Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Smaranda Demian"'
Autor:
Florin Tripon, Claudia Bănescu, Adrian P. Trifa, Andrei G. Crauciuc, Valeriu G. Moldovan, Alina Boglis, Istvan Benedek, Smaranda Demian, Carmen Duicu, Mihaela Iancu
Publikováno v:
Archives of Medical Science, Vol 18, Iss 1, Pp 103-111 (2021)
Introduction The aim of the study was to investigate the contribution of TERT rs2736100 and rs2853669 gene polymorphisms in defining the genetic predisposition to acute myeloid leukaemia (AML), their association with different prognostic markers, and
Externí odkaz:
https://doaj.org/article/304e5b9c4e694c6aa67e408f9282e133
Publikováno v:
Romanian Journal of Medical Practice, Vol 15, Iss 2, Pp 231-236 (2020)
The primary cutaneous diffuse large B-cell lymphoma leg type (PCDLBCL-LT) is a rare form of cutaneous lymphoma with aggressive and unpredictable evolution. The patients are often aged and with comorbid conditions so that immunochemotherapy can be poo
Externí odkaz:
https://doaj.org/article/e992f0ef8d8b4e46aa6952667b8a037c
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 24, Iss 2, Pp 228-231 (2016)
Externí odkaz:
https://doaj.org/article/e51331e329c44f91998d614e6da1d88f
Publikováno v:
F1000Research, Vol 5 (2016)
Myeloid sarcoma results from the extramedullary homing and proliferation of immature myeloid precursors. We present the timeline, events and diagnostic pitfalls related to a 66 year-old male patient’s case, admitted to the Hematology Clinic for pan
Externí odkaz:
https://doaj.org/article/d96ab436233a4f13866b5ae3ee783a19
Publikováno v:
Journal of Interdisciplinary Medicine. 7:74-77
Introduction: Schnitzler syndrome (SchS), first described in 1972, is a rare autoinflammatory condition characterized by chronic urticaria and monoclonal gammopathy of IgM or, exceptionally, IgG profile. Additional features include recurrent fever, e
Publikováno v:
Romanian Journal of Medical Practice, Vol 15, Iss 2, Pp 231-236 (2020)
The primary cutaneous diffuse large B-cell lymphoma leg type (PCDLBCL-LT) is a rare form of cutaneous lymphoma with aggressive and unpredictable evolution. The patients are often aged and with comorbid conditions so that immunochemotherapy can be poo
Autor:
Mirela Liana Gliga, Ioan Tilea, Smaranda Demian, Mariana-Cornelia Tilinca, Andreea Varga, Dorina Nastasia Petra
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 3269, p 3269 (2020)
Journal of Clinical Medicine
Volume 9
Issue 10
Journal of Clinical Medicine
Volume 9
Issue 10
Introduction. Cardiovascular risk factors, pre-existing comorbidities, molecular factors, and the direct effects of second- and third-generation BCR-ABL1 tyrosine kinase inhibitors on the vascular endothelium contribute to the progression of cardiova
Autor:
Alina, Bogliş, Cristina Georgiana, Radu, F, Tripon, A G, Crauciuc, Smaranda, Demian, Carmen, Duicu, Claudia, Bănescu
Publikováno v:
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi. 120(3)
XRCC1 polymorphisms may alter the individual’s capacity to repair DNA damages and may increase the risk for developing different types of cancer, including Non-Hodgkin Lymphoma (NHL). The purpose of our study was to investigate the association betw
Autor:
Florin Tripon, István Benedek, Adrian P. Trifa, Smaranda Demian, Valeriu Moldovan, Carmen Duicu, Claudia Bănescu, Mihaela Iancu, Alina Bogliş, Andrei Crauciuc
Publikováno v:
Archives of medical science : AMS. 18(1)
IntroductionObjectiv. To investigate the contribution of TERT rs2736100 and rs2853669 gene polymorphisms in defining the genetic predisposition to AML, their association with different prognostic markers and their impact on survival, outcome and the
Autor:
Adrian P. Trifa, Delia Dima, Claudia Bănescu, Smaranda Demian, Carmen Duicu, Erzsebeth Benedek Lazar, Minodora Dobreanu
Publikováno v:
BioMed Research International, Vol 2014 (2014)
BioMed Research International
BioMed Research International
The genetic polymorphisms of X-ray repair cross complementing group 1 (XRCC1), X-ray repair cross complementing group 3 (XRCC3), and xeroderma pigmentosum complementation group D (XPD) repair genes may lead to genetic instability and leukemogenesis.