Read Secondary Schizophrenia Online

Authors: Perminder S. Sachdev

Secondary Schizophrenia (128 page)

28. Jones P., Rodgers B., Murray R., et
their relatives. J Nerv Ment Dis,

Morrow B.,
et al.
Schizophrenia

al. Child development risk factors

1994.
182
:476–8.

susceptibility associated with

for adult schizophrenia in the

9. Papolos D. F., Faedda G. L., Veit

interstitial deletions of

British 1946 birth cohort. Lancet,

S.,
et al.
Bipolar spectrum

chromosome 22q11. Proc Natl

1994.
344
:1398–1402.

disorders in patients diagnosed

Acad Sci USA, 1995.
92
:7612–16.

29. Scutt L. E., Chow E. W., Weksberg

with velocardio-facial syndrome:

20. Arinami T., Ohtsuki T., Takase K.,

R.,
et al.
Patterns of dysmorphic
does a hemizygous deletion of

et al.
Screening for 22q11

features in schizophrenia. Am J

chromosome 22q11 result in

deletions in a schizophrenia

Med Genet, 2001.
105
:713–23.

321

Organic Syndromes of Schizophrenia – Section 3

30. Walker E. F., Savoie T., Davis D.

caudate volume in

49. Rapoport J. L., Castellanos F. X.,

Neuromotor precursors of

neuroleptic-naive psychotic

Gogate N.,
et al.
Imaging normal
schizophrenia. Schizophr Bull,

patients. Am J Psychiatry, 1998.

and abnormal brain development:

1994.
20
:441–51.

155;774–8.

new perspectives for child

31. Hollis C. Child and adolescent

40. Zipursky R. B., Lambe E. K.,

psychiatry. Aust N Z J Psychiatry,

(juvenile onset) schizophrenia. A

Kapur S.,
et al.
Cerebral gray

2001.
35
:272–81.

case control study of premorbid

matter volume deficits in first

50. Zecevic N., Bourgeois J. P., Rakic

developmental impairments. Br J

episode psychosis. Arch Gen

P. Changes in synaptic density in

Psychiatry, 1995.
166
:489–95.

Psychiatry, 1998. 55:540–6.

motor cortex of rhesus monkey

32. Pantelis C., Maruff P. The

41. DeQuardo J. R., Keshavan M. S.,

during fetal and postnatal life.

cognitive neuropsychiatric

Bookstein F. L.,
et al.
Landmark-Brain Res Dev Brain Res, 1989.

approach to investigating the

based morphometric analysis of

50
:11–32.

neurobiology of schizophrenia

first-episode schizophrenia. Biol

51. Huttenlocher P. R., Dabholkar

and other disorders. J Psychosom

Psychiatry, 1999.
45
:1321–8.

A. S. Regional differences in

Res, 2002.
53
:655–64.

42. Shenton M. E., Dickey C. C.,

synaptogenesis in human cerebral

33. Kessler R. C., Demler O., Frank R.

Frumin M.,
et al.
A review of MRI
cortex. J Comp Neurol, 1997.
387
:
G.,
et al.
Prevalence and treatment
findings in schizophrenia.

167–78.

of mental disorders, 1990 to 2003.

Schizophr Res, 2001.
49
:1–52.

52. Giedd J. N., Clasen L. S., Lenroot

N Engl J Med, 2005.
352
:
43. Molina V., Sanchez J., Reig S.,

R.,
et al.
(2006) Puberty-related
2515–23.

et al.
N-acetyl-aspartate levels in
influences on brain development.

34. Cornblatt B. A., Erlenmeyer-

the dorsolateral prefrontal cortex

Mol Cell Endocrinol, 2006.

Kimling L. Global attentional

in the early years of schizophrenia

254–5:154–62.

deviance as a marker of risk for

are inversely related to disease

53. Sowell E. R., Thompson P. M.,

schizophrenia: specificity and

duration. Schizophr Res, 2005.

Leonard C. M.,
et al.
Longitudinal
predictive validity. J Abnorm

73
:209–19.

mapping of cortical thickness and

Psychol, 1985.
94
:470–86.

44. Nelson M. D., Saykin A. J.,

brain growth in normal children.

35. Niemi L. T., Suvisaari J. M.,

Flashman L. A.,
et al.

J Neurosci, 2004.
24
:8223–31.

Tuulio-Henriksson A.,
et al.

Hippocampal volume reduction

54. Thompson P. M., Vidal C., Giedd

Childhood developmental

in schizophrenia as assessed by

J. N.,
et al.
Mapping adolescent
abnormalities in schizophrenia:

magnetic resonance imaging: a

brain change reveals dynamic

evidence from high-risk studies.

meta-analytic study. Arch Gen

wave of accelerated grey matter

Schizophr Res, 2003.
60
:239–
Psychiatry, 1998.
55
:433–40.

loss in very early-onset

58.

45. Konick L. C., Friedman L.

schizophrenia. Proc Natl Acad Sci

36. Morey R. A., Inan S., Mitchell T.

Meta-analysis of thalamic size in

USA, 2001.
98
:11650–5.

V.,
et al.
Imaging frontostriatal
schizophrenia. Biol Psychiatry,

55. McGlashan T. H., Hoffman R. E.

function in ultra-high-risk, early,

2001.
49
:28–38.

Schizophrenia as a disorder of

and chronic schizophrenia during

46. Choi J. S., Kang D. H., Kim J. J.,

developmentally reduced synaptic

executive processing. Arch Gen

et al.
Decreased caudal anterior
connectivity. Arch Gen Psychiatry,

Psychiatry, 2005.
62
:254–62.

cingulate gyrus volume and

2000.
57
:637–48.

