Read Secondary Schizophrenia Online
Authors: Perminder S. Sachdev
Association (IHA) and the World
10
:167–76.
R. H.,
et al.
Evidence of
Federation of Neurology (WFN)
5. Lyon R. L. Huntington’s chorea in
presymptomatic cognitive decline
Research Group on Huntington’s
the Moray Firth area. Br Med J,
in Huntington’s disease. J Clin
Chorea. Guidelines for the
1962.
1
:1301–6.
Exp Neuropsychol, 1992.
14
:
molecular genetics predictive test
6. Wexler N. S., Bonilla E., Young A.
961–75.
in Huntington’s disease.
B.,
et al.
Huntington’s disease in
16. Foroud T., Siemers E., Kleindorfer
Neurology, 1994.
44
:1533–6.
Venezuela and gene linkage.
D.,
et al.
Cognitive scores of
25. Schulman J. D., Black S. H.,
Cytogenet Cell Genet, 1984.
carriers of Huntingont’s disease
Handyside A.,
et al.
37
:605. (Abstract).
gene compared to non-carriers.
Preimplantation genetic testing
7. Gusella J. F., Wexler N. S.,
Ann Neurol, 1995.
37
:657–64.
for Huntington disease and
Conneally P. M.,
et al.
A
17. Leroi I., O’Hearn E., Marsh L.,
certain other dominantly
polymorphic DNA marker
et al.
Psychopathology in patients
inherited disorders. Clin Genet,
genetically linked to Huntington’s
with degenerative cerebellar
1996.
49
:57–8.
disease. Nature, 1983.
306
:
diseases: a comparison to
26. Kremer B., Goldberg P., Andrew S.
234–8.
Huntington’s disease. Am J
E.,
et al.
A worldwide study of the
8. Huntington’s Disease
Psychiatry, 2002.
159
:1306–
Huntington’s disease mutation.
Collaborative Research Group.
14.
The sensitivity and sensitivity of
A novel gene containing a
18. Folstein S. E., Abbott M. H.,
measuring CAG repeats. N Engl J
trinucleotide repeat that is
Chase G. A.,
et al.
The association
Med, 1994.
330
:1401–6.
expanded and unstable on
of affective disorder with
27. Margolis R. L., Ross C. A.
Huntington’s disease
Huntington’s disease in a case
Diagnosis of Huntington disease.
chromosomes. Cell, 1993.
series and in families. Psychol
Clin Chem, 2003.
49
:1726–32.
72
:971–83.
Med, 1983.
13
:537–42.
28. McInnis M. G. Anticipation: an
9. Morris M. Dementia and
19. Reed T. E., Chandler J. H.
old idea in new genes. Am J Hum
cognitive changes in Huntington’s
Huntington’s chorea in Michigan:
Genet, 1996.
59
:973–9.
disease. Adv Neurol, 1995.
I. Demography and genetics. Am J
29. Duyao M., Ambrose C., Myers R.,
65
:187–200.
Hum Genet, 1958.
10
:210–25.
et al.
Trinucleotide repeat length
10. Saint-Cyr J. A., Taylor A. E., Lang
20. Young A. B., Shoulson I., Penney
instability and age of onset in
A. E. Procedural learning and
J. B.,
et al.
Huntington’s disease in
Huntington’s disease. Nat Genet,
neostriatal dysfunction in man.
Venezuela: neurologic features
1993.
4
:387–92.
Brain, 1988.
111
:941–59.
and functional decline. Neurology,
30. MacDonald M. E., Vonsattel J. P.,
11. Shoulson I. Huntington’s disease:
1986.
36
:244–9.
Shrinidhi J.,
et al.
Evidence for the
cognitive and psychiatric features.
21. Jernigan T. L., Salmon D. P.,
GluR6 gene associated with
Neuropsychiatry Neuropsychol
Butters N.,
et al.
Cerebral
younger onset age of Huntington’s
Behav Neurol, 1990.
3
:15–
structure on MRI. Part II: specific
disease. Neurology, 1999.
47
:155–
355
22.
changes in Alzheimer’s and
60.
Organic Syndromes of Schizophrenia – Section 3
31. Panas M., Avramopoulos D.,
Huntington’s Disease and
trinucleotide repeats. Nat Genet,
Karadima0 G.,
et al.
schizophrenia-like psychosis in a
1992.
2
:186–91.
Apolipoprotein E and presenilin-1
Huntington’s disease pedigree.
51. Cummings J. L. Frontal-
genotypes in Huntington’s
Clin Pract Epidemiol Ment Health,
subcortical circuits and human
disease. J Neurol, 1999.
2006.
2
:1.
behaviour. Arch Neurol, 1993.
246
:574–7.
42. Basset A. S., Honer W. G.
50
:873–80.
32. Duyao M. P., Auerbach A. B.,
Evidence for anticipation in
52. Rajkowska G., Selemon L. D.,
Ryan A.,
et al.
Inactivation of the
schizophrenia. Am J Hum Genet,
Goldman-Rakic P. S. Neuronal
mouse Huntington’s disease gene
1994.
54
:864–70.
and glial somal size in the
homolog Hdh. Science, 1995.
269
:
43. ODonovan M. C., Guy C.,
prefrontal cortex: a postmortem
407–10.
Craddock N.,
et al.
Expanded
morphometric study of
33. Everett C. M., Wood N. W.
CAG repeats in schizophrenia and
schizophrenia and Huntington’s
Trinucleotide repeats and
bipolar disorder. Nat Genet, 1995.
disease. Arch Gen Psychiatry,
neurodegenerative disease. Brain,
10
:380–1.
1998.
55
:215–24.
2004.
127
:2385–405.
