Read Secondary Schizophrenia Online

Authors: Perminder S. Sachdev

Secondary Schizophrenia (89 page)

hexosaminidase activity in an

psychiatry Clin Neurosci, 1998.

development of normal and

exceptional case of Tay-Sachs

10
:10–19.

abnormal function during

disease with additional storage of

28. Zaroff C., Neudorfer O. Morrison

adolescence. J Comp Neurol, 2002.

kidney globoside in visceral

C.,
et al.
Neuropsychological

453
:116–30.

organs. Life Sci, 1968.

assessment of patients with

9. Sachs B. On amaurotic family

7
:283–8.

late-onset GM2 gangliosidosis.

idiocy. A disease chiefly of the

19. Neudorfer O., Pastores G. M.,

Neurology, 2004.
62
:2283–6.

grey matter of the central nervous

Zeng B. J.,
et al.
Late-onset

29. Frey L., Ringel S., Filley C. The

system. J Nerv Ment Dis, 1903.

Tay-Sachs disease: phenotypic

natural history of cognitive

30
:1–13.

characterization and genotypic

dysfunction in late-onset GM2

10. Sachs B. On arrested cerebral

correlation in 21 affected patients.

gangliosidosis. Arch Neurol, 2005.

223

development, with special

Genet Med, 2005.
7
:119–23.

62
:989–94.

Organic Syndromes of Schizophrenia – Section 3

30. Streifler J., Golomb M., Gadoth N.

(Eds.). New York: McGraw Hill,

50. Blom T., Linder M., Snow K.,
et al.

Psychiatric features of adult GM2

pp. 2625–39.

Defective endocytic trafficking of

gangliosidosis. Br J Psychiatry,

40. Spence M., Callahan J. (1989). The

NPC1 and NPC2 underlying

1989.
155
:410–3.

Niemann-Pick group of diseases.

infantile Niemann-Pick type C

31. Jacobs J., Willemsen M.,

The Metabolic Basis of Inherited

disease. Hum Mol Genet, 2003.

Groot-Loonen J.,
et al.
Allogenic

Diseases. 6th Ed. New York:

12
:257–72.

BMT followed by substrate

McGraw-Hill, pp. 1655–76.

51. Zervas M., Dobrenis K., Walkley

reduction therapy in a child with

S. Neurons in Niemann-Pick type

41. Crocker A. Niemann-Pick

subacute Tay-Sachs disease. Bone

C accumulate gangliosides as well

disease: A review of fifteen

Marrow Transplant, 2005.

as unesterified cholesterol and

patients. Medicine (Baltimore),

36
:925–6.

undergo dendritic and axonal

1958.
37
:1–95.

32. Navon R., Argov Z., Frisch A.

alterations. J Neuropathol Exp

42. Millat G., Marcais C., Rafi M.,

Hexosaminidase deficiency in

Neurol, 2001.
60
:49–64.

et al.
Niemann-Pick C1 disease:

adults. Am J Med Genet, 1986.

52. Suzuki K., Parker C., Pentchev P.,

the I1061T substitution is a

24
:179–96.

et al.
Neurofibrillary tangles in

frequent mutant allele in patients

33. Oates C., Bosch E., Hart M.

Niemann-Pick disease type C.

of Western European descent and

Movement disorders associated

Acta Neuropathol (Berl), 1995.

correlates with a classic juvenile

with chronic GM2 gangliosidosis:

89
:227–38.

phenotype. Am J Human Genet,

case report and review of the

1999.
65
:1321–9.

53. Saito Y., Suzuki K., Nanba E.,
et al.

literature. Eur Neurol, 1986.

Niemann-Pick type C disease:

25
:154–9.

43. Kobayashi T., Beuchat M.,

accelerated neurofibrillary tangle

Lindsay M.,
et al.
Late endosomal

34. Streifler J., Gornish M., Hadar H.,

formation and amyloid B

membranes rich in

et al.
Brain imaging in late-onset

deposition associated with

lysobisphosphatidic acid regulate

GM2 gangliosidosis. Neurology,

apolipoprotein E4 homozygosity.

cholesterol transport. Nat Cell

1993.
43
:2055–8.

Ann Neurol, 2002.
52
:351–5.

Biol, 1999.
1
:113–8.

35. Renshaw P., Stern T., Welch C.

54. Liscum L. Niemann-Pick type C

44. Naureckiene S., Sleat D., Lackland

Electroconvulsive therapy

mutations cause lipid traffic jam.

H.,
et al.
Identification of HE1 as

treatment of depression in a

Traffic, 2000.
1
:218–25.

the second gene of Niemann-Pick

patient with adult GM2

C disease. Science, 2000.
290
:
55. Nixon R. Niemann-Pick type C

gangliosidosis. Ann Neurol, 1992.

2227–9.

disease and Alzheimer’s disease:

31
:342–4.

the APP endosome connection

45. Carstea E., Morris J., Coleman K.,

36. Rosebush P., MacQueen G.,

fattens up. Am J Pathol, 2004.

et al.
Niemann-Pick C1 disease

Mazurek M. Late-onset Tay-Sachs

164
:757–61.

gene: homology to mediators of

disease presenting as catatonic

56. Goodrum J., Pentchev P.

cholesterol homeostasis. Science,

schizophrenia: diagnostic and

Cholesterol reutilization during

1997.
277
:228–31.

treatment issues. J Clin Psychiatry,

myelination of regenerating PNS

1995.
56
:347–53.

