Read Secondary Schizophrenia Online
Authors: Perminder S. Sachdev
Chapter 1 – Neurobiology and etiology of primary schizophrenia: current status
abnormal auditory circuitry in
schizophrenia. Neuroimage, 2004.
to neuroscience, Oxford: Oxford
early-onset psychosis. Cereb
22
(3):1247–54.
University Press.
Cortex, 2008.
18
(2):371–8. [Epub
41. Steen R. G.,
et al.
Brain volume in
51. Keshavan M. S.,
et al.
Jun 8, 2007.]
first-episode schizophrenia:
Neurobiology of early psychosis.
31. Kerns J. G.,
et al.
Anterior
systematic review and
Br J Psychiatry, 2005.
48
(Suppl):
cingulate conflict monitoring and
meta-analysis of magnetic
s8–18.
adjustments in control. Science,
resonance imaging studies. Br J
52. Ho B. C.,
et al.
Progressive
2004.
303
(5660):1023–6.
Psychiatry, 2006.
188
:510–8.
structural brain abnormalities and
32. Carter C. S.,
et al.
Anterior
42. Ward K. E.,
et al.
Meta-analysis of
their relationship to clinical
cingulate cortex activity and
brain and cranial size in
outcome: a longitudinal magnetic
impaired self-monitoring of
schizophrenia. Schizophr Res,
resonance imaging study early in
performance in patients with
1996.
22
(3):197–213.
schizophrenia. Arch Gen
schizophrenia: an event-related
43. Wright I. C.,
et al.
Meta-analysis
Psychiatry, 2003.
60
(6):585–94.
fMRI study. Am J Psychiatry,
of regional brain volumes in
53. DeLisi L. E.,
et al.
Cerebral
2001.
158
(9):1423–8.
schizophrenia. Am J Psychiatry,
ventricular change over the first
33. Kerns J. G.,
et al.
Decreased
2000.
157
(1):16–25.
10 years after the onset of
conflict-and error-related activity
44. Woodruff P. W., McManus I. C.,
schizophrenia. Psychiatry Res,
in the anterior cingulate cortex in
David A. S. Meta-analysis of
2004.
130
(1):57–70.
subjects with schizophrenia. Am J
corpus callosum size in
54. Whitworth A. B.,
et al.
Psychiatry, 2005.
162
(10):1833–9.
schizophrenia. J Neurol Neurosurg
Longitudinal volumetric MRI
34. Fletcher P.,
et al.
Abnormal
Psychiatry, 1995.
58
(4):457–
study in first-and multiple-
cingulate modulation of
61.
episode male schizophrenia
fronto-temporal connectivity in
45. Nelson M. D.,
et al.
Hippocampal
patients. Psychiatry Res, 2005.
schizophrenia. Neuroimage, 1999.
140
(3):225–37.
9
(3):337–42.
schizophrenia as assessed by
55. Lawrie S. M.,
et al.
Magnetic
35. LeDoux J. The emotional brain,
magnetic resonance imaging: a
resonance imaging of brain in
fear, and the amygdala. Cell Mol
meta-analytic study. Arch Gen
people at high risk of developing
Neurobiol, 2003.
23
(4–5):727–
Psychiatry, 1998.
55
(5):
schizophrenia. Lancet, 1999.
38.
433–40.
353
(9146):30–3.
36. Eichenbaum H. Hippocampus:
46. Lawrie S. M., Abukmeil S. S. Brain
56. Keshavan M. S.,
et al.
Magnetic
cognitive processes and neural
abnormality in schizophrenia. A
resonance imaging and
representations that underlie
systematic and quantitative review
spectroscopy in offspring at risk
declarative memory. Neuron,
of volumetric magnetic resonance
for schizophrenia: preliminary
2004.
44
(1):109–20.
imaging studies. Br J Psychiatry,
studies. Prog Neuropsychophar-
37. Adolphs R., Baron-Cohen S.,
1998.
172
:110–20.
macol Biol Psychiatry, 1997.
Tranel D. Impaired recognition of
47. Konick L. C., Friedman L. Meta-
21
(8):1285–95.
social emotions following
analysis of thalamic size in
57. Boos H. B.,
et al.
Brain volumes in
amygdala damage. J Cogn
schizophrenia. Biol Psychiatry,
relatives of patients with
Neurosci, 2002.
14
(8):
2001.
49
(1):28–38.
schizophrenia: a meta-analysis.
1264–74.
48. Honea R.,
et al.
Regional deficits
Arch Gen Psychiatry, 2007.
64
(3):
38. Aleman A., Kahn R. S. Strange
in brain volume in schizophrenia:
297–304.
feelings: do amygdala
a meta-analysis of voxel-based
58. Job D. E.,
et al.
Voxel-based
abnormalities dysregulate the
morphometry studies. Am J
morphometry of grey matter
emotional brain in schizophrenia?
Psychiatry, 2005.
162
(12):
densities in subjects at high risk of
Prog Neurobiol, 2005.
77
(5):
2233–45.
schizophrenia. Schizophr Res,
283–98.
49. Antonova E.,
et al.
The
2003.
64
(1):1–13.
39. Hempel A.,
et al.
Impairment in
relationship between brain
59. Diwadkar V. A.,
et al.
Genetically
basal limbic function in
structure and neurocognition in
predisposed offspring with
schizophrenia during affect
schizophrenia: a selective review.
schizotypal features: an ultra
recognition. Psychiatry Res, 2003.
