Read Secondary Schizophrenia Online
Authors: Perminder S. Sachdev
112. Hitomi T., Mezaki T., Tsujii T.,
and adrenomyeloneuropathy.
presenting as neurologically pure
et al.
Improvement of central
J R Soc Med, 1984.
77
:882–4.
familial spastic paraparesis.
motor conduction after bone
92. Sereni C., Ruel M., Iba-zizen T.,
Neurology, 1995.
45
:
marrow transplantation in
et al.
Adult adrenoleuko-
1101–4.
adrenoleukodystrophy. J Neurol
dystrophy: a sporadic case?
254
103. Schwankhaus J. D., Katz D. A.,
Neurosurg Psychiatry, 2003.
J Neurol Sci, 1987.
80
:121–8.
Eldridge R.,
et al.
Clinical and
74
:3:373–5.
Chapter 18 – Psychosis associated with leukodystrophies
113. Spurek M., Taylor-Gjevre R., Van
123. Saraste M. Oxidative
with special reference to
Uum S.,
et al.
Adrenomyelo-
phosphorylation at the fin de
extra-neuromuscular
neuropathy as a cause of primary
siecle. Science, 1999.
283
:1488–93.
abnormalities. Acta Pathol Jpn,
adrenal insufficiency and
124. Lerman-Sagie T., Leshinsky-Silver
1992.
42
:818–25.
spastic paraparesis. Can Med
E., Watemberg N.,
et al.
White
133. Clark J. M., Marks M. P.,
Assoc J, 2004.
171
(9):
matter involvement in
Adalsteinsson E.,
et al.
MELAS:
1073–7.
mitochondrial diseases. Mol Genet
Clinical and pathologic
114. Mukherjee S., Newby E., Harvey J.
and Metab, 2005.
84
:127–36.
correlations with MRI, xenon/CT,
N. Adrenomyeloneuropathy in
125. Kovacs G. G., Hoftberger R.,
and MR spectroscopy. Neurology,
patients with ‘Addison’s disease’:
Majtenyi K.,
et al.
Neuropathology
1996.
46
:223–7.
genetic case analysis. J R Soc Med,
of white matter disease in Leber’s
134. Campos Y., Garcia A., Eiris J.,
2006.
99
:245–9.
hereditary optic neuropathy.
et al.
Mitochondrial myopathy,
115. Castellote A., Vera J., Vasquez E.,
Brain, 2005.
128
:35–41.
cardiomyopathy and psychiatric
et al.
MR in adrenoleuko-
126. Sedel F., Tourbah A., Fontaine B.,
illness in a Spanish family
dystrophy: atypical presentation
et al.
Leukoencephalopathies
harbouring the mtDNA 3303C>T
as bilateral frontal demyelination.
associated with inborn errors of
mutation. J Inherit Metab Dis,
AJNR Am J Neuroradiol, 1995.
metabolism in adults. J Inherit
2001.
24
:685–7.
16
(Suppl 4):814–15.
Metab Dis, 2008.
31
:295–307.
135. Desnuelle C., Pellissier J. F.,
116. Close P. J., Sinnott S. J., Nolan K.
127. Barragan-Campos H. M., Vallee
Serratrice G.,
et al.
Kearns-Sayre
T. Adrenoleukodystrophy: a case
J. N., Lo D., Barrera-Ramirez C. F.,
syndrome: mitochondrial
report demonstrating unilateral
et al.
Brain magnetic resonance
encephalomyopathy caused by
abnormalities. Pediatr Radiol,
imaging findings in patients with
deficiency of the repiratory chain.
1993.
23
:400–1.
mitochondrial cytopathies. Arch
Rev Neurol, 1989.
145
:842–50.
117. MacDonald J. T., Stauffer A. E.,
Neurol, 2005.
62
:737–42.
136. Prayson R. A., Wang N.
Heitoff K. Adrenoleukodystrophy:
128. Anglin R., Mazurek M. F.,
Mitochondrial myopathy,
early frontal lobe involvement on
Noseworthy M.,
et al.
