Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alexander Linev"'
Autor:
Dimitar Nikolov, Vili K. Stoyanova, Ludmila Vladimirova-Kitova, Alexander Linev, Georgi Nikolov, Spas Kitov
Publikováno v:
Folia Medica, Vol 64, Iss 6, Pp 896-904 (2022)
Introduction: Diabetic nephropathy is a major microangiopathic complication of type 2 diabetes and a leading cause of chronic kidney disease (CKD).Aim: To improve the diagnostic approach to early diagnosis of diabetic nephropathy in patients with typ
Externí odkaz:
https://doaj.org/article/31d741b84b144fcf9cfc28441c7139d5
Autor:
Veselina Goranova-Marinova, Alexander Linev, Hristo J. Ivanov, Ivan Zheljazkov, Vily Stoyanova, Zhanet Grudeva-Popova
Publikováno v:
Folia Medica, Vol 63, Iss 5, Pp 670-675 (2021)
Introduction: The T315I mutation in patients with chronic myeloid leukemia (CML) has been associated with therapeutic resistance and an unfavourable prognosis.Aim: To study the frequency of T315I mutation in patients with CML, BCR-ABL (+), their clin
Externí odkaz:
https://doaj.org/article/9d41668abf8c485680a9a44d9030b0d5
Autor:
Hristo J. Ivanov, Zhanet Grudeva-Popova, Ivan Zheljazkov, Alexander Linev, Vily Stoyanova, Veselina Goranova-Marinova
Publikováno v:
Folia Medica, Vol 63, Iss 5, Pp 670-675 (2021)
Introduction: The T315I mutation in patients with chronic myeloid leukemia (CML) has been associated with therapeutic resistance and an unfavourable prognosis. Aim: To study the frequency of T315I mutation in patients with CML, BCR-ABL(+), their clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e74d5b0b55f8e0a9019a9439b466eed7
https://doi.org/10.3897/folmed.63.e63366
https://doi.org/10.3897/folmed.63.e63366
Autor:
Krum Enchev, Alexander Linev, Zhanet Grudeva-Popova, Ivanka S Nenova, Hristo Y Ivanov, Ivan Zheliazkov, Teodora Gogova, Elina Beleva
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 21:S365-S366
Context Splanchnic thrombosis (ST) is a characteristic feature of MPN-associated prothrombotic state. Objective To determine the prevalence of subclinical ST in patients with myelofibrosis and assess disease-related and hereditary factors as potentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f35aa69ab2adfea1c25de1f094987ad
https://doi.org/10.1016/s2152-2650(21)01839-5
https://doi.org/10.1016/s2152-2650(21)01839-5
Autor:
Elina Beleva, Hristo Ivanov, Teodora Gogova, Krum Enchev, Ivan Zheliazkov, Alexander Linev, Ivanka Nenova, Zhanet Grudeva-Popova
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 21:S232
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fbec55f94bd36061be72d53f66b935e
https://doi.org/10.1016/s2152-2650(21)01462-2
https://doi.org/10.1016/s2152-2650(21)01462-2
Autor:
Ivan Ivanov, S. Ivanov, Vili K. Stoyanova, Hristo Hy Ivanov, L Balabanski, Radoslava Vazharova, Alexander Linev, Draga Toncheva
Publikováno v:
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 21, Iss 2, Pp 59-62 (2018)
Balkan Journal of Medical Genetics, Vol 21, Iss 2, Pp 59-62 (2018)
Intellectual disability is affecting 3.0-4.0% of the general population. Copy number variants (CNVs) are a significant cause leading to neurodevelopmental disorders such as intellectual disability, epilepsy, autism spectrum disorders and developmenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dcf2c6b7e21ac01e301fb7ee57be51f
https://pubmed.ncbi.nlm.nih.gov/30984527
https://pubmed.ncbi.nlm.nih.gov/30984527