Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Girma Belay"'
Autor:
Ketema Bizuwork Gebremedhin, Engida Yisma, Haile Alemayehu, Girmay Medhin, Girma Belay, Shubhada Bopegamage, Wondwosson Amogne, Tadesse Eguale
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundUrinary tract infections (UTIs) and antibacterial resistance (ABR) are important public health problems, but they are not well-studied among people living with human immunodeficiency virus (PLHIV) globally, especially in low-income countrie
Externí odkaz:
https://doaj.org/article/1007e88c015c4e1185f67fb29a495dfd
Publikováno v:
Pathogens, Vol 10, Iss 4, p 435 (2021)
The most frequent human prion disease is Creutzfeldt–Jakob disease (CJD). It occurs as sporadic (sCJD), genetic (gCJD), iatrogenic (iCJD) form and as variant CJD. The genetic form represents about 10–15% of confirmed cases worldwide, in Slovakia
Externí odkaz:
https://doaj.org/article/d6443fb2ade14f879c5622a7255294b8
Autor:
Girma, Belay
Publikováno v:
International Journal of Education, Technology & Science; 2022, Vol. 2 Issue 4, p486-502, 17p
Publikováno v:
Pathogens
Volume 10
Issue 4
Pathogens, Vol 10, Iss 435, p 435 (2021)
Volume 10
Issue 4
Pathogens, Vol 10, Iss 435, p 435 (2021)
The most frequent human prion disease is Creutzfeldt–Jakob disease (CJD). It occurs as sporadic (sCJD), genetic (gCJD), iatrogenic (iCJD) form and as variant CJD. The genetic form represents about 10–15% of confirmed cases worldwide, in Slovakia
Autor:
Girma, Belay
Publikováno v:
Journal of Science and Sustainable Development; Vol. 7 No. 1 (2019); 43-52
The main objective of this study was to investigate the challenges and opportunities of developing students’ communicative competence. To this end, a total of three schools from three different zones such as Sheka, Bench-Maji and Kafa were selected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60ce846240528af6f23acfb1ae0274d8
Autor:
Eva Mitrova, Dana Záková-Slivarichová, Alzbeta Janakova, Silvia Koščová, Martin Stelzer, Girma Belay
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 66
Three monozygotic twin pairs with the Creutzfeldt-Jakob diseases-specific mutation E200K are described. All three have been concordant for genetic CJDE200K and discordant for the age at death and the duration of the disease. Twin pairs have been comp
Autor:
Dana Kosorinova, Martin Stelzer, Ivana Tomeckova, Dana Slivarichova, Katarina Melicherova, Silvia Koščová, Alzbeta Janakova, Girma Belay, Eva Mitrova
Publikováno v:
Molecular neurobiology. 54(8)
Creutzfeldt-Jakob disease is a rare, but rapidly progressive, up to now untreatable and fatal neurodegenerative disorder. Clinical diagnosis of Creutzfeldt-Jakob disease (CJD) is difficult; however, it can be facilitated by suitable biomarkers. Aim o
Autor:
Eva Mitrova, Gabor G. Kovacs, Christa Jarius, Johannes A. Hainfellner, Herbert Budka, Girma Belay
Publikováno v:
Scopus-Elsevier
We have compared the immunomorphological spectrum of the deposition of the disease-associated prion protein (PrP(Sc)) in the cerebral and cerebellar cortex of 32 Creutzfeldt-Jakob disease (CJD) patients with the PrP gene (PRNP) E200K mutation to 45 s
Autor:
Gabor G. Kovacs, Ellen Gelpi, Richard Knight, Herbert Budka, Sara Nocentini, Cornelia M. van Duijn, Anikó Gál, Mária Judit Molnár, Piero Parchi, Anna Poleggi, Uta Heinemann, Sabina Capellari, Claudia Giannattasio, Matthew Bishop, Eva Mitrova, Thomas Ströbel, Pascual Sánchez-Juan, Agnes Bakos, Inga Zerr, Maaike Schuur, Girma Belay
Publikováno v:
Kovacs, G G, Sanchez-Juan, P, Ströbel, T, Schuur, M, Poleggi, A, Nocentini, S, Giannattasio, C, Belay, G, Bishop, M, Capellari, S, Parchi, P, Gelpi, E, Gal, A, Bakos, A, Molnar, M J, Heinemann, U, Zerr, I, Knight, R S G, Mitrova, E, Van Duijn, C & Budka, H 2010, ' Cathepsin D (C224T) polymorphism in sporadic and genetic creutzfeldt-jakob disease ', Alzheimer Disease and Associated Disorders, vol. 24, no. 1, pp. 104-107 . https://doi.org/10.1097/WAD.0b013e3181ad378c
Alzheimer Disease & Associated Disorders, 24(1), 104-107. Lippincott Williams & Wilkins
Alzheimer Disease and Associated Disorders, 24(1), 104-107. Lippincott Williams and Wilkins
Alzheimer Disease & Associated Disorders, 24(1), 104-107. Lippincott Williams & Wilkins
Alzheimer Disease and Associated Disorders, 24(1), 104-107. Lippincott Williams and Wilkins
Accumulation of cathepsin D immunoreactive lysosomes correlates with tissue pathology in sporadic Creutzfeldt-Jakob disease (CJD) brains. The C-to-T transition within exon 2 of the cathepsin D (CTSD) gene is associated with altered enzymatic activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9215efde25b4bf48b31058c4ba15ac
https://research.vumc.nl/en/publications/c96cd3e1-8268-425d-9389-b07ed57e60af
https://research.vumc.nl/en/publications/c96cd3e1-8268-425d-9389-b07ed57e60af
Autor:
Eva Mitrova, Girma Belay
Publikováno v:
European Journal of Epidemiology. 16:353-355
Creutzfeldt-Jakob disease (CJD) is the most important human transmissible spongiform encephalopathy (prion disease), recognised in sporadic, genetic but also iatrogenic forms. The identification of 8 health care workers in a group of 114 definitive C