The
encephalopathy, lactic acidosis,
computed tomography. J Comput
psychiatric profile of
and strokelike episodes (MELAS)
Assist Tomogr, 1984.
8
:128–
mitochondrial disorders: clinical
syndrome: an autopsy report.
30.
presentation and MR
Arch Pathol Lab Med, 1998.
118. Young R. S., Ramer J. C., Towfighi
spectroscopy findings. Society for
122
:978–81.
J.,
et al.
Adrenoleukodystrophy:
Neuroscience Annual Meeting, San
137. Sartor H., Loose R., Tucha O., et
unusual computed tomographic
Diego, November 2007.
al. MELAS: a neuropsychological
appearance. Arch Neurol, 1982.
129. Fattal O., Budur K., Vaughan A. J.,
and radiological follow-up study.
39
:782–3.
et al.
Review of the Literature on
Mitochondrial encephalo-
119. Farrell D. F., Hamilton S. R.,
Major Mental Disorders in Adult
myopathy, lactic acidosis and
Krauss T. A.,
et al.
Xlinked
Patients with Mitochondrial
stroke. Acta Neurol Scand, 2002.
adrenoleukodystrophy: adult
Diseases. Psychosomatics, 2006.
106
:309–13.
cerebral variant. Neurology, 1993.
47
:1–7.
138. Lacey C. J., Salzberg M. R.
43
:1518–22.
130. Ahn M. S., Sims K. B., Frazier J. A.
Obsessive-compulsive disorder
120. Moser A. B., Kreiter N., Bezman
Risperidone-induced psychosis
with mitochondrial disease
L.,
et al.
Plasma very long chain
and depression in a child with a
Psychosomatics, 2008.
49
:540–2.
fatty acids in 3,000 peroxisome
mitochondrial disorder. J Child
139. Chinnery P., Majamaa K.,
disease patients and 29,000
Adolesc Psychopharmacol, 2005.
Turnbull D.,
et al.
Treatment for
controls. Ann Neurol, 1999.
15
:520–5.
mitochondrial disorders.
45
:100–10.
131. Apostolova L. G., White M.,
Cochrane Database Syst Rev, 2006.
121. Moser H. W., Raymond G. V., Lu
Moore S. A.,
et al.
Deep white
1:CD004426.
S. E.,
et al.
Followup of 89
matter pathologic features in
140. Brockmann K., Dechent P.,
asymptomatic patients with
watershed regions: a novel of
Wilken B.,
et al.
Proton MRS
adrenoleukodystrophy treated
central nervous system
profile of cerebral metabolic
with Lorenzo’s oil. Arch Neurol,
involvement in MELAS. Arch
abnormalities in Krabbe disease.
2005.
62
:1073–80.
Neurol, 2005.
62
:1154–6.
Neurology, 2003.
60
:819–25.
122. Siva N. Positive effects with
132. Ban S., Mori N., Saito K.,
et al.
An
141. Suzuki K. Twenty five years of the
Lorenzo’s oil (Letter). Lancet,
autopsy case of mitochondrial
“Psychosine Hypothesis”: a
255
2005.
4
:529.
encephalomyopathy (MELAS)
personal perspective of its history
Organic Syndromes of Schizophrenia – Section 3
and present status. Neurochem
Pelizaeus-Merzbacher disease
157. Maurer I., Moller H. G. Inhibition
Res, 1998.
23
:251–9.
phenotype of adult onset, without
of complex 1 by neuroleptics in
142. Suzuki K., Suzuki Y., Suzuki K.
mutation of proteolipid protein
normal human brain cortex
(1995). Galactosylceramide
gene. Acta Neuropathol, 2000.
parallels the extrapyramidal
lipidosis: globoid-cell
99
:7–13.
toxicity of neuroleptics. Mol Cell
leukodystrophy (Krabbe disease).
