The prolactin (hPRL) level in the serum of 17 patients (10 females, 7 males) with primary depression (manic-depressive disease) was determined before and after prophylactic treatment with lithium salts. All patients were free of acute psychotic-depressive symptomes. However, 9 of 17 patients received moderate doses of additional antidepressive medication continuously for 4 weeks. No significant changes of the serum hPRL were observed in the group as a whole, the lithium serum levels being within the normal therapeutic range. The mean hPRL level in patients with concomitant antidepressive medication was significantly higher as compared to the "only lithium" group, but never exceeded the normal range in both groups. Considering similar results of other authors, it is suggested that lithium does not influence the hPRL serum level, at least if no special methods of hPRL stimulation are used. However, with regard to recent communications suggesting that besides dopaminergic influences also serotonergic mechanisms play an important part in hPRL regulation, it is held that the prolactin response in lithium-treated patients warrants further investigations using serotonergic stimulation methods.
{"title":"[The influence of lithium salts and antidepressive medication on the serum prolactin level (author's transl)].","authors":"H Mühlbauer, W Hardt","doi":"10.1055/s-2007-1019633","DOIUrl":"https://doi.org/10.1055/s-2007-1019633","url":null,"abstract":"<p><p>The prolactin (hPRL) level in the serum of 17 patients (10 females, 7 males) with primary depression (manic-depressive disease) was determined before and after prophylactic treatment with lithium salts. All patients were free of acute psychotic-depressive symptomes. However, 9 of 17 patients received moderate doses of additional antidepressive medication continuously for 4 weeks. No significant changes of the serum hPRL were observed in the group as a whole, the lithium serum levels being within the normal therapeutic range. The mean hPRL level in patients with concomitant antidepressive medication was significantly higher as compared to the \"only lithium\" group, but never exceeded the normal range in both groups. Considering similar results of other authors, it is suggested that lithium does not influence the hPRL serum level, at least if no special methods of hPRL stimulation are used. However, with regard to recent communications suggesting that besides dopaminergic influences also serotonergic mechanisms play an important part in hPRL regulation, it is held that the prolactin response in lithium-treated patients warrants further investigations using serotonergic stimulation methods.</p>","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 4","pages":"213-7"},"PeriodicalIF":0.0,"publicationDate":"1980-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019633","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18454044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A 31-year-old white woman developed bilateral papilloedema whilst on lithium carbonate therapy for five years because of manic depressive illness. Oedema of the optic disc disappeared after lithium administration had been discontinued. To our knowledge this is the second case of this kind which has been reported in literature.
{"title":"Bilateral papilloedema in long term therapy with lithium carbonate.","authors":"P Pesando, G Nuzzi, G Maraini","doi":"10.1055/s-2007-1019636","DOIUrl":"https://doi.org/10.1055/s-2007-1019636","url":null,"abstract":"<p><p>A 31-year-old white woman developed bilateral papilloedema whilst on lithium carbonate therapy for five years because of manic depressive illness. Oedema of the optic disc disappeared after lithium administration had been discontinued. To our knowledge this is the second case of this kind which has been reported in literature.</p>","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 4","pages":"235-9"},"PeriodicalIF":0.0,"publicationDate":"1980-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019636","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17830739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
W M Herrmann, D Kropf, K Fichte, B Müller-Oerlinghausen
{"title":"[Electroencephalographic and psychoexperimental studies in healthy subjects on lithium medication (author's transl)].","authors":"W M Herrmann, D Kropf, K Fichte, B Müller-Oerlinghausen","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 4","pages":"200-12"},"PeriodicalIF":0.0,"publicationDate":"1980-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18454043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Extrapyramidal side effects (EPS) as a result of treatment with lithium ion is an uncom· mon, but weil documented, phenomenon (Bien, 1976; Branchey et al., 1976; DiMascio et al., 1976; and Shopsin and Gershon, 1975). Such lithium induced cogwheel rigidity has been reported in the V.S. but has not been confirmed by European observers. Treatment of these particular lithium induced side effects has remained problematic. Bien (1976) reported one patient on lithium treatment whose cogwheel rigidity did not respond to either intramuscular benztropine, 4 mg, or diphenhydramine, 50 mg. Shopsin and Gershon (1975) gave intravenous benztropine, 4 mg, to nine patients on lithium treatment who exhibited cogwheel rigidity, and only two of their patients showed even minimal amelioration. We wish to report a single case of a young woman who developed EPS in association with lithium treatment, which responded minimally to benztropine and diphenhydramine, and markedly to amantadine.
