol 11, Iss 3, pp 321-323. Address: A. Feigin, N Shore Univ Hosp, Dept Neurol, 300 Community Dr, Manhasset, NY 11030 USA. Abstract available in Current Contents.
Fiandaca, M.S.; Gash, D.M. "New insights and technologies in brain grafting." Clin Neurosurg, 1992; 39 482-508
Filoteo, J.V.; Delis, D.C.; Roman, M.J.; Demadura, T.; Ford, E.; Butters, N.; Salmon, D.P.; Paulsen, J.; Shults, C.W.; Swenson, M.; et al. "Visual attention and perception in patients with Huntington's disease: comparisons with other subcortical and cortical dementias." J Clin Exp Neuropsychol, 1995 Oct; 17 (5): 654-67
Fisher, L.J.; Gage, F.H. "Intracerebral transplantation: basic and clinical applications to the neostriatum." FASEB J, 1994 May; 8 (8): 489-96
Fricker, R.A., Barker, R.A., Fawcett, J.W., Dunnett, S.B. "A comparative study of preparation techniques for improving the viability of striatal grafts using vital stains, in vitro cultures, and in vivo grafts." Cell Transplantation, 1996, Vol 5, Iss 6, pp 599-611. Address: Dunnett SB, Univ Cambridge, MRC, Cambridge Ctr Brain Repair, Forvie Site, Robinson Way, Cambridge CB2 2PY, ENGLAND. Abstract available in Current Contents.
Frontali, M., A. Novelletto, et al. (1999). "CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci." Philos Trans R Soc Lond B Biol Sci 354(1386): 1089-94.
Frontali, M., Sabbadini, G., Novelletto, A., Jodice, C., Naso, F., Spadaro, M., Giunti, P., Jacopini, A.G., Veneziano, L., Mantuano, E., Malaspina, P., Ulizzi, L., Brice, A., Durr, A., Terrenato, L. "Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: A population genetics model for CAG repeat expansions." Annals of Human Genetics, 1996, Vol 60, Part 5, pp 423-435 Language: English Address: Frontali M, CNR, Ist Med Sperimentale, Viale Marx 15, I-00137 Rome, ITALY. Abstract available in Current Contents.
Funk, Sandra L. "Teens and HD and Adolescent Reaction to HD." Horizon, No. 77, Huntington Society of Canada, Fall 1993.
Furtado, J.C.S., Mazurek, M.F. "Behavioral characterization of quinolinate-induced lesions of the medial striatum: Relevance for Huntington's disease." Experimental Neurology, 1996, Vol 138, Iss 1, pp 158-168. Address: Furtado JCS, Mcmaster Univ, Med Ctr, Dept Biomed Sci Neurosci, Hamilton, ON L8N 3Z5, CANADA. Abstract available in Current Contents.
Furtado, S.; Suchowersky, O.; Rewcastle, B.; Graham, L.; Klimek, M.L.; Garber, A. "Relationship between trinucleotide repeats and neuropathological changes in Huntington's disease." Ann Neurol, 1996 Jan; 39 (1): 132-6
Ge, J.A., Barnes, N.M. "Alterations in angiotensin AT(1) and AT(2) receptor subtype levels in brain regions from patients with neurodegenerative disorders." European Journal of Pharmacology, 1996, Vol 297, Iss 3, pp 299-306. Address: Ge JA, Univ Birmingham, Sch Med, Dept Pharmacol, Birmingham B15 2TT, W Midlands, ENGLAND. Abstract available in Current Contents.
Gellera, C., Meoni, C., Castellotti, B., Zappacosta, B., Girotti, F., Taroni, F., DiDonato, S. "Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene." American Journal of Human Genetics, 1996, Vol 59, Iss 2, pp 475-477. Language: English. Address: Taroni F, Ist Nazl Neurol Carlo Besta, Dept Biochem & Genet, Div Biochem & Genet, Via Celoria 11, I-20133 Milan, ITALY. Abstract available in Current Contents.
Georgiou, N., Bradshaw, J.L., Phillips, J.G., Chiu, E. "The effect of Huntington's disease and Gilles de la Tourette's syndrome on the ability to hold and shift attention." Neuropsychologia, 1996 Sep; 34 (9): 843-51. Address: Department of Psychology, Monash University, Clayton, Victoria, Australia. N.Georgiou@sci.monash.edu.au. Abstract available in Medline.
