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Secondary Schizophrenia (101 page)

BOOK: Secondary Schizophrenia
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J Neuropsychiatr Clin Neurosci,

with early neurological signs.

transplantation. J Child Neurol,

2006.
18
:450–9.

Psychiatr Genet, 2007.
17
:85–91.

1999.
14
:222–8.

73. Puck J. M., Willard H. F.

54. Reider-Grosswasser I., Bornstein
64. Learish R., Ohashi T., Robbins P.

X-inactivation in females with

N. CT and MRI in late-onset

A.,
et al.
Retroviral gene transfer
Xlinked disease. N Engl J Med,

metachromatic leukodystrophy.

and sustained expression of

1998.
338
:325–8.

Acta Neurol Scand, 1987.
75
:64–9.

human arylsulfatase A. Gene

74. Schmidt S., Traber F., Block W., et
Therapy, 1996.
3
:343–9.

55. Taylor W. D., Hsu E., Krishnan K.

al. Phenotype assignment in

R. R.,
et al.
Diffusion tensor
65. Nevo Y., Pestronk A., Lopate G.,
symptomatic female carriers of

imaging: background, potential

et al.
Neuropathy of

Xlinked adrenoleukodystrophy.

and utility in psychiatric research.

metachromatic leukodystrophy:

J Neurol, 2001.
248
:36–44.

Biol Psychiatry, 2004.
55
:201–7.

improvement with

75. Moser H. W., Raymond G. V.,

immunomodulation. Pediatr

56. Patay Z. Diffusion-weighted MR

Dubey P. Adrenoleukodystrophy:

Neurol, 1996.
15
:237–9.

imaging in leukodystrophies. Eur

new approaches to a

Radiol, 2005.
15
:2284–303.

66. von Figura K., Steckel F., Hasilik
neurogenetive disease. JAMA,

A. Juvenile and adult

2005.
294
:3131–4.

57. Porter M. T., Fluharty A. L.,

metachromatic leukodystrophy:

Kihara H. Correction of abnormal

partial restoration of arylsulfatase
76. Mahmood A., Dubey P., Moser H.

cerebroside sulfate metabolism in

A (cerebroside sulfatase) activity

W.,
et al.
Xlinked

cultured metachromatic

by inhibitors of thiol proteinases.

adrenoleukodystrophy:

leukodystrophy fibroblasts.

Proc Natl Acad Sci, 1983.

therapeutic approaches to distinct

Science, 1971.
172
:1263–5.

80
:6066–70.

phenotypes. Pediatr Transplant,

2005.
9
(Suppl 7):55–62.

58. Greene H. L., Hug G., Schubert W.

67. Moser H. W., Smith K. D., Moser

K. Metachromatic

A. (1995). Xlinked

77. Moser H. W., Moser A. E., Singh

leukodystrophy. Treatment with

adrenoleukodystrophy. In The

I.,
et al.
Adrenoleukodystrophy:
arylsulfatase-A. Arch Neurol,

Metabolic and Molecular Basis of

survey of 303 cases: biochemistry,

1969.
20
:147–53.

Inherited Diseases, 7th ed., Scriver
diagnosis, and therapy. Ann

Neurol, 1984.
16
:628–41.

59. Austin J. H. Studies in

C. R., Beaudet A. L., Sly W. S.,

metachromatic leukodystrophy

et al.
(Eds.). New York:

78. Moser H. W., Moser A. B., Naidu

XI. Therapeutic considerations,

McGraw-Hill, pp. 2325–49.

S.,
et al.
Clinical aspects of
1972. Birth Defects: Original

68. Moser H. W.

adrenoleukodystrophy and

Article Series, 1973.
9
:125–9.

Adrenoleukodystrophy:

adrenomyeloneuropathy. Dev

60. Bayever E., Ladisch S., Philippart
phenotype, genetics, pathogenesis

Neurosci, 1991.
13
:254–61.

M.,
et al.
Bone-marrow

and therapy. Brain, 1997.