37. Kern R. S., Green M. F.,

positive symptoms in

56. Gill M., Vallada H., Collier D.,

Nuechterlein K. H.,
et al.

schizophrenia. Psychiatry Res,

et al.
A combined analysis of

NIMH-MATRICS survey on

2005.
139
:239–47.

D22S278 marker alleles in

assessment of neurocognition in

47. Keshavan M. S., Diwadkar V. A.,

affected sib-pairs: support for a

schizophrenia. Schizophr Res,

Montrose D. M.,
et al.
Premorbid
susceptibility locus for

2004.
72
:11–19.

indicators and risk for

schizophrenia at chromosome

38. Degreef G., Ashtari M., Bogerts

schizophrenia: a selective review

22q12. Schizophrenia

B.,
et al.
Volumes of ventricular
and update. Schizophr Res, 2005.

Collaborative Linkage Group

system subdivisions measured

79
:45–57.

(Chromosome 22). Am J Med

from magnetic resonance images

48. Giedd J. N., Snell J. W., Lange N.,
Genet, 1996.
67
:40–5.

in first-episode schizophrenic

et al.
Quantitative magnetic

57. Shprintzen R. J., Goldberg R. B.,

patients. Arch Gen Psychiatry,

resonance imaging of human

Young D.,
et al.
The

1992.
49
:531–7.

brain development: ages 4–18.

velocardio-facial syndrome: a

39. Keshavan M. S., Rosenberg D.,

Cereb Cortex, 1996.

clinical and genetic analysis.

322

Sweeney J. A.,
et al.
Decreased

6
:551–60.

Pediatrics, 1981.
67
:167–72.

Chapter 24 – Velocardiofacial syndrome

58. Swillen A., Devriendt K., Legius

67. Bish J. P., Ferrante S. M.,

75. Heineman-de Boer J. A., Van

E.,
et al.
Intelligence and

Donald-McGinn D.,
et al.

Haelst M. J., Cordia-de H. M.,

psychosocial adjustment in

Maladaptive conflict monitoring

et al.
Behavior problems and

velocardiofacial syndrome: a

as evidence for executive

personality aspects of 40 children

study of 37 children and

dysfunction in children with

with velocardio-facial syndrome.

adolescents with VCFS. J Med

chromosome 22q11.2 deletion

Genet Couns, 1999.
10
:89–93.

Genet, 1997.
34
:453–8.

syndrome. Dev Sci, 2005.
8
:36–43.

76. Feinstein C., Eliez S., Blasey C.,

59. Moss E. M., Batshaw M. L., Solot

68. Simon T. J., Bearden C. E.,

et al.
Psychiatric disorders and
C. B.,
et al.
Psychoeducational

Mc-Ginn D. M.,
et al.
Visuospatial
behavioral problems in children

profile of the 22q11.2

and numerical cognitive deficits

with velocardiofacial syndrome:

microdeletion: a complex pattern.

in children with chromosome

usefulness as phenotypic

J Pediatr, 1999.
134
:193–8.

22q11.2 deletion syndrome.

indicators of schizophrenia risk.

60. Woodin M., Wang P. P., Aleman

Cortex, 2005a.
41
:145–55.

Biol Psychiatry, 2002.
51
:312–18.

D.,
et al.
Neuropsychological

69. Lewandowski K. E., Shashi V.,

77. Murphy K. C., Owen M. J.

profile of children and adolescents

Berry P. M.,
et al.
Schizophrenic-Velo-cardiofacial syndrome: a
with the 22q11.2 microdeletion.

like neurocognitive deficits in

model for understanding the

Genet Med, 2001.
3
:34–9.

children and adolescents with

genetics and pathogenesis of

61. Glaser B., Mumme D. L., Blasey

22q11 deletion syndrome. Am J

schizophrenia. Br J Psychiatry,

C.,
et al.
Language skills in

Med Genet, B Neuropsychiatr

2001.
179
:397–402.

children with velocardiofacial

Genet, 2007.
144
:27–36.

78. Murphy K. C. Annotation:

syndrome (deletion 22q11.2).

70. Buchanan R. W., Francis A.,

velocardio-facial syndrome.

J Pediatr, 2002.
140
:753–8.

Arango C.,
et al.
Morphometric

J Child Psychol Psychiatry, 2005.

62. Gerdes M., Solot C., Wang P. P.,

assessment of the heteromodal

46
:563–71.

et al.
Cognitive and behavior

association cortex in

79. Debbane M., Glaser B., David M.

profile of preschool children with

schizophrenia. Am J Psychiatry,

K.,
et al.
(2006a) Psychotic

chromosome 22q11.2 deletion.

2004.
161
:322–31.

symptoms in children and

Am J Med Genet, 1999
85
:127–33.

71. Swillen A., Devriendt K., Legius

adolescents with 22q11.2 deletion

63. Sobin C., Kiley-Brabeck K.,

E.,
et al.
The behavioural

syndrome: Neuropsychological

Daniels S.,
et al.

phenotype in velocardio-facial

and behavioral implications.

Neuropsychological

syndrome (VCFS): from infancy

Schizophr Res, 2006a.
84
:187–93.

characteristics of children with

to adolescence. Genet Couns,

80. Baker K. D., Skuse D. H.

the 22q11 Deletion Syndrome: a

1999.
10
:79–88.

Adolescents and young adults

descriptive analysis. Child

72. Swillen A., Vogels A., Devriendt

with 22q11 deletion syndrome:

Neuropsychol, 2005a.
11
:39–53.

K.,
et al.
Chromosome 22q11

psychopathology in an at-risk

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