نتایج جستجو برای: change of diagnosis
تعداد نتایج: 21233115 فیلتر نتایج به سال:
objectives this study aimed to understand the patients’ experience of tuberculosis treatment according to dots in iran. patients and methods this study is a qualitative study, using content analysis to examine patients’ experience of tb treatment and to understand their compliance during dots. in this study, a semi-structured interview with open questions was answered by 40 patients, who had a ...
in semiarid regions such as saida, the steppe ecosystem is currently submitted to desertification under the combined effect of human activity and climate change. our study is a contribution to the assessment of the biodiversity of steppe formations through a phytoecological diagnosis at the south zone of the wilaya of saida. to achieve the objective of this study, a methodological approach base...
Backgrounds Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare genetic disorder caused from mutations in the Cadherin 3 (CDH3) gene. Results In the present study, we reported an Iranian family with three affected members born to a consanguineous parent. Mutational analysis using whole exome sequencing has revealed a nucleotide change in CDH3 gene (NM_001793:exon8:c.830delG) which l...
the present study has tried to accomplish an analysis of margaret atwood’s novels oryx and crake, and the year of the flood in the light of posthuman and cyborg theories. considering posthumanism as a critical reading of some notions of humanism focus of which in this thesis has been identity, new definitions for humanity and human identity are formed. haraway’s cyborg, as one possible new figu...
MicroRNAs regulate gene expression at the post-transcriptional level. Differential expression of miRNAs can potentially be used as biomarkers for early diagnosis and prediction for outcomes. Failure in validation of miRNA profiles is often caused by variations in experimental parameters. In this study, the performance of five extraction kits and three RT-qPCR systems were evaluated using BioMar...
purpose: retinitis pigmentosa (rp) is a hereditary eye disease in human beings. it commences at childhood and continues by nyctalopia and gradual reduction of visual field and ends up by blindness. it may be inherited in three forms of autosomal dominant, autosomal recessive and sex-linked. in this investigation we intend to study rp type as a sex-linked disease and its location on x chromosome...
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