Results 31 to 40 of about 303 (163)
Novel homozygous nonsynonymous variant of CNNM4 gene in a Chinese family with Jalili syndrome
Molecular Genetics &Genomic Medicine, Volume 10, Issue 3, March 2022., 2022 We described the detailed clinical features of a Chinese family with Jalili syndrome (JS) and identified a novel homozygous nonsynonymous variant in CNNM4 gene. Our findings broadened the phenotypes and mutation spectrum of JS in Chinese population, as well as are helpful in the diagnosis of this rare disorder.
Huajin Li +3 more
wiley +1 more source
Critical Ethnography and Research Relationships: Some Ethical Dilemmas
Anthropology and Humanism, Volume 46, Issue 2, Page 300-314, December 2021., 2021 Summary Ethnography can be a deeply challenging form of research in which the researcher has to navigate the boundaries of acceptable observation and avoid the pitfalls of intrusion. In the last twenty years, legalistic and contractual ethical codes have gained prominence and influence in social research.
Andrew Ryder
wiley +1 more source
Rationale for extent of operation choice in rectal cancer
Journal of Education, Health and Sport, 2021 Introduction. Colorectal cancer (CRC) remains relevant occupying one of the leading places in morbidity and mortality among oncological diseases. It reaches 13.5% in the structure of tumor diseases tending to increase.
R. Nikitenko +3 more
doaj +1 more source
Business Ethics, the Environment &Responsibility, Volume 30, Issue S1, Page 87-102, September 2021., 2021 Abstract This study contributes to the burgeoning research on corporate social responsibility (CSR) at the individual level of analysis, in a hitherto largely neglected developing country context. Using survey information collected from 297 employees in public and private enterprises in Kosovo, this study examines how and to what extent employees ...
Sonja Grabner‐Kräuter +2 more
wiley +1 more source
The role of sentinel lymph nodes in breast cancer
Journal of Education, Health and Sport, 2022 Introduction. The problem of improving early diagnosis and prognosis of breast cancer remains one of the most actual for current oncological practice.
R. Nikitenko +3 more
doaj +1 more source
LITERARY AND MYSTIC INTERTWINES: KAFKA, RAMADANI, DIBRA [PDF]
Езиков свят, 2023 Despite his late occurrence in Albanian literature, Franz Kafka’s influence has been particularly noticed in Musa Ramadani’s (1944-2020) novel “The Prophet from Prague” in Kosovo and Ridvan Dibra’s (1959) novel “Franz Kafka Writes to His Son”.
Vjollca DIBRA +2 more
doaj +1 more source
HBIM IMPLEMENTATION FOR AN OTTOMAN MOSQUE. CASE OF STUDY: SULTAN MEHMET FATIH II MOSQUE IN KOSOVO [PDF]
The International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, 2019 National Strategy For Cultural Heritage 2017–2027 is a Kosovo Government document that aims the enhancement of the system for the protection and preservation of Kosovan cultural heritage.
F. Di Stefano +4 more
doaj +1 more source
Strategy tools in use: New empirical insights from the strategy-as-practice perspective
Management : Journal of Contemporary Management Issues, 2020 This paper examines the usage of strategy tools from the strategy-as-practice perspective. In general, there is a lack of empirical evidence regarding the use of strategy tools, particularly in transition economies.
Albana Berisha Qehaja, Enver Kutllovci
doaj +1 more source
Про поліноміальність нарізно сталих функцій
Karpatsʹkì Matematičnì Publìkacìï, 2014 Вивчається, які необхідні і які достатні умови має задовольняти підмножина $E$ числової площини $\mathbb{R}^2$ для того, щоб кожна нарізно стала функція $f:E\to \mathbb{R}$ була поліноміальною і разом з тим існувала нарізно стала і не стала функція $f_0 ...
V.M. Kosovan, V.K. Maslyuchenko
doaj +1 more source
Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene. [PDF]
PLoS ONE, 2013 Jalili syndrome denotes a recessively inherited combination of an eye disease (cone-rod dystrophy) and a dental disorder (amelogenesis imperfecta), which is caused by mutations in the CNNM4 gene.
Hans U Luder +3 more
doaj +1 more source