{"title":"Lithium induced cogwheel rigidity: treatment with amantadine.","authors":"A A Abrams, D L Braff","doi":"10.1055/s-2007-1019637","DOIUrl":"https://doi.org/10.1055/s-2007-1019637","url":null,"abstract":"Extrapyramidal side effects (EPS) as a result of treatment with lithium ion is an uncom· mon, but weil documented, phenomenon (Bien, 1976; Branchey et al., 1976; DiMascio et al., 1976; and Shopsin and Gershon, 1975). Such lithium induced cogwheel rigidity has been reported in the V.S. but has not been confirmed by European observers. Treatment of these particular lithium induced side effects has remained problematic. Bien (1976) reported one patient on lithium treatment whose cogwheel rigidity did not respond to either intramuscular benztropine, 4 mg, or diphenhydramine, 50 mg. Shopsin and Gershon (1975) gave intravenous benztropine, 4 mg, to nine patients on lithium treatment who exhibited cogwheel rigidity, and only two of their patients showed even minimal amelioration. We wish to report a single case of a young woman who developed EPS in association with lithium treatment, which responded minimally to benztropine and diphenhydramine, and markedly to amantadine.","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 4","pages":"240-2"},"PeriodicalIF":0.0,"publicationDate":"1980-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019637","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18454891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A Kukopulos, D Reginaldi, P Laddomada, G Floris, G Serra, L Tondo
The course of 434 bipolar patients (256 women, 178 men) was studied longitudinally. The prevailing patterns of the manic-depressive cycles at the end of the observation time were: mania followed by depression (usually mild), 28%; depression followed by mania (usually hypomania), 25%; and continuous circular course, with long cycles, 19%, or with short (rapid) cycles, 20%. The cycles followed an irregular pattern in 8% of the patients.
{"title":"Course of the manic-depressive cycle and changes caused by treatment.","authors":"A Kukopulos, D Reginaldi, P Laddomada, G Floris, G Serra, L Tondo","doi":"10.1055/s-2007-1019628","DOIUrl":"https://doi.org/10.1055/s-2007-1019628","url":null,"abstract":"The course of 434 bipolar patients (256 women, 178 men) was studied longitudinally. The prevailing patterns of the manic-depressive cycles at the end of the observation time were: mania followed by depression (usually mild), 28%; depression followed by mania (usually hypomania), 25%; and continuous circular course, with long cycles, 19%, or with short (rapid) cycles, 20%. The cycles followed an irregular pattern in 8% of the patients.","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 4","pages":"156-67"},"PeriodicalIF":0.0,"publicationDate":"1980-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019628","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17174907","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The paper reports on an open study of flupirilene administration in ten previously untreated female outpatients with paranoid symptomatology who were of advanced age. In eight of the ten patients who had been included in the 12-week study the authors observed a remission particularly of delusion dynamics, delusional intuitions, delusional perceptions, and restlessness as well as excitment. The therapy failed in two patients. Preexisting cerebro-organic impairments deteriorated partly, whereas vegetative and extrapyramidal side effects were of only moderate intensity. Hence, fluspirilene proved to be a depot neuroleptic with good antipsychotic effect in outpatient treatment of paranoid psychoses of patients of advanced age. However, especially in patients of advanced age. However, especially patients with preorganic brain syndrome, the obviously sedating and retarding effects of this drug must be taken into account, since they may contribute to further disturbance of the impaired cerebral function.
{"title":"[Experience with fluspirilene in gerontopsychiatry (author's transl)].","authors":"S Kanowski, R Paur","doi":"10.1055/s-2007-1019623","DOIUrl":"https://doi.org/10.1055/s-2007-1019623","url":null,"abstract":"<p><p>The paper reports on an open study of flupirilene administration in ten previously untreated female outpatients with paranoid symptomatology who were of advanced age. In eight of the ten patients who had been included in the 12-week study the authors observed a remission particularly of delusion dynamics, delusional intuitions, delusional perceptions, and restlessness as well as excitment. The therapy failed in two patients. Preexisting cerebro-organic impairments deteriorated partly, whereas vegetative and extrapyramidal side effects were of only moderate intensity. Hence, fluspirilene proved to be a depot neuroleptic with good antipsychotic effect in outpatient treatment of paranoid psychoses of patients of advanced age. However, especially in patients of advanced age. However, especially patients with preorganic brain syndrome, the obviously sedating and retarding effects of this drug must be taken into account, since they may contribute to further disturbance of the impaired cerebral function.</p>","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 3","pages":"137-43"},"PeriodicalIF":0.0,"publicationDate":"1980-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019623","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18406126","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The antidepressant effect of amitriptyline was studied in 28 endogenous depressive patients. They received 150 mg amitriptyline once nightly in a sustained release form for 4 weeks. Blood samples were drawn 12 hrs. after medication. Amitriptyline concentrations were between 35--300 ng/ml Nortriptyline concentrations were between 20--330 ng/ml. No correlations were found between plasma concentrations of amitriptyline, nortriptyline, or their sum, and the clinical outcome of treatment. Plasma levels of amitriptyline depended on neither the age nor the sex of the patients. A significant correlation was found between the ratio of nortriptyline to amitriptyline concentrations in serum (demethylation ratio) and clinical improvement. The demethylation ratio appeared to be relatively constant after a few days of treatment. The results suggest that monitoring the demethylation ratio of endogenous depressive patients treated with amitriptyline may predict therapeutic effects of the treatment. They also suggest that a balance between noradrenergic and serotonergic mechanisms is necessary to improve antidepressant treatment with amitriptyline.
