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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    BJOG 77 (1970), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Amniotic fluid was obtained from 100 patients at the induction of labour by hindwater puncture of the membranes using a Drew-Smythe catheter. Biochemical estimations of lactate, pyruvate, glucose, urea and Astrup gas analysis of the amniotic fluid were performed. An effort was made to correlate the biochemical findings in the amniotic fluid at the induction of labour with the subsequent occurrence of fetal distress during labour and with the Apgar score at delivery.No significant correlation was found between the various factors analyzed and the later status of the fetus. High levels of lactate were found in the amniotic fluid together with low levels of pH and buffer base associated with high Pco2 values.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of gynecology and obstetrics 7 (1875), S. 107-125 
    ISSN: 1432-0711
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 5 (1972), S. 81-86 
    ISSN: 1432-1041
    Keywords: Nasal flow/resistance ; common cold ; phenylephrine ; nasal patency ; rhinometry ; nasal decongestant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Although nasal airways flow/resistance (R n) measurements distinguish drug-induced changes in nasal patency better than investigator observations, it has not been shown that these alterations reflect useful clinical effects. Forty-eight patients with elevatedR n values from colds were studied for their responses to 10.0, 15.0 and 25.0 mg single doses of phenylephrine, and to placebo, given orally in a double-blind crossover protocol. Nasal flow/resistance was determined by electronic posterior rhinometry, and subjective estimates of nasal congestion using a five-ranked scale, before and over 120 min after, therapy each day. The meanR n changes observed for all three drug doses were significantly better than those following placebo at 14 of 15 time periods, with like significance for the mean subjective scores. Mean per cent changes inR n separated the effects of 25.0 mg from 10.0 and 15.0 mg doses of phenylephrine, and distinguished all three active tablet doses from placebo, whereas the subjective estimates could only differentiate the three phenylephrine doses from placebo, but not from one another. While these data confirm the sharp ranking of nasal decongestant potency possible withR n recording, contrasted with more blurred patient impressions, they suggest that statistically valid changes in nasal airways flow/resistance commonly imply favorable clinical activity as well as increased nasal passage patency.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: Key wordsNeuroleptics ; Antipsychotic drugs ; Thalamus ; Fos immunohistochemistry ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The thalamus has been proposed as a site which may be involved in the production of the syndrome of schizophrenia and the response of schizophrenic symptoms to treatment. These studies test whether, consistent with this hypothesis, the activation of thalamic nuclei is a shared property of neuroleptic antipsychotic drugs. Rats were given single doses of the typical high and low potency neuroleptics haloperidol (1 mg/kg) and chlorpromazine (20 mg/kg), the atypical neuroleptics thiroridazine (20 mg/kg) and clozapine (20 mg/kg), the specific dopamine antagonist raclopride (3 mg/kg), the mixed dopamine/serotonin antagonist risperidone (3 mg/kg) or drug-free vehicle. Increased expression of Fos-like protein was utilized as a marker of cellular activation. All drugs tested, including typical and atypical antipsychotic agents, led to similar effects on the midline thalamic paraventricular, centromedian and rhomboid nuclei and the nucleus reuniens. These results suggest that midline thalamic nuclei may participate in neural circuits mediating some of the shared effects of antipsychotic drugs.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2072
    Keywords: Key words Dopamine ; Polymorphism ; Antipsychotic ; Receptor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The dopamine D4 receptor may be a site through which the clinical effects of antipsychotic drugs are mediated. Polymorphisms of a 48 base pair repeat in the third exon of the DRD4 gene code for different length segments in the third intracytoplasmic loop of the D4 receptor. The most common long (seven repeat) form of the D4 receptor has been shown in both physiologic and pharmacologic experiments to respond differently to dopamine agonists and antagonists than do shorter forms of D4. Thus, variants of D4 may partly determine patient response to antipsychotic drugs and, in particular, response to typical neuroleptics, which have a relatively low affinity for the D4 receptor, as compared to clozapine, which has a relatively high affinity for D4. DRD4 polymorphisms in the third intron were characterized in 28 patients with chronic psychosis who responded well to typical neuroleptics, 32 patients who responded well to clozapine, and 57 healthy comparison subjects. Patients responding to typical neuroleptics carried the allele for the long (seven repeat) form of the D4 receptor (allele frequency 8.9%) less frequently than patients responding to clozapine (allele frequency 23.4%, P = 0.046) or healthy comparison subjects (allele frequency 26.3%, P = 0.004). The results of this study suggest that inherited variants of D4 may explain some of the interindividual variation seen in patient response to different classes of antipsychotic medication.
    Type of Medium: Electronic Resource
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