| 1. |
- Basic, Goran, 1972-
(författare)
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Pomirenje i nepomirljivost u pričama preživjelih poslije rata u Bosni i Hercegovini : Reconciliation and Implacability in Narratives of Survivors after the War in Bosnia and Herzegovina.
- 2015
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Ingår i: Criminal Justice Issues. - 1512-5505 .- 2637-269X. ; 15:1-2, s. 75-96
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Tidskriftsartikel (refereegranskat)abstract
- Reason(s) for writing and research problem(s): Previous research on post-war society emphasized structural violence with subsequent reconciliation processes. Aims of the paper (scientific and/or social): Researchers have focused on the importance of narratives, but they have neither highlighted narratives about reconciliation nor analyzed conditions for reconciliation in post-war interviews. One aim of the article is analyzing markers for reconciliation and implacability, the second is describing conditions for reconciliation which are actualized in those stories. Methodology/Design: This article analyzes retold experiences of 27 survivors from the war in Bosnia and Herzegovina between 1992 and 1995. The material for the study was gathered through qualitative interviews with 27 individuals who survived the war in north-western Bosnia and Herzegovina. Research/paper limitations: Interactive dynamics which prevailed during the war associate post-war reconciliation with the war time. Results/Findings: These stories of reconciliation, implacability and conditions for reconciliation, are not created in relation to the war as a whole only but also in relation to one’s own and other’s personal actions during the war. General conclusion: These stories on reconciliation become a forum for confrontation between us and them – not least through dissociation from others war actions. In the interviewees stories implacability is predominant however reconciliation is said to be possible if certain conditions are met. These conditions are, among others, justice for war victims, that the perpetrators’ recognize their crimes and display strong emotions (for example remorse and shame).
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| 2. |
- Marisavljević, Dragomir, et al.
(författare)
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Abnormalnosti hromozoma 17 kod bolesnika sa primarnim mijeloidisplasticnih sindromima : incidencija i bioloski znacaj
- 2004
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Ingår i: Srpski Arhiv Za Celokupno Lekarstvo. - 0370-8179. ; 132:1-2, s. 3-10
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Tidskriftsartikel (refereegranskat)abstract
- Cytogenetic analysis has proven to be a mandatory part of the diagnosis of myelodysplastic syndromes (MDS) as well as a major indicator for predicting clinical course and outcome. Aside from the 5q-syndrome, no specific clinico-cytogenetic entity has been reported. To determine the incidence and clinical significance of acquired abnormalities of chromosome 17 in adult primary MDS, we reviewed the cytogenetic features of 271 patients detected at our institution during a 10-year period. Clonal cytogenetic abnormalities were identified in 109 cases. Among them, abnormalities of chromosome 17 were identified in 13 patients (11.9%). Five patients had "single" defects, while in eight patients abnormalities of chromosome 17 were associated with other chromosomal rearrangements ("complex" defects). After chromosomes 5, 7, 8 and 1, abnormalities of chromosome 17 were the most frequent chromosomal rearrangements in our patients with MDS. Following "single" defects of chromosome 17 were identified: del(17)(p12) in two cases, and i(17)(q10), del(17)(q21;q23) and del(17)(q12;q22) in one case each. Two patients with del(17p), one with RAEB-t and the other one with CMML, had an aggressive course of the disease with accelerated leukemic transformation and short survival. Patient with i(17q) had RARS subtype and died soon after diagnosis, while other two cases with interstitial deletions of the long arm of chromosome 17 had RAEB subtype and stable, no progressive course of the disease. Among "complex" karyotypes with abnormalities of chromosome 17 we identified der(17) in four, monosomy 17 in two, and del(17p) and l(17q) in one case each. Most of these patients transformed to acute leukemia and had very short survival. The results of this study suggest that abnormalities of chromosome 17 are frequent finding in MDS. Loss of genetic material in 17p, both in "single" and "complex" defects, seems to be closely related to poor prognosis of MDS patients.
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| 3. |
- Pilka, Radovan, et al.
