Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study.

Standard

Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study. / Pickar, D; Bunney, W E; Douillet, P; Sethi, B B; Sharma, M; Vartanian, M E; Lideman, R P; Naber, Dieter; Leibl, K; Yamashita, I.

In: BIOL PSYCHIAT, Vol. 25, No. 4, 4, 1989, p. 440-448.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Pickar, D, Bunney, WE, Douillet, P, Sethi, BB, Sharma, M, Vartanian, ME, Lideman, RP, Naber, D, Leibl, K & Yamashita, I 1989, 'Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study.', BIOL PSYCHIAT, vol. 25, no. 4, 4, pp. 440-448. <http://www.ncbi.nlm.nih.gov/pubmed/2539206?dopt=Citation>

APA

Pickar, D., Bunney, W. E., Douillet, P., Sethi, B. B., Sharma, M., Vartanian, M. E., Lideman, R. P., Naber, D., Leibl, K., & Yamashita, I. (1989). Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study. BIOL PSYCHIAT, 25(4), 440-448. [4]. http://www.ncbi.nlm.nih.gov/pubmed/2539206?dopt=Citation

Vancouver

Pickar D, Bunney WE, Douillet P, Sethi BB, Sharma M, Vartanian ME et al. Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study. BIOL PSYCHIAT. 1989;25(4):440-448. 4.

Bibtex

@article{67e52ec3774a47518ca22e50e3d493ee,
title = "Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study.",
abstract = "In the context of a previous WHO collaborative study, six research centers reported that naloxone (0.3 mg/kg) produced significant improvement in symptomatology in neuroleptic-treated patients. In the current Phase II WHO study, repeated (4 days) naloxone (0.3 mg/kg) administration was performed in schizophrenic patients (n = 43) from five WHO collaborating centers using a double-blind, placebo-controlled design. Both naloxone and placebo administrations were associated with significant reductions in symptoms. Naloxone, however, was not superior to placebo. These data are discussed in relation to endorphin hypotheses of schizophrenia.",
author = "D Pickar and Bunney, {W E} and P Douillet and Sethi, {B B} and M Sharma and Vartanian, {M E} and Lideman, {R P} and Dieter Naber and K Leibl and I Yamashita",
year = "1989",
language = "Deutsch",
volume = "25",
pages = "440--448",
journal = "BIOL PSYCHIAT",
issn = "0006-3223",
publisher = "Elsevier USA",
number = "4",

}

RIS

TY - JOUR

T1 - Repeated naloxone administration in schizophrenia: a phase II World Health Organization Study.

AU - Pickar, D

AU - Bunney, W E

AU - Douillet, P

AU - Sethi, B B

AU - Sharma, M

AU - Vartanian, M E

AU - Lideman, R P

AU - Naber, Dieter

AU - Leibl, K

AU - Yamashita, I

PY - 1989

Y1 - 1989

N2 - In the context of a previous WHO collaborative study, six research centers reported that naloxone (0.3 mg/kg) produced significant improvement in symptomatology in neuroleptic-treated patients. In the current Phase II WHO study, repeated (4 days) naloxone (0.3 mg/kg) administration was performed in schizophrenic patients (n = 43) from five WHO collaborating centers using a double-blind, placebo-controlled design. Both naloxone and placebo administrations were associated with significant reductions in symptoms. Naloxone, however, was not superior to placebo. These data are discussed in relation to endorphin hypotheses of schizophrenia.

AB - In the context of a previous WHO collaborative study, six research centers reported that naloxone (0.3 mg/kg) produced significant improvement in symptomatology in neuroleptic-treated patients. In the current Phase II WHO study, repeated (4 days) naloxone (0.3 mg/kg) administration was performed in schizophrenic patients (n = 43) from five WHO collaborating centers using a double-blind, placebo-controlled design. Both naloxone and placebo administrations were associated with significant reductions in symptoms. Naloxone, however, was not superior to placebo. These data are discussed in relation to endorphin hypotheses of schizophrenia.

M3 - SCORING: Zeitschriftenaufsatz

VL - 25

SP - 440

EP - 448

JO - BIOL PSYCHIAT

JF - BIOL PSYCHIAT

SN - 0006-3223

IS - 4

M1 - 4

ER -