46. Loftus S., Morris J., Carstea E.,

axons is impaired in

et al.
Murine model of

37. Hurowitz G., Silver J., Brin M., et

Niemann-Pick disease type C

Niemann-Pick C disease:

al. Neuropsychiatric aspects of

mice. J Neurosci Res, 1997.

mutation in a cholesterol

adult-onset Tay-Sachs disease:

49
:389–92.

homeostasis gene. Science, 1997.

two case reports with several new

57. Karten B., Vance D., Campenot

277
:232–5.

findings. J Neuropsychiatry Clin

R.,
et al.
Trafficking of cholesterol
Neurosci, 1993.
5
:30–6.

47. Vincent I., Bu B., Erickson R.

from cell bodies to distal axons in

Understanding of Niemann-Pick

38. Vanier M., Suzuki K. Recent

Niemann Pick C1-deficiant

type C disease: a fat problem. Curr

advances in elucidating

neurons. J Biol Chem, 2003.
278
:
Opin Neurol, 2003.
16
:155–61.

Niemann-Pick C disease. Brain

4168–75.

Pathol, 1998.
8
:163–74.

48. Ory D. Niemann-Pick type C: A

58. Palmeri S., Battisti C., Federico

disorder of cellular cholesterol

39. Pentchev P., Vanier M., Suzuki K.,

A.,
et al.
Hypoplasia of the corpus

trafficking. Biochim Biophys Acta,

et al.
(1995). Niemann-Pick

callosum in Niemann-Pick type C

2000.
1529
:331–9.

disease Type C: a cellular

disease. Neuroradiology, 1994.

cholesterol lipidosis. In The

49. Ioannou Y. The structure and

36
:20–2.

Metabolic and Molecular Bases of

function of the Niemann-Pick C1

59. Ong W., Kumar U., Switzer R.,

Inherited Disease, 7th Ed. Scriver

protein. Mol Genet Metab, 2000.

et al.
Neurodegeneration in

224

C., Beaudet A., Sly W., Valle D.,

71
:175–81.

Niemann-Pick type C disease

Chapter 16 – Storage disorders and psychosis

mice. Exp Brain Res, 2001.
141
:
Niemann-Pick disease type C.

beta deposition in sporadic

218–31.

Neurology, 1989.
39
:1040–9.

Alzheimer’s disease and Down

60. German D. C., Liang C. L., Song

69. Brady R. O., Filling-Katz M. R.,

syndrome: differential effects of

T.,
et al.
Neurodegeneration in the

Barton N. W.,
et al.
Niemann-Pick

APOE genotype and presenelin

Niemann-Pick C mouse: glial

disease types C and D. Neurol

mutations. Am J Pathol, 2000.

involvement. Neuroscience, 2002.

Clin, 1989.
7
:75–88.

157
:277–86.

109
:437–50.

79. Hulette C., Earl N., Anthony D.,

70. Millat G., Chikh K., Naureckienne

61. Harzer K., Schlote W., Peiffer J.,

et al.
Adult onset Niemann-Pick

S.,
et al.
Niemann-Pick disease

et al.
Neurovisceral lipidosis

disease type C presenting with

type C: spectrum of HE1

compatible with Niemann-Pick

dementia and absent

mutations and genotype/

disease type C: morphological and

organomegaly. Clin Neuropathol,

phenotype correlations in the

biochemical studies of a late

1992.
11
:293–7.

NPC2 group. Am J Human Genet,

infantile case and enzyme and

2001.
69
:1013–21.

80. Campo J., Stowe R., Slomka G.,

lipid assays in a prenatal case of

et al.
Psychosis as a presentation

71. Shulman L., Lang A., Jankovic J.,

the same family. Acta

of physical disease in adolescence:

et al.
Case 1, 1995: psychosis,

Neuropathol, 1978.
43
:97–104.

a case of Niemann-Pick disease

dementia, chorea, ataxia and

62. Elleder M., Jirasek A., Smid F.,

type C. Dev Med Child Neurol,

supranuclear gaze dysfunction.

et al.
Niemann-Pick disease type

1998.
40
:126–9.

Mov Disord, 1995.
10
(3):257–62.

C. Study on the nature of the

81. Velakoulis D., Pantelis C. What

72. Schiffman R. Niemann-Pick

cerebral storage process. Acta

have we learned from functional

disease type C: from bench to

Neuropathol, 1985.
66
:325–66.

imaging studies in schizophrenia?

bedside. JAMA, 1996.

63. March P., Thrall M., Brown D.,

The role of frontal, striatal and

276
(7):561–4.

et al.
GABAergic neuroaxonal

temporal areas. Aust NZ J

dystrophy and other

73. Lossos A., Schlesigner I., Okon E.,

Psychiatry, 1996.
30
:195–209.

cytopathological alterations in

et al.
Adult-onset Niemann-Pick

82. Heckers S. Neuropathology of

feline Niemann-Pick disease type

type C disease: clinical,

schizophrenia: cortex, thalamus,

C. Acta Neuropathol, 1997.

biochemical and genetic study.

basal ganglia, and

94
:164–72.

Arch Neurol, 1997.
54
:1536–41.

neurotransmitter-specific

64. Paul C., Boegle A., Maue R.

74. Tedeschi G., Bonavita S., Barton

projection systems. Schizophr

Before the loss: neuronal

N.,
et al.
Proton magnetic

Bull, 1997.
23
:403–21.

dysfunction in Niemann-Pick

resonance spectroscopic imaging

83. Walterfang M., Wood S.,

type C disease. Biochim Biophys

in the clinical evaluation of

Velakoulis D.,
et al.

Acta, 2004.
1685
:63–76.

patients with Niemann-Pick type

Other books

Girl Gone Nova by Pauline Baird Jones
All the Dead Are Here by Pete Bevan
Slocum #422 by Jake Logan
On Her Knees by Jenika Snow
Lost by Devon, Gary;
Doctor Who: Galaxy Four by William Emms
Star Cruise - Outbreak by Veronica Scott
Loving Lord Ash by Sally MacKenzie