{"title":"On the relationship of nortriptyline: amitriptyline ratio to clinical improvement of amitriptyline treated depressive patients.","authors":"G Jungkunz, H J Kuss","doi":"10.1055/s-2007-1019620","DOIUrl":"https://doi.org/10.1055/s-2007-1019620","url":null,"abstract":"<p><p>The antidepressant effect of amitriptyline was studied in 28 endogenous depressive patients. They received 150 mg amitriptyline once nightly in a sustained release form for 4 weeks. Blood samples were drawn 12 hrs. after medication. Amitriptyline concentrations were between 35--300 ng/ml Nortriptyline concentrations were between 20--330 ng/ml. No correlations were found between plasma concentrations of amitriptyline, nortriptyline, or their sum, and the clinical outcome of treatment. Plasma levels of amitriptyline depended on neither the age nor the sex of the patients. A significant correlation was found between the ratio of nortriptyline to amitriptyline concentrations in serum (demethylation ratio) and clinical improvement. The demethylation ratio appeared to be relatively constant after a few days of treatment. The results suggest that monitoring the demethylation ratio of endogenous depressive patients treated with amitriptyline may predict therapeutic effects of the treatment. They also suggest that a balance between noradrenergic and serotonergic mechanisms is necessary to improve antidepressant treatment with amitriptyline.</p>","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 3","pages":"111-6"},"PeriodicalIF":0.0,"publicationDate":"1980-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019620","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18406125","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
G L Corona, P Pinelli, F Zerbi, L Fenoglio, G Santagostino, P Frattini, M L Cucchi
The relationship between the plasma levels of amitriptyline and its metabolite nortriptyline, as well as their side-effects and clinical response, were studied in 102 depressed female in-patients, treated with different dosages of amitriptyline. For 50 and 100 mg dosages, significant positive correlations were found between amitriptyline concentration and the Hamilton amelioration scores, as well as between Hamilton final values and side effects. For depressive neurosis and involutional melancholia best therapeutic responses were yielded at a dosage of 50 mg, while in the treatment of manic-depressive illness, comparable results occurred at a 150 mg dosage. In the depressive neurosis and in the involutional melancholia the upper plasma concentration limits for the therapeutic effect of nortriptyline were identified. The lower plasma concentration limits of amitriptyline and nortriptyline in the treatment of manic-depressive illness were also pointed out.
{"title":"Amitriptyline, nortriptyline plasma levels and clinical response in women with affective disorders.","authors":"G L Corona, P Pinelli, F Zerbi, L Fenoglio, G Santagostino, P Frattini, M L Cucchi","doi":"10.1055/s-2007-1019619","DOIUrl":"https://doi.org/10.1055/s-2007-1019619","url":null,"abstract":"<p><p>The relationship between the plasma levels of amitriptyline and its metabolite nortriptyline, as well as their side-effects and clinical response, were studied in 102 depressed female in-patients, treated with different dosages of amitriptyline. For 50 and 100 mg dosages, significant positive correlations were found between amitriptyline concentration and the Hamilton amelioration scores, as well as between Hamilton final values and side effects. For depressive neurosis and involutional melancholia best therapeutic responses were yielded at a dosage of 50 mg, while in the treatment of manic-depressive illness, comparable results occurred at a 150 mg dosage. In the depressive neurosis and in the involutional melancholia the upper plasma concentration limits for the therapeutic effect of nortriptyline were identified. The lower plasma concentration limits of amitriptyline and nortriptyline in the treatment of manic-depressive illness were also pointed out.</p>","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 3","pages":"102-10"},"PeriodicalIF":0.0,"publicationDate":"1980-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019619","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18406124","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
J Schley, M Nündel, M Siegert, E Riedel, B Müller-Oerlinghausen
By means of gel-chromatography we have found recently a high affinity protein binding of perazine in native human sera. The affinity constant could be determined as 5.42 x 10 I/mol (Sch/ey et al., 1979), and the binding was clearly shown to be reversible. The affmity constant of perazine to human albumin is approximately more than 2 potencies less (Kinawi and Min, 1979). No evidence could be gained that formation of perazine radicals might be responsible for the high affinity binding, nor that a dissociation of the complex took place during the chromatographic run.