150. Moghadasian M. H., Salen G.,
Biochem, 1997.
174
:255–9.
In The Metabolic Basis of Inherited
Frohlich J. J.,
et al.
158. Burkhardt C., Kelly J. P., Lim Y.,
Disease, Scriver C. R., Beaudet A.
Cerebrotendinous xanthomatosis:
et al.
Neuroleptic medications
L., Sly W. S.,
et al.
(Eds.). Eighth
a rare disease with diverse
inhibit complex I of the electron
Ed., vol 2. New York:
manifestations. Arch Neurol, 2002.
transport chain. Ann Neurol,
McGraw-Hill, pp. 2671–92.
59
:527–9.
1993.
33
:512–17.
143. Husain A. M., Altuwaijri M.,
151. Moghadasian M. H.
159. Lullman H., Lullman-Ranch R.,
Aldosari M. Krabbe disease:
Cerebrotendinous xanthomatosis:
Wassermann D. Lipidosis induced
neurophysiologic studies and MRI
clinical course, genotypes and
by amphiphilic cationic drugs.
correlations. Neurology, 2004.
metabolic backgrounds. Clin
Biochem Pharmacol, 1978.
63
:617–20.
Invest Med, 2004.
27
:42–50.
27
:1103–8.
144. Lyon G., Hagberg B., Evrard P., et
152. Berginer V. M., Foster N. L.,
160. Shapiro B. E., Hatters-Friedman
al. Symptomatology of late onset
Sadowsky M.,
et al.
Psychiatric
S., Fernandes-Filho J. A.,
et al.
Krabbe’s leukodystrophy: the
disorders in patients with
Late-onset Tay-Sachs disease:
European experience. Dev
cerebrotendinous xanthomatosis.
adverse effects of medications and
Neurosci, 1991.
13
(4–5):
Am J Psychiatry, 1988.
145
:354–7.
implications for treatment.
240–4.
153. Brenner M., Johnson A. B.,
Neurology, 2006.
67
:
145. Escolar M. L., Poe M. D.,
Boespflug-Tanguy O.,
et al.
875–7.
Provenzsale J. M.,
et al.
Mutations in GFAP, encoding glial
161. MacQueen G. M., Rosebush P. I.,
Transplantation of umbilical-cord
fibrillary acidic protein, are
Mazurek M. F. Neuropsychiatric
blood in babies with infantile
associated with Alexander disease.
aspects of the adult-onset
Krabbe’s disease. N Eng J Med,
Nat Genet, 2001.
27
:117–20.
variant of Tay-Sachs disease.
2005.
352
:2069–81.
154. Berger J., Moser H. W.,
J Neuropsychiatry Clin Neurosci,
146. Krivit W., Shapiro E. G., Peters C.,
Forss-Petter S. Leukodystrophies:
1998.
10
:10–19.
et al.
Hematopoietic stem-cell
recent developments in genetics,
162. Neustadt J., Pieczenik S. R.
transplantation in globoid-cell
molecular biology, pathogenesis
Medication-induced
leukodystrophy. N Eng J Med,
and treatment. Curr Opin Neurol,
mitochondrial damage and
1998.
338
:1119–26.
2001.
14
:305–12.
disease. Mol Nutr Food Re, 2008.
147. Koeppen A. H. A brief history of
155. Paloneva J., Kestila M., Wu J.,
52
:780–8.
Pelizaeus-Merzbacher disease and
et al.
Loss-of-function mutations
163. Pacia S. V., Devinsky O.
proteolipid protein. J Neurol Sci,
in TYROBP (DAP12) result in a
Clozapine-related seizures:
2005.
228
:198–200.
presenile dementia with bone
experience with 5,629 patients.
148. Koeppen A. H., Robitaille Y.
cyst. Nat Genet, 2000.
25
:357–
Neurology, 1994.
44
:2247–9.
Pelizaeus-Merzbacher disease.
61.
164. Sevin C., Aubourg P., Cartier N.