79. Schaumburg H. H., Powers J. M.,

transplantation for

120
:1485–508.

Raine C. S.,
et al.

metachromatic leucodystrophy.

69. Aubourg P., Mosser J., Douar A.

Adrenoleukodystrophy: a clinical

Lancet, 1985.
2
:471–3.

M.,
et al.
Adrenoleukodystrophy
and pathological study of 17 cases.

61. Krivit W., Lipton M. E., Lockman
gene: unexpected homology to a

Arch Neurol, 1975.
32
:577–91.

L. A.,
et al.
Prevention of

protein involved in peroxisome

80. Van Geel B. M., Assies J., Wanders
deterioration in metachromatic

biogenesis. Biochimie 1993.

J. A.
et al.
X linked adreno-

leukodystrophy by bone marrow

75
:293–302.

leukodystrophy: clinical

transplantation. Am J Med Sci,

70. Mosser J., Lutz Y., Stoeckel M. E.,
presentation, diagnosis, and

1987.
294
:80–5.

et al.
The gene responsible for
therapy. J Neurol Neurosurg

62. Dhuna A., Toro C., Torres F.,
et al.

adrenoleukodystrophy encodes a

Psychiatry, 1997.
63
:4–14.

Longitudinal neurophysiologic

peroxisomal membrane protein.

81. Gray A. M. Addison’s disease and
studies in a patient with

Hum Mol Genet, 1994.
3
:265–71.

diffuse cerebral sclerosis. J Neurol
metachromatic leukodystrophy

71. Higgins C. F. ABC transporters:

Neurosurg Psychiatry, 1969.

following bone marrow

from microorganisms to man.

32
:344–7.

transplantation. Arch Neurol,

Ann Rev Cell Biol, 1992.
8
:67–113.

82. Budka H., Sluga E., Heiss W. D.

1992.
49
:1088–92.

72. Anglin R. E., Rosebush P. I.,

Spastic paraplegia associated with

63. Kapaun P., Dittmann R. W.,

Mazurek M. F. The

Addison’s disease: adult variant of

Granitzny B.,
et al.
Slow

neuropsychiatric profile of

adrenoleukodystrophy. J Neurol,

253

progression of juvenile

Addison’s disease: revisiting a

1976.
213
:237–50.

Organic Syndromes of Schizophrenia – Section 3

83. Scully R. E., Galdabini J. J.,

93. Simpson R. H., Rodda J., Reinecke
pathological features of an

McNeely B. U. Case 18–1979:

C. J. Adrenoleukodystrophy in a

autosomal dominant, adult-onset

Case records of the Massachusetts

mother and son. J Neurol

leukodystrophy simulating

General Hospital. N Engl J Med,

Neurosurg Psychiatry 1987.

chronic progressive multiple

1979.
300
:1037–45.

50
:1165–72.

sclerosis. Arch Neurol, 1994.

84. Davis L. E., Snyder R. D., Orth D.

94. Jeffcoate W. J., McGivern D.,

51
:757–66.

N.,
et al.
Adrenoleukodystrophy
Cotton R. E.,
et al.
Late-onset
104. Afifi A. K., Menezes A. H., Reed L.

and adrenomyeloneuropathy

adrenoleukodystrophy (Letter).

A.,
et al.
Atypical presentation of
associated with partial adrenal

J Neurol Neurosurg Psychiatry,

Xlinked adrenoleukodystrophy

insufficiency in three generations

1987.
50
:1238–9.

with an unusual magnetic

of a kindred. Am J Med, 1979.

95. Menza M. A., Blake J., Goldberg

resonance imaging pattern.

66
:342–7.

L. Affective symptoms and

J Child Neurol, 1996.
11
:497–9.

85. Weiss G. M., Nelson R. L., O’Neill
adrenoleukodystrophy: a report of

105. Crum B. A., Carter J. L. 26 year
B. P.,
et al.
Use of adrenal biopsy
two cases. Psychosomatics, 1988.

old man with hyperpigmentation

in diagnosing adrenoleukomyelo-

29
:442–5.

of skin and lower extremity

neuropathy. Arch Neurol, 1980.