Schizophr Res, 2004.
70
(2–3):
high-risk group for
122
(2):115–24.
117–45.
schizophrenia? Prog
40. Takahashi H.,
et al.
An fMRI
50. Lawrie S., Johnstone E.,
Neuropsychopharmacol Biol
study of differential neural
Weinberger D. (Eds.) (2004).
Psychiatry, 2006.
30
(2):
13
response to affective pictures in
Schizophrenia: from neuroimaging
230–8.
Introduction – Section 1
60. Job D. E.,
et al.
Grey matter
70. Kumra S.,
et al.
Reduced frontal
subjects at risk for schizophrenia.
changes over time in high risk
white matter integrity in
Schizophr Res, 2006.
87
(1–3):
subjects developing
early-onset schizophrenia: a
81–8.
schizophrenia. Neuroimage, 2005.
preliminary study. Biol Psychiatry,
80. Pettegrew J. W.,
et al.
Alterations
25
(4):1023–30.
2004.
55
(12):1138–45.
in brain high-energy phosphate
61. Pantelis C.,
et al.
71. Lindstrom L. H.,
et al.
Increased
and membrane phospholipid
Neuroanatomical abnormalities
dopamine synthesis rate in medial
metabolism in first-episode,
before and after onset of
prefrontal cortex and striatum in
drug-naive schizophrenics. A
psychosis: a cross-sectional and
schizophrenia indicated by
pilot study of the dorsal prefrontal
longitudinal MRI comparison.
L-(beta-11C) DOPA and PET.
cortex by in vivo phosphorus 31
Lancet, 2003.
361
(9354):
Biol Psychiatry, 1999.
46
(5):681–8.
nuclear magnetic resonance
281–8.
72. Zakzanis K. K., Hansen K. T.
spectroscopy. Arch Gen
62. Thompson P. M.,
et al.
Mapping
Dopamine D2 densities and the
Psychiatry, 1991.
48
(6):563–8.
adolescent brain change reveals
schizophrenic brain. Schizophr
81. Feinberg I. Schizophrenia and late
dynamic wave of accelerated gray
Res, 1998.
32
(3):201–6.
maturational brain changes in
matter loss in very early-onset
73. Erritzoe D.,
et al.
Positron
man. Psychopharmacol Bull, 1982.
schizophrenia. Proc Natl Acad Sci
emission tomography and single
18
:29–31.
USA, 2001.
98
(20):11650–5.
photon emission CT molecular
82. Stanley J. A.,
et al.
An in vivo
63. Thompson P. M.,
et al.
Structural
imaging in schizophrenia.
study of the prefrontal cortex of
MRI and brain development. Int
Neuroimaging Clin N Am, 2003.
schizophrenic patients at different
Rev Neurobiol, 2005.
67
:285–
13
(4):817–32.
stages of illness via phosphorus
323.
74. Laruelle M. The role of
magnetic resonance spectroscopy.
64. Toga A. W., Thompson P. M.,
endogenous sensitization in the
Arch Gen Psychiatry, 1995.
52
(5):
Sowell E. R. Mapping brain
pathophysiology of schizophrenia:
399–406.
maturation. Trends Neurosci,
implications from recent brain
83. Williamson P.,
et al.
Localized
2006.
29
(3):148–59.
imaging studies. Brain Res Brain
phosphorus 31 magnetic
65. Gogtay N.,
et al.
Cortical brain
Res Rev, 2000.
31
(2–3):371–84.
resonance spectroscopy in
development in nonpsychotic
75. Weinberger D. R. The biological
chronic schizophrenia patients
siblings of patients with
basis of schizophrenia: new
and normal controls. Arch Gen
childhood-onset schizophrenia.
directions. J Clin Psychiatry, 1997.
Psychiatry, 1991.
48
:578.
Arch Gen Psychiatry, 2007.
64
(7):
58
:22–7.
84. Fukuzako H.,
et al.
Changes in
772–80.
76. Steen R. G., Hamer R. M.,
levels of phosphorus metabolites
66. Klingberg T.,
et al.
Myelination
Lieberman J. A. Measurement of
in temporal lobes of drug-naive
and organization of the frontal
brain metabolites by 1H magnetic
schizophrenic patients. Am J
white matter in children: a
resonance spectroscopy in
Psychiatry, 1999.
156
(8):1205–8.
diffusion tensor MRI study.
patients with schizophrenia: a
85. Volz H. R.,
et al.
Reduced
Neuroreport, 1999.
10
(13):
systematic review and meta-
phosphodiesters and high-energy
2817–21.
analysis. Neuropsychopharma-
phosphates in the frontal lobe of
67. Nagy Z., Westerberg H.,
cology, 2005.
30
(11):1949–62.
schizophrenic patients: a (31)P
Klingberg T. Maturation of white
77. Keshavan M. S., Stanley J. A.,
chemical shift spectroscopic-
matter is associated with the
Pettegrew J. W. Magnetic
imaging study. Biol Psychiatry,
development of cognitive
resonance spectroscopy in
2000.
47
(11):954–61.
functions during childhood.
schizophrenia: methodological
86. Smesny S.,
et al.
Metabolic
J Cogn Neurosci, 2004.
16
(7):
issues and findings–part II. Biol
mapping using 2D (31)P-MR
1227–33.
Psychiatry, 2000.
48
(5):
spectroscopy reveals frontal and
68. Liston C.,
et al.
Frontostriatal
369–80.