(författare)
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Nove matrix metaloproteinazy v cyklickem endometriu
- 2004
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Ingår i: Ceska gynekologie / Ceska lekarska spolecnost J. Ev. Purkyne. - 1210-7832. ; 69:4, s. 262-266
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Tidskriftsartikel (refereegranskat)abstract
- OBJECTIVE: To examine the expression pattern of some novel matrix metalloproteinases (MMPs) in cycling endometrium. DESIGN: Experimental study. SETTING: Department of Obstetrics and Gynecology of the Palacky University Medical School and University Hospital, Olomouc, Czech Republic, Department of Obstetrics and Gynecology, University Hospital, Lund, Sweden. METHODS: We studied MMP-12, -16, -17, -19 and -26 mRNA in 39 normal endometrial samples obtained across the menstrual cycle. Based on histological examination, all specimens were classified according to an ideal 28 day menstrual cycle as early (n=8), mid (n=6) and late (n=7) proliferative phase, early (n=4), mid (n=4) and late (n=8) secretory phase and menstrual (n=3) phase. Cycle variation was examined in frozen samples using in situ hybridization. RESULTS: Three distinct pattern of MMP mRNA expression were detected in cycling endometrium. MMP-12 was expressed predominantly in perimenstrual period, MMP-16, -17 and 19 were expressed throughout the cycle and MMP-26 was found to be maximal in periovulatory period. CONCLUSION: Different endometrial expression patterns of novel MMPs during menstrual cycle may indicate their specific roles for menstruation, endometrial growth and remodelling and implantation.
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| 4. |
- Resic, Sanimir
(författare)
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Ratnicka cast
- 2001
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Ingår i: Polemos. Journal of Interdisciplinary Research on War and Peace. - 1331-5595. ; 4:8 July-December 2001, s. 123-146
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Tidskriftsartikel (refereegranskat)
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| 5. |
- Silkeberg, Marie, 1961
(författare)
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Teologija
- 2013
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Ingår i: Sarajevo Poetry Days, Programblad. - Sarajevo : Sarajevo Poetry Days.
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Publ på bosniska i övers av Refik Licina
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| 6. |
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| 7. |
- Suvajdzić-Vuković, Nada, et al.
(författare)
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Rezultati lecenja trombozne trombocitopenijske purpure na 36 bolesnika
- 2004
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Ingår i: Vojnosanitetski Pregled. - 0042-8450. ; 61:6, s. 7-621
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Tidskriftsartikel (refereegranskat)abstract
- Thirty-six patients (pts.) with thrombotic thrombocytopenic purpura (TTP) were treated between May 1990 and May 2003. There were 31 women and 5 men; the average age was 37 years. Twenty-five cases were idiopathic and 11 secondary (3 infection--related, 5 occurred during pregnancy and 3 were drug--associated). The mean lag period between the first symptoms and the diagnosis was 8.5 days (in 14 pts. < or = 5; in 22 > 5). On diagnosis neurological symptoms were present in 31, bleeding in 33, fever in 21 and renal impairment in 27 patients. The mean hemoglobin was 67.5 g/L, the mean platelet count was 10 x 10(9)/L, and the mean reticulocytosis was 17%. The mean serum LDH was 1457 IU. Treatment included plasma exchange (PE) in 24 pts. and only plasma infusions in 12 pts. There were 24 complete responders (20 on PE) and 12 deaths (4 on PE); PE significantly improved survival (p < 0.01). There were 5 treatment-related complications due to the infection and bleeding, 17 exacerbations and 4 relapses. The mean time delay before the onset of symptoms and the treatment initiation lasted for 9 days suggesting the poor disease recognition; the mean time delay from diagnosis to PE institution was 6 days, indicating postponed PE. The mean treatment duration in all patients was 18 days; the mean number of PE cycles needed for the platelet count stabilization was 9. Good prognostic indicators of survival were: the longer prodromal period (> 5 days), the secondary form of TTP and the absence of coma at presentation. The use of PE significantly improved survival. TTP is a severe disorder requiring early recognition and diagnosis in general medical care facilities, which should lead to the timely treatment with PE.
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