96. Ladenson P. W. Adrenoleuko-

spasticity. Mayo Clin Proc, 1997.

37
:634–6.

dystrophy. JAMA, 1989.

72
:479–82.

86. Probst A., Ulrich J., Heitz U.,
et al.

262
:1504–6.

106. Munchau A., Hagel C., Vogel P.

Adrenomyeloneuropathy: a

97. Elrington G. M., Bateman D. E.,

Adrenoleukodystrophy of very

protracted pseudosystemic

Jeffrey M. J.,
et al.

late onset. J Neurol, 1997.

variant of adrenoleukodystrophy.

Adrenoleukodystrophy:

244
:595–9.

Acta Neuropathol, 1980.

heterogeneity in two brothers.

107. Garside S., Rosebush P. I.,

49
:105–15.

J Neurol Neurosurg Psychiatry,

Levinson A. J.,
et al.
Late-onset
87. O’Neill B. P., Marmion L. C.,

1989.
52
:310–13.

adrenoleukodystrophy associated

Feringa E. R. The adrenoleuko-

98. Panegyres P. K., Goldswain P.,

with longstanding psychiatric

myeloneuropathy complex:

Kakulas B. A. Adult-onset

symptoms. J Clin Psychiatry, 1999.

expression in four generations.

adrenoleukodystrophy

60
:460–8.

Neurology, 1981.
31
:151–6.

manifesting as dementia. Am J

108. Kopala L. C., Tan S., Shea C.,
et al.

88. Peckham R. S., Marshall M. C.,

Med, 1989.
87
:481–3.

Adrednoleukodystrophy

Rosman P. M.,
et al.
A variant of
99. Weller M., Liedtke W., Peterson

associated with psychosis (Letter).

adrenomyeloneuropathy with

D.,
et al.
Very-late-onset

Schizophr Res, 2000.
45
:263–5.

hypothalamic-pituitary

adrenoleukodystrophy: possible

109. Gothelf D., Levite R., Gadoth N.

dysfunction and neurologic

precipitation of demyelination by

Bipolar affective disorder

remission after glucocorticoid

cerebral contusion. Neurology,

heralding cerebral demyelination

replacement therapy. Am J Med,

1992.
42
:367–70.

in adrenomyelo-leukodystrophy.

1982.
72
:173–6.

100. Angus B., de Silva R., Davidson
Brain Dev, 2000.
22
:184–7.

89. Kuroda S., Hirano A., Yuasa S.

R.,
et al.
A family with adult-onset
110. Luda E., Barisone M. G. Adult-

Adrenoleukodystrophy-cerebello-

cerebral adrenoleucodystrophy.

onset adrenoleukodystrophy: a

brainstem dominant case. Acta

J Neurol, 1994.
241
:497–9.

clinical and neuropsychological

Neuropathol, 1983.
60
:
101. Sobue G., Ueno-Natsukari I.,

study. Neurol Sci, 2001.
22
:21–5.

149–52.

Okamoto H.,
et al.
Phenotypic
111. Sakakibara R., Fukutake T., Arai
90. Ohno T., Tsuchiya H., Fukuhara

heterogeneity of an adult form of

K., et al.Unilateral caudate head

N.,
et al.
Adrenoleukodystrophy:
adrenoleukodystrophy in

lesion simulating brain tumour in

a clinical variant presenting as

monozygotic twins. Ann Neurol,

Xlinked adult onset

olivopontocerebellar atrophy.

1994.
36
:912–15.

adrenoleukodystrophy (Letter).

J Neurol, 1984.
231
:167–9.

102. Maris T., Androulidakis E. J.,

J Neurol Neurosurg Psychiatry,

91. James A. C., Kaplan P., Lees A.,
Tzagournissakis M.,
et al.

2001.
70
:3:414–15.

et al.
Schizophreniform psychosis
Xlinked adrenoleukodystrophy

BOOK: Secondary Schizophrenia
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