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386


Effect of cycloheximide on corticosteroid-induced changes in

Zorgniotti, A W; Adler, L; Peselow, E; Corwin, J; Rotrosen, J University Medical Center and Psychiatry Service, Veterans Administration Medical Center, New York, NY 10016 United States; Aleksic, S; Greco, M A; Reuben, R; Margolis, S; Epstein, F; Feigin, I; Charney, A N; Wallach, J D; Donowitz, M; Johnstone, N
13 cases of Goldenhar-Gorlin syndrome are presented in which numerous central nervous system anomalies have been found. These others. Pertinent literature has been reviewed. It is concluded that any part of the central nervous system can be involved in this condition and that careful evaluation is indicated in order to rule
EMBASE:22024188
ISSN: 0007-1250
CID: 4775032

Human platelet phospholipid methylation

Cordasco DM; Segarnick DJ; Rotrosen J
PMID: 6798348
ISSN: 0024-3205
CID: 23644

Effect of lithium on glycine levels in patients with affective disorders

Deutsch SI; Peselow ED; Banay-Schwartz M; Gershon S; Virgilio J; Fieve RR; Rotrosen J
PMID: 6786113
ISSN: 0002-953x
CID: 23645

THE EFFECT OF A NOVEL PSYCHOTROPIC AGENT, TREBENZOMINE, ON BRAIN AND PLATELET UPTAKE SYSTEMS

Friedman, E; Hallock, M; Rotrosen, J; Dallob, A
ISI:A1981NG14900001
ISSN: 0362-2428
CID: 30326

DETERMINATION OF GLYCINE IN ULTRAFILTRATES OF PLASMA AND RBC LYSATES BY A DANSYLATION THIN-LAYER CHROMATOGRAPHIC METHOD

DEUTSCH, SI; PESELOW, ED; TRAFICANTE, LJ; VIRGILIO, J; STANLEY, M; ROTROSEN, J
ISI:A1981MW42200001
ISSN: 0362-2428
CID: 40472

Discrimination of functionally heterogeneous receptor subpopulations: antipsychotic and antidopaminergic properties of metoclopramide [proceedings]

Rotrosen J; Stanley M; Lautin A; Wazer D; Gershon S
PMID: 6262853
ISSN: 0048-5764
CID: 23646

A double-blind comparison of trebenzomine and thioridazine in the treatment of schizophrenia

Georgotas A; Gerbino L; Jordan B; McCarthy M; Gershon S; Kleinberg D; Lautin A; Stanley M; Rotrosen J
Forty inpatient volunteers with diagnoses of schizophrenia were randomly assigned to treatment either with trebenzomine or thioridazine in a double-blind study of clinical antipsychotic efficacy following a 1-week placebo treatment. Psychopathology was rated using the Brief Psychiatric Rating Scale (BPRS) and Clinical Global Impression (CGI). There was a significant difference in therapeutic response to the two drugs in that psychopathology decreased significantly for the thioridazine group, but not for the trebenzomine group. Serum prolactin was elevated during treatment with thioridazine, but not with trebenzomine. Side effects were more frequently reported for the thioridazine group. These results fail to confirm previous reports of clinical antipsychotic efficacy for trebenzomine
PMID: 6113618
ISSN: 0033-3158
CID: 23647

SYMPOSIUM ON ALZHEIMERS-DISEASE

Serby, M; Corwin, J; Groher, M; Rotrosen, J
ISI:A1981MR48900011
ISSN: 0197-4580
CID: 30187

RELATIONSHIPS BETWEEN RESPONSES TO DOPAMINE AGONISTS PSYCHO PATHOLOGY NEUROLEPTIC TREATMENT RESPONSE AND NEED FOR NEUROLEPTIC MAINTENANCE IN SCHIZOPHRENIC SUBJECTS

ANGRIST B; PESELOW E; ROTROSEN J; GERSHON S
BIOSIS:PREV198222045035
ISSN: 0065-3446
CID: 106740

Relationships between responses to dopamine agonists, psychopathology, neuroleptic treatment response, and need for neuroleptic maintenance in schizophrenic subjects

Angrist, B; Peselow, E; Rotrosen, J; Gershon, S
Sensitivity to the emetic effect of apomorphine was not different in unmedicated schizophrenic and control subjects. Sensitivity to apomorphine emesis also did not correlate with schizophrenics' level of psychopathology before treatment. Floridity of baseline psychopathology was found to predict improvement with treatment. Change in psychopathology after amphetamine correlated inversely with apomorphine emesis sensitivity and statistically predicted improvement after neuroleptic treatment. Clinically meaningful improvement after neuroleptics was rare in subjects whose psychopathology did not change after amphetamine. In a separate study, clear increases in psychopathology after amphetamine appeared to predict rapid relapse after neuroleptic discontinuation. These later data are preliminary.
SCOPUS:49149136718
ISSN: 0065-3446
CID: 579852