Gilman, S. "Research trends in Alzheimer's disease and other neurodegenerative disorders: The Michigan Alzheimer's disease Research Center." Alzheimer's Disease (Series: Facts and Research in Gerontology), 1996, pp 95-109 Address: Gilman S, Univ Michigan, Med Ctr, Michigan Alzheimers Dis Res Ctr, 1500 E Med Ctr Dr, Tc 1914-0316, Ann Arbor, MI 48109 USA. Abstract available in Current Contents.
Giordani, B.; Berent, S.; Boivin, M. J.; Penney, J. B.; Lehtinen, S.; Markel, D. S.; Hollingsworth, Z.; Butterbaugh, G.; Hichwa, R. D.; Gusella, J. F.; Young, A. B. "Longitudinal neuropsychological and genetic linkage analysis of persons at risk for Huntington's disease." Arch. Neurol. 52: 59-64, 1995.
Giron, Louis T. "Critical survey and update on the epidemiology of Huntington's disease." In Handbook of neuroepidemiology. New York : M. Dekker, 1994. xii, 622 p. Series: Neurological disease and therapy ; v. 29. ISBN: 0824792424 (acid-free paper)
Goedert, M. (1999). "Filamentous nerve cell inclusions in neurodegenerative diseases: tauopathies and alpha-synucleinopathies." Philos Trans R Soc Lond B Biol Sci 354(1386): 1101-18.
Goldberg, Y. P.; Andrew, S. E.; Theilmann, J.; Kremer, B.; Squitieri, F.; Telenius, H.; Brown, J. D.; Hayden, M. R. "Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases." J. Med. Genet. 30: 987-990, 1993.
Goldberg, Y. P.; Kalchman, M. A.; Metzler, M.; Nasir, J.; Zeisler, J.; Graham, R.; Koide, H. B.; O'Kusky, J.; Sharp, A. H.; Ross, C. A.; Jirik, F.; Hayden, M. R. "Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript." Hum. Molec. Genet. 5: 177-185, 1996.
Goldberg, Y.P.; McMurray, C.T.; Zeisler, J.; Almqvist, E.; Sillence, D.; Richards, F.; Gacy, A.M.; Buchanan, J.; Telenius, H.; Hayden, M.R. "Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population." Hum Mol Genet, 1995 Oct; 4 (10): 1911-8
Goldberg, Y.P., Nicholson, D.W., Rasper, D.M., Kalchman, M.A., Koide, H.B., Graham, R.K., Bromm, M., Kazemi-Esfarjani, P., Thornberry, N.A., Vaillancourt, J.P., & Hayden, M.R., "Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract." Nature Genetics. Aug. 1996 (v. 13, no. 4) pp. 442-449. Abstract available in Current Contents. Summary by Dr. Mark Guttman available at: http://www.interlog.com/~rlaycock/abs001.html
Goldberg, Y. P.; Rommens, J. M.; Andrew, S. E.; Hutchinson, G. B.; Lin, B.; Theilmann, J.; Graham, R.; Glaves, M. L.; Starr, E.; McDonald, H.; Nasir, J.; Schappert, K.; Kalchman, M. A.; Clarke, L. A.; Hayden, M. R. "Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease." Nature 362: 370-373, 1993.
GomezTortosa, E., delBarrio, A., Barroso, T., Ruiz, PJG. "Visual processing disorders in patients with Huntington's disease and asymptomatic carriers." Journal of Neurology, 1996, Vol 243, Iss 3, pp 286-292. Address: GomezTortosa E, Fdn Jimenez Diaz, Dept Neurol, Avda Reyes Catolicos 2, E-28040 Madrid, SPAIN. Abstract available in Current Contents.
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Trottier, Y.; Biancalana, V.; Mandel, J.-L. "Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset." J. Med. Genet. 31: 377-382, 1994.
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Watanabe, M., Abe, K., Aoki, M., Kameya, T., Itoyama, Y., Shoji, M., Ikeda, M., Iizuka, T., Hirai, S. "A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea." Neurological Research, 1996, Vol. 18, Iss. 1, pp. 16-18. Language: English. Address: Watanabe M, Gunma Univ, Sch Med, Dept Neurol, 3-39-15 Showa Machi, Maebashi, Gumma 371, JAPAN. Abstract available in Current Contents.
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Last updated: Dec. 27, 2002
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