GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Vereinigung zur Kritik der politischen Okonomie e.V. ; 2013
    In:  PROKLA. Zeitschrift für kritische Sozialwissenschaft Vol. 43, No. 173 ( 2013-12-01)
    In: PROKLA. Zeitschrift für kritische Sozialwissenschaft, Vereinigung zur Kritik der politischen Okonomie e.V., Vol. 43, No. 173 ( 2013-12-01)
    Abstract: The article discusses the June Uprising in Turkey in the specific context of neoliberal authoritarianism and Islamic conservatism. It is argued that the occupation of the Gezi-Park and the spontaneous formation of the “Gezi Commune” revealed a communitarian and libertarian political practice in resistance to the accelerated accumulation by dispossession and in opposition to the Kulturkampf tradition fostered by the ruling party.
    Type of Medium: Online Resource
    ISSN: 2700-0311 , 0342-8176
    RVK:
    RVK:
    Language: Unknown
    Publisher: Vereinigung zur Kritik der politischen Okonomie e.V.
    Publication Date: 2013
    detail.hit.zdb_id: 2533452-9
    detail.hit.zdb_id: 1112215-8
    SSG: 3,6
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Antiviral Therapy, SAGE Publications, Vol. 13, No. 8 ( 2008-11), p. 1039-1046
    Abstract: A saquinavir/ritonavir-containing regimen is one option for the prevention of mother-to-child transmission of HIV during pregnancy. We evaluated the pharmaco-kinetics, efficacy and safety of saquinavir/ritonavir 1,000/100 mg twice daily plus nucleos(t)ide reverse transcriptase inhibitors in 13 women during late pregnancy and compared the results to those of 15 non-pregnant women. Methods Protease inhibitor plasma concentration profiles were assessed at 12 h using a standardized therapeutic drug monitoring procedure and measured by LC-MS/MS. Minimum and maximum concentrations (C min and C max ), area under the plasma concentration–time curve (AUC 0–12 h ), and total clearance (CL total ) were compared between the groups and correlated to demographic, physiological and clinical cofactors. Antiviral and immunological efficacy and safety were investigated. Results The geometric means (90% confidence interval [CI]) for saquinavir C min , C max and AUC 0–12 h of pregnant versus non-pregnant women were 572 (437–717) versus 765 (485–1,052, P=0.064) ng/ml, 2,168 (1,594–2,807) versus 3,344 (2,429–4,350; P=0.045) ng/ml and 15,512 (11,657–19,943) versus 24,027 (17,454–31,548, P=0.029) ng•h/ml. The geometric means (90% CI) for ritonavir C min , C max and AUC 0–12 h were 190 (148–234) versus 310 (240–381, P=0.011) ng/ml, 781 (580–999) versus 1,552 (1,127–2,007, P=0.004) ng/ml and 5,576 (4,303–7,006) versus 10,528 (8,131–13,177, P=0.003) ng•h/ml. Age, weight, saquinavir dose per weight and body mass index differed significantly; saquinavir C min and AUC 0–12 h were correlated with ritonavir C min and saquinavir dose per weight. After a mean of 11 weeks treatment, 12 of 13 pregnant women had a viral load 〈 400 copies/ml, which was similar to the results of non-pregnant women. Conclusions Although saquinavir plasma concentrations were significantly lower in pregnant women compared with non-pregnant women, all pregnant women displayed a saquinavir AUC 0–12 h 〉 10,000 ng•h/ml, 92.3% had a viral load 〈 400 copies/ml at birth. Saquinavir was well tolerated by the mothers and all newborn children were HIV type-1 negative at 18 months of age.
    Type of Medium: Online Resource
    ISSN: 1359-6535 , 2040-2058
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2008
    detail.hit.zdb_id: 2118396-X
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: Antimicrobial Agents and Chemotherapy, American Society for Microbiology, Vol. 52, No. 6 ( 2008-06), p. 2273-2275
    Abstract: The human immunodeficiency virus protease inhibitor combination of atazanavir (ATV)-lopinavir-ritonavir was reported to exhibit a mutual pharmacoenhancement of plasma lopinavir and ATV concentrations which may be beneficial for salvage patients. We identified 17 patients in our pharmacokinetic database taking this combination and found conflicting results. Plasma concentrations of both ATV and lopinavir were modestly, although not significantly, decreased when the drugs were coadministered. Therefore, patients should be selected carefully for this regimen and frequent clinical and therapeutic drug monitoring is strongly advised.
    Type of Medium: Online Resource
    ISSN: 0066-4804 , 1098-6596
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2008
    detail.hit.zdb_id: 1496156-8
    SSG: 12
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: Medizinische Klinik, Springer Science and Business Media LLC, Vol. 103, No. 2 ( 2008-2), p. 69-74
    Type of Medium: Online Resource
    ISSN: 0723-5003 , 1615-6722
    RVK:
    Language: German
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2008
    detail.hit.zdb_id: 2233632-1
    detail.hit.zdb_id: 2636049-4
    detail.hit.zdb_id: 2017822-0
    SSG: 7,52
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    In: Antiviral Therapy, SAGE Publications, Vol. 12, No. 8 ( 2007-11), p. 1237-1246
    Abstract: To evaluate predictive factors for therapy outcome of a boosted double-protease inhibitor (PI) regimen in 58 extensively pre-treated patients with HIV. Methods Patients received lopinavir/ritonavir 400/100 mg and saquinavir 1,000 mg twice daily without reverse transcriptase inhibitors (RTI). The primary outcome parameter was HIV RNA 〈 400 copies/ml at week 48, secondary parameters were HIV-1 RNA and CD4 + T-cell count changes from baseline to week 48. Pharmacokinetics, genotypic resistance and clinical and individual parameters were correlated with the clinical outcome in regression analyses. Covariates for the analyses were minimum plasma concentration (C min ), maximum plasma concentration, area under the concentration versus time curve, half-life and clearance of lopinavir and saquinavir, the genotypic inhibitory quotients (GIQ) of archived (GIQ arch ) and baseline PI resistance mutations, previously taken antiretrovirals, archived and baseline viral resistance mutations, baseline HIV-1 RNA and CD4 + T-cell count. Results The analyses detected correlations between the primary outcome parameter and several factors: baseline CD4 + T-cell count ( P=0.001); absence of mutations at V82T/A/F/I/S plus I54M/V/L ( P=0.002) or K20M/R ( P=0.010); and lopinavir C min GIQ arch ( P=0.046). This regression model had a predictability of 97.0% for response to therapy. Covariates for the decrease of HIV-1 RNA from baseline to week 48 were baseline HIV-1 RNA ( P 〈 0.001), lopinavir C min GIQ arch ( P=0.013), presence/absence of mutations at V82T/A/F/I/S or I84A/V plus L10I/R/V/F, I54M/V/L or L63P ( P=0.018), and previously taken antiretrovirals ( P=0.034). Conclusions Baseline HIV-1 RNA 〈 5.0 log 10 and CD4 + T-cell count 〉 200 cells/μl, lopinavir C min GIQ arch 〉 2,000 ng/ml and the absence of viral resistance mutations at V82T/A/F/I/S and I54M/V/L are highly predictive for therapeutic success of a regimen of saquinavir/lopinavir/ ritonavir without RTI in a heterogenic cohort of patients with an extensive pre-treatment history and highly variable pharmacokinetics.
    Type of Medium: Online Resource
    ISSN: 1359-6535 , 2040-2058
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2007
    detail.hit.zdb_id: 2118396-X
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...