44. Morris A. G., Gaitonde E.,
53. Gold J. M., Goldberg T. E.,
34. Folstein S. E., Chase G. A., Wahl
McKenna P. J.,
et al.
CAG repeat
Weinberger D. R. Prefrontal
W. E.,
et al.
Huntington disease in
expansions and schizophrenia:
function and schizophrenic
Maryland: clinical aspects of
association with disease in females
symptoms. Neuropsychiatry
racial variation. Am J Hum Genet,
and with early age-at-onset. Hum
Neuropsychol Behav Neurol, 1992.
1987.
41
:168–79.
Mol Genet, 1995.
4
:1957–61.
5
:253–61.
35. Shiwach R. Psychopathology in
45. Rubinsztein D. C., Leggo J.,
54. Tamlyn D., McKenna P. J.,
Huntington’s disease patients.
Goodburn S.,
et al.
Huntington’s
Mortimer A. M.,
et al.
Memory
Acta Psychiatr Scand, 1994.
Disease (HD) gene CAG repeats
impairment in schizophrenia: its
90
:241–6.
in schizophrenic patients shows
extent, affiliations and
36. Beckson M., Cummings J. L.
overlap of the normal and HD
neuropsychological character.
Psychosis in basal ganglia
affected ranges but absence of
Psychol Med, 1992.
22
:101–15.
disorders. Neuropsychiatry
correlation with schizophrenia. J
55. Hanes K. R., Andrewes D. G.,
Neuropsychol Behav Neurol, 1992.
Med Genet, 1994.
31
:690–3.
Pantelis C.,
et al.
Subcortical
5
:126–31.
46. Jain S., Leggo J., De Lisi L. E.,
et al.
dysfunction in schizophrenia:
37. McHugh P. R., Folstein M. F.
Analysis of thirteen trinucleotide
comparison with Parkinson’s
(1975). Psychiatric syndromes of
repeat loci as candidate genes for
disease and Huntington’s
Huntington’s chorea. In
schizophrenia and bipolar
disease. Schizophr Res, 1996.
19
:
Psychiatric Aspects of Neurological
disorder. Am J Med Genet
121–8.
Disease, Benson D. F., Bulmer D.
(Neuropsychiatr Genet), 1996.
56. Dallocchio C., Buffa C., Tinelli C.,
(Eds.). New York: Grune &
67
:139–46.
et al.
Effectiveness of risperidone
Stratton, pp. 267–86.
47. MacMillan J. C., Snell R. G., Tyler
in Huntington chorea patients.
38. Lovestone S., Hodgson S., Sham
A.,
et al.
Molecular analysis and
J Clin Psychopharmacol, 1999.
P.,
et al.
Familial psychiatric
clinical correlations of the
19
:101–3.
presentation of Huntington’s
Huntington’s disease mutation.
57. Parsa M. A., Szigethy E., Voci J.
disease. J Med Genet, 1996.
Lancet, 1993.
342
:954–8.
M.,
et al.
Risperidone in treatment
33
:128–31.
48. Weigell-Weber M., Schmid W.,
of choreoathetosis of Huntington’s
39. Tsuang D., DiGiacomo L., Lipe
Spiegel R. Psychiatric symptoms
disease. J Clin Psychopharmacol,
H.,
et al.
Familial aggregation of
and CAG expansion in
1997.
17
:134–5.
schizophrenia-like symptoms in
Huntington’s disease. Am J Med
58. Bogelman G., Hirschmann S.,
Huntington’s disease. Am J Med
Genet, 1996.
67
:53–7.
Modai I. Olanzapine and
Genet, 1999.
81
:323–7.
49. Wang S., Sun C. E., Walczak C. A.,
Huntington’s disease. J Clin
40. Tsuang D., Almqvist E., Lipe H.,
et al.
Evidence for a susceptibility
Psychopharmacol, 2001.
21
:245–6.
et al.
Familial aggregation of
locus for schizophrenia on
59. Reveley M. A., Dursum S. M.,
psychotic symptoms in
chromosome 6pter-p22.
Andrews H. A. Comparative trial
Huntington’s disease. Am J
Nat Genet, 1995.
10
:41–6.
use of sulpiride and risperidone in
Psychiatry, 2000.
157
:1955–9.
50. Riggins G. J., Lokey L. K.,
Huntington’s disease: a pilot
41. Correa B. B., Xavier M.,
Chastain J. L.,
et al.
Human genes
study. J Clin Psychopharmacol,
356
Guimaraes J. Association of
containing polymorphic
1996.
10
:162–5.
Chapter 28 – Huntington’s Disease and related disorders
60. van Vugt J., Siesling S., Vergeer
cystamine. Nat Med, 2002.
65. Andreasen N. C., Nopoulos P.,
M.,
et al.
Clozapine versus
8
:143–9.
O’Leary D. S.,
et al.
Defining the
placebo in Huntington’s disease:
phenotype of schizophrenia:
62. Schmahmann J. D., Pandya D. N.
a double blind randomised
cognitive dysmetria and its neural
The cerebrocerebellar system. Int
comparative study. J Neurol
mechanisms. Biol Psychiatry,
Rev Neurobiol, 1997.
41
:31–60.
Neurosurg Psychiatry, 1997.
1999.
46
:908–20.
63
:35–9.
63. Schmahmann J. D., Sherman J. C.
66. Kutty I. N., Prendes J. L. Psychosis
Cerebellar cognitive affective
61. Karpuj M. V., Becher M. W.,
and cerebellar degeneration.
syndrome. Int Rev Neurobiol,
Springer J. E.,
et al.
Prolonged
J Nerv Ment Dis, 1981.
169
:390–1.