{"title":"High affinity binding of perazine and desmethylperazine to human alpha 1-acid glycoprotein.","authors":"J Schley, M Nündel, M Siegert, E Riedel, B Müller-Oerlinghausen","doi":"10.1055/s-2007-1019624","DOIUrl":"https://doi.org/10.1055/s-2007-1019624","url":null,"abstract":"By means of gel-chromatography we have found recently a high affinity protein binding of perazine in native human sera. The affinity constant could be determined as 5.42 x 10 I/mol (Sch/ey et al., 1979), and the binding was clearly shown to be reversible. The affmity constant of perazine to human albumin is approximately more than 2 potencies less (Kinawi and Min, 1979). No evidence could be gained that formation of perazine radicals might be responsible for the high affinity binding, nor that a dissociation of the complex took place during the chromatographic run.","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 3","pages":"144-5"},"PeriodicalIF":0.0,"publicationDate":"1980-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019624","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17171580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E Lehmann, H Quadbeck, J Tegeler, M Fararuni, K Heinrich
The treatment of schizophrenic patients with high-dosed neuroleptics is discussed. The drug-response difference between a low dose and a high dose of Fluphenazine-Decanoate was investigated in 40 chronic schizophrenic patients. All patients were resistant to standard doses of neuroleptics and were therefore treated with higher doses. All patients entering the study were treated for at least three months with high doses of Fluphenazine-Decanoate, i.e. 100 mg or more within three weeks. From this pool of 40 patients two groups were created at random for the doubleblind study: In one group the high dose was continued (average dose 225 mg/in 14 days), in the other group Fluphenazine-Decanoate was reduced to a standard-dose of 25 mg in 14 days. During the 24 weeks of investigation the somatic and psychopathological state of the patient was evaluated by means of the AMP-System. Furthermore the self-rating scale EWL-K was used. After 24 weeks the patients of the high-dosed group were more often rated as unchanged, while the patients in the standard-dosed group were evaluated significantly more often as better or worse. Average condition-differences between the both groups could not be found in a covariance-analysis. A factorial covariance-analysis showed that differences in the initial hostility-syndrome and catatonic-syndrome scores are predictors for a syndrom-relevant differential dosage per group. Patients with low hostility- and low catatonic-syndrome-scores improved after reduction of the doses in the apathic, the halluzinatoric-desintegrative and the neurological syndrome, whereas patients with high initial hostility- and catatonic-syndrome-scores became psychopathologically worse after dosage reduction. Finally the possibilities of generalizing from the results obtained to the relevance of high and standard neuropletic therapy are discussed.
{"title":"[Drug-response differences of high and standard dosage of fluphenazine-decanoate in relation to schizophrenic symptoms (author's transl)].","authors":"E Lehmann, H Quadbeck, J Tegeler, M Fararuni, K Heinrich","doi":"10.1055/s-2007-1019621","DOIUrl":"https://doi.org/10.1055/s-2007-1019621","url":null,"abstract":"<p><p>The treatment of schizophrenic patients with high-dosed neuroleptics is discussed. The drug-response difference between a low dose and a high dose of Fluphenazine-Decanoate was investigated in 40 chronic schizophrenic patients. All patients were resistant to standard doses of neuroleptics and were therefore treated with higher doses. All patients entering the study were treated for at least three months with high doses of Fluphenazine-Decanoate, i.e. 100 mg or more within three weeks. From this pool of 40 patients two groups were created at random for the doubleblind study: In one group the high dose was continued (average dose 225 mg/in 14 days), in the other group Fluphenazine-Decanoate was reduced to a standard-dose of 25 mg in 14 days. During the 24 weeks of investigation the somatic and psychopathological state of the patient was evaluated by means of the AMP-System. Furthermore the self-rating scale EWL-K was used. After 24 weeks the patients of the high-dosed group were more often rated as unchanged, while the patients in the standard-dosed group were evaluated significantly more often as better or worse. Average condition-differences between the both groups could not be found in a covariance-analysis. A factorial covariance-analysis showed that differences in the initial hostility-syndrome and catatonic-syndrome scores are predictors for a syndrom-relevant differential dosage per group. Patients with low hostility- and low catatonic-syndrome-scores improved after reduction of the doses in the apathic, the halluzinatoric-desintegrative and the neurological syndrome, whereas patients with high initial hostility- and catatonic-syndrome-scores became psychopathologically worse after dosage reduction. Finally the possibilities of generalizing from the results obtained to the relevance of high and standard neuropletic therapy are discussed.</p>","PeriodicalId":76325,"journal":{"name":"Pharmakopsychiatrie, Neuro-Psychopharmakologie","volume":"13 3","pages":"117-29"},"PeriodicalIF":0.0,"publicationDate":"1980-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-